Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yiğit Köroğlu"'
Publikováno v:
Turkish Archives of Otorhinolaryngology, Vol 61, Iss 2, Pp 52-57 (2023)
Objective:Fabry disease is a rare hereditary lysosomal storage disease caused by the deficiency of alpha-galactosidase A (α-GLA). Although sensorineural hearing loss is common in Fabry disease, there are no studies in the literature that have screen
Externí odkaz:
https://doaj.org/article/fc1b305ae5004599a40d8a45b63a55b8
Publikováno v:
Kafkas Journal of Medical Sciences. 13:78-81
Publikováno v:
Ankara Üniversitesi Tıp Fakültesi Mecmuas, Vol 71, Iss 2, Pp 96-104 (2018)
Blood product transfusions are frequently performed during critical illnesses. Primarily; erythrocyte suspension, platelet suspension and fresh frozen plasma transfusions are performed. It should not be forgotten that these procedures, which have pos
Autor:
Andrée Wallin, Robh Ruppel, Irvin Rodriguez, Loïc Zimmermann, Stéphan Brisson, Elise Frappier, Jack Zhang, Tomasz Jedruszek, Min Yum, Anto Juricic Toni, Yiğit Köroğlu, Tomasz Strzalkowski, Rudolf Herczog, Justin Yun, Kekai Kotaki, Rodrigo Lloret Crespo, Richard Anderson, Gábor Kis-Juhász, Rebeca Puebla Paniagua, Wei-Che(Jason) Juan, Jason Seiler, David Moratilla Amago, Alexey Egorov, Pascal Ackermann, Andrew Hickinbottom, Maurice Panisch, Eric Zhang, Marcin Jakubowski, Serge Birault, Matt Gaser, Jeffrey Simpson, Marek Denko, Valérie Villeuneuve, Lois van Baarle, Fabricio Moraes, Miguel Alba Gutiérrez, Chase Stone, Mariusz Kozik, Neil Maccormack, Jose Alves da Silva, Eduardo Peña, Viktor Fretyán, Andrew Finch, Chee Ming Wong, Michal Suchánek, Christer Wibert, Vitaly Bulgarov, Ignacio Bazán Lazcano, Michal Lisowski, István Vastag, Simon Dominic, Jiema
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eccc53909c638be716c84c0c24fe0101
https://doi.org/10.1016/b978-0-240-52210-4.50056-1
https://doi.org/10.1016/b978-0-240-52210-4.50056-1