Mathews KD - Search Results

1

Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies.

Michele DE, Barresi R, Kanagawa M, Saito F, Cohn RD, Satz JS, Dollar J, Nishino I, Kelley RI, Somer H, Straub V, Mathews KD, Moore SA, Campbell KP. Michele DE, et al. Among authors: mathews kd. Nature. 2002 Jul 25;418(6896):417-22. doi: 10.1038/nature00837. Nature. 2002. PMID: 12140558

2

A syntrophin gene maps to mouse chromosome 8 and is not the myodystrophy gene.

Mills KA, Sunada Y, Campbell KP, Mathews KD. Mills KA, et al. Among authors: mathews kd. Mamm Genome. 1995 Sep;6(9):664-5. doi: 10.1007/BF00352377. Mamm Genome. 1995. PMID: 8535078 No abstract available.

3

Presentation, management and follow-up of Schilder's disease.

Garell PC, Menezes AH, Baumbach G, Moore SA, Nelson G, Mathews K, Afifi AK. Garell PC, et al. Pediatr Neurosurg. 1998 Aug;29(2):86-91. doi: 10.1159/000028695. Pediatr Neurosurg. 1998. PMID: 9792962 Review.

4

FSH dystrophy 4q35 deletion in patients presenting with facial-sparing scapular myopathy.

Felice KJ, North WA, Moore SA, Mathews KD. Felice KJ, et al. Among authors: mathews kd. Neurology. 2000 May 23;54(10):1927-31. doi: 10.1212/wnl.54.10.1927. Neurology. 2000. PMID: 10822431

5

Limb-girdle muscular dystrophies.

Piccolo F, Moore SA, Mathews KD, Campbell KP. Piccolo F, et al. Among authors: mathews kd. Adv Neurol. 2002;88:273-91. Adv Neurol. 2002. PMID: 11908231 Review. No abstract available.

6

Limb-girdle muscular dystrophy.

Mathews KD, Moore SA. Mathews KD, et al. Curr Neurol Neurosci Rep. 2003 Jan;3(1):78-85. doi: 10.1007/s11910-003-0042-9. Curr Neurol Neurosci Rep. 2003. PMID: 12507416 Review.

7

Multiminicore myopathy, central core disease, malignant hyperthermia susceptibility, and RYR1 mutations: one disease with many faces?

Mathews KD, Moore SA. Mathews KD, et al. Arch Neurol. 2004 Jan;61(1):27-9. doi: 10.1001/archneur.61.1.27. Arch Neurol. 2004. PMID: 14732615 Review. No abstract available.

8

Limb-girdle muscular dystrophy in the United States.

Moore SA, Shilling CJ, Westra S, Wall C, Wicklund MP, Stolle C, Brown CA, Michele DE, Piccolo F, Winder TL, Stence A, Barresi R, King N, King W, Florence J, Campbell KP, Fenichel GM, Stedman HH, Kissel JT, Griggs RC, Pandya S, Mathews KD, Pestronk A, Serrano C, Darvish D, Mendell JR. Moore SA, et al. Among authors: mathews kd. J Neuropathol Exp Neurol. 2006 Oct;65(10):995-1003. doi: 10.1097/01.jnen.0000235854.77716.6c. J Neuropathol Exp Neurol. 2006. PMID: 17021404

9

Exercise-induced left ventricular systolic dysfunction in women heterozygous for dystrophinopathy.

Weiss RM, Kerber RE, Jones JK, Stephan CM, Trout CJ, Lindower PD, Staffey KS, Campbell KP, Mathews KD. Weiss RM, et al. Among authors: mathews kd. J Am Soc Echocardiogr. 2010 Aug;23(8):848-53. doi: 10.1016/j.echo.2010.05.007. Epub 2010 Jun 19. J Am Soc Echocardiogr. 2010. PMID: 20646909 Free PMC article.

10

Myoglobinuria and muscle pain are common in patients with limb-girdle muscular dystrophy 2I.

Mathews KD, Stephan CM, Laubenthal K, Winder TL, Michele DE, Moore SA, Campbell KP. Mathews KD, et al. Neurology. 2011 Jan 11;76(2):194-5. doi: 10.1212/WNL.0b013e3182061ad4. Neurology. 2011. PMID: 21220724 Free PMC article. No abstract available.

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