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Clinical Pharmacology and Therapeutics
|
May 28, 2010
Long-term follow-up of bezafibrate treatment in patients with the myopathic form of carnitine palmitoyltransferase 2 deficiency
J P Bonnefont, J Bastin, P Laforêt, et al.
Revue Neurologique
|
October 16, 2018
Myopathy with MTCYB mutation mimicking Multiple Acyl-CoA Dehydrogenase Deficiency
E Kaphan, H Bou Ali, M Gastaldi, et al.
Neuromuscular Disorders : NMD
|
July 26, 2008
Electron microscopy in myofibrillar myopathies reveals clues to the mutated gene
K G Claeys, M Fardeau, R Schröder, et al.
Acta Neurologica Scandinavica
|
April 11, 2018
Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndrome
N Witting, P Laforêt, N C Voermans, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 24, 2014
Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolution
N Deconinck, P Richard, V Allamand, et al.
Journal of Neurology
|
September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations
N C Voermans, R C van der Bilt, J IJspeert, et al.
European Journal of Neurology
|
October 14, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathies
R 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 FLNC
D Avila-Smirnow, L Gueneau, S Batonnet-Pichon, et al.
Muscle & Nerve
|
April 7, 2026
Limb Girdle Muscular Dystrophy Associated With TRIM32 Variants: A National Cohort Study
Alexandre Guérémy, V Morel, T Stojkovic, et al.
Journal of Neuroimmunology
|
May 31, 2015
MuSK autoantibodies in myasthenia gravis detected by cell based assay--A multinational study
A I Tsonis, P Zisimopoulou, K Lazaridis, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Clinical Pharmacology and Therapeutics
|
May 28, 2010
Long-term follow-up of bezafibrate treatment in patients with the myopathic form of carnitine palmitoyltransferase 2 deficiency
J P Bonnefont, J Bastin, P Laforêt, et al.
Revue Neurologique
|
October 16, 2018
Myopathy with MTCYB mutation mimicking Multiple Acyl-CoA Dehydrogenase Deficiency
E Kaphan, H Bou Ali, M Gastaldi, et al.
Neuromuscular Disorders : NMD
|
July 26, 2008
Electron microscopy in myofibrillar myopathies reveals clues to the mutated gene
K G Claeys, M Fardeau, R Schröder, et al.
Acta Neurologica Scandinavica
|
April 11, 2018
Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndrome
N Witting, P Laforêt, N C Voermans, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 24, 2014
Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolution
N Deconinck, P Richard, V Allamand, et al.
Journal of Neurology
|
September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations
N C Voermans, R C van der Bilt, J IJspeert, et al.
European Journal of Neurology
|
October 14, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathies
R 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 FLNC
D Avila-Smirnow, L Gueneau, S Batonnet-Pichon, et al.
Muscle & Nerve
|
April 7, 2026
Limb Girdle Muscular Dystrophy Associated With TRIM32 Variants: A National Cohort Study
Alexandre Guérémy, V Morel, T Stojkovic, et al.
Journal of Neuroimmunology
|
May 31, 2015
MuSK autoantibodies in myasthenia gravis detected by cell based assay--A multinational study
A I Tsonis, P Zisimopoulou, K Lazaridis, et al.
Page
of 3