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Annals of Neurology|November 18, 2000

Multi-minicore disease--searching for boundaries: phenotype analysis of 38 casesA Ferreiro, B Estournet, D Chateau, et al.

Acta Neurologica Scandinavica|April 11, 2018

Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndromeN Witting, P Laforêt, N C Voermans, et al.

Neuromuscular Disorders : NMD|January 31, 2009

Four Caucasian patients with mutations in the fukutin gene and variable clinical phenotypeS Vuillaumier-Barrot, S Quijano-Roy, C Bouchet-Seraphin, et al.

Neurology|May 1, 1997

Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophyB Eymard, N B Romero, F Leturcq, et al.

European Journal of Neurology|February 14, 2018

Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.

European Journal of Neurology|October 14, 2020

Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathiesR Guimarães-Costa, G Fernández-Eulate, K Wahbi, et al.

Revue Neurologique|September 17, 2016

Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNCD Avila-Smirnow, L Gueneau, S Batonnet-Pichon, et al.

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Showing results (31-40 of 37) with videos related to

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You have reached the last page of results.This site can display upto 37 results.

Annals of Neurology|November 18, 2000

Multi-minicore disease--searching for boundaries: phenotype analysis of 38 casesA Ferreiro, B Estournet, D Chateau, et al.

Acta Neurologica Scandinavica|April 11, 2018

Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndromeN Witting, P Laforêt, N C Voermans, et al.

Neuromuscular Disorders : NMD|January 31, 2009

Four Caucasian patients with mutations in the fukutin gene and variable clinical phenotypeS Vuillaumier-Barrot, S Quijano-Roy, C Bouchet-Seraphin, et al.

Neurology|May 1, 1997

Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophyB Eymard, N B Romero, F Leturcq, et al.

European Journal of Neurology|February 14, 2018

Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.

European Journal of Neurology|October 14, 2020

Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathiesR Guimarães-Costa, G Fernández-Eulate, K Wahbi, et al.

Revue Neurologique|September 17, 2016

Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNCD Avila-Smirnow, L Gueneau, S Batonnet-Pichon, et al.

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