Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Chiraag Gangahar"'
Publikováno v:
Case Reports in Pediatrics, Vol 2018 (2018)
Background. Omphalocele is a rare congenital abdominal wall defect. It is frequently associated with genetic abnormality and other congenital anomalies, although isolated omphalocele cases do exist. Data have shown that omphalocele with co-occurring
Externí odkaz:
https://doaj.org/article/3c00578591394c1399900f776c194394
Publikováno v:
Journal of the American Society of Cytopathology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8b3fd6922874909229039c97bb96d14
http://europepmc.org/articles/PMC8495498
http://europepmc.org/articles/PMC8495498
Publikováno v:
Case Reports in Pediatrics
Case Reports in Pediatrics, Vol 2018 (2018)
Case Reports in Pediatrics, Vol 2018 (2018)
Background. Omphalocele is a rare congenital abdominal wall defect. It is frequently associated with genetic abnormality and other congenital anomalies, although isolated omphalocele cases do exist. Data have shown that omphalocele with co-occurring
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32be3e7d2e5462b1f709b331f6ab3d53
http://europepmc.org/articles/PMC6257893
http://europepmc.org/articles/PMC6257893
Publikováno v:
American Journal of Clinical Pathology. 152:S34-S34
Background Heparin-induced thrombocytopenia (HIT) is a life-threatening complication of exposure to heparin that is caused by autoantibodies against heparin-PF4 complexes. We recently changed our in-house HIT screening platform from a manual, daily b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6de49a277521c89c98cea635e4e8e17
https://doi.org/10.1093/ajcp/aqz112.064
https://doi.org/10.1093/ajcp/aqz112.064