The Relevance of Family History Taking in the Detection and Management of Birt-Hogg-Dubé Syndrome-Reference-Cited by-同舟云学术

The Relevance of Family History Taking in the Detection and Management of Birt-Hogg-Dubé Syndrome

Published:2019 Issue:2 Volume:98 Page:125-132
ISSN:0025-7931
Container-title:Respiration
language:en
Short-container-title:Respiration

Author:

Torricelli Elena,Occhipinti Mariaelena^ORCID,Cavigli Edoardo,Tancredi Giorgia,Rosi Elisabetta,Rossi Cesare,Bonaguro Michela,Candita Luisa,Papi Laura,Novelli Luca,Bezzi Michela,Bargagli Elena,Voltolini Luca,Pistolesi Massimo

Publisher

S. Karger AG

Subject

Pulmonary and Respiratory Medicine

Reference37 articles.

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2. Schmidt LS, Nickerson ML, Warren MB, Glenn GM, Toro JR, Merino MJ, et al. Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dubé syndrome. Am J Hum Genet. 2005 Jun;76(6):1023–33.

3. Nickerson ML, Warren MB, Toro JR, Matrosova V, Glenn G, Turner ML, et al. Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome. Cancer Cell. 2002 Aug;2(2):157–64.

4. Tomassetti S, Carloni A, Chilosi M, Maffè A, Ungari S, Sverzellati N, et al. Pulmonary features of Birt-Hogg-Dubé syndrome: cystic lesions and pulmonary histiocytoma. Respir Med. 2011 May;105(5):768–74.

5. Abolnik IZ, Lossos IS, Zlotogora J, Brauer R. On the inheritance of primary spontaneous pneumothorax. Am J Med Genet. 1991 Aug;40(2):155–8.

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