Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Burak Baser"'
Autor:
Malik Ejder Yildirim, Hande Kucuk Kurtulgan, Ozturk Ozdemir, Hasan Kilicgun, Didem S. Aydemir, Burak Baser, Ilhan Sezgin
Publikováno v:
Annals of Saudi Medicine, Vol 39, Iss 6, Pp 382-387 (2019)
BACKGROUND: Familial Mediterranean fever (FMF), an autosomal recessive, autoinflammatory disease that is common in Arabs, Jews, Armenians and Turks, is caused by mutations in the MEFV gene, which encodes a protein called pyrin. The disease is charact
Externí odkaz:
https://doaj.org/article/007e1e1917cc4faca68662cd59df76a7
Publikováno v:
American Journal of Medical Genetics Part A. 185:2198-2203
Filippi syndrome (MIM #272440), one of the craniodigital syndromes, is a rare genetic entity with autosomal recessive inheritance and characterized by pre- and postnatal growth retardation, microcephaly, distinctive facial appearance, developmental d
Autor:
Malik Ejder Yildirim, Gokhan Bagci, Mansur Kayataş, Hande Küçük Kurtulgan, Meryem Timucin, Ilhan Sezgin, Burak Baser, Suleyman Koz
Publikováno v:
Turkish Journal of Nephrology. 29:304-309
Autor:
Hasan Kilicgun, Malik Ejder Yildirim, Ilhan Sezgin, Hande Küçük Kurtulgan, Öztürk Özdemir, Burak Baser, Didem S. Aydemir
Publikováno v:
Annals of Saudi Medicine
Annals of Saudi Medicine, Vol 39, Iss 6, Pp 382-387 (2019)
Annals of Saudi Medicine, Vol 39, Iss 6, Pp 382-387 (2019)
BACKGROUND: Familial Mediterranean fever (FMF), an autosomal recessive, autoinflammatory disease that is common in Arabs, Jews, Armenians and Turks, is caused by mutations in the MEFV gene, which encodes a protein called pyrin. The disease is charact
Publikováno v:
Journal of gynecology obstetrics and human reproduction. 48(7)
Objective Chromosomal abnormalities are more common in the first trimester abortions. We aimed to investigate the types and prevalence of chromosomal abnormalities in couples with recurrent first trimester miscarriages in Sivas, Turkey. Materials and
Publikováno v:
Cornea. 38(3)
WOS: 000464539300021
PubMed ID: 30394912
Purpose: To present ocular findings and anterior segment-optical coherence tomography (AS-OCT) imaging findings of 2 cases of fish-eye disease (FED) involving 2 novel genetic variants of the lecithin
PubMed ID: 30394912
Purpose: To present ocular findings and anterior segment-optical coherence tomography (AS-OCT) imaging findings of 2 cases of fish-eye disease (FED) involving 2 novel genetic variants of the lecithin
Publikováno v:
SAE Technical Paper Series.
Autor:
Burak Baser, Ronnie Törnqvist
Publikováno v:
SAE Technical Paper Series.