Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Huri Sema Aymelek"'
Publikováno v:
Medicine Science, Vol 10, Iss 3, Pp 1049-53 (2021)
Multiple Pterygium syndrome (MPS) is characterized by antecubital, popliteal pterygium, short stature, dysmorphic face, kyphoscoliosis, club foot, genital and cardiac malformations. Mutation in the acetylcholine nicotinergic receptor gamma polypeptid
Externí odkaz:
https://doaj.org/article/9fe9d7b389c442a981de421c9a2b3ef6
Autor:
Kamuran Karaman, Eyüp Yürektürk, Hadi Geylan, Akkız Şahin Yaşar, Serap Karaman, Huri Sema Aymelek, Mecnun Çetin, Ahmet Fayik Oner
Publikováno v:
Platelets, Vol 32, Iss 2, Pp 238-242 (2021)
Glanzmann’s thrombasthenia (GT) is an autosomal recessive disorder in which the underlying problem is the lack or dysfunction of the GpIIb/IIIa receptor on the platelet surface. The present study determines the genetic mutation typology and analyze
Externí odkaz:
https://doaj.org/article/fd04d405f9504f739929fde27b30e2fe
Autor:
Ümmet Abur, Gönül Oğur, Ömer Salih Akar, Engin Altundağ, Huri Sema Aymelek, Düzgün Özatlı, Mehmet Turgut
Publikováno v:
Turkish Journal of Hematology, Vol 35, Iss 1, Pp 61-65 (2018)
Objective: This study evaluates the impact of CLLU1 expression and fluorescent in situ hybridization (FISH) analysis of a group of Turkish chronic lymphocytic leukemia (CLL) patients. Materials and Methods: A total of 156 CLL patients were analyzed b
Externí odkaz:
https://doaj.org/article/9ae6477089e042378aedb2400bb50333
Autor:
Onur Karaaslan, Ali Kolusari, Gökçe Naz Küçükbaş, Deniz Dirik, Erbil Karaman, Hanım Güler Şahin, Abdülaziz Gül, Huri Sema Aymelek
Publikováno v:
Eastern Journal Of Medicine. 26:600-605
Autor:
Eyüp Yürektürk, Akkız Şahin Yaşar, Serap Karaman, Huri Sema Aymelek, Kamuran Karaman, Mecnun Çetin, Ahmet Fayik Öner, Hadi Geylan
Publikováno v:
Platelets. 32:238-242
Glanzmann's thrombasthenia (GT) is an autosomal recessive disorder in which the underlying problem is the lack or dysfunction of the GpIIb/IIIa receptor on the platelet surface. The present study determines the genetic mutation typology and analyzes
Publikováno v:
Andrologia. 53
Gynaecomastia in adolescents is a benign glandular proliferation of the male breast. Secondary causes of gynaecomastia in adolescents are relatively rare and may result from a wide variety of rare pathological conditions. Among these, klinefelter syn
Autor:
Eda Çelebi Bitkin, Huri Sema Aymelek
Publikováno v:
The Turkish Journal of Pediatrics. 64:585
Autor:
Düzgün Özatlı, Ummet Abur, Omer Salih Akar, Mehmet Turgut, Gonul Ogur, Engin Altundag, Huri Sema Aymelek
Publikováno v:
Turkish Journal of Hematology
Turkish Journal of Hematology, Vol 35, Iss 1, Pp 61-65 (2018)
Turkish Journal of Hematology, Vol 35, Iss 1, Pp 61-65 (2018)
This study evaluates the impact of CLLU1 expression and fluorescent in situ hybridization (FISH) analysis of a group of Turkish chronic lymphocytic leukemia (CLL) patients.A total of 156 CLL patients were analyzed by FISH method; 47 of them were also
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::527e4e6490ff0e7c591abc9d670770e7
https://hdl.handle.net/20.500.12712/12037
https://hdl.handle.net/20.500.12712/12037
Autor:
Engin Altundaǧ, Handan Celik, Erdal Malatyalıoǧlu, Emel Kurtoǧlu, Omer Salih Akar, Huri Sema Aymelek, Miǧraci Tosun, Ummet Abur, Tayfun Alper, Gonul Ogur
Publikováno v:
Journal of Medical Ultrasound
WOS: 000513789000004 PubMed: 31867191 Objective: Genetic burden, fetal malformations, and fetal outcomes of 93 fetuses with cystic hygroma (CH) are reported from a single center in Turkey. Patients and Methods: Pregnancies, having a diagnosis of feta