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B Eymard

Showing results (141-150 of 160) with videos related to

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Neurology|August 28, 2002
Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophyA J van der Kooi, G Bonne, B Eymard, et al.
The Journal of Clinical Endocrinology and Metabolism|June 24, 2005
Breast inflammatory gigantomastia in a context of immune-mediated diseasesP Touraine, N Youssef, M A Alyanakian, et al.
Revue Neurologique|September 7, 2013
The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe diseaseP Laforêt, K Laloui, B Granger, et al.
Revue Neurologique|April 4, 2016
Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic diseaseA Béhin, C Acquaviva-Bourdain, S Souvannanorath, et al.
Revue Neurologique|January 29, 2005
[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations]R Ben Yaou, H-M Bécane, L Demay, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|December 24, 2014
Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolutionN Deconinck, P Richard, V Allamand, et al.
Journal of Neurology|September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigationsN C Voermans, R C van der Bilt, J IJspeert, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Towards the molecular elucidation of congenital myasthenic syndromes: identification of mutations in MuSKF Chevessier, B Faraut, A Ravel-Chapuis, et al.
Neurology|September 4, 2008
Distinct muscle imaging patterns in myofibrillar myopathiesD Fischer, R A Kley, K Strach, et al.
Pageof 16

Showing results (141-150 of 160) with videos related to

Sort By:
Pageof 16
Neurology|August 28, 2002
Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophyA J van der Kooi, G Bonne, B Eymard, et al.
The Journal of Clinical Endocrinology and Metabolism|June 24, 2005
Breast inflammatory gigantomastia in a context of immune-mediated diseasesP Touraine, N Youssef, M A Alyanakian, et al.
Revue Neurologique|September 7, 2013
The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe diseaseP Laforêt, K Laloui, B Granger, et al.
Revue Neurologique|April 4, 2016
Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic diseaseA Béhin, C Acquaviva-Bourdain, S Souvannanorath, et al.
Revue Neurologique|January 29, 2005
[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations]R Ben Yaou, H-M Bécane, L Demay, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|December 24, 2014
Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolutionN Deconinck, P Richard, V Allamand, et al.
Journal of Neurology|September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigationsN C Voermans, R C van der Bilt, J IJspeert, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Towards the molecular elucidation of congenital myasthenic syndromes: identification of mutations in MuSKF Chevessier, B Faraut, A Ravel-Chapuis, et al.
Neurology|September 4, 2008
Distinct muscle imaging patterns in myofibrillar myopathiesD Fischer, R A Kley, K Strach, et al.
Pageof 16