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B Eymard

Showing results (111-120 of 160) with videos related to

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Circulation|September 1, 1996
Blunted coronary reserve in myotonic dystrophy. An early and gene-related phenomenonD Annane, P Merlet, H Radvanyi, et al.
Brain : a Journal of Neurology|March 6, 2007
Zaspopathy in a large classic late-onset distal myopathy familyR Griggs, A Vihola, P Hackman, et al.
Revue Neurologique|March 5, 2013
[Congenital myasthenic syndromes: difficulties in the diagnosis, course and prognosis, and therapy--The French National Congenital Myasthenic Syndrome Network experience]B Eymard, T Stojkovic, D Sternberg, et al.
Archives of Neurology|May 1, 1997
Localized proton magnetic resonance spectroscopy in patients with adult adrenoleukodystrophy. Increase of choline compounds in normal appearing white matterA Tourbah, J L Stievenart, M T Iba-Zizen, et al.
Revue Neurologique|March 6, 2003
[Exploration of exercise intolerance by 31P NMR spectroscopy of calf muscles coupled with MRI and ergometry]P Laforêt, C Wary, S Duteil, et al.
European Journal of Neurology|March 6, 2015
Diagnostic power of the non-ischaemic forearm exercise test in detecting glycogenosis type VJ-Y Hogrel, F van den Bogaart, I Ledoux, et al.
European Journal of Neurology|November 22, 2016
Prediction of long-term prognosis by heteroplasmy levels of the m.3243A>G mutation in patients with the mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndromeA Fayssoil, P Laforêt, W Bougouin, et al.
Archives of Physical Medicine and Rehabilitation|July 7, 2009
Periodic salbutamol in facioscapulohumeral muscular dystrophy: a randomized controlled trialC A Payan, J Y Hogrel, E H Hammouda, et al.
Neurology|May 29, 2008
Dilative arteriopathy and basilar artery dolichoectasia complicating late-onset Pompe diseaseP Laforêt, P Petiot, M Nicolino, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Impaired cerebral glucose metabolism in myotonic dystrophy: a triplet-size dependent phenomenonD Annane, M Fiorelli, B Mazoyer, et al.
Pageof 16

Showing results (111-120 of 160) with videos related to

Sort By:
Pageof 16
Circulation|September 1, 1996
Blunted coronary reserve in myotonic dystrophy. An early and gene-related phenomenonD Annane, P Merlet, H Radvanyi, et al.
Brain : a Journal of Neurology|March 6, 2007
Zaspopathy in a large classic late-onset distal myopathy familyR Griggs, A Vihola, P Hackman, et al.
Revue Neurologique|March 5, 2013
[Congenital myasthenic syndromes: difficulties in the diagnosis, course and prognosis, and therapy--The French National Congenital Myasthenic Syndrome Network experience]B Eymard, T Stojkovic, D Sternberg, et al.
Archives of Neurology|May 1, 1997
Localized proton magnetic resonance spectroscopy in patients with adult adrenoleukodystrophy. Increase of choline compounds in normal appearing white matterA Tourbah, J L Stievenart, M T Iba-Zizen, et al.
Revue Neurologique|March 6, 2003
[Exploration of exercise intolerance by 31P NMR spectroscopy of calf muscles coupled with MRI and ergometry]P Laforêt, C Wary, S Duteil, et al.
European Journal of Neurology|March 6, 2015
Diagnostic power of the non-ischaemic forearm exercise test in detecting glycogenosis type VJ-Y Hogrel, F van den Bogaart, I Ledoux, et al.
European Journal of Neurology|November 22, 2016
Prediction of long-term prognosis by heteroplasmy levels of the m.3243A>G mutation in patients with the mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndromeA Fayssoil, P Laforêt, W Bougouin, et al.
Archives of Physical Medicine and Rehabilitation|July 7, 2009
Periodic salbutamol in facioscapulohumeral muscular dystrophy: a randomized controlled trialC A Payan, J Y Hogrel, E H Hammouda, et al.
Neurology|May 29, 2008
Dilative arteriopathy and basilar artery dolichoectasia complicating late-onset Pompe diseaseP Laforêt, P Petiot, M Nicolino, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Impaired cerebral glucose metabolism in myotonic dystrophy: a triplet-size dependent phenomenonD Annane, M Fiorelli, B Mazoyer, et al.
Pageof 16