| DOUBKOVÁ, Martina, Jakub TRIZULJAK, Anna HRAZDIROVÁ, Zuzana VRZALOVÁ, Ivona BLAHÁKOVÁ, Lenka RADOVÁ, Šárka POSPÍŠILOVÁ a Michael DOUBEK. A rare diagnosis: Hermansky-Pudlak syndrome i a patient eith pulmonary fibrosis, oculocutaneous albinism and thrombocytopathy. In European Respiratory Journal 2019, 54, Suppl. 63, PA1400. doi:10.1183/13993003.congress-219.PA1400. 2019. |
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@proceedings{1589846,
author = {Doubková, Martina and Trizuljak, Jakub and Hrazdirová, Anna and Vrzalová, Zuzana and Blaháková, Ivona and Radová, Lenka and Pospíšilová, Šárka and Doubek, Michael},
booktitle = {European Respiratory Journal 2019, 54, Suppl. 63, PA1400},
doi = {http://dx.doi.org/10.1183/13993003.congress-219.PA1400},
title = {A rare diagnosis: Hermansky-Pudlak syndrome i a patient eith pulmonary fibrosis, oculocutaneous albinism and thrombocytopathy},
year = {2019}
}
TY - CONF
ID - 1589846
AU - Doubková, Martina - Trizuljak, Jakub - Hrazdirová, Anna - Vrzalová, Zuzana - Blaháková, Ivona - Radová, Lenka - Pospíšilová, Šárka - Doubek, Michael
PY - 2019
TI - A rare diagnosis: Hermansky-Pudlak syndrome i a patient eith pulmonary fibrosis, oculocutaneous albinism and thrombocytopathy
ER -
DOUBKOVÁ, Martina, Jakub TRIZULJAK, Anna HRAZDIROVÁ, Zuzana VRZALOVÁ, Ivona BLAHÁKOVÁ, Lenka RADOVÁ, Šárka POSPÍŠILOVÁ a Michael DOUBEK. A rare diagnosis: Hermansky-Pudlak syndrome i a patient eith pulmonary fibrosis, oculocutaneous albinism and thrombocytopathy. In \textit{European Respiratory Journal 2019, 54, Suppl. 63, PA1400}. doi:10.1183/13993003.congress-219.PA1400. 2019.
|
