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. 2019. Dostupné z: https://dx.doi.org/10.1183/13993003.congress-219.PA1400.
@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}. 2019. Dostupné z: https://dx.doi.org/10.1183/13993003.congress-219.PA1400.