Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Serap Teber Tıras"'
Publikováno v:
Klinische Pädiatrie. 234:52-55
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2436c0f542e5b70713174e6f32550cf3
https://doi.org/10.1055/a-1478-4528
https://doi.org/10.1055/a-1478-4528
Autor:
Ebru Azapagasi, Tanıl Kendirli, Gokcen Oz Tunçer, Oktay Perk, Selen Yilmaz Isikhan, Serap Teber Tıras, Zeynep Eyileten, Erdal Ince, Adnan Uysalel, Ahmet Rüçhan Akar
We aimed at evaluating acute neurologic complications (ANC) and clinical outcome at a 2-year follow-up in children after extracorporeal membrane oxygenation (ECMO).We conducted a single-center, retrospective review of our patient cohort aged between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0342ac60301738a0bd426a3aeec75ecb
https://avesis.gazi.edu.tr/publication/details/77a3ab4e-8a73-488a-9930-b00cf3ad1b80/oai
https://avesis.gazi.edu.tr/publication/details/77a3ab4e-8a73-488a-9930-b00cf3ad1b80/oai
Autor:
Hasan Fatih Çakmaklı, Mehmet Ertem, Zümrüt Uysal, Esra Pekpak, Serap Teber Tıras, Elif İnce, Ercan Tutar, Talia Ileri, Tayfun Uçar
Publikováno v:
Journal of pediatric hematology/oncology. 43(5)
Introduction Thrombosis is rare in children and antithrombolytic treatment is controversial. Most commonly used thrombolytic agent is tissue plasminogen activator (t-PA) in pediatrics. In this study, we report our experience in the use of thrombolyti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d86d624819c2f0e876e49b3187b56972
https://pubmed.ncbi.nlm.nih.gov/33480646
https://pubmed.ncbi.nlm.nih.gov/33480646
Publikováno v:
Thrombosis Research. 120:47-52
Introduction High plasma levels of sEPCR lead to dysfunction of the EPCR-mediated coagulation. We have evaluated the role of EPCR A3 haplotype with its representative promoter variant 1651 C–G in a total of twenty-seven pediatric stroke patients an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84ffbf193a8380a580a2ad863db96c86
https://doi.org/10.1016/j.thromres.2006.08.004
https://doi.org/10.1016/j.thromres.2006.08.004
Autor:
Suat Fitoz, Zeynep Şıklar, Bülent Hacıhamdioğlu, Serap Teber Tıras, Gulhiz Deda, Gönül Öcal, Merih Berberoğlu, Şenay Savaş Erdeve
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Genoa syndrome was first described by Camera et al in 1993 in two patients with semilobar holoprosencephaly (HPE), craniosynostosis and abnormal small hands with cone−shaped epiphyses and hypoplastic terminal phalanges of fingers (OMIM: 601370). In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aefbe6d85269fd580966ba630a162518
https://pubmed.ncbi.nlm.nih.gov/21274346
https://pubmed.ncbi.nlm.nih.gov/21274346