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20 Mutual control of mitochondrial bioenergetics

Mitochondrion, 2007-12, Vol.7 (6), p.409

2007

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53 Bioenergetics of tumors: Investigation of mitochondrial function, structure and composition in human lung cancer

Mitochondrion, 2007-12, Vol.7 (6), p.419

2007

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Ataxie proprioceptive et carence en cuivre masquée

Revue neurologique, 2010-08, Vol.166 (8), p.734-736

2010

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Atteintes du système nerveux périphérique et du muscle squelettique au cours des paraplégies associées au virus HTLV1 : étude de 70 cas observés en Martinique

Revue neurologique, 1995, Vol.151 (3), p.190-195

1995

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AUTOSOMAL DOMINANT CEREBELLAR ATAXIA IN A CARIBBEAN FAMILY LINKED TO THE SCA 2 LOCUS ON CHROMOSOME 12q: PATHOLOGICAL STUDY OF TWO CASES

Journal of neuropathology and experimental neurology, 1995-05, Vol.54 (3), p.443

1995

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AUTOSOMAL DOMINANT CEREBELLAR ATAXIA IN A CARIBBEAN FAMILY LINKED TO THE SCA 2 LOCUS ON CHROMOSOME 12q: PATHOLOGICAL STUDY OF TWO CASES: 130

Journal of neuropathology and experimental neurology, 1995-05, Vol.54 (3), p.443-443

1995

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Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies) : clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families

Brain (London, England : 1878), 1995-12, Vol.118 (6), p.1573-1581

1995

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Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies) : genetic analysis of three unrelated SCA2 families

Human genetics, 1996-05, Vol.97 (5), p.671-676

1996

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Bioenergetics of lung tumors: Alteration of mitochondrial biogenesis and respiratory capacity

The international journal of biochemistry & cell biology, 2009-12, Vol.41 (12), p.2566-2577

2009

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Caractéristiques de la neurofibromatose de type 1 en Martinique : étude préliminaire

Annales de dermatologie et de vénéréologie, 2015-01, Vol.142 (1), p.50-51

2015

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Cerebrovascular complications of sickle-cell anemia

Revue neurologique, 1988, Vol.144 (8-9), p.465-473

1988

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Clinical characteristics of HTLV-1 associated dermato-polymyositis

Acta neurologica Scandinavica, 1995-09, Vol.92 (3), p.206-212

1995

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Clinical characteristics of HTLV-1 associated dermato-polymyositis : seven cases from Martinique

Acta neurologica Scandinavica, 1995-09, Vol.92 (3), p.206-212

1995

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Complications cérébro-vasculaires de la drépanocytose

Revue neurologique, 1988, Vol.144 (8-9), p.465-473

1988

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CONGENITAL MYOPATHIES (CNM)

Neuromuscular disorders : NMD, 2018-10, Vol.28, p.S71

2018

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CONGENITAL MYOPATHIES (CNM): P.140Clinical changes over time in a European and North-american cohort of patients with X-linked myotubular myopathy

Neuromuscular disorders : NMD, 2018-10, Vol.28, p.S71-S71

2018

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Current clinical management of CIDP with immunoglobulins in France: An expert opinion

Revue neurologique, 2023-10, Vol.179 (8), p.914-922

2023

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Different HLA class II (DRB1 and DQB1) alleles determine either susceptibility or resistance to NMO and multiple sclerosis among the French Afro-Caribbean population

Multiple sclerosis, 2011-01, Vol.17 (1), p.24-31

2011

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Direct Aldol-Reduction Process using Difluoromethyl Aryl Ketones and Aryl Aldehydes in the Presence of Potassium tert-Butoxide: One-Pot Efficient Stereoselective Synthesis of Symmetrical and Unsymmetrical anti-2,2-Difluoropropane-1,3-diols

Advanced synthesis & catalysis, 2010-11, Vol.352 (16), p.2787-2790

2010

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The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care

Orphanet journal of rare diseases, 2019-06

2019

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La dysphonie et les anticorps anti-MI2 sont indépendamment associés à la dysphagie au cours des myopathies inflammatoires en Martinique

La revue de medecine interne, 2024-06, Vol.45, p.A61-A62

2024

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Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene

Neuromuscular disorders : NMD, 2004, Vol.14 (1), p.10-18

2004

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Feeding mice with diets containing mercury-contaminated fish flesh from French Guiana: a model for the mercurial intoxication of the Wayana Amerindians

Environmental health, 2008-10, Vol.7 (1), p.53-53, Article 53

2008

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Functional dynamic compartmentalization of respiratory chain intermediate substrates: Implications for the control of energy production and mitochondrial diseases

The international journal of biochemistry & cell biology, 2008, Vol.40 (8), p.1543-1554

2008

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Guidance for the care of neuromuscular patients during the COVID-19 pandemic outbreak from the French Rare Health Care for Neuromuscular Diseases Network

Revue neurologique, 2020-06, Vol.176 (6), p.507-515

2020

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20 Mutual control of mitochondrial bioenergetics

53 Bioenergetics of tumors: Investigation of mitochondrial function, structure and composition in human lung cancer

Ataxie proprioceptive et carence en cuivre masquée

Atteintes du système nerveux périphérique et du muscle squelettique au cours des paraplégies associées au virus HTLV1 : étude de 70 cas observés en Martinique

AUTOSOMAL DOMINANT CEREBELLAR ATAXIA IN A CARIBBEAN FAMILY LINKED TO THE SCA 2 LOCUS ON CHROMOSOME 12q: PATHOLOGICAL STUDY OF TWO CASES

AUTOSOMAL DOMINANT CEREBELLAR ATAXIA IN A CARIBBEAN FAMILY LINKED TO THE SCA 2 LOCUS ON CHROMOSOME 12q: PATHOLOGICAL STUDY OF TWO CASES: 130

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies) : clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies) : genetic analysis of three unrelated SCA2 families

Bioenergetics of lung tumors: Alteration of mitochondrial biogenesis and respiratory capacity

Caractéristiques de la neurofibromatose de type 1 en Martinique : étude préliminaire

Cerebrovascular complications of sickle-cell anemia

Clinical characteristics of HTLV-1 associated dermato-polymyositis

Clinical characteristics of HTLV-1 associated dermato-polymyositis : seven cases from Martinique

Complications cérébro-vasculaires de la drépanocytose

CONGENITAL MYOPATHIES (CNM)

CONGENITAL MYOPATHIES (CNM): P.140Clinical changes over time in a European and North-american cohort of patients with X-linked myotubular myopathy

Current clinical management of CIDP with immunoglobulins in France: An expert opinion

Different HLA class II (DRB1 and DQB1) alleles determine either susceptibility or resistance to NMO and multiple sclerosis among the French Afro-Caribbean population

Direct Aldol-Reduction Process using Difluoromethyl Aryl Ketones and Aryl Aldehydes in the Presence of Potassium tert-Butoxide: One-Pot Efficient Stereoselective Synthesis of Symmetrical and Unsymmetrical anti-2,2-Difluoropropane-1,3-diols

The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care

La dysphonie et les anticorps anti-MI2 sont indépendamment associés à la dysphagie au cours des myopathies inflammatoires en Martinique

Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene

Feeding mice with diets containing mercury-contaminated fish flesh from French Guiana: a model for the mercurial intoxication of the Wayana Amerindians

Functional dynamic compartmentalization of respiratory chain intermediate substrates: Implications for the control of energy production and mitochondrial diseases

Guidance for the care of neuromuscular patients during the COVID-19 pandemic outbreak from the French Rare Health Care for Neuromuscular Diseases Network

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