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Cobblestone Malformation in LAMA2 Congenital Muscular Dystrophy (MDC1A).
Jayakody H, Zarei S, Nguyen H, Dalton J, Chen K, Hudgins L, Day J, Withrow K, Pandya A, Teasley J, Dobyns WB, Mathews KD, Moore SA. Jayakody H, et al. Among authors: moore sa. J Neuropathol Exp Neurol. 2020 Sep 1;79(9):998-1010. doi: 10.1093/jnen/nlaa062. J Neuropathol Exp Neurol. 2020. PMID: 32827036 Free PMC article.
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. Among authors: moore sa. Pediatr Neurosurg. 1998 Aug;29(2):86-91. doi: 10.1159/000028695. Pediatr Neurosurg. 1998. PMID: 9792962 Review.
Limb-girdle muscular dystrophies.
Piccolo F, Moore SA, Mathews KD, Campbell KP. Piccolo F, et al. Among authors: moore sa. Adv Neurol. 2002;88:273-91. Adv Neurol. 2002. PMID: 11908231 Review. No abstract available.
Limb-girdle muscular dystrophy.
Mathews KD, Moore SA. Mathews KD, et al. Among authors: moore sa. 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.
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. 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
Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severity.
Pace RA, Peat RA, Baker NL, Zamurs L, Mörgelin M, Irving M, Adams NE, Bateman JF, Mowat D, Smith NJ, Lamont PJ, Moore SA, Mathews KD, North KN, Lamandé SR. Pace RA, et al. Among authors: moore sa. Ann Neurol. 2008 Sep;64(3):294-303. doi: 10.1002/ana.21439. Ann Neurol. 2008. PMID: 18825676 Free PMC article.
617 results