Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Roongaroon Phuangtham"'
Autor:
Laura Blouin, Roongaroon Phuangtham, Mathieu Fiore, Sentot Santoso, Yoann Huguenin, Gregor Bein, Behnaz Bayat
Publikováno v:
Journal of Thrombosis and Haemostasis. 19:255-261
Essentials The c.1544+1G>A mutation was identified in Gypsy Glanzmann thrombasthenia (GT) patients. Gypsy GT patients express normal αv β3 carrying HPA-1b epitopes. To demonstrate HPA-1a alloimmunization by modified antigen capture assays. Gypsy GT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24cf669e25d37f7c03fa6b564020c6a7
https://doi.org/10.1111/jth.15117
https://doi.org/10.1111/jth.15117
Autor:
Haoqiang Ding, Sentot Santoso, Patcharee Komvilaisak, Chanvit Leelayuwat, Roongaroon Phuangtham, Amornrat Romphruk
Publikováno v:
Transfusion. 60:847-854
BACKGROUND Anti-CD36s, developing after transfusion or during pregnancy, play an important role in immune-mediated bleeding disorders among Asian populations. Currently, little is known about the clinical relevance of anti-CD36. Here, we aimed to det
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aacccd69585cff30f88103958dcfe4e4
https://doi.org/10.1111/trf.15737
https://doi.org/10.1111/trf.15737
Autor:
Silke Schmidt, Sentot Santoso, Lars Fischer, Roongaroon Phuangtham, Sarah Theresa Holzwarth, Jieqing Zhu, Doris Boeckelmann, Lida Röder, Behnaz Bayat, Gregor Bein, Heike Berghöfer
Publikováno v:
Transfusion
Background Fetal and neonatal alloimmune thrombocytopenia (FNAIT) is caused by the destruction of platelets in the fetus or newborn by maternal platelet alloantibodies, mostly against human platelet antigen (HPA)-1a. Recent studies indicate that two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af29212f5c5160d87d0c4def68e1df01
https://europepmc.org/articles/PMC8020566/
https://europepmc.org/articles/PMC8020566/
Autor:
Mathieu, Fiore, Behnaz, Bayat, Roongaroon, Phuangtham, Laura, Blouin, Yoann, Huguenin, Gregor, Bein, Sentot, Santoso
Publikováno v:
Journal of thrombosis and haemostasis : JTHREFERENCES. 19(1)
Essentials The c.1544+1GA mutation was identified in Gypsy Glanzmann thrombasthenia (GT) patients. Gypsy GT patients express normal α
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::af19584156b88f1dac7516e684295a57
https://pubmed.ncbi.nlm.nih.gov/33090654
https://pubmed.ncbi.nlm.nih.gov/33090654