Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Derya Karaer"'
Publikováno v:
Clinical Dysmorphology. 31:167-173
Neurodevelopmental disorder with microcephaly, ataxia, and seizures (NEDMAS) syndrome is a rare neurodevelopmental disorder characterized by moderate intellectual disability (ID), thin body habitus, microcephaly, seizures, ataxia, muscle weakness, an
Publikováno v:
Pamukkale Medical Journal.
Purpose: Familial Mediterranean Fever (FMF) is a hereditary auto inflammatory disease (MIM#249100). The most common symptoms are high fever, abdominal pain and arthralgia. FMF is the result of variations in the MEditerraneanFeVer (MEFV) gene, which i
Publikováno v:
Volume: 14, Issue: 3 620-625
Pamukkale Tıp Dergisi
Pamukkale Tıp Dergisi
Amaç: İnfertilite çiftlerin %15’inde görülen bir problemdir. Oligozoospermi ve azoospermi kaynaklı erkek infertilitesi tanısı alanların %30’unun etiyolojisinde genetik nedenler sorumludur. Bu retrospektif çalışmada, merkezimize başvu
Autor:
MUSTAFA NECMİ İLHAN, DERYA KARAER, MEHMET ALİ ERGÜN, SEYHAN YAĞAR, ZELİHA ASLI DEMİR, AYŞEGÜL ÖZGÖK, BAHAR AYDINLI
Publikováno v:
Volume: 41, Issue: 6 1037-1041
Turkish Journal of Medical Sciences
Turkish Journal of Medical Sciences
To evaluate dose-related genotoxicity of desflurane. In the literature, there are studies with equivocal data regarding the potential genotoxicity of inhalational anesthetics. However, it is important to know about the genotoxic safety of an anesthet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf6e32a3c75850b6c3d7bc47e197d870
https://dergipark.org.tr/tr/pub/tbtkmedical/issue/12301/147182
https://dergipark.org.tr/tr/pub/tbtkmedical/issue/12301/147182