Valberg SJ - Search Results

1

Fatal infantile neuromuscular presentation of glycogen storage disease type IV.

Tay SK, Akman HO, Chung WK, Pike MG, Muntoni F, Hays AP, Shanske S, Valberg SJ, Mickelson JR, Tanji K, DiMauro S. Tay SK, et al. Among authors: valberg sj. Neuromuscul Disord. 2004 Apr;14(4):253-60. doi: 10.1016/j.nmd.2003.12.006. Neuromuscul Disord. 2004. PMID: 15019703

2

Cloning of bovine muscle glycogen phosphorylase cDNA and identification of a mutation in cattle with myophosphorylase deficiency, an animal model for McArdle's disease.

Tsujino S, Shanske S, Valberg SJ, Cardinet GH 3rd, Smith BP, DiMauro S. Tsujino S, et al. Among authors: valberg sj. Neuromuscul Disord. 1996 Jan;6(1):19-26. doi: 10.1016/0960-8966(95)00014-3. Neuromuscul Disord. 1996. PMID: 8845714

3

Insulin sensitivity and skeletal muscle glucose transport in horses with equine polysaccharide storage myopathy.

Annandale EJ, Valberg SJ, Mickelson JR, Seaquist ER. Annandale EJ, et al. Among authors: valberg sj. Neuromuscul Disord. 2004 Oct;14(10):666-74. doi: 10.1016/j.nmd.2004.05.007. Neuromuscul Disord. 2004. PMID: 15351424

4

Glycogen branching enzyme (GBE1) mutation causing equine glycogen storage disease IV.

Ward TL, Valberg SJ, Adelson DL, Abbey CA, Binns MM, Mickelson JR. Ward TL, et al. Among authors: valberg sj. Mamm Genome. 2004 Jul;15(7):570-7. doi: 10.1007/s00335-004-2369-1. Mamm Genome. 2004. PMID: 15366377

5

Polysaccharide storage myopathy phenotype in quarter horse-related breeds is modified by the presence of an RYR1 mutation.

McCue ME, Valberg SJ, Jackson M, Borgia L, Lucio M, Mickelson JR. McCue ME, et al. Among authors: valberg sj. Neuromuscul Disord. 2009 Jan;19(1):37-43. doi: 10.1016/j.nmd.2008.10.001. Epub 2008 Dec 3. Neuromuscul Disord. 2009. PMID: 19056269

6

Polysaccharide storage myopathy associated with recurrent exertional rhabdomyolysis in horses.

Valberg SJ, Cardinet GH 3rd, Carlson GP, DiMauro S. Valberg SJ, et al. Neuromuscul Disord. 1992;2(5-6):351-9. doi: 10.1016/s0960-8966(06)80006-4. Neuromuscul Disord. 1992. PMID: 1284408

7

Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosis.

McCue ME, Valberg SJ, Miller MB, Wade C, DiMauro S, Akman HO, Mickelson JR. McCue ME, et al. Among authors: valberg sj. Genomics. 2008 May;91(5):458-66. doi: 10.1016/j.ygeno.2008.01.011. Epub 2008 Mar 20. Genomics. 2008. PMID: 18358695 Free PMC article.

8

Glycogen synthase 1 (GYS1) mutation in diverse breeds with polysaccharide storage myopathy.

McCue ME, Valberg SJ, Lucio M, Mickelson JR. McCue ME, et al. Among authors: valberg sj. J Vet Intern Med. 2008 Sep-Oct;22(5):1228-33. doi: 10.1111/j.1939-1676.2008.0167.x. Epub 2008 Aug 6. J Vet Intern Med. 2008. PMID: 18691366 Free article.

9

The genetics of skeletal muscle disorders in horses.

Mickelson JR, Valberg SJ. Mickelson JR, et al. Among authors: valberg sj. Annu Rev Anim Biosci. 2015;3:197-217. doi: 10.1146/annurev-animal-022114-110653. Epub 2014 Sep 12. Annu Rev Anim Biosci. 2015. PMID: 25387114 Review.

10

Glycogen branching enzyme deficiency in quarter horse foals.

Valberg SJ, Ward TL, Rush B, Kinde H, Hiraragi H, Nahey D, Fyfe J, Mickelson JR. Valberg SJ, et al. J Vet Intern Med. 2001 Nov-Dec;15(6):572-80. doi: 10.1892/0891-6640(2001)015<0572:gbediq>2.3.co;2. J Vet Intern Med. 2001. PMID: 11817063 Free article.

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