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Cutis verticis gyrata : une dermatose finalement souvent primitive

Annales de Dermatologie et de Vénéréologie - FMC, 2022-11, Vol.2 (8), p.A208-A209

2022

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Koebner phenomenon in systemic lupus erythematosus after subcutaneous injections of methotrexate

Annales de dermatologie et de vénéréologie, 2022-06, Vol.149 (2), p.135-136

2022

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Atteinte cutanée périnéale gravissime de maladie de Crohn traitée par risankizumab

Annales de Dermatologie et de Vénéréologie - FMC, 2023-12, Vol.3 (8), p.A255-A256

2023

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Infection cutanée à Vibrio alginolyticus après séjour au Cap Ferret

Annales de Dermatologie et de Vénéréologie - FMC, 2023-12, Vol.3 (8), p.A222

2023

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Intérêt de la PCR digitale pour la détection d’ADN tumoral circulant dans les lymphomes cutanés diffus à grandes cellules de type jambe

Annales de Dermatologie et de Vénéréologie - FMC, 2023-12, Vol.3 (8), p.A156-A157

2023

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La Conférence de sept Parfums

2017

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Encorafénib-binimétinib : des résultats encourageants notamment en intracrânien

Annales de dermatologie et de vénéréologie, 2020-12, Vol.147 (12), p.A310-A311

2020

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Ophtalmoplégie isolée au cours d’un traitement par double immunothérapie pour un mélanome métastatique

La revue de medecine interne, 2019-12, Vol.40, p.A195-A195

2019

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Food processing and allergenicity

Food and chemical toxicology, 2015-06, Vol.80, p.223-240

2015

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An international compendium of mutations in the SCN5A -encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

Heart rhythm, 2010-01, Vol.7 (1), p.33-46

2010

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Influence of the water vapor on the activity of CuO/SBA-15 SOx adsorbents

Catalysis today, 2022-08, Vol.397-399, p.436-448

2022

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Study of the reversible/irreversible character of the deactivation of CuO/SBA–15 SOx adsorbents in wet conditions under SO2 adsorption/regeneration cycling experiments

Chemical engineering journal (Lausanne, Switzerland : 1996), 2022-12, Vol.450 (2), p.138056, Article 138056

2022

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Mutations in dynamin 2 cause dominant centronuclear myopathy

Nature genetics, 2005-11, Vol.37 (11), p.1207-1209

2005

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Mutations in the selenocysteine insertion sequence-binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans

The Journal of clinical investigation, 2010-12, Vol.120 (12), p.4220-4235

2010

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Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia

Circulation research, 2002-10, Vol.91 (8), p.e21-e26

2002

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SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome

Circulation. Cardiovascular genetics, 2009-12, Vol.2 (6), p.552-557

2009

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Correlative SICM‐FCM reveals changes in morphology and kinetics of endocytic pits induced by disease‐associated mutations in dynamin

The FASEB journal, 2019-07, Vol.33 (7), p.8504-8518

2019

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Toxicological evaluation of proteins introduced into food crops

Critical reviews in toxicology, 2013-11, Vol.43 (S2), p.25-42

2013

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Dynamin-2 mutations linked to Centronuclear Myopathy impair actin-dependent trafficking in muscle cells

Scientific reports, 2017-07, Vol.7 (1), p.4580-16, Article 4580

2017

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Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients

Journal of medical genetics, 2005-11, Vol.42 (11), p.863-870

2005

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Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization

Neuropathology and applied neurobiology, 2011-04, Vol.37 (3), p.271-284

2011

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R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation

Heart rhythm, 2011-01, Vol.8 (1), p.48-55

2011

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Mutations of the Selenoprotein N Gene, Which Is Implicated in Rigid Spine Muscular Dystrophy, Cause the Classical Phenotype of Multiminicore Disease: Reassessing the Nosology of Early-Onset Myopathies

American journal of human genetics, 2002-10, Vol.71 (4), p.739-749

2002

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Cutis verticis gyrata : une dermatose finalement souvent primitive

Koebner phenomenon in systemic lupus erythematosus after subcutaneous injections of methotrexate

Atteinte cutanée périnéale gravissime de maladie de Crohn traitée par risankizumab

Infection cutanée à Vibrio alginolyticus après séjour au Cap Ferret

Intérêt de la PCR digitale pour la détection d’ADN tumoral circulant dans les lymphomes cutanés diffus à grandes cellules de type jambe

La Conférence de sept Parfums

Encorafénib-binimétinib : des résultats encourageants notamment en intracrânien

Ophtalmoplégie isolée au cours d’un traitement par double immunothérapie pour un mélanome métastatique

Food processing and allergenicity

An international compendium of mutations in the SCN5A -encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

Influence of the water vapor on the activity of CuO/SBA-15 SOx adsorbents

Study of the reversible/irreversible character of the deactivation of CuO/SBA–15 SOx adsorbents in wet conditions under SO2 adsorption/regeneration cycling experiments

Mutations in dynamin 2 cause dominant centronuclear myopathy

Mutations in the selenocysteine insertion sequence-binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans

Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia

Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study

SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome

Correlative SICM‐FCM reveals changes in morphology and kinetics of endocytic pits induced by disease‐associated mutations in dynamin

Toxicological evaluation of proteins introduced into food crops

Dynamin-2 mutations linked to Centronuclear Myopathy impair actin-dependent trafficking in muscle cells

Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients

Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation

Mutations of the Selenoprotein N Gene, Which Is Implicated in Rigid Spine Muscular Dystrophy, Cause the Classical Phenotype of Multiminicore Disease: Reassessing the Nosology of Early-Onset Myopathies

Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes

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