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NOONAN SENDROMU’NUN PRENATAL TANISINDA PTPN11 GEN ANALİZLERİNİN ETKİNLİĞİ
(2021)
Amaç: Hücre büyüme, farklılaşma, yaşlanma ve siklus düzenlenmesindeönemli rol oynayan RAS-MAPK (Rat-sarcoma-Mitogen-activated-protein-kinase) yolağında bulunan 29 gendeki dominantpatojenik varyantların yol açtığı klinik ...
The right temporal variant of frontotemporal dementia is not genetically sporadic: A case series
(2021)
© 2021 - IOS Press. All rights reserved.Background: Right temporal variant frontotemporal dementia (rtvFTD) has been generally considered as a right sided variant of semantic variant primary progressive aphasia (svPPA), ...
COVID-19’da Antikor Bağımlı İmmünpataloji, Monoklonal Antikorlar ve Mutasyonlar
(2020)
CoV-2) etiyolojik etken olduğu koronavirus 19 hastalığı (COVID-19)
pandemisi mevcut ve olası sonuçları ile tüm dünyayı etkisi altına almıştır. COVID-19 ile mücadelede ve SARS-CoV-2 enfeksiyonun önlenmesinde aşı dizaynı ...
Mutational landscape of severe combined immunodeficiency patients from Turkey.
Severe combined immunodeficiency (SCID) has a diverse genetic aetiology, where a clinical phenotype, caused by single and/or multiple gene variants, can give rise to multiple presentations. The advent of next-generation ...
Traditional Chinese medicine practices used in COVID-19 (Sars-cov 2/Coronavirus-19) treatment in clinic and their effects on the cardiovascular system COVID-19 (Sars-cov 2/Koronavirüs-19) tedavisinde klinikte kullanilan geleneksel Çin tibbi bitkileri ve kardiyovasküler sisteme etkileri
(2020)
Objective: The aim of this study was to evaluate the effectiveness of plants used in the formulations of traditional Chinese medicine (TCM), which were also used in clinical trials to treat patients with the novel coronavirus ...
Application of Multifrequency Bioelectrical Impedance Analysis Method for the Detection of Dehydration Status in Professional Divers
Background and Objective. The level of dehydration has been known to be a predisposing factor for the development of decompression sickness in divers. The aim of this study was to determine the level of dehydration in ...
A rare urea cycle disorder in a neonate: N-acetylglutamate synthetase deficiency
(2020)
Urea cycle disorders (UCD), are genetically inherited diseases that may have a poor outcome due to to profound hyperammonemia. We report the case of a baby girl diagnosed as N-acetylglutamate synthase (NAGS) deficiency. ...
Abruptio placentae after amnioreduction in twin to twin transfusion syndrome.
(2017)
özeti ektedir
Comparison of MPV and High Sensitive CRP Levels between Patients with and without Diabetic Microvascular Complication
(2015)
Aim: Diabetes is an important cause of mortality and morbidity affecting especially individuals with its complications. We aimed to draw attention to the fact that MPV and hsCRP can be evaluated as warning parameters in ...