Our most recent publications

2022
Lung disease

Mornex J-F, Balduyck M, 
Bouchecareih M, et al.

French clinical practice guidelines for the diagnosis and management of lung disease with alpha 1-antitrypsin deficiency.

 

Manuscripts
2024
Hereditary angioedema

Boccon-Gibod I, Gobert D, Gauthier M, et al.
Evaluation of Adherence to Berotralstat in Patients with Hereditary Angioedema: A Prospective Survey in Community Pharmacies. Journal of Allergy and Clinical Immunology. 2024;153(2):AB8.

Manuscripts
2024
Amyloidosis

Oghina S, Legallois D, 
Fournier P, et al.
Evaluating the current physicians’ knowledge and patients’ pathways for diagnosing transthyretin cardiac amyloidosis (ATTR-CM) in France: An extensive survey of diverse medical specialists. Archives of Cardiovascular Diseases.

Manuscripts
2023
Hereditary angioedema

Launay D, Bouillet L, Boccon-gibod I, et al.

Mise au point sur les angiœdèmes héréditaires et leurs nouvelles thérapeutiques. La Revue de Médecine Interne. 2023;44.

Manuscripts
2022
Hereditary angioedema

Bouillet L, Fain O, Armengol G, et al.

Long-term prophylaxis in hereditary angioedema management: Current practices in France and unmet needs. Allergy and Asthma Proceedings. 2022;43.

Manuscripts
2021
Chylomicronemia

Bouillet L, Fain O, Armengol G, et al.

ATHENEE : enquête sur les besoins non couverts dans la prise en charge de l’angiœdème héréditaire (AOH) en France. Revue Française d’Allergologie. 2021;61(4):306.

Manuscripts
2021
Chylomicronemia

Bouillet L, Fain O, Armengol G, et al.

ATHENEE : enquête sur les besoins non couverts dans la prise en charge de l’angiœdème héréditaire (AOH) en France. Revue Française d’Allergologie. 2021;61(4):306.

Manuscripts
2021
Hereditary angioedema

Bouillet L, Fain O, Armengol G, et al.
ATHENEE : enquête sur les besoins non couverts dans la prise en charge de l’angiœdème héréditaire (AOH) en France. Revue Française d’Allergologie. 2021;61(4):306.

Manuscripts
Mai 2019
Chylomicronemia

IN-FOCUS France: an epidemiological survey on severe hypertriglyceridaemiae assessing the comparative burden of illness of familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS) Endocrine abstracts (May 2019)]

Abstracts, posters and presentations
2018
Pulmonary fibrosis

Cottin V, Bergot E, Bonniaud P, et al.

Enquête sur le vécu et les attentes des patients atteints de fibrose pulmonaire. Revue des Maladies Respiratoires. 2018;35:A33.

Manuscripts
2017
Pulmonary fibrosis

Cottin V, Bourdin A, Crestani B, et al.

Healthcare pathway and patients’ expectations in pulmonary fibrosis. ERJ Open Res. 2017;3(2).

Manuscripts
2015
Pulmonary fibrosis

Cottin V, Bergot E, Bourdin A, et al.

Adherence to guidelines in idiopathic pulmonary fibrosis: A follow-up national survey. ERJ Open Research. 2015;1:00032-2015.

Manuscripts
2015
Pulmonary fibrosis

Cottin V, Bergot E, Bourdin A, et al.

Seconde enquête de pratique sur la prise en charge de la fibrose pulmonaire idiopathique en France. Revue des Maladies Respiratoires. 2015;32:A27-A28.

Manuscripts
2014
Pulmonary fibrosis

Cottin V, Bourdin A, Crestani B, et al.

Enquête sur le vécu, le parcours de soin, et les attentes des patients atteints de fibrose pulmonaire. Revue des Maladies Respiratoires. 2014;31:A43.

Manuscripts
2014
Pulmonary fibrosis

Cottin V, Cadranel J, Crestani B, et al.

Management of idiopathic pulmonary fibrosis in France: a survey of 1244 pulmonologists. Respir Med. 2014;108(1):195-202.

Manuscripts
2014
Pulmonary fibrosis

Cottin V, Crestani B, Valeyre D, et al.

Diagnosis and management of idiopathic pulmonary fibrosis: French practical guidelines. Eur Respir Rev. 2014;23(132):193-214.

Manuscripts

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