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X-chromosome inactivation in female patients with Fabry disease

Clinical genetics, 2016-01, Vol.89 (1), p.44-54

2016

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Classification of the cardiomyopathies: a position statement from the european society of cardiology working group on myocardial and pericardial diseases

European heart journal, 2008-01, Vol.29 (2), p.270-276

2008

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Long-term observational study of sporadic inclusion body myositis

Brain (London, England : 1878), 2011-11, Vol.134 (11), p.3176-3184

2011

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Triage strategy for urgent management of cardiac tamponade: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

European heart journal, 2014-09, Vol.35 (34), p.2279-2284

2014

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Eosinophilic fasciitis (Shulman disease): new insights into the therapeutic management from a series of 34 patients

Rheumatology (Oxford, England), 2012-03, Vol.51 (3), p.557-561

2012

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Developments in hereditary neuropathies

Revue neurologique, 2012-12, Vol.168 (12), p.983-985

Dubourg, O

2012

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Actualités dans les neuropathies héréditaires

Revue neurologique, 2012-12, Vol.168 (12), p.983-985

Dubourg, O.

2012

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Ischemic stroke: A not so unusual complication of SMART syndrome?

Revue neurologique, 2021-10, Vol.177 (8), p.1013-1015

2021

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Prevention of atrial fibrillation onset by beta-blocker treatment in heart failure: a meta-analysis

European heart journal, 2007-02, Vol.28 (4), p.457-462

2007

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Bilateral papillitis concomitant with cytomegalovirus primo-infection in an immunocompetent patient

Revue neurologique, 2021-04, Vol.177 (4), p.442-443

2021

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Gunshot suicides caused by cane-gun and alarm garden gun cannon: Two cases report.

Journal of forensic and legal medicine, 2021-01, Vol.77, p.102090-102090, Article 102090

2021

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La kétamine en pratique militaire

Douleur et analgésie, 2021-03, Vol.34 (1), p.46-52

2021

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New CT index to quantify arterial obstruction in pulmonary embolism: comparison with angiographic index and echocardiography

American journal of roentgenology (1976), 2001-06, Vol.176 (6), p.1415-1420

2001

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Sexually transmitted infections among victims attending a French sexual offence centre

Sexually transmitted infections, 2017-09, Vol.93 (6), p.451-451

2017

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Phenotypic spectrum of Charcot−Marie−Tooth disease due to LITAF/SIMPLE mutations: a study of 18 patients

European journal of neurology, 2017-03, Vol.24 (3), p.530-538

2017

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Pulmonary embolism detection: prospective evaluation of dual-section helical CT versus selective pulmonary arteriography in 157 patients

Radiology, 2000-11, Vol.217 (2), p.447-455

2000

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Oedematous myositis: An original subtype of autoimmune myopathy characterised by intense C5-b9 deposits

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S212-S212

2016

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Experience from clinical genetics in hypertrophic cardiomyopathy: proposal for new diagnostic criteria in adult members of affected families

Heart (British Cardiac Society), 1997-02, Vol.77 (2), p.130-132

1997

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Charcot–Marie–Tooth type 4B1 ( MTMR2 gene): Confounding clinical presentation and report of 5 original mutations

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S285-S285

2015

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Violence in schools: Prospective study conducted in an emergency reception center for victims of aggression

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2016-12, Vol.23 (12), p.1240-1246

2016

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Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations

Neurology, 2006-08, Vol.67 (4), p.602-606

2006

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Abnormal TDP-43 and FUS proteins in muscles of sporadic IBM: similarities in a TARDBP-linked ALS patient

Journal of neurology, neurosurgery and psychiatry, 2011-12, Vol.82 (12), p.1414-1416

2011

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Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1

Neurology, 2007-01, Vol.68 (4), p.295-297

2007

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Electron microscopy in myofibrillar myopathies reveals clues to the mutated gene

Neuromuscular disorders : NMD, 2008-08, Vol.18 (8), p.656-666

2008

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Stem cell transplantation in a patient with late-onset nemaline myopathy and gammopathy

Neurology, 2008-08, Vol.71 (7), p.531-532

2008

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X-chromosome inactivation in female patients with Fabry disease

Classification of the cardiomyopathies: a position statement from the european society of cardiology working group on myocardial and pericardial diseases

Long-term observational study of sporadic inclusion body myositis

Triage strategy for urgent management of cardiac tamponade: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

Eosinophilic fasciitis (Shulman disease): new insights into the therapeutic management from a series of 34 patients

Developments in hereditary neuropathies

Actualités dans les neuropathies héréditaires

Ischemic stroke: A not so unusual complication of SMART syndrome?

Prevention of atrial fibrillation onset by beta-blocker treatment in heart failure: a meta-analysis

Bilateral papillitis concomitant with cytomegalovirus primo-infection in an immunocompetent patient

Gunshot suicides caused by cane-gun and alarm garden gun cannon: Two cases report.

La kétamine en pratique militaire

New CT index to quantify arterial obstruction in pulmonary embolism: comparison with angiographic index and echocardiography

Sexually transmitted infections among victims attending a French sexual offence centre

Phenotypic spectrum of Charcot−Marie−Tooth disease due to LITAF/SIMPLE mutations: a study of 18 patients

Pulmonary embolism detection: prospective evaluation of dual-section helical CT versus selective pulmonary arteriography in 157 patients

Oedematous myositis: An original subtype of autoimmune myopathy characterised by intense C5-b9 deposits

Experience from clinical genetics in hypertrophic cardiomyopathy: proposal for new diagnostic criteria in adult members of affected families

Charcot–Marie–Tooth type 4B1 ( MTMR2 gene): Confounding clinical presentation and report of 5 original mutations

Violence in schools: Prospective study conducted in an emergency reception center for victims of aggression

Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations

Abnormal TDP-43 and FUS proteins in muscles of sporadic IBM: similarities in a TARDBP-linked ALS patient

Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1

Electron microscopy in myofibrillar myopathies reveals clues to the mutated gene

Stem cell transplantation in a patient with late-onset nemaline myopathy and gammopathy

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