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B Girerd

Showing results (1-10 of 9) with videos related to

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Revue Des Maladies Respiratoires|February 12, 2021
[Screening for pulmonary veno-occlusive disease: A specific approach]D Montani, B Girerd, M Humbert
European Respiratory Review : an Official Journal of the European Respiratory Society|October 20, 2010
Fatal rupture of pulmonary arteriovenous malformation in hereditary haemorrhagic telangiectasis and severe PAHD Montani, L C Price, B Girerd, et al.
The European Respiratory Journal|January 3, 2012
Circulating fibrocytes and pulmonary arterial hypertensionN Gambaryan, S Cohen-Kaminsky, D Montani, et al.
Clinical Pharmacology and Therapeutics|May 21, 2014
CYP2C9, SLCO1B1, SLCO1B3, and ABCB11 polymorphisms in patients with bosentan-induced liver toxicityM Roustit, X Fonrose, D Montani, et al.
Revue Des Maladies Respiratoires|February 13, 2016
Pulmonary complications of type 1 neurofibromatosisL Reviron-Rabec, B Girerd, A Seferian, et al.
Revue Des Maladies Respiratoires|March 5, 2018
[Pulmonary veno-occlusive disease]A Boucly, B Girerd, D Bourlier, et al.
Clinical Genetics|June 10, 2011
ACVRL1 germinal mosaic with two mutant alleles in hereditary hemorrhagic telangiectasia associated with pulmonary arterial hypertensionM Eyries, F Coulet, B Girerd, et al.
Arthritis and Rheumatism|June 18, 2010
Association of a KCNA5 gene polymorphism with systemic sclerosis-associated pulmonary arterial hypertension in the European Caucasian populationJ Wipff, P Dieudé, M Guedj, et al.
Revue Des Maladies Respiratoires|July 29, 2022
[French clinical practice guidelines for the diagnosis and management of lung disease with alpha 1-antitrypsin deficiency]J-F Mornex, M Balduyck, M Bouchecareilh, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Revue Des Maladies Respiratoires|February 12, 2021
[Screening for pulmonary veno-occlusive disease: A specific approach]D Montani, B Girerd, M Humbert
European Respiratory Review : an Official Journal of the European Respiratory Society|October 20, 2010
Fatal rupture of pulmonary arteriovenous malformation in hereditary haemorrhagic telangiectasis and severe PAHD Montani, L C Price, B Girerd, et al.
The European Respiratory Journal|January 3, 2012
Circulating fibrocytes and pulmonary arterial hypertensionN Gambaryan, S Cohen-Kaminsky, D Montani, et al.
Clinical Pharmacology and Therapeutics|May 21, 2014
CYP2C9, SLCO1B1, SLCO1B3, and ABCB11 polymorphisms in patients with bosentan-induced liver toxicityM Roustit, X Fonrose, D Montani, et al.
Revue Des Maladies Respiratoires|February 13, 2016
Pulmonary complications of type 1 neurofibromatosisL Reviron-Rabec, B Girerd, A Seferian, et al.
Revue Des Maladies Respiratoires|March 5, 2018
[Pulmonary veno-occlusive disease]A Boucly, B Girerd, D Bourlier, et al.
Clinical Genetics|June 10, 2011
ACVRL1 germinal mosaic with two mutant alleles in hereditary hemorrhagic telangiectasia associated with pulmonary arterial hypertensionM Eyries, F Coulet, B Girerd, et al.
Arthritis and Rheumatism|June 18, 2010
Association of a KCNA5 gene polymorphism with systemic sclerosis-associated pulmonary arterial hypertension in the European Caucasian populationJ Wipff, P Dieudé, M Guedj, et al.
Revue Des Maladies Respiratoires|July 29, 2022
[French clinical practice guidelines for the diagnosis and management of lung disease with alpha 1-antitrypsin deficiency]J-F Mornex, M Balduyck, M Bouchecareilh, et al.
Pageof 1