Mathews KD - Search Results

1

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.

2

Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35.

Mathews KD, Mills KA, Bosch EP, Ionasescu VV, Wiles KR, Buetow KH, Murray JC. Mathews KD, et al. Am J Hum Genet. 1992 Aug;51(2):428-31. Am J Hum Genet. 1992. PMID: 1642242 Free PMC article.

3

Phenotypic and pathologic evaluation of the myd mouse. A candidate model for facioscapulohumeral dystrophy.

Mathews KD, Rapisarda D, Bailey HL, Murray JC, Schelper RL, Smith R. Mathews KD, et al. J Neuropathol Exp Neurol. 1995 Jul;54(4):601-6. doi: 10.1093/whq/54.4.601. J Neuropathol Exp Neurol. 1995. PMID: 7602333

4

The molecular genetics of human facioscapulohumeral muscular dystrophy and the myodystrophy mouse model.

Mathews KD, Mills KA. Mathews KD, et al. Curr Opin Neurol. 1996 Oct;9(5):394-9. Curr Opin Neurol. 1996. PMID: 8894417 Review.

5

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.

6

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

7

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.

8

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

9

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.

10

Muscular dystrophy overview: genetics and diagnosis.

Mathews KD. Mathews KD. Neurol Clin. 2003 Nov;21(4):795-816. doi: 10.1016/s0733-8619(03)00065-3. Neurol Clin. 2003. PMID: 14743650 Review.

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