A Rare Cause of Interstitial Lung Disease: Hermansky-Pudlak Syndrome

Autor: Akin Kaya, Nurdan Kokturk, Celik G, Aydın Çiledağ, Cirit Koçer B, Numan Numanoglu

Publikováno v: Tuberkuloz ve Toraks. 59:85-88

Hermansky-Pudlak syndrome is a rare disease characterized by bleeding diathesis, oculocutaneous albinism and lysosomal ceroid lipofuscin pigment deposits. Pulmonary fibrosis may also accompany with the disease. A 48-year-old male patient with a diagn

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2090a0fb287c81c31260eba5b00805f8
https://doi.org/10.5578/tt.2433

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Retrospective evaluation of patients with organizing pneumonia: is cryptogenic organizing pneumonia different from secondary organizing pneumonia?

Autor: Yılmaz S, Akıncı Özyürek B; Clinic of Chest Diseases, Ankara Ataturk Chest Diseases and Chest Surgery Training and Research Hospital, Ankara, Turkey. drberna_1982@yahoo.com., Erdoğan Y, Cirit Koçer B, Demirağ F, Dadalı Y, Büyükyaylacı Özden S

Publikováno v: Tuberkuloz ve toraks [Tuberk Toraks] 2017 Mar; Vol. 65 (1), pp. 1-8.