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Muscle & Nerve. Supplement|January 1, 1995
Various classes of mutations in patients with phosphofructokinase deficiency (Tarui's disease)N Raben, J B Sherman, E Adams, et al.Muscle & Nerve. Supplement|January 1, 1995
A new variant case of muscle phosphofructokinase deficiency, coexisting with gastric ulcer, gouty arthritis, and increased hemolysisC Nakagawa, I Mineo, M Kaido, et al.Muscle & Nerve. Supplement|January 1, 1995
Genetic defects in patients with glycogenosis type II (acid maltase deficiency)N Raben, R C Nichols, C Boerkoel, et al.Muscle & Nerve. Supplement|January 1, 1995
Heteroplasmic mitochondrial tRNA(Lys) mutation and its complementation in MERRF patient-derived mitochondrial transformantsM Yoneda, T Miyatake, G AttardiMuscle & Nerve. Supplement|January 1, 1995
Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35J C van Deutekom, M H Hofker, S Romberg, et al.Muscle & Nerve. Supplement|January 1, 1995
Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analysesK Arahata, T Ishihara, H Fukunaga, et al.Muscle & Nerve. Supplement|January 1, 1995
Early onset facioscapulohumeral muscular dystrophyO F Brouwer, G W Padberg, E Bakker, et al.Muscle & Nerve. Supplement|January 1, 1995
Clinical variability of facioscapulohumeral muscular dystrophy in RussiaV M Kazakov, D I RudenkoMuscle & Nerve. Supplement|January 1, 1997
Clinicophysiologic concepts of spasticity and motor dysfunction in adults with an upper motoneuron lesionN H MayerPageof 11