Ara
Toplam kayıt 514, listelenen: 31-40
A homozygous TPO gene duplication (c. 1184_1187dup4) causes congenital hypothyroidism in three siblings born to a consanguineous family
(Georg Thieme Verlag, 2015)
Congenital hypothyroidism (CH) is the most common neonatal endocrine disease, and germ-line mutations in the TPO gene cause the inherited form of the disease. Our aim in this study was to determine the genetic basis of ...
Oxidative stress markers are increased in non-alcoholic fatty liver disease patients with high serum alanine aminotransferase levels
(Termedia Publishing House Ltd, 2019)
Introduction: Non- alcoholic fatty liver disease (NAFLD) is a pathological disease that causes chronic damage in the liver without alcohol consumption. Aim of the research: To determine oxidative stress and inflammation ...
The prevalence of restless legs syndrome and comorbid condition among patient with type 2 diabetic mellitus visiting primary healthcare
(2019)
AIM: The aim of this study was to determine the prevalence of restless legs syndrome (RLS) and Pittsburgh Sleep Quality Index (PSQI) in patients with type 2 diabetes mellitus (T2DM) attending primary healthcare. SUBJECTS ...
Is there a relationship between microvascular complications and the severity of type 2 diabetes mellitus?
(Erciyes University Faculty Of Medicine, 2020)
Objective: The aim of this study was to determine the relationship between microvascular Type 2 diabetes mellitus (T2DM) complications and the severity and duration of diabetes in the light of sociodemographic and lifestyle ...
Exome sequencing in a large family with Tourette Syndrome/Chronic Tic Disorder
(Nature Publishing Group, 2018)
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Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism
(Nature Publishing Group, 2018)
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Investigation of vitamin utilization in primary care in Istanbul
(Oxford University Press, 2020)
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Infectious epidemiology in multiple myeloma patients after autologous stem cell transplantation: A single-center analysis from Turkey
(Nature Publishing Group, 2018)
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Patient-specific induced pluripotent stem cells for cardiac disease modeling
(Walter de Gruyter GMBH, 2019)
Reprogramming of human somatic cells to induced pluripotent stem cells (iPSCs) via induction of pluripotency genes is one of the most influential scientific breakthroughs during the last decade. Behind this breakthrough ...