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Balance control impairments in Fabry disease

Frontiers in neurology, 2022-09, Vol.13, p.856946-856946

2022

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Intra-venous bevacizumab in hereditary hemorrhagic telangiectasia (HHT): A retrospective study of 46 patients

PloS one, 2017-11, Vol.12 (11), p.e0188943-e0188943

2017

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Validity of the global anti-phospholipid syndrome score to predict thrombosis: a prospective multicentre cohort study

Rheumatology, 2015-11, Vol.54 (11), p.2071-2075

2015

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Pulmonary hypertension subtypes associated with hereditary haemorrhagic telangiectasia: Haemodynamic profiles and survival probability

PloS one, 2017-10, Vol.12 (10), p.e0184227-e0184227

2017

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Lack of correlation between the ventilatory response to CO2 and lung function impairment in myotonic dystrophy patients: Evidence for a dysregulation at central level

Neuromuscular disorders : NMD, 2015-05, Vol.25 (5), p.403-408

2015

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The French Gaucher's disease registry: clinical characteristics, complications and treatment of 562 patients

Orphanet journal of rare diseases, 2012-10, Vol.7 (1), p.77-77

2012

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Exertional Heat Stroke and Susceptibility to Malignant Hyperthermia in an Athlete: Evidence for a Link?

Journal of athletic training, 2015-11, Vol.50 (11), p.1212-1214

2015

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Atrial Flutter or Fibrillation is the Most Frequent and Life-Threatening Arrhythmia in Myotonic Dystrophy

Pacing and clinical electrophysiology, 2014-03, Vol.37 (3), p.329-335

2014

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Age, conduction defects and restrictive lung disease independently predict cardiac events and death in myotonic dystrophy

International journal of cardiology, 2013-01, Vol.162 (3), p.172-178

2013

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Subacute myopathy in a mature patient due to multiple acyl‐coenzyme a dehydrogenase deficiency

Muscle & nerve, 2011-03, Vol.43 (3), p.444-446

2011

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Iliopsoas Hematoma in Gaucher's Disease

Internal Medicine, 2011, Vol.50(21), pp.2643-2647

2011

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Leukocyte Differential for Acute Abdominal Pain in Adults

Laboratory hematology, 2011-03, Vol.17 (1), p.1-5

2011

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Stratégies thérapeutiques actuelles dans les maladies lysosomales

La Presse médicale (1983), 2014-11, Vol.43 (11), p.1174-1184

2014

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Current therapeutic strategies in lysosomal disorders

La Presse médicale (1983), 2014-11, Vol.43 (11), p.1174-1184

2014

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Central nervous system involvement of granulomatosis with polyangiitis: clinical-radiological presentation distinguishes different outcomes

Rheumatology, 2015-03, Vol.54 (3), p.424-432

2015

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Angioedema induced by angiotensin converting enzyme inhibitors, potentiated by m-TOR inhibitors: successful treatment with icatibant

Intensive care medicine, 2014-06, Vol.40 (6), p.893-894

2014

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Stratégies thérapeutiques actuelles dans les maladies lysosomales

La Presse médicale (1983), 2014-11, Vol.43 (11), p.1174-1184

2014

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Health-related quality of life, remission and low lupus disease activity state in patients with systemic lupus erythematosus

Rheumatology (Oxford, England), 2024-05, Vol.63 (5), p.1447-1455

2024

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Responsiveness of the 36-item Short Form Health Survey and the Lupus Quality of Life questionnaire in SLE

Rheumatology (Oxford, England), 2015-05, Vol.54 (5), p.940-949

2015

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The mediating effect of fatigue in impaired quality of life in systemic lupus erythematosus: mediation analysis of the French EQUAL cohort

Rheumatology (Oxford, England), 2023-09, Vol.62 (9), p.3051-3058

2023

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Increasing risk of tumors in myotonic dystrophy type 1

La Presse médicale (1983), 2013-09, Vol.42 (9 Pt 1), p.e281-e284

2013

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Supine changes in lung function correlate with chronic respiratory failure in myotonic dystrophy patients

Respiratory physiology & neurobiology, 2014-03, Vol.193, p.43-51

2014

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Regional body composition and functional impairment in patients with myotonic dystrophy

Muscle & nerve, 2011-10, Vol.44 (4), p.503-508

2011

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Organ dysfunction and muscular disability in myotonic dystrophy type 1

Medicine (Baltimore), 2011-07, Vol.90 (4), p.262-268

2011

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Intra-venous bevacizumab in hereditary hemorrhagic telangiectasia

PloS one, 2017-11, Vol.12 (11), p.e0188943

2017

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Balance control impairments in Fabry disease

Intra-venous bevacizumab in hereditary hemorrhagic telangiectasia (HHT): A retrospective study of 46 patients

Validity of the global anti-phospholipid syndrome score to predict thrombosis: a prospective multicentre cohort study

Pulmonary hypertension subtypes associated with hereditary haemorrhagic telangiectasia: Haemodynamic profiles and survival probability

Lack of correlation between the ventilatory response to CO2 and lung function impairment in myotonic dystrophy patients: Evidence for a dysregulation at central level

The French Gaucher's disease registry: clinical characteristics, complications and treatment of 562 patients

Exertional Heat Stroke and Susceptibility to Malignant Hyperthermia in an Athlete: Evidence for a Link?

Atrial Flutter or Fibrillation is the Most Frequent and Life-Threatening Arrhythmia in Myotonic Dystrophy

Age, conduction defects and restrictive lung disease independently predict cardiac events and death in myotonic dystrophy

Subacute myopathy in a mature patient due to multiple acyl‐coenzyme a dehydrogenase deficiency

Iliopsoas Hematoma in Gaucher's Disease

Leukocyte Differential for Acute Abdominal Pain in Adults

Stratégies thérapeutiques actuelles dans les maladies lysosomales

Current therapeutic strategies in lysosomal disorders

Central nervous system involvement of granulomatosis with polyangiitis: clinical-radiological presentation distinguishes different outcomes

Angioedema induced by angiotensin converting enzyme inhibitors, potentiated by m-TOR inhibitors: successful treatment with icatibant

Stratégies thérapeutiques actuelles dans les maladies lysosomales

Health-related quality of life, remission and low lupus disease activity state in patients with systemic lupus erythematosus

Responsiveness of the 36-item Short Form Health Survey and the Lupus Quality of Life questionnaire in SLE

The mediating effect of fatigue in impaired quality of life in systemic lupus erythematosus: mediation analysis of the French EQUAL cohort

Increasing risk of tumors in myotonic dystrophy type 1

Supine changes in lung function correlate with chronic respiratory failure in myotonic dystrophy patients

Regional body composition and functional impairment in patients with myotonic dystrophy

Organ dysfunction and muscular disability in myotonic dystrophy type 1

Intra-venous bevacizumab in hereditary hemorrhagic telangiectasia

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