| Year |
Citation |
Score |
| 2023 |
Ekenstedt KJ, Minor KM, Shelton GD, Hammond JJ, Miller AD, Taylor SM, Huang Y, Mickelson JR. A SACS deletion variant in Great Pyrenees dogs causes autosomal recessive neuronal degeneration. Human Genetics. PMID 37758910 DOI: 10.1007/s00439-023-02599-1 |
0.311 |
|
| 2023 |
Jankelunas L, Murthy VD, Chen AV, Minor KM, Friedenberg SG, Cullen JN, Guo LT, Mickelson JR, Shelton GD. Novel COL6A3 frameshift variant in American Staffordshire Terrier dogs with Ullrich-like congenital muscular dystrophy. Journal of Veterinary Internal Medicine. PMID 37706358 DOI: 10.1111/jvim.16862 |
0.36 |
|
| 2022 |
Beckers E, Cornelis I, Bhatti SFM, Smets P, Shelton GD, Guo LT, Peelman L, Broeckx BJG. A Nonsense Variant in the Gene Causes X-Linked Muscular Dystrophy in the Maine Coon Cat. Animals : An Open Access Journal From Mdpi. 12. PMID 36359052 DOI: 10.3390/ani12212928 |
0.323 |
|
| 2022 |
Stevens R, Kanazono S, Petesch S, Guo LT, Shelton GD. Dystrophin-Deficient Muscular Dystrophy in Two Male Juvenile Brittanys. Journal of the American Animal Hospital Association. 58: 292-296. PMID 36315862 DOI: 10.5326/JAAHA-MS-7255 |
0.341 |
|
| 2022 |
Shelton GD, Minor KM, Vieira NM, Kunkel LM, Friedenberg SG, Cullen JN, Guo LT, Zatz M, Mickelson JR. Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype. Neuromuscular Disorders : Nmd. PMID 36041985 DOI: 10.1016/j.nmd.2022.08.001 |
0.303 |
|
| 2022 |
Shelton GD, Minor KM, Guo LT, Thomas-Hollands A, Walsh KA, Friedenberg SG, Cullen JN, Mickelson JR. An Nonsense Mutation Associated with Congenital Dyserythropoietic Anemia and Polymyopathy in Labrador Retriever Littermates. Genes. 13. PMID 36011338 DOI: 10.3390/genes13081427 |
0.315 |
|
| 2022 |
Krenzke LR, Cameron S, Pritchard JC, Webb DB, Guo LT, Shelton GD. Glossitis in an older non-corgi dog: Diagnosis and long-term follow-up. The Canadian Veterinary Journal = La Revue Veterinaire Canadienne. 63: 825-829. PMID 35919473 |
0.322 |
|
| 2021 |
Shelton GD, Minor KM, Thomovsky S, Guo LT, Friedenberg SG, Cullen JN, Mickelson JR. Congenital muscular dystrophy in a dog with a LAMA2 gene deletion. Journal of Veterinary Internal Medicine. PMID 34854126 DOI: 10.1111/jvim.16330 |
0.373 |
|
| 2021 |
Christen M, Indzhova V, Guo LT, Jagannathan V, Leeb T, Shelton GD, Brocal J. Nonsense Variant in an Italian Greyhound with Congenital Muscular Dystrophy. Genes. 12. PMID 34828429 DOI: 10.3390/genes12111823 |
0.375 |
|
| 2021 |
Shelton GD, Minor KM, Guo LT, Friedenberg SG, Cullen JN, Hord JM, Venzke D, Anderson ME, Devereaux M, Prouty SJ, Handelman C, Campbell KP, Mickelson JR. Muscular dystrophy-dystroglycanopathy in a family of Labrador retrievers with a LARGE1 mutation. Neuromuscular Disorders : Nmd. PMID 34654610 DOI: 10.1016/j.nmd.2021.07.016 |
0.328 |
|
| 2020 |
Vernau KM, Struys E, Letko A, Woolard KD, Aguilar M, Brown EA, Cissell DD, Dickinson PJ, Shelton GD, Broome MR, Gibson KM, Pearl PL, König F, Van Winkle TJ, O'Brien D, et al. A Missense Variant in Associated with Canine Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD) in the Saluki Dog. Genes. 11. PMID 32887425 DOI: 10.3390/Genes11091033 |
0.326 |
|
| 2020 |
Bradbury AM, Bagel JH, Nguyen D, Lykken EA, Pesayco Salvador J, Jiang X, Swain GP, Assenmacher CA, Hendricks IJ, Miyadera K, Hess RS, Ostrager A, ODonnell P, Sands MS, Ory DS, ... Shelton GD, et al. Krabbe disease successfully treated via monotherapy of intrathecal gene therapy. The Journal of Clinical Investigation. PMID 32773406 DOI: 10.1172/Jci133953 |
0.307 |
|
| 2020 |
Mariné AF, Granger N, Bertolani C, Boixeda JM, Shelton GD, Feliu‐Pascual AL. Long‐term outcome of Miniature Schnauzers with genetically confirmed demyelinating polyneuropathy: 12 cases Journal of Veterinary Internal Medicine. PMID 32738000 DOI: 10.1111/Jvim.15861 |
0.348 |
|
| 2020 |
Jahns H, Vernau KM, Nolan CM, O’Neill EJ, Shiel RE, Shelton GD. Polyneuropathy in Young Siberian Huskies Caused by Degenerative and Inflammatory Diseases. Veterinary Pathology. 57: 666-674. PMID 32578500 DOI: 10.1177/0300985820934112 |
0.384 |
|
| 2020 |
Bolduc V, Minor KM, Hu Y, Kaur R, Friedenberg SG, Van Buren S, Guo LT, Glennon JC, Marioni-Henry K, Mickelson JR, Bönnemann CG, Shelton GD. Pathogenic variants in COL6A3 cause Ullrich-like congenital muscular dystrophy in young Labrador Retriever dogs. Neuromuscular Disorders : Nmd. PMID 32439203 DOI: 10.1016/J.Nmd.2020.03.005 |
0.435 |
|
| 2020 |
Olby NJ, Friedenberg S, Meurs K, DeProspero D, Guevar J, Lau J, Yost O, Guo LT, Shelton GD. A mutation in MTM1 causes X-Linked myotubular myopathy in Boykin spaniels. Neuromuscular Disorders : Nmd. PMID 32417001 DOI: 10.1016/J.Nmd.2020.02.021 |
0.435 |
|
| 2019 |
Tsai KL, Vernau KM, Winger K, Zwueste DM, Sturges BK, Knipe M, Williams DC, Anderson KJ, Evans JM, Guo LT, Clark LA, Shelton GD. Congenital myasthenic syndrome in Golden Retrievers is associated with a novel COLQ mutation. Journal of Veterinary Internal Medicine. PMID 31769119 DOI: 10.1111/Jvim.15667 |
0.316 |
|
| 2019 |
Papageorgiou S, Gnirs K, Quinton J, Shelton GD. Clinical and serologic remission of acquired myasthenia gravis in a domestic ferret (Mustela putorius furo) Javma-Journal of the American Veterinary Medical Association. 254: 1192-1195. PMID 31039095 DOI: 10.2460/Javma.254.10.1192 |
0.318 |
|
| 2019 |
Murphy SC, Recio A, de la Fuente C, Guo LT, Shelton GD, Clark LA. A glycine transporter SLC6A5 frameshift mutation causes startle disease in Spanish greyhounds. Human Genetics. PMID 30847549 DOI: 10.1007/S00439-019-01986-X |
0.353 |
|
| 2019 |
Meurs KM, Friedenberg SG, Olby NJ, Condit J, Weidman J, Rosenthal S, Shelton GD. A QIL1 Variant Associated with Ventricular Arrhythmias and Sudden Cardiac Death in the Juvenile Rhodesian Ridgeback Dog. Genes. 10. PMID 30795627 DOI: 10.3390/Genes10020168 |
0.333 |
|
| 2019 |
Meurs KM, Friedenberg SG, Kolb J, Saripalli C, Tonino P, Woodruff K, Olby NJ, Keene BW, Adin DB, Yost OL, DeFrancesco TC, Lahmers S, Tou S, Shelton GD, Granzier H. A missense variant in the titin gene in Doberman pinscher dogs with familial dilated cardiomyopathy and sudden cardiac death. Human Genetics. PMID 30715562 DOI: 10.1007/S00439-019-01973-2 |
0.344 |
|
| 2018 |
Amengual‐Batle P, Rusbridge C, José‐López R, Golini L, Shelton GD, Mellersh CS, Gutierrez‐Quintana R. Two mixed breed dogs with sensory neuropathy are homozygous for an inversion disrupting FAM134B previously identified in Border Collies. Journal of Veterinary Internal Medicine. 32: 2082-2087. PMID 30307654 DOI: 10.1111/Jvim.15312 |
0.389 |
|
| 2018 |
Rossman PM, Thomovsky SA, Schafbuch RM, Guo LT, Shelton GD. Myositis, Ganglioneuritis, and Myocarditis with Distinct Perifascicular Muscle Atrophy in a 2-Year-Old Male Boxer. Frontiers in Veterinary Science. 5: 20. PMID 29516006 DOI: 10.3389/fvets.2018.00020 |
0.346 |
|
| 2018 |
Sánchez L, Beltrán E, de Stefani A, Guo LT, Shea A, Shelton GD, De Risio L, Burmeister LM. Clinical and genetic characterisation of dystrophin-deficient muscular dystrophy in a family of Miniature Poodle dogs. Plos One. 13: e0193372. PMID 29474464 DOI: 10.1371/Journal.Pone.0193372 |
0.421 |
|
| 2018 |
Jeandel A, Garosi LS, Davies L, Guo LT, Salgüero R, Shelton GD. Late-onset Becker-type muscular dystrophy in a Border terrier dog. The Journal of Small Animal Practice. PMID 29377139 DOI: 10.1111/jsap.12824 |
0.303 |
|
| 2018 |
Bradbury AM, Rafi MA, Bagel J, Brisson BK, Marshall MS, Pesayco Salvador J, Jiang X, Swain GP, Prociuk ML, O'Donnell P, Fitzgerald C, Ory DS, Bongarzone ER, Shelton GD, Wenger DA, et al. AAVrh10 gene therapy ameliorates central and peripheral nervous system disease in canine globoid cell leukodystrophy (Krabbe disease). Human Gene Therapy. PMID 29316812 DOI: 10.1089/Hum.2017.151 |
0.345 |
|
| 2017 |
Blakey TJ, Michaels JR, Guo LT, Hodshon AJ, Shelton GD. Congenital Myasthenic Syndrome in a Mixed Breed Dog. Frontiers in Veterinary Science. 4: 173. PMID 29090216 DOI: 10.3389/Fvets.2017.00173 |
0.457 |
|
| 2017 |
Becker D, Minor KM, Letko A, Ekenstedt KJ, Jagannathan V, Leeb T, Shelton GD, Mickelson JR, Drögemüller C. A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs. Bmc Genomics. 18: 662. PMID 28841859 DOI: 10.1186/S12864-017-4081-Z |
0.368 |
|
| 2017 |
Cox ML, Evans JM, Davis AG, Guo LT, Levy JR, Starr-Moss AN, Salmela E, Hytönen MK, Lohi H, Campbell KP, Clark LA, Shelton GD. Exome sequencing reveals independent SGCD deletions causing limb girdle muscular dystrophy in Boston terriers. Skeletal Muscle. 7: 15. PMID 28697784 DOI: 10.1186/S13395-017-0131-0 |
0.461 |
|
| 2017 |
Mayousse V, Jeandel A, Blanchard-Gutton N, Escriou C, Gnirs K, Shelton GD, Blot S. Evaluation of coexisting polymyositis in feline myasthenia gravis: A case series. Neuromuscular Disorders : Nmd. 27: 804-815. PMID 28687435 DOI: 10.1016/J.Nmd.2017.06.006 |
0.375 |
|
| 2017 |
Wolf Z, Vernau K, Safra N, Shelton GD, King J, Owen J, Weich K, Bannasch D. Association of early onset myasthenia gravis in Newfoundland dogs with the canine major histocompatibility complex class I. Neuromuscular Disorders : Nmd. PMID 28262470 DOI: 10.1016/J.Nmd.2017.01.020 |
0.318 |
|
| 2016 |
Taylor S, Minor K, Shmon CL, Shelton GD, Patterson EE, Mickelson JR. Border Collie Collapse: Owner Survey Results and Veterinary Description of Videotaped Episodes. Journal of the American Animal Hospital Association. PMID 27685362 DOI: 10.5326/Jaaha-Ms-6436 |
0.359 |
|
| 2016 |
Forman OP, Hitti RJ, Pettitt L, Jenkins CA, O’Brien DP, Shelton GD, Risio LD, Quintana RG, Beltran E, Mellersh C. An Inversion Disrupting FAM134B Is Associated with Sensory Neuropathy in the Border Collie Dog Breed G3: Genes, Genomes, Genetics. 6: 2687-2692. PMID 27527794 DOI: 10.1534/G3.116.027896 |
0.331 |
|
| 2016 |
Taylor S, Shmon C, Su L, Epp T, Minor K, Mickelson J, Patterson E, Shelton GD. Evaluation of Dogs with Border Collie Collapse, Including Response to Two Standardized Strenuous Exercise Protocols. Journal of the American Animal Hospital Association. PMID 27487345 DOI: 10.5326/Jaaha-Ms-6361 |
0.312 |
|
| 2016 |
Evans JM, Cox ML, Huska J, Li F, Gaitero L, Guo LT, Casal ML, Granzier HL, Shelton GD, Clark LA. Exome sequencing reveals a nebulin nonsense mutation in a dog model of nemaline myopathy. Mammalian Genome : Official Journal of the International Mammalian Genome Society. PMID 27215641 DOI: 10.1007/S00335-016-9644-9 |
0.442 |
|
| 2016 |
Shelton GD. Myasthenia gravis and congenital myasthenic syndromes in dogs and cats: A history and mini-review Neuromuscular Disorders. 26: 331-334. PMID 27080328 DOI: 10.1016/J.Nmd.2016.03.002 |
0.391 |
|
| 2015 |
Biegen VR, McCue JP, Donovan TA, Shelton GD. Metabolic Encephalopathy and Lipid Storage Myopathy Associated with a Presumptive Mitochondrial Fatty Acid Oxidation Defect in a Dog. Frontiers in Veterinary Science. 2: 64. PMID 26664991 DOI: 10.3389/Fvets.2015.00064 |
0.32 |
|
| 2015 |
Wiedmer M, Oevermann A, Borer-Germann SE, Gorgas D, Shelton GD, Jagannathan V, Henke D, Leeb T. A RAB3GAP1 SINE Insertion in Alaskan Huskies with Polyneuropathy, Ocular Abnormalities and Neuronal Vacuolation (POANV) Resembling Human Warburg Micro Syndrome 1 (WARBM1). G3 (Bethesda, Md.). PMID 26596647 DOI: 10.1534/G3.115.022707 |
0.363 |
|
| 2015 |
Rinz CJ, Lennon VA, James F, Thoreson JB, Tsai KL, Starr-Moss AN, Humphries HD, Guo LT, Palmer AC, Clark LA, Shelton GD. A CHRNE frameshift mutation causes congenital myasthenic syndrome in young Jack Russell Terriers. Neuromuscular Disorders : Nmd. PMID 26429099 DOI: 10.1016/J.Nmd.2015.09.005 |
0.35 |
|
| 2015 |
Gandolfi B, Grahn RA, Creighton EK, Williams DC, Dickinson PJ, Sturges BK, Guo LT, Shelton GD, Leegwater PA, Longeri M, Malik R, Lyons LA. COLQ variant associated with Devon Rex and Sphynx feline hereditary myopathy. Animal Genetics. 46: 711-5. PMID 26374066 DOI: 10.1111/Age.12350 |
0.412 |
|
| 2015 |
Vieira NM, Guo LT, Estrela E, Kunkel LM, Zatz M, Shelton GD. Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype. Neuromuscular Disorders : Nmd. 25: 363-70. PMID 25813339 DOI: 10.1016/J.Nmd.2015.02.012 |
0.475 |
|
| 2015 |
Shelton GD, Rider BE, Child G, Tzannes S, Guo LT, Moghadaszadeh B, Troiano EC, Haase B, Wade CM, Beggs AH. X-linked myotubular myopathy in Rottweiler dogs is caused by a missense mutation in Exon 11 of the MTM1 gene. Skeletal Muscle. 5: 1. PMID 25664165 DOI: 10.1186/S13395-014-0025-3 |
0.466 |
|
| 2015 |
Snead EC, Taylor SM, van der Kooij M, Cosford K, Beggs AH, Shelton GD. Clinical phenotype of X-linked myotubular myopathy in labrador retriever puppies. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 29: 254-60. PMID 25581576 DOI: 10.1111/Jvim.12513 |
0.353 |
|
| 2014 |
Gandolfi B, Daniel RJ, O'Brien DP, Guo LT, Youngs MD, Leach SB, Jones BR, Shelton GD, Lyons LA. A novel mutation in CLCN1 associated with feline myotonia congenita. Plos One. 9: e109926. PMID 25356766 DOI: 10.1371/Journal.Pone.0109926 |
0.41 |
|
| 2014 |
Ekenstedt KJ, Becker D, Minor KM, Shelton GD, Patterson EE, Bley T, Oevermann A, Bilzer T, Leeb T, Drögemüller C, Mickelson JR. An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogs. Plos Genetics. 10: e1004635. PMID 25275565 DOI: 10.1371/Journal.Pgen.1004635 |
0.422 |
|
| 2014 |
Rinz CJ, Levine J, Minor KM, Humphries HD, Lara R, Starr-Moss AN, Guo LT, Williams DC, Shelton GD, Clark LA. A COLQ missense mutation in Labrador Retrievers having congenital myasthenic syndrome. Plos One. 9: e106425. PMID 25166616 DOI: 10.1371/Journal.Pone.0106425 |
0.384 |
|
| 2014 |
Eminaga S, Cherubini GB, Shelton GD. Identification of the mutation causing centronuclear myopathy in a border collie. The Veterinary Record. 175: 124. PMID 25081885 DOI: 10.1136/Vr.G4883 |
0.304 |
|
| 2014 |
Utsugi S, Saito M, Shelton GD. Resolution of polyneuropathy in a hypothyroid dog following thyroid supplementation. Journal of the American Animal Hospital Association. 50: 345-9. PMID 25028439 DOI: 10.5326/Jaaha-Ms-6035 |
0.357 |
|
| 2014 |
Chapman MA, Zhang J, Banerjee I, Guo LT, Zhang Z, Shelton GD, Ouyang K, Lieber RL, Chen J. Disruption of both nesprin 1 and desmin results in nuclear anchorage defects and fibrosis in skeletal muscle. Human Molecular Genetics. 23: 5879-92. PMID 24943590 DOI: 10.1093/Hmg/Ddu310 |
0.404 |
|
| 2014 |
Cortes CJ, Ling SC, Guo LT, Hung G, Tsunemi T, Ly L, Tokunaga S, Lopez E, Sopher BL, Bennett CF, Shelton GD, Cleveland DW, La Spada AR. Muscle expression of mutant androgen receptor accounts for systemic and motor neuron disease phenotypes in spinal and bulbar muscular atrophy. Neuron. 82: 295-307. PMID 24742458 DOI: 10.1016/J.Neuron.2014.03.001 |
0.422 |
|
| 2014 |
Spoo JW, Shelton GD. Recurrent gastric dilatation and intestinal dysmotility possibly resulting from autonomic neuropathy in a Great Dane. Journal of the American Animal Hospital Association. 50: 221-6. PMID 24659724 DOI: 10.5326/Jaaha-Ms-6176 |
0.373 |
|
| 2014 |
Gambino AN, Mouser PJ, Shelton GD, Winand NJ. Emergent presentation of a cat with dystrophin-deficient muscular dystrophy. Journal of the American Animal Hospital Association. 50: 130-5. PMID 24446404 DOI: 10.5326/Jaaha-Ms-5973 |
0.372 |
|
| 2014 |
Morgan BR, Coates JR, Johnson GC, Shelton GD, Katz ML. Characterization of thoracic motor and sensory neurons and spinal nerve roots in canine degenerative myelopathy, a potential disease model of amyotrophic lateral sclerosis. Journal of Neuroscience Research. 92: 531-41. PMID 24375814 DOI: 10.1002/Jnr.23332 |
0.338 |
|
| 2014 |
Domenighetti AA, Chu PH, Wu T, Sheikh F, Gokhin DS, Guo LT, Cui Z, Peter AK, Christodoulou DC, Parfenov MG, Gorham JM, Li DY, Banerjee I, Lai X, Witzmann FA, ... ... Shelton GD, et al. Loss of FHL1 induces an age-dependent skeletal muscle myopathy associated with myofibrillar and intermyofibrillar disorganization in mice. Human Molecular Genetics. 23: 209-25. PMID 23975679 DOI: 10.1093/Hmg/Ddt412 |
0.443 |
|
| 2013 |
Bannykh SI, Balch WE, Kelly JW, Page LJ, Shelton GD. Formation of gelsolin amyloid fibrils in the rough endoplasmic reticulum of skeletal muscle in the gelsolin mouse model of inclusion body myositis: comparative analysis to human sporadic inclusion body myositis. Ultrastructural Pathology. 37: 304-11. PMID 24047347 DOI: 10.3109/01913123.2013.810684 |
0.369 |
|
| 2013 |
Böhm J, Vasli N, Maurer M, Cowling BS, Cowling B, Shelton GD, Kress W, Toussaint A, Prokic I, Schara U, Anderson TJ, Weis J, Tiret L, Laporte J. Altered splicing of the BIN1 muscle-specific exon in humans and dogs with highly progressive centronuclear myopathy. Plos Genetics. 9: e1003430. PMID 23754947 DOI: 10.1371/Journal.Pgen.1003430 |
0.456 |
|
| 2013 |
Vernau KM, Runstadler JA, Brown EA, Cameron JM, Huson HJ, Higgins RJ, Ackerley C, Sturges BK, Dickinson PJ, Puschner B, Giulivi C, Shelton GD, Robinson BH, DiMauro S, Bollen AW, et al. Genome-wide association analysis identifies a mutation in the thiamine transporter 2 (SLC19A3) gene associated with Alaskan Husky encephalopathy. Plos One. 8: e57195. PMID 23469184 DOI: 10.1371/Journal.Pone.0057195 |
0.367 |
|
| 2013 |
Bagel JH, Sikora TU, Prociuk M, Pesayco JP, Mizisin AP, Shelton GD, Vite CH. Electrodiagnostic testing and histopathologic changes confirm peripheral nervous system myelin abnormalities in the feline model of niemann-pick disease type C. Journal of Neuropathology and Experimental Neurology. 72: 256-62. PMID 23399903 DOI: 10.1097/Nen.0B013E318286587F |
0.347 |
|
| 2013 |
Bruun CS, Jäderlund KH, Berendt M, Jensen KB, Spodsberg EH, Gredal H, Shelton GD, Mickelson JR, Minor KM, Lohi H, Bjerkås I, Stigen O, Espenes A, Rohdin C, Edlund R, et al. A Gly98Val mutation in the N-Myc downstream regulated gene 1 (NDRG1) in Alaskan Malamutes with polyneuropathy. Plos One. 8: e54547. PMID 23393557 DOI: 10.1371/Journal.Pone.0054547 |
0.353 |
|
| 2012 |
Maurer M, Mary J, Guillaud L, Fender M, Pelé M, Bilzer T, Olby N, Penderis J, Shelton GD, Panthier JJ, Thibaud JL, Barthélémy I, Aubin-Houzelstein G, Blot S, Hitte C, et al. Centronuclear myopathy in Labrador retrievers: a recent founder mutation in the PTPLA gene has rapidly disseminated worldwide. Plos One. 7: e46408. PMID 23071563 DOI: 10.1371/Journal.Pone.0046408 |
0.383 |
|
| 2012 |
Nakamura RK, Russell NJ, Shelton GD. Adult-onset nemaline myopathy in a dog presenting with persistent atrial standstill and primary hypothyroidism. The Journal of Small Animal Practice. 53: 357-60. PMID 22647214 DOI: 10.1111/j.1748-5827.2012.01221.x |
0.31 |
|
| 2012 |
Shelton GD, Johnson GC, O'Brien DP, Katz ML, Pesayco JP, Chang BJ, Mizisin AP, Coates JR. Degenerative myelopathy associated with a missense mutation in the superoxide dismutase 1 (SOD1) gene progresses to peripheral neuropathy in Pembroke Welsh corgis and boxers. Journal of the Neurological Sciences. 318: 55-64. PMID 22542607 DOI: 10.1016/J.Jns.2012.04.003 |
0.446 |
|
| 2011 |
Sykes JE, Dubey JP, Lindsay LL, Prato P, Lappin MR, Guo LT, Mizisin AP, Shelton GD. Severe myositis associated with Sarcocystis spp. infection in 2 dogs. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 25: 1277-83. PMID 22092617 DOI: 10.1111/J.1939-1676.2011.00828.X |
0.317 |
|
| 2011 |
Gill JL, Capper D, Vanbellinghen JF, Chung SK, Higgins RJ, Rees MI, Shelton GD, Harvey RJ. Startle disease in Irish wolfhounds associated with a microdeletion in the glycine transporter GlyT2 gene. Neurobiology of Disease. 43: 184-9. PMID 21420493 DOI: 10.1016/J.Nbd.2011.03.010 |
0.386 |
|
| 2010 |
Bader HL, Ruhe AL, Wang LW, Wong AK, Walsh KF, Packer RA, Mitelman J, Robertson KR, O'Brien DP, Broman KW, Shelton GD, Apte SS, Neff MW. An ADAMTSL2 founder mutation causes Musladin-Lueke Syndrome, a heritable disorder of beagle dogs, featuring stiff skin and joint contractures. Plos One. 5. PMID 20862248 DOI: 10.1371/Journal.Pone.0012817 |
0.313 |
|
| 2010 |
Guo LT, Moore SA, Forcales S, Engvall E, Shelton GD. Evaluation of commercial dysferlin antibodies on canine, mouse and human skeletal muscle. Neuromuscular Disorders : Nmd. 20: 820-5. PMID 20817457 DOI: 10.1016/J.Nmd.2010.07.278 |
0.411 |
|
| 2010 |
Shelton GD. Routine and specialized laboratory testing for the diagnosis of neuromuscular diseases in dogs and cats. Veterinary Clinical Pathology / American Society For Veterinary Clinical Pathology. 39: 278-95. PMID 20726955 DOI: 10.1111/J.1939-165X.2010.00244.X |
0.431 |
|
| 2010 |
Beggs AH, Böhm J, Snead E, Kozlowski M, Maurer M, Minor K, Childers MK, Taylor SM, Hitte C, Mickelson JR, Guo LT, Mizisin AP, Buj-Bello A, Tiret L, Laporte J, ... Shelton GD, et al. MTM1 mutation associated with X-linked myotubular myopathy in Labrador Retrievers. Proceedings of the National Academy of Sciences of the United States of America. 107: 14697-702. PMID 20682747 DOI: 10.1073/Pnas.1003677107 |
0.447 |
|
| 2010 |
Thieman KM, Krahwinkel DJ, Sims MH, Shelton GD. Histopathological confirmation of polyneuropathy in 11 dogs with laryngeal paralysis. Journal of the American Animal Hospital Association. 46: 161-7. PMID 20439938 DOI: 10.5326/0460161 |
0.389 |
|
| 2010 |
Shelton GD. Acquired laryngeal paralysis in dogs: evidence accumulating for a generalized neuromuscular disease. Veterinary Surgery : Vs. 39: 137-8. PMID 20210959 DOI: 10.1111/J.1532-950X.2009.00646.X |
0.33 |
|
| 2010 |
Rohdin C, Karlstam E, Jäderlund KH, Shelton GD. Acquired motor neuron loss causing severe pelvic limb contractures in a young cat. Journal of Feline Medicine and Surgery. 12: 237-40. PMID 20193915 DOI: 10.1016/J.Jfms.2010.01.007 |
0.42 |
|
| 2010 |
Walmsley GL, Arechavala-Gomeza V, Fernandez-Fuente M, Burke MM, Nagel N, Holder A, Stanley R, Chandler K, Marks SL, Muntoni F, Shelton GD, Piercy RJ. A duchenne muscular dystrophy gene hot spot mutation in dystrophin-deficient cavalier king charles spaniels is amenable to exon 51 skipping. Plos One. 5: e8647. PMID 20072625 DOI: 10.1371/Journal.Pone.0008647 |
0.379 |
|
| 2010 |
Zhang J, Felder A, Liu Y, Guo LT, Lange S, Dalton ND, Gu Y, Peterson KL, Mizisin AP, Shelton GD, Lieber RL, Chen J. Nesprin 1 is critical for nuclear positioning and anchorage. Human Molecular Genetics. 19: 329-41. PMID 19864491 DOI: 10.1093/Hmg/Ddp499 |
0.388 |
|
| 2009 |
Abelson AL, Shelton GD, Whelan MF, Cornejo L, Shaw S, O'Toole TE. Use of mycophenolate mofetil as a rescue agent in the treatment of severe generalized myasthenia gravis in three dogs. Journal of Veterinary Emergency and Critical Care (San Antonio, Tex. : 2001). 19: 369-74. PMID 25164637 DOI: 10.1111/J.1476-4431.2009.00433.X |
0.32 |
|
| 2009 |
Couturier J, Huynh M, Boussarie D, Cauzinille L, Shelton GD. Autoimmune myasthenia gravis in a ferret. Journal of the American Veterinary Medical Association. 235: 1462-6. PMID 20001782 DOI: 10.2460/Javma.235.12.1462 |
0.408 |
|
| 2009 |
King J, LeCouteur RA, Aleman M, Williams DC, Moore PF, Guo LT, Mizisin AP, Shelton GD. Vacuolar myopathy in a dog resembling human sporadic inclusion body myositis. Acta Neuropathologica. 118: 711-7. PMID 19718499 DOI: 10.1007/S00401-009-0588-Y |
0.375 |
|
| 2009 |
Ginman AA, Kline KL, Shelton GD. Severe polymyositis and neuritis in a cat. Journal of the American Veterinary Medical Association. 235: 172-5. PMID 19601738 DOI: 10.2460/Javma.235.2.172 |
0.447 |
|
| 2009 |
Nanai B, Phillips L, Christiansen J, Shelton GD. Life threatening complication associated with anesthesia in a dog with masticatory muscle myositis. Veterinary Surgery : Vs. 38: 645-9. PMID 19573068 DOI: 10.1111/J.1532-950X.2009.00515.X |
0.424 |
|
| 2009 |
Rossmeisl JH, Duncan RB, Inzana KD, Panciera DL, Shelton GD. Longitudinal study of the effects of chronic hypothyroidism on skeletal muscle in dogs. American Journal of Veterinary Research. 70: 879-89. PMID 19566473 DOI: 10.2460/Ajvr.70.7.879 |
0.425 |
|
| 2009 |
Page LJ, Suk JY, Bazhenova L, Fleming SM, Wood M, Jiang Y, Guo LT, Mizisin AP, Kisilevsky R, Shelton GD, Balch WE, Kelly JW. Secretion of amyloidogenic gelsolin progressively compromises protein homeostasis leading to the intracellular aggregation of proteins. Proceedings of the National Academy of Sciences of the United States of America. 106: 11125-30. PMID 19549824 DOI: 10.1073/Pnas.0811753106 |
0.392 |
|
| 2009 |
Wells RJ, Sedacca CD, Aman AM, Hackett TB, Twedt DC, Shelton GD. Successful management of a dog that had severe rhabdomyolysis with myocardial and respiratory failure. Journal of the American Veterinary Medical Association. 234: 1049-54. PMID 19366338 DOI: 10.2460/Javma.234.8.1049 |
0.375 |
|
| 2009 |
Awano T, Johnson GS, Wade CM, Katz ML, Johnson GC, Taylor JF, Perloski M, Biagi T, Baranowska I, Long S, March PA, Olby NJ, Shelton GD, Khan S, O'Brien DP, et al. Genome-wide association analysis reveals a SOD1 mutation in canine degenerative myelopathy that resembles amyotrophic lateral sclerosis. Proceedings of the National Academy of Sciences of the United States of America. 106: 2794-9. PMID 19188595 DOI: 10.1073/Pnas.0812297106 |
0.37 |
|
| 2009 |
Taylor SM, Shmon CL, Adams VJ, Mickelson JR, Patterson EN, Shelton GD. Evaluations of labrador retrievers with exercise-induced collapse, including response to a standardized strenuous exercise protocol. Journal of the American Animal Hospital Association. 45: 3-13. PMID 19122058 DOI: 10.5326/0450003 |
0.301 |
|
| 2008 |
Martin PT, Shelton GD, Dickinson PJ, Sturges BK, Xu R, LeCouteur RA, Guo LT, Grahn RA, Lo HP, North KN, Malik R, Engvall E, Lyons LA. Muscular dystrophy associated with alpha-dystroglycan deficiency in Sphynx and Devon Rex cats. Neuromuscular Disorders : Nmd. 18: 942-52. PMID 18990577 DOI: 10.1016/J.Nmd.2008.08.002 |
0.36 |
|
| 2008 |
Vanhaesebrouck AE, Couturier J, Cauzinille L, Mizisin AP, Shelton GD, Granger N. Demyelinating polyneuropathy with focally folded myelin sheaths in a family of Miniature Schnauzer dogs. Journal of the Neurological Sciences. 275: 100-5. PMID 18809183 DOI: 10.1016/J.Jns.2008.07.031 |
0.358 |
|
| 2008 |
Patterson EE, Minor KM, Tchernatynskaia AV, Taylor SM, Shelton GD, Ekenstedt KJ, Mickelson JR. A canine DNM1 mutation is highly associated with the syndrome of exercise-induced collapse. Nature Genetics. 40: 1235-9. PMID 18806795 DOI: 10.1038/Ng.224 |
0.343 |
|
| 2008 |
Bishop TM, Glass EN, De Lahunta A, Shelton GD. Imaging diagnosis--masticatory muscle myositis in a young dog. Veterinary Radiology & Ultrasound : the Official Journal of the American College of Veterinary Radiology and the International Veterinary Radiology Association. 49: 270-2. PMID 18546784 DOI: 10.1111/J.1740-8261.2008.00364.X |
0.386 |
|
| 2008 |
Delaunay A, Bromberg KD, Hayashi Y, Mirabella M, Burch D, Kirkwood B, Serra C, Malicdan MC, Mizisin AP, Morosetti R, Broccolini A, Guo LT, Jones SN, Lira SA, Puri PL, ... Shelton GD, et al. The ER-bound RING finger protein 5 (RNF5/RMA1) causes degenerative myopathy in transgenic mice and is deregulated in inclusion body myositis. Plos One. 3: e1609. PMID 18270596 DOI: 10.1371/Journal.Pone.0001609 |
0.418 |
|
| 2008 |
Li ZF, Wu X, Jiang Y, Liu J, Wu C, Inagaki M, Izawa I, Mizisin AP, Engvall E, Shelton GD. Non-pathogenic protein aggregates in skeletal muscle in MLF1 transgenic mice. Journal of the Neurological Sciences. 264: 77-86. PMID 17854834 DOI: 10.1016/J.Jns.2007.07.027 |
0.384 |
|
| 2007 |
Wu X, Li ZF, Brooks R, Komives EA, Torpey JW, Engvall E, Gonias SL, Shelton GD. Autoantibodies in canine masticatory muscle myositis recognize a novel myosin binding protein-C family member. Journal of Immunology (Baltimore, Md. : 1950). 179: 4939-44. PMID 17878394 DOI: 10.4049/Jimmunol.179.7.4939 |
0.411 |
|
| 2007 |
Shelton GD, Engvall E. Gross muscle hypertrophy in whippet dogs is caused by a mutation in the myostatin gene. Neuromuscular Disorders : Nmd. 17: 721-2. PMID 17651971 DOI: 10.1016/J.Nmd.2007.06.008 |
0.42 |
|
| 2007 |
Shelton GD. From dog to man: the broad spectrum of inflammatory myopathies. Neuromuscular Disorders : Nmd. 17: 663-70. PMID 17629703 DOI: 10.1016/J.Nmd.2007.06.466 |
0.371 |
|
| 2007 |
Baltzer WI, Calise DV, Levine JM, Shelton GD, Edwards JF, Steiner JM. Dystrophin-deficient muscular dystrophy in a Weimaraner. Journal of the American Animal Hospital Association. 43: 227-32. PMID 17615404 DOI: 10.5326/0430227 |
0.333 |
|
| 2007 |
Berdeaux R, Goebel N, Banaszynski L, Takemori H, Wandless T, Shelton GD, Montminy M. SIK1 is a class II HDAC kinase that promotes survival of skeletal myocytes. Nature Medicine. 13: 597-603. PMID 17468767 DOI: 10.1038/Nm1573 |
0.315 |
|
| 2007 |
Shelton GD, Sturges BK, Lyons LA, Williams DC, Aleman M, Jiang Y, Mizisin AP. Myopathy with tubulin-reactive inclusions in two cats. Acta Neuropathologica. 114: 537-42. PMID 17393175 DOI: 10.1007/S00401-007-0217-6 |
0.393 |
|
| 2007 |
Paciello O, Shelton GD, Papparella S. Expression of major histocompatibility complex class I and class II antigens in canine masticatory muscle myositis. Neuromuscular Disorders : Nmd. 17: 313-20. PMID 17360184 DOI: 10.1016/J.Nmd.2007.01.012 |
0.342 |
|
| 2007 |
Cameron JM, Maj MC, Levandovskiy V, MacKay N, Shelton GD, Robinson BH. Identification of a canine model of pyruvate dehydrogenase phosphatase 1 deficiency. Molecular Genetics and Metabolism. 90: 15-23. PMID 17095275 DOI: 10.1016/J.Ymgme.2006.09.011 |
0.34 |
|
| 2007 |
Kelmer E, Shelton GD, Williams DA, Ruaux CG, Kerl ME, O'Brien DP. Organic acidemia in a young cat associated with cobalamin deficiency Journal of Veterinary Emergency and Critical Care. 17: 299-304. DOI: 10.1111/J.1476-4431.2007.00234.X |
0.3 |
|
| 2006 |
Platt SR, McConnell JF, Garosi LS, Ladlow J, de Stefani A, Shelton GD. Magnetic resonance imaging in the diagnosis of canine inflammatory myopathies in three dogs. Veterinary Radiology & Ultrasound : the Official Journal of the American College of Veterinary Radiology and the International Veterinary Radiology Association. 47: 532-7. PMID 17153060 DOI: 10.1111/J.1740-8261.2006.00181.X |
0.361 |
|
| 2006 |
Aleman M, Watson JL, Williams DC, LeCouteur RA, Nieto JE, Shelton GD. Myopathy in horses with pituitary pars intermedia dysfunction (Cushing's disease). Neuromuscular Disorders : Nmd. 16: 737-44. PMID 17005399 DOI: 10.1016/J.Nmd.2006.07.019 |
0.319 |
|
| 2006 |
Homma S, Iwasaki M, Shelton GD, Engvall E, Reed JC, Takayama S. BAG3 deficiency results in fulminant myopathy and early lethality. The American Journal of Pathology. 169: 761-73. PMID 16936253 DOI: 10.2353/Ajpath.2006.060250 |
0.413 |
|
| 2006 |
Hankel S, Shelton GD, Engvall E. Sarcolemma-specific autoantibodies in canine inflammatory myopathy. Veterinary Immunology and Immunopathology. 113: 1-10. PMID 16824619 DOI: 10.1016/J.Vetimm.2006.03.025 |
0.375 |
|
| 2006 |
Shelton GD, Hoffman EP, Ghimbovschi S, Peters IR, Day MJ, Mullins M, Moore PF, Nagaraju K. Immunopathogenic pathways in canine inflammatory myopathies resemble human myositis. Veterinary Immunology and Immunopathology. 113: 200-14. PMID 16797723 DOI: 10.1016/J.Vetimm.2006.05.005 |
0.368 |
|
| 2006 |
Shelton GD, Paciello O. Evidence for MHC-1-restricted CD8+ T-cell-mediated immunopathology in canine masticatory muscle myositis and polymyositis. Muscle & Nerve. 34: 122; author reply 12. PMID 16583372 DOI: 10.1002/Mus.20547 |
0.315 |
|
| 2006 |
Kube SA, Vernau KM, LeCouteur RA, Mizisin AP, Shelton GD. Congenital myopathy with abundant nemaline rods in a cat. Neuromuscular Disorders : Nmd. 16: 188-91. PMID 16487709 DOI: 10.1016/J.Nmd.2005.12.005 |
0.45 |
|
| 2006 |
Li FY, Cuddon PA, Song J, Wood SL, Patterson JS, Shelton GD, Duncan ID. Canine spongiform leukoencephalomyelopathy is associated with a missense mutation in cytochrome b. Neurobiology of Disease. 21: 35-42. PMID 16026996 DOI: 10.1016/J.Nbd.2005.06.009 |
0.311 |
|
| 2005 |
Dickinson PJ, Sturges BK, Shelton GD, LeCouteur RA. Congenital myasthenia gravis in Smooth-Haired Miniature Dachshund dogs. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 19: 920-3. PMID 16355692 DOI: 10.1892/0891-6640(2005)19[920:Cmgism]2.0.Co;2 |
0.396 |
|
| 2005 |
Galano HR, Olby NJ, Howard JF, Shelton GD. Myokymia and neuromyotonia in a cat. Journal of the American Veterinary Medical Association. 227: 1608-12, 1591. PMID 16313038 DOI: 10.2460/Javma.2005.227.1608 |
0.416 |
|
| 2005 |
Guo LT, Shelton GD, Wewer UM, Engvall E. ADAM12 overexpression does not improve outcome in mice with laminin alpha2-deficient muscular dystrophy. Neuromuscular Disorders : Nmd. 15: 786-9. PMID 16198565 DOI: 10.1016/J.Nmd.2005.06.019 |
0.379 |
|
| 2005 |
Garosi LS, Rossmeisl JH, de Lahunta A, Shelton GD, Lennox G. Primary orthostatic tremor in Great Danes. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 19: 606-9. PMID 16095183 DOI: 10.1111/J.1939-1676.2005.Tb02736.X |
0.352 |
|
| 2005 |
Levine JM, Bergman RL, Coates JR, Shelton GD. Myasthenia gravis and hypothyroidism in a dog with meningomyelitis. Journal of the American Animal Hospital Association. 41: 247-51. PMID 15995162 DOI: 10.5326/0410247 |
0.347 |
|
| 2005 |
Ryckman LR, Krahwinkel DJ, Sims MH, Donnell RL, Moore PF, Shelton GD. Dysphagia as the primary clinical abnormality in two dogs with inflammatory myopathy. Journal of the American Veterinary Medical Association. 226: 1519-23, 1501. PMID 15882004 DOI: 10.2460/Javma.2005.226.1519 |
0.424 |
|
| 2005 |
Salvadori C, Peters IR, Day MJ, Engvall E, Shelton GD. Muscle regeneration, inflammation, and connective tissue expansion in canine inflammatory myopathy. Muscle & Nerve. 31: 192-8. PMID 15736299 DOI: 10.1002/Mus.20252 |
0.419 |
|
| 2005 |
Evans J, Katz ML, Levesque D, Shelton GD, de Lahunta A, O'Brien D. A variant form of neuronal ceroid lipofuscinosis in American bulldogs. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 19: 44-51. PMID 15715047 DOI: 10.1111/J.1939-1676.2005.Tb02657.X |
0.341 |
|
| 2005 |
Aleman M, Lecouteur RA, Nieto JE, Williams DC, Stanke NJ, Shelton GD. Sarcoplasmic masses in equine skeletal muscle. Neuromuscular Disorders : Nmd. 15: 147-53. PMID 15694136 DOI: 10.1016/J.Nmd.2004.10.014 |
0.306 |
|
| 2005 |
Shelton GD, Engvall E. Canine and feline models of human inherited muscle diseases. Neuromuscular Disorders : Nmd. 15: 127-38. PMID 15694134 DOI: 10.1016/J.Nmd.2004.10.019 |
0.441 |
|
| 2005 |
Li ZF, Shelton GD, Engvall E. Elimination of myostatin does not combat muscular dystrophy in dy mice but increases postnatal lethality. The American Journal of Pathology. 166: 491-7. PMID 15681832 DOI: 10.1016/S0002-9440(10)62271-7 |
0.4 |
|
| 2005 |
Lohi H, Young EJ, Fitzmaurice SN, Rusbridge C, Chan EM, Vervoort M, Turnbull J, Zhao XC, Ianzano L, Paterson AD, Sutter NB, Ostrander EA, André C, Shelton GD, Ackerley CA, et al. Expanded repeat in canine epilepsy. Science (New York, N.Y.). 307: 81. PMID 15637270 DOI: 10.1126/Science.1102832 |
0.321 |
|
| 2005 |
He Q, Lowrie C, Shelton GD, Castellani RJ, Menotti-Raymond M, Murphy W, O'Brien SJ, Swanson WF, Fyfe JC. Inherited motor neuron disease in domestic cats: a model of spinal muscular atrophy. Pediatric Research. 57: 324-30. PMID 15635053 DOI: 10.1203/01.Pdr.0000153625.46892.6F |
0.377 |
|
| 2004 |
Evans J, Levesque D, Shelton GD. Canine inflammatory myopathies: a clinicopathologic review of 200 cases. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 18: 679-91. PMID 15515585 DOI: 10.1892/0891-6640(2004)18<679:Cimacr>2.0.Co;2 |
0.443 |
|
| 2004 |
Schatzberg SJ, Shelton GD. Newly identified neuromuscular disorders. The Veterinary Clinics of North America. Small Animal Practice. 34: 1497-524. PMID 15474686 DOI: 10.1016/J.Cvsm.2004.06.001 |
0.305 |
|
| 2004 |
Shelton GD. Muscle pain, cramps and hypertonicity. The Veterinary Clinics of North America. Small Animal Practice. 34: 1483-96. PMID 15474685 DOI: 10.1016/J.Cvsm.2004.05.019 |
0.357 |
|
| 2004 |
Shelton GD. Rhabdomyolysis, myoglobinuria, and necrotizing myopathies. The Veterinary Clinics of North America. Small Animal Practice. 34: 1469-82. PMID 15474684 DOI: 10.1016/J.Cvsm.2004.05.020 |
0.389 |
|
| 2004 |
Shelton GD, Sammut V, Homma S, Takayama S, Mizisin AP. Myofibrillar myopathy with desmin accumulation in a young Australian Shepherd dog. Neuromuscular Disorders : Nmd. 14: 399-404. PMID 15210162 DOI: 10.1016/J.Nmd.2004.03.010 |
0.405 |
|
| 2004 |
Pumarola M, Moore PF, Shelton GD. Canine inflammatory myopathy: analysis of cellular infiltrates. Muscle & Nerve. 29: 782-9. PMID 15170610 DOI: 10.1002/Mus.20043 |
0.35 |
|
| 2004 |
Dickinson PJ, Anderson PJ, Williams DC, Powell HC, Shelton GD, Morris JG, LeCouteur RA. Assessment of the neurologic effects of dietary deficiencies of phenylalanine and tyrosine in cats. American Journal of Veterinary Research. 65: 671-80. PMID 15141890 DOI: 10.2460/Ajvr.2004.65.671 |
0.366 |
|
| 2004 |
Jones BR, Brennan S, Mooney CT, Callanan JJ, McAllister H, Guo LT, Martin PT, Engvall E, Shelton GD. Muscular dystrophy with truncated dystrophin in a family of Japanese Spitz dogs. Journal of the Neurological Sciences. 217: 143-9. PMID 14706216 DOI: 10.1016/J.Jns.2003.09.002 |
0.417 |
|
| 2003 |
Abramson CJ, Platt SR, Jakobs C, Verhoeven NM, Dennis R, Garosi L, Shelton GD. L-2-Hydroxyglutaric aciduria in Staffordshire Bull Terriers. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 17: 551-6. PMID 12892307 DOI: 10.1111/J.1939-1676.2003.Tb02477.X |
0.301 |
|
| 2003 |
Shelton GD, Podell M, Poncelet L, Schatzberg S, Patterson E, Powell HC, Mizisin AP. Inherited polyneuropathy in Leonberger dogs: a mixed or intermediate form of Charcot-Marie-Tooth disease? Muscle & Nerve. 27: 471-7. PMID 12661049 DOI: 10.1002/Mus.10350 |
0.42 |
|
| 2003 |
Huang C, Zhou Q, Liang P, Hollander MS, Sheikh F, Li X, Greaser M, Shelton GD, Evans S, Chen J. Characterization and in vivo functional analysis of splice variants of cypher. The Journal of Biological Chemistry. 278: 7360-5. PMID 12499364 DOI: 10.1074/Jbc.M211875200 |
0.384 |
|
| 2002 |
Coates JR, O'Brien DP, Kline KL, Storts RW, Johnson GC, Shelton GD, Patterson EE, Abbott LC. Neonatal cerebellar ataxia in Coton de Tulear dogs. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 16: 680-9. PMID 12465765 DOI: 10.1111/J.1939-1676.2002.Tb02408.X |
0.375 |
|
| 2002 |
Mizisin AP, Shelton GD, Burgers ML, Powell HC, Cuddon PA. Neurological complications associated with spontaneously occurring feline diabetes mellitus. Journal of Neuropathology and Experimental Neurology. 61: 872-84. PMID 12387453 DOI: 10.1093/Jnen/61.10.872 |
0.338 |
|
| 2002 |
Bergman RL, Inzana KD, Monroe WE, Shell LG, Liu LA, Engvall E, Shelton GD. Dystrophin-deficient muscular dystrophy in a Labrador retriever. Journal of the American Animal Hospital Association. 38: 255-61. PMID 12022412 DOI: 10.5326/0380255 |
0.428 |
|
| 2002 |
Shelton GD. Myasthenia gravis and disorders of neuromuscular transmission. The Veterinary Clinics of North America. Small Animal Practice. 32: 189-206, vii. PMID 11785729 DOI: 10.1016/S0195-5616(03)00085-8 |
0.302 |
|
| 2002 |
Shelton GD, Engvall E. Muscular dystrophies and other inherited myopathies. The Veterinary Clinics of North America. Small Animal Practice. 32: 103-24. PMID 11785725 DOI: 10.1016/S0195-5616(03)00081-0 |
0.447 |
|
| 2001 |
O'Brien DP, Johnson GC, Liu LA, Guo LT, Engvall E, Powell HC, Shelton GD. Laminin alpha 2 (merosin)-deficient muscular dystrophy and demyelinating neuropathy in two cats. Journal of the Neurological Sciences. 189: 37-43. PMID 11535231 DOI: 10.1016/S0022-510X(01)00559-7 |
0.408 |
|
| 2001 |
Shelton GD, Liu LA, Guo LT, Smith GK, Christiansen JS, Thomas WB, Smith MO, Kline KL, March PA, Flegel T, Engvall E. Muscular dystrophy in female dogs. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 15: 240-4. PMID 11380033 DOI: 10.1111/J.1939-1676.2001.Tb02317.X |
0.471 |
|
| 2001 |
Shelton GD, Skeie GO, Kass PH, Aarli JA. Titin and ryanodine receptor autoantibodies in dogs with thymoma and late-onset myasthenia gravis. Veterinary Immunology and Immunopathology. 78: 97-105. PMID 11182151 DOI: 10.1016/S0165-2427(00)00255-5 |
0.304 |
|
| 2000 |
Wetterman CA, Harkin KR, Cash WC, Nietfield JC, Shelton GD. Hypertrophic muscular dystrophy in a young dog. Journal of the American Veterinary Medical Association. 216: 878-81, 864. PMID 22570900 DOI: 10.2460/Javma.2000.216.878 |
0.471 |
|
| 2000 |
Allgoewer I, Blair M, Basher T, Davidson M, Hamilton H, Jandeck C, Ward D, Wolfer J, Shelton GD. Extraocular muscle myositis and restrictive strabismus in 10 dogs. Veterinary Ophthalmology. 3: 21-26. PMID 11397278 |
0.317 |
|
| 1999 |
Shelton GD, Calcutt NA, Garrett RS, Gu D, Sarvetnick N, Campana WM, Powell HC. Necrotizing myopathy induced by overexpression of interferon-gamma in transgenic mice. Muscle & Nerve. 22: 156-65. PMID 10024128 DOI: 10.1002/(Sici)1097-4598(199902)22:2<156::Aid-Mus3>3.0.Co;2-U |
0.303 |
|
| 1998 |
Delauche AJ, Cuddon PA, Podell M, Devoe K, Powell HC, Shelton GD. Nemaline rods in canine myopathies: 4 case reports and literature review. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 12: 424-30. PMID 9857334 DOI: 10.1111/J.1939-1676.1998.Tb02145.X |
0.411 |
|
| 1998 |
Podell M, Chen E, Shelton GD. Feline immunodeficiency virus associated myopathy in the adult cat. Muscle & Nerve. 21: 1680-5. PMID 9843069 DOI: 10.1002/(Sici)1097-4598(199812)21:12<1680::Aid-Mus9>3.0.Co;2-F |
0.424 |
|
| 1998 |
Shelton GD, Nyhan WL, Kass PH, Barshop BA, Haas RH. Analysis of organic acids, amino acids, and carnitine in dogs with lipid storage myopathy. Muscle & Nerve. 21: 1202-5. PMID 9703448 DOI: 10.1002/(Sici)1097-4598(199809)21:9<1202::Aid-Mus13>3.0.Co;2-T |
0.406 |
|
| 1998 |
Hanson SM, Smith MO, Walker TL, Shelton GD. Juvenile-onset distal myopathy in Rottweiler dogs. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 12: 103-8. PMID 9560767 DOI: 10.1111/J.1939-1676.1998.Tb02103.X |
0.458 |
|
| 1997 |
Dewey CW, Bailey CS, Shelton GD, Kass PH, Cardinet GH. Clinical forms of acquired myasthenia gravis in dogs: 25 cases (1988-1995). Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 11: 50-7. PMID 9127290 DOI: 10.1111/J.1939-1676.1997.Tb00073.X |
0.459 |
|
| 1995 |
Hill SL, Shelton GD, Lenehan TM. Myotonia in a cocker spaniel. Journal of the American Animal Hospital Association. 31: 506-9. PMID 8581546 DOI: 10.5326/15473317-31-6-506 |
0.34 |
|
| 1988 |
Shelton GD, Cardinet GH, Bandman E. Expression of fiber type specific proteins during ontogeny of canine temporalis muscle. Muscle & Nerve. 11: 124-32. PMID 3343987 DOI: 10.1002/Mus.880110207 |
0.379 |
|
| 1987 |
Shelton GD, Cardinet GH, Bandman E. Canine masticatory muscle disorders: a study of 29 cases. Muscle & Nerve. 10: 753-66. PMID 3317035 DOI: 10.1002/Mus.880100812 |
0.427 |
|
| 1985 |
Shelton GD, Cardinet GH, Bandman E, Cuddon P. Fiber type-specific autoantibodies in a dog with eosinophilic myositis. Muscle & Nerve. 8: 783-90. PMID 4079956 DOI: 10.1002/Mus.880080907 |
0.412 |
|
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