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Items: 1 to 50 of 239

1.

Clinical and serologic remission of acquired myasthenia gravis in a domestic ferret (Mustela putorius furo).

Papageorgiou S, Gnirs K, Quinton JF, Shelton GD.

J Am Vet Med Assoc. 2019 May 15;254(10):1192-1195. doi: 10.2460/javma.254.10.1192.

PMID:
31039095
2.

Author Correction: Applications and efficiencies of the first cat 63 K DNA array.

Gandolfi B, Alhaddad H, Abdi M, Bach LH, Creighton EK, Davis BW, Decker JE, Dodman NH, Ginns EI, Grahn JC, Grahn RA, Haase B, Haggstrom J, Hamilton MJ, Helps CR, Kurushima JD, Lohi H, Longeri M, Malik R, Meurs KM, Montague MJ, Mullikin JC, Murphy WJ, Nilson SM, Pedersen NC, Peterson CB, Rusbridge C, Saif R, Shelton GD, Warren WC, Wasim M, Lyons LA.

Sci Rep. 2019 Mar 12;9(1):4664. doi: 10.1038/s41598-018-38073-6.

3.

A glycine transporter SLC6A5 frameshift mutation causes startle disease in Spanish greyhounds.

Murphy SC, Recio A, de la Fuente C, Guo LT, Shelton GD, Clark LA.

Hum Genet. 2019 May;138(5):509-513. doi: 10.1007/s00439-019-01986-x. Epub 2019 Mar 7.

PMID:
30847549
4.

A QIL1 Variant Associated with Ventricular Arrhythmias and Sudden Cardiac Death in the Juvenile Rhodesian Ridgeback Dog.

Meurs KM, Friedenberg SG, Olby NJ, Condit J, Weidman J, Rosenthal S, Shelton GD.

Genes (Basel). 2019 Feb 21;10(2). pii: E168. doi: 10.3390/genes10020168.

5.

A missense variant in the titin gene in Doberman pinscher dogs with familial dilated cardiomyopathy and sudden cardiac death.

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.

Hum Genet. 2019 May;138(5):515-524. doi: 10.1007/s00439-019-01973-2. Epub 2019 Feb 4.

PMID:
30715562
6.

Two mixed breed dogs with sensory neuropathy are homozygous for an inversion disrupting FAM134B previously identified in Border Collies.

Amengual-Batle P, Rusbridge C, José-López R, Golini L, Shelton GD, Mellersh CS, Gutierrez-Quintana R.

J Vet Intern Med. 2018 Nov;32(6):2082-2087. doi: 10.1111/jvim.15312. Epub 2018 Oct 11.

7.

Author Correction: Applications and efficiencies of the first cat 63K DNA array.

Gandolfi B, Alhaddad H, Abdi M, Bach LH, Creighton EK, Davis BW, Decker JE, Dodman NH, Ginns EI, Grahn JC, Grahn RA, Haase B, Haggstrom J, Hamilton MJ, Helps CR, Kurushima JD, Lohi H, Longeri M, Malik R, Meurs KM, Montague MJ, Mullikin JC, Murphy WJ, Nilson SM, Pedersen NC, Peterson CB, Rusbridge C, Saif R, Shelton GD, Warren WC, Wasim M, Lyons LA.

Sci Rep. 2018 Jun 4;8(1):8746. doi: 10.1038/s41598-018-26885-5.

8.

Trismus, masticatory myositis and antibodies against type 2M fibers in a mixed breed cat.

Blazejewski SW, Shelton GD.

JFMS Open Rep. 2018 Apr 26;4(1):2055116918764993. doi: 10.1177/2055116918764993. eCollection 2018 Jan-Jun.

9.

Applications and efficiencies of the first cat 63K DNA array.

Gandolfi B, Alhaddad H, Abdi M, Bach LH, Creighton EK, Davis BW, Decker JE, Dodman NH, Ginns EI, Grahn JC, Grahn RA, Haase B, Haggstrom J, Hamilton MJ, Helps CR, Kurushima JD, Lohi H, Longeri M, Malik R, Meurs KM, Montague MJ, Mullikin JC, Murphy WJ, Nilson SM, Pedersen NC, Peterson CB, Rusbridge C, Saif R, Shelton GD, Warren WC, Wasim M, Lyons LA.

Sci Rep. 2018 May 4;8(1):7024. doi: 10.1038/s41598-018-25438-0. Erratum in: Sci Rep. 2018 Jun 4;8(1):8746. Sci Rep. 2019 Mar 12;9(1):4664.

10.

Canine NAPEPLD-associated models of human myelin disorders.

Minor KM, Letko A, Becker D, Drögemüller M, Mandigers PJJ, Bellekom SR, Leegwater PAJ, Stassen QEM, Putschbach K, Fischer A, Flegel T, Matiasek K, Ekenstedt KJ, Furrow E, Patterson EE, Platt SR, Kelly PA, Cassidy JP, Shelton GD, Lucot K, Bannasch DL, Martineau H, Muir CF, Priestnall SL, Henke D, Oevermann A, Jagannathan V, Mickelson JR, Drögemüller C.

Sci Rep. 2018 Apr 11;8(1):5818. doi: 10.1038/s41598-018-23938-7.

11.

Myositis, Ganglioneuritis, and Myocarditis with Distinct Perifascicular Muscle Atrophy in a 2-Year-Old Male Boxer.

Rossman PM, Thomovsky SA, Schafbuch RM, Guo LT, Shelton GD.

Front Vet Sci. 2018 Feb 20;5:20. doi: 10.3389/fvets.2018.00020. eCollection 2018.

12.

Clinical and genetic characterisation of dystrophin-deficient muscular dystrophy in a family of Miniature Poodle dogs.

Sánchez L, Beltrán E, de Stefani A, Guo LT, Shea A, Shelton GD, De Risio L, Burmeister LM.

PLoS One. 2018 Feb 23;13(2):e0193372. doi: 10.1371/journal.pone.0193372. eCollection 2018.

13.

What Is Your Neurologic Diagnosis?

Kowal JB, Thomovsky SA, Shelton GD, Bentley RT.

J Am Vet Med Assoc. 2018 Feb 15;252(4):405-408. doi: 10.2460/javma.252.4.405. No abstract available.

PMID:
29393743
14.

Dysphagia and esophageal dysfunction due to dystrophin deficient muscular dystrophy in a male Spanish water spaniel.

McAtee BB, Heseltine JC, Guo LT, Willard MD, Shelton GD.

Vet Q. 2018 Dec;38(1):28-32. doi: 10.1080/01652176.2018.1435939. No abstract available.

PMID:
29384432
15.

Late-onset Becker-type muscular dystrophy in a Border terrier dog.

Jeandel A, Garosi LS, Davies L, Guo LT, Salgüero R, Shelton GD.

J Small Anim Pract. 2018 Jan 29. doi: 10.1111/jsap.12824. [Epub ahead of print]

PMID:
29377139
16.

Dysphagia secondary to focal inflammatory myopathy and consequent dorsiflexion of the tongue in a dog.

Strøm PC, Marks SL, Rivera JA, Shelton GD.

J Small Anim Pract. 2018 Nov;59(11):714-718. doi: 10.1111/jsap.12819. Epub 2018 Jan 22.

PMID:
29355995
17.

AAVrh10 Gene Therapy Ameliorates Central and Peripheral Nervous System Disease in Canine Globoid Cell Leukodystrophy (Krabbe Disease).

Bradbury AM, Rafi MA, Bagel JH, Brisson BK, Marshall MS, Pesayco Salvador J, Jiang X, Swain GP, Prociuk ML, ODonnell PA, Fitzgerald C, Ory DS, Bongarzone ER, Shelton GD, Wenger DA, Vite CH.

Hum Gene Ther. 2018 Jul;29(7):785-801. doi: 10.1089/hum.2017.151. Epub 2018 Mar 14.

PMID:
29316812
18.

Congenital Myasthenic Syndrome in a Mixed Breed Dog.

Blakey TJ, Michaels JR, Guo LT, Hodshon AJ, Shelton GD.

Front Vet Sci. 2017 Oct 17;4:173. doi: 10.3389/fvets.2017.00173. eCollection 2017.

19.

A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs.

Becker D, Minor KM, Letko A, Ekenstedt KJ, Jagannathan V, Leeb T, Shelton GD, Mickelson JR, Drögemüller C.

BMC Genomics. 2017 Aug 25;18(1):662. doi: 10.1186/s12864-017-4081-z.

20.

Exome sequencing reveals independent SGCD deletions causing limb girdle muscular dystrophy in Boston terriers.

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.

Skelet Muscle. 2017 Jul 11;7(1):15. doi: 10.1186/s13395-017-0131-0.

21.

Evaluation of coexisting polymyositis in feline myasthenia gravis: A case series.

Mayousse V, Jeandel A, Blanchard-Gutton N, Escriou C, Gnirs K, Shelton GD, Blot S.

Neuromuscul Disord. 2017 Sep;27(9):804-815. doi: 10.1016/j.nmd.2017.06.006. Epub 2017 Jun 16.

PMID:
28687435
22.

Association of early onset myasthenia gravis in Newfoundland dogs with the canine major histocompatibility complex class I.

Wolf Z, Vernau K, Safra N, Shelton GD, King J, Owen J, Weich K, Bannasch D.

Neuromuscul Disord. 2017 May;27(5):409-416. doi: 10.1016/j.nmd.2017.01.020. Epub 2017 Jan 30.

PMID:
28262470
23.

Clinical Phenotype of Musladin-Lueke Syndrome in 2 Beagles.

Packer RA, Logan MA, Guo LT, Apte SS, Bader H, O'Brien DP, Johnson G, Shelton GD.

J Vet Intern Med. 2017 Mar;31(2):532-538. doi: 10.1111/jvim.14654. Epub 2017 Feb 3.

24.

Border Collie Collapse: Owner Survey Results and Veterinary Description of Videotaped Episodes.

Taylor S, Minor K, Shmon CL, Shelton GD, Patterson EE, Mickelson JR.

J Am Anim Hosp Assoc. 2016 Nov/Dec;52(6):364-370. Epub 2016 Sep 29.

PMID:
27685362
25.

An Inversion Disrupting FAM134B Is Associated with Sensory Neuropathy in the Border Collie Dog Breed.

Forman OP, Hitti RJ, Pettitt L, Jenkins CA, O'Brien DP, Shelton GD, De Risio L, Quintana RG, Beltran E, Mellersh C.

G3 (Bethesda). 2016 Sep 8;6(9):2687-92. doi: 10.1534/g3.116.027896.

26.

Evaluation of Dogs with Border Collie Collapse, Including Response to Two Standardized Strenuous Exercise Protocols.

Taylor S, Shmon C, Su L, Epp T, Minor K, Mickelson J, Patterson E, Shelton GD.

J Am Anim Hosp Assoc. 2016 Sep-Oct;52(5):281-90. doi: 10.5326/JAAHA-MS-6361. Epub 2016 Aug 3.

PMID:
27487345
27.

Total laryngectomy for management of chronic aspiration pneumonia in a myopathic dog.

Vernau KM, Marks SL, Kuhn MA, Culp WT, Owens TJ, Shelton GD, Siddiqui T, Pollard R, Belafsky PC.

Can Vet J. 2016 Jul;57(7):761-6.

28.

Major Histocompatibility Complex I and II Expression and Lymphocytic Subtypes in Muscle of Horses with Immune-Mediated Myositis.

Durward-Akhurst SA, Finno CJ, Barnes N, Shivers J, Guo LT, Shelton GD, Valberg SJ.

J Vet Intern Med. 2016 Jul;30(4):1313-21. doi: 10.1111/jvim.14371. Epub 2016 Jun 28.

29.

Exome sequencing reveals a nebulin nonsense mutation in a dog model of nemaline myopathy.

Evans JM, Cox ML, Huska J, Li F, Gaitero L, Guo LT, Casal ML, Granzier HL, Shelton GD, Clark LA.

Mamm Genome. 2016 Oct;27(9-10):495-502. doi: 10.1007/s00335-016-9644-9. Epub 2016 May 23.

30.

Myasthenia gravis and congenital myasthenic syndromes in dogs and cats: A history and mini-review.

Shelton GD.

Neuromuscul Disord. 2016 Jun;26(6):331-4. doi: 10.1016/j.nmd.2016.03.002. Epub 2016 Mar 10. Review.

PMID:
27080328
31.

A Homozygous RAB3GAP1:c.743delC Mutation in Rottweilers with Neuronal Vacuolation and Spinocerebellar Degeneration.

Mhlanga-Mutangadura T, Johnson GS, Ashwini A, Shelton GD, Wennogle SA, Johnson GC, Kuroki K, O'Brien DP.

J Vet Intern Med. 2016 May;30(3):813-8. doi: 10.1111/jvim.13921. Epub 2016 Mar 10.

32.

Distal polyneuropathy in an adult Birman cat with toxoplasmosis.

Mari L, Shelton GD, De Risio L.

JFMS Open Rep. 2016 Feb 10;2(1):2055116916630335. doi: 10.1177/2055116916630335. eCollection 2016 Jan-Jun.

33.

Metabolic Encephalopathy and Lipid Storage Myopathy Associated with a Presumptive Mitochondrial Fatty Acid Oxidation Defect in a Dog.

Biegen VR, McCue JP, Donovan TA, Shelton GD.

Front Vet Sci. 2015 Nov 26;2:64. doi: 10.3389/fvets.2015.00064. eCollection 2015.

34.

A mutation in the Warburg syndrome gene, RAB3GAP1, causes a similar syndrome with polyneuropathy and neuronal vacuolation in Black Russian Terrier dogs.

Mhlanga-Mutangadura T, Johnson GS, Schnabel RD, Taylor JF, Johnson GC, Katz ML, Shelton GD, Lever TE, Giuliano E, Granger N, Shomper J, O'Brien DP.

Neurobiol Dis. 2016 Feb;86:75-85. doi: 10.1016/j.nbd.2015.11.016. Epub 2015 Nov 25.

35.

Acetazolamide-responsive paroxysmal dyskinesia in a 12-week-old female golden retriever dog.

Royaux E, Bhatti S, Harvey R, Garosi L, Shelton GD, Van Ham L.

Vet Q. 2016;36(1):45-9. doi: 10.1080/01652176.2015.1123822. Epub 2015 Dec 24. No abstract available.

PMID:
26598936
36.

A RAB3GAP1 SINE Insertion in Alaskan Huskies with Polyneuropathy, Ocular Abnormalities, and Neuronal Vacuolation (POANV) Resembling Human Warburg Micro Syndrome 1 (WARBM1).

Wiedmer M, Oevermann A, Borer-Germann SE, Gorgas D, Shelton GD, Drögemüller M, Jagannathan V, Henke D, Leeb T.

G3 (Bethesda). 2015 Nov 23;6(2):255-62. doi: 10.1534/g3.115.022707.

37.

A CHRNE frameshift mutation causes congenital myasthenic syndrome in young Jack Russell Terriers.

Rinz CJ, Lennon VA, James F, Thoreson JB, Tsai KL, Starr-Moss AN, Humphries HD, Guo LT, Palmer AC, Clark LA, Shelton GD.

Neuromuscul Disord. 2015 Dec;25(12):921-7. doi: 10.1016/j.nmd.2015.09.005. Epub 2015 Sep 8.

PMID:
26429099
38.

COLQ variant associated with Devon Rex and Sphynx feline hereditary myopathy.

Gandolfi B, Grahn RA, Creighton EK, Williams DC, Dickinson PJ, Sturges BK, Guo LT, Shelton GD, Leegwater PA, Longeri M, Malik R, Lyons LA.

Anim Genet. 2015 Dec;46(6):711-5. doi: 10.1111/age.12350. Epub 2015 Sep 16.

39.

Risk Factors and Outcomes in Cats with Acquired Myasthenia Gravis (2001-2012).

Hague DW, Humphries HD, Mitchell MA, Shelton GD.

J Vet Intern Med. 2015 Sep-Oct;29(5):1307-12. doi: 10.1111/jvim.13596. Epub 2015 Aug 26.

40.

Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype.

Vieira NM, Guo LT, Estrela E, Kunkel LM, Zatz M, Shelton GD.

Neuromuscul Disord. 2015 May;25(5):363-70. doi: 10.1016/j.nmd.2015.02.012. Epub 2015 Mar 3.

PMID:
25813339
41.

X-linked myotubular myopathy in Rottweiler dogs is caused by a missense mutation in Exon 11 of the MTM1 gene.

Shelton GD, Rider BE, Child G, Tzannes S, Guo LT, Moghadaszadeh B, Troiano EC, Haase B, Wade CM, Beggs AH.

Skelet Muscle. 2015 Jan 27;5(1):1. doi: 10.1186/s13395-014-0025-3. eCollection 2015.

42.

Nitrocobinamide, a new cyanide antidote that can be administered by intramuscular injection.

Chan A, Jiang J, Fridman A, Guo LT, Shelton GD, Liu MT, Green C, Haushalter KJ, Patel HH, Lee J, Yoon D, Burney T, Mukai D, Mahon SB, Brenner M, Pilz RB, Boss GR.

J Med Chem. 2015 Feb 26;58(4):1750-9. doi: 10.1021/jm501565k. Epub 2015 Feb 16.

43.

Dystrophin-deficient muscular dystrophy in two lurcher siblings.

Giannasi C, Tappin SW, Guo LT, Shelton GD, Palus V.

J Small Anim Pract. 2015 Sep;56(9):577-80. doi: 10.1111/jsap.12331. Epub 2015 Jan 27.

PMID:
25622540
44.

Clinical phenotype of X-linked myotubular myopathy in Labrador Retriever puppies.

Snead EC, Taylor SM, van der Kooij M, Cosford K, Beggs AH, Shelton GD.

J Vet Intern Med. 2015 Jan;29(1):254-60. doi: 10.1111/jvim.12513. Epub 2015 Jan 8.

45.

Muscular dystrophy due to a sarcoglycan deficiency in a female Dobermann dog.

Munday JS, Shelton GD, Willox S, Kingsbury DD.

J Small Anim Pract. 2015 Jun;56(6):414-6. doi: 10.1111/jsap.12306. Epub 2014 Dec 5.

PMID:
25482856
46.

Suspected congenital centronuclear myopathy in an Arabian-cross foal.

Polle F, Andrews FM, Gillon T, Eades SC, McConnico RS, Strain GM, Valberg SJ, Guo LT, Shelton GD.

J Vet Intern Med. 2014 Nov-Dec;28(6):1886-91. doi: 10.1111/jvim.12438. No abstract available.

47.

A novel mutation in CLCN1 associated with feline myotonia congenita.

Gandolfi B, Daniel RJ, O'Brien DP, Guo LT, Youngs MD, Leach SB, Jones BR, Shelton GD, Lyons LA.

PLoS One. 2014 Oct 30;9(10):e109926. doi: 10.1371/journal.pone.0109926. eCollection 2014.

48.

Dystrophin-deficient muscular dystrophy in a Norfolk terrier.

Beltran E, Shelton GD, Guo LT, Dennis R, Sanchez-Masian D, Robinson D, De Risio L.

J Small Anim Pract. 2015 May;56(5):351-4. doi: 10.1111/jsap.12292. Epub 2014 Oct 29.

PMID:
25353637
49.

An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogs.

Ekenstedt KJ, Becker D, Minor KM, Shelton GD, Patterson EE, Bley T, Oevermann A, Bilzer T, Leeb T, Drögemüller C, Mickelson JR.

PLoS Genet. 2014 Oct 2;10(10):e1004635. doi: 10.1371/journal.pgen.1004635. eCollection 2014 Oct.

50.

Sarcocystis caninum and Sarcocystis svanai n. spp. (Apicomplexa: Sarcocystidae) Associated with Severe Myositis and Hepatitis in the Domestic Dog (Canis familiaris).

Dubey JP, Sykes JE, Shelton GD, Sharp N, Verma SK, Calero-Bernal R, Viviano J, Sundar N, Khan A, Grigg ME.

J Eukaryot Microbiol. 2015 May-Jun;62(3):307-17. doi: 10.1111/jeu.12182. Epub 2014 Oct 27.

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