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Neuromuscular Disorders : NMD|October 26, 2002
Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish familiesGeorgios M Hadjigeorgiou, Menachem Sadeh, Olimpia Musumeci, et al.Neuromuscular Disorders : NMD|December 4, 2001
Autosomal dominant Emery-Dreifuss muscular dystrophy: a new family with late diagnosisJ Colomer, C Iturriaga, G Bonne, et al.Neuromuscular Disorders : NMD|December 4, 2001
Autosomal dominant distal spinal muscular atrophy: an Italian family not linked to 12q24 and 7p14M V De Angelis, V Gatta, L Stuppia, et al.Neuromuscular Disorders : NMD|December 4, 2001
Expression of dystrophin-associated proteins during neuronal differentiation of P19 embryonal carcinoma cellsMarina Ceccarini, Pompeo Macioce, Barbara Panetta, et al.Neuromuscular Disorders : NMD|December 4, 2001
A novel nonsense mutation (Q352X) in the mitochondrial cytochrome b gene associated with a combined deficiency of complexes I and IIIEleonora Lamantea, Franco Carrara, Caterina Mariotti, et al.Neuromuscular Disorders : NMD|December 4, 2001
A point mutation of mitochondrial ATPase 6 gene in Leigh syndromeMotohiro Akagi, Koji Inui, Hiroko Tsukamoto, et al.Neuromuscular Disorders : NMD|July 19, 2003
Facioscapulohumeral muscular dystrophy (FSHD) myoblasts demonstrate increased susceptibility to oxidative stressSara T Winokur, Kathy Barrett, Jorge H Martin, et al.Neuromuscular Disorders : NMD|December 7, 2002
Relocalization of neuronal nitric oxide synthase (nNOS) as a marker for complete restoration of the dystrophin associated protein complex in skeletal muscleKim E Wells, Silvia Torelli, Qi Lu, et al.Neuromuscular Disorders : NMD|December 7, 2002
Early and severe presentation of X-linked myotubular myopathy in a girl with skewed X-inactivationH Jungbluth, C A Sewry, A Buj-Bello, et al.Pageof 340