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Results: 1 to 20 of 198

1.

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.

2.

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.

PMID:
25650735
3.

Dystrophin-deficient muscular dystrophy in two lurcher siblings.

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

J Small Anim Pract. 2015 Jan 27. doi: 10.1111/jsap.12331. [Epub ahead of print]

PMID:
25622540
4.

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.

5.

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

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

J Small Anim Pract. 2014 Dec 5. doi: 10.1111/jsap.12306. [Epub ahead of print]

PMID:
25482856
6.

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.

PMID:
25410957
7.

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.

8.

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. 2014 Oct 29. doi: 10.1111/jsap.12292. [Epub ahead of print]

PMID:
25353637
9.

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.

10.

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. 2014 Sep 24. doi: 10.1111/jeu.12182. [Epub ahead of print]

PMID:
25256157
11.

Electrophysiologic confirmation of heterogenous motor polyneuropathy in young cats.

Aleman M, Dickinson PJ, Williams DC, Sturges BK, LeCouteur RA, Vernau KM, Shelton GD.

J Vet Intern Med. 2014 Nov-Dec;28(6):1789-98. doi: 10.1111/jvim.12439. Epub 2014 Sep 17.

PMID:
25231268
12.

A COLQ missense mutation in Labrador Retrievers having congenital myasthenic syndrome.

Rinz CJ, Levine J, Minor KM, Humphries HD, Lara R, Starr-Moss AN, Guo LT, Williams DC, Shelton GD, Clark LA.

PLoS One. 2014 Aug 28;9(8):e106425. doi: 10.1371/journal.pone.0106425. eCollection 2014.

13.

Identification of the mutation causing centronuclear myopathy in a border collie.

Eminaga S, Cherubini GB, Shelton GD.

Vet Rec. 2014 Aug 2;175(5):124. doi: 10.1136/vr.g4883. No abstract available.

PMID:
25081885
14.

Resolution of polyneuropathy in a hypothyroid dog following thyroid supplementation.

Utsugi S, Saito M, Shelton GD.

J Am Anim Hosp Assoc. 2014 Sep-Oct;50(5):345-9. doi: 10.5326/JAAHA-MS-6035. Epub 2014 Jul 15.

PMID:
25028439
15.

Necrotizing and eosinophilic masticatory myositis in farmed mink: a preliminary description.

Needle DB, Hollinger C, Shelton GD, Fitzgerald SD.

J Comp Pathol. 2014 Aug-Oct;151(2-3):217-27. doi: 10.1016/j.jcpa.2014.04.017. Epub 2014 Jul 10.

PMID:
25016423
16.

Disruption of both nesprin 1 and desmin results in nuclear anchorage defects and fibrosis in skeletal muscle.

Chapman MA, Zhang J, Banerjee I, Guo LT, Zhang Z, Shelton GD, Ouyang K, Lieber RL, Chen J.

Hum Mol Genet. 2014 Nov 15;23(22):5879-92. doi: 10.1093/hmg/ddu310. Epub 2014 Jun 18.

PMID:
24943590
17.

Muscle expression of mutant androgen receptor accounts for systemic and motor neuron disease phenotypes in spinal and bulbar muscular atrophy.

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.

Neuron. 2014 Apr 16;82(2):295-307. doi: 10.1016/j.neuron.2014.03.001.

PMID:
24742458
18.

Recurrent gastric dilatation and intestinal dysmotility possibly resulting from autonomic neuropathy in a Great Dane.

Spoo JW, Shelton GD.

J Am Anim Hosp Assoc. 2014 May-Jun;50(3):221-6. doi: 10.5326/JAAHA-MS-6176. Epub 2014 Mar 21.

PMID:
24659724
19.

Emergent presentation of a cat with dystrophin-deficient muscular dystrophy.

Gambino AN, Mouser PJ, Shelton GD, Winand NJ.

J Am Anim Hosp Assoc. 2014 Mar-Apr;50(2):130-5. doi: 10.5326/JAAHA-MS-5973. Epub 2014 Jan 20.

PMID:
24446404
20.

Characterization of thoracic motor and sensory neurons and spinal nerve roots in canine degenerative myelopathy, a potential disease model of amyotrophic lateral sclerosis.

Morgan BR, Coates JR, Johnson GC, Shelton GD, Katz ML.

J Neurosci Res. 2014 Apr;92(4):531-41. doi: 10.1002/jnr.23332. Epub 2013 Dec 21.

PMID:
24375814
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