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Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2

Neurology, 2003-06, Vol.60 (11), p.1854

2003

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Immunohistochemical localization of cytokines, C5b-9 and ICAM-1 in peripheral nerve of Guillain–Barré Syndrome

Journal of the neurological sciences, 2000-03, Vol.174 (1), p.16-21

2000

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Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategy

Mitochondrion, 2008-03, Vol.8 (2), p.136-145

2008

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Block of neural Kv1.1 potassium channels for neuroinflammatory disease therapy

Annals of neurology, 2006-11, Vol.60 (5), p.586-596

2006

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Avant-propos. Myofasciites à macrophages

Revue neurologique, 2007, Vol.163 (10), p.979-980

2007

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Value of fetal autopsy after medical termination of pregnancy

Forensic science international, 2004-08, Vol.144 (1), p.7-10

2004

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‘Cap myopathy’: Case report of a family

Neuromuscular disorders : NMD, 2006-04, Vol.16 (4), p.277-281

2006

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Mitochondrial respiratory failure in skeletal muscle from patients with Parkinson's disease and multiple system atrophy

Journal of the neurological sciences, 1994-08, Vol.125 (1), p.95-101

1994

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Myopathy with lobulated muscle fibers: evidence for heterogeneous etiology and clinical presentation

Neuromuscular disorders : NMD, 2002, Vol.12 (1), p.4-12

2002

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Nécrose laminaire corticale : aspects en imagerie par résonance magnétique et étude anatomoclinique

Revue neurologique, 2007-03, Vol.163 (3), p.365-368

2007

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Fasciite avec éosinophilie : discussion de la responsabilité d’un inhibiteur de l’enzyme de conversion de l’angiotensine

Revue neurologique, 2007-02, Vol.163 (2), p.241-243

2007

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J - 22 Myosite à inclusions et poliomyélite : un cas

Revue neurologique, 2007-04, Vol.163 (4), p.98-98

2007

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Pièges diagnostiques dans les myopathies inflammatoires

Revue neurologique, 2007-04, Vol.163 (4), p.217-217

2007

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75 Prevalence of mitochondrial gene defects in maternally inherited diabetes and deafness and in neuromuscular presentations suggesting respiratory chain dysfunction: Screening of the entire mitochondrial genome in 100 patients

Mitochondrion, 2007-12, Vol.7 (6), p.426

2007

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X-linked myopathy with excessive autophagy: a clinicopathological study of five new families

Neuromuscular disorders : NMD, 2001-05, Vol.11 (4), p.376-388

2001

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Linear Insertion of Atrioventricular Valves without Septal Defect: A New Anatomical Landmark for Down’s Syndrome?

Fetal diagnosis and therapy, 2002-05, Vol.17 (3), p.188-192

2002

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Le syndrome d’Andersen : une forme particulière de paralysie périodique avec dysrythmie cardiaque

Revue neurologique, 2004, Vol.160 (5), p.38-42

2004

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Congenital myopathy with central cores and fingerprint bodies in association with malignant hyperthermia susceptibility

Neuromuscular disorders : NMD, 2001-09, Vol.11 (6), p.538-541

2001

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Erratum to ‘Sequence of expression of MyoD1 and various cell surface and cytoskeletal proteins in regenerating mouse muscle fibers following treatment with sodium dihydrogen phosphate’: [J. Neurol. Sci. 165 (1999) 106–115]

Journal of the neurological sciences, 1999-11, Vol.170 (2), p.149-149

1999

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Sequence of expression of MyoD1 and various cell surface and cytoskeletal proteins in regenerating mouse muscle fibers following treatment with sodium dihydrogen phosphate

Journal of the neurological sciences, 1999-06, Vol.165 (2), p.106-115

1999

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Sequence of expression of MyoD1 and various cell surface and cytoskeletal proteins in regenerating mouse muscle fibers following treatment with sodium dihydrogen phosphate

Journal of the neurological sciences, 1999-11, Vol.170 (2), p.151-160

1999

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Adult onset reducing body myopathy

Neuromuscular disorders : NMD, 1999-12, Vol.9 (8), p.580-586

1999

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Syndrome de Leigh avec déficit en cytochrome c oxydase lié à une mutation homozygote du gène SURF1

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2005-05, Vol.12 (5), p.568-571

2005

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Multinévrite sensitive et nodules cutanés

La revue de medecine interne, 2003-06, Vol.24, p.76s-76s

2003

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Magnetic resonance spectroscopy and histological study of tubular aggregates in a familial myopathy

Journal of the neurological sciences, 1996-07, Vol.139 (1), p.149-155

1996

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Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2

Immunohistochemical localization of cytokines, C5b-9 and ICAM-1 in peripheral nerve of Guillain–Barré Syndrome

Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategy

Block of neural Kv1.1 potassium channels for neuroinflammatory disease therapy

Avant-propos. Myofasciites à macrophages

Value of fetal autopsy after medical termination of pregnancy

‘Cap myopathy’: Case report of a family

Mitochondrial respiratory failure in skeletal muscle from patients with Parkinson's disease and multiple system atrophy

Myopathy with lobulated muscle fibers: evidence for heterogeneous etiology and clinical presentation

Nécrose laminaire corticale : aspects en imagerie par résonance magnétique et étude anatomoclinique

Fasciite avec éosinophilie : discussion de la responsabilité d’un inhibiteur de l’enzyme de conversion de l’angiotensine

J - 22 Myosite à inclusions et poliomyélite : un cas

Pièges diagnostiques dans les myopathies inflammatoires

75 Prevalence of mitochondrial gene defects in maternally inherited diabetes and deafness and in neuromuscular presentations suggesting respiratory chain dysfunction: Screening of the entire mitochondrial genome in 100 patients

X-linked myopathy with excessive autophagy: a clinicopathological study of five new families

Linear Insertion of Atrioventricular Valves without Septal Defect: A New Anatomical Landmark for Down’s Syndrome?

Le syndrome d’Andersen : une forme particulière de paralysie périodique avec dysrythmie cardiaque

Congenital myopathy with central cores and fingerprint bodies in association with malignant hyperthermia susceptibility

Erratum to ‘Sequence of expression of MyoD1 and various cell surface and cytoskeletal proteins in regenerating mouse muscle fibers following treatment with sodium dihydrogen phosphate’: [J. Neurol. Sci. 165 (1999) 106–115]

Sequence of expression of MyoD1 and various cell surface and cytoskeletal proteins in regenerating mouse muscle fibers following treatment with sodium dihydrogen phosphate

Sequence of expression of MyoD1 and various cell surface and cytoskeletal proteins in regenerating mouse muscle fibers following treatment with sodium dihydrogen phosphate

Adult onset reducing body myopathy

Syndrome de Leigh avec déficit en cytochrome c oxydase lié à une mutation homozygote du gène SURF1

Multinévrite sensitive et nodules cutanés

Magnetic resonance spectroscopy and histological study of tubular aggregates in a familial myopathy

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