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Toplam kayıt 5, listelenen: 1-5
BRAF V600E mutation in papillary thyroid cancer is correlated with adverse clinicopathological features but not with iodine exposure
(Via Medica, 2019)
Introduction: BRAF(V600E) activating mutation is the most frequent genetic abnormality in the pathogenesis of papillary thyroid carcinoma. We aimed to evaluate the association between BRAF(V600E )mutation and well-established ...
Cryptosporidiosis in Humans with Reference to the First Case of Cryptosporidium hominis Infection in Turkey
(Galenos Yayincilik, 2017)
Aim: Cryptosporidiosis is a worldwide zoonosis. Microscopic examinations may fail due to indistinctive morphological peculiarities of causative species. Hence, molecular diagnostics has become more important. Methods: Stool ...
Borrelia burgdorferi s.l. and Rickettsia spp. in Ticks Collected from European Part of Turkey
(Kafkas Univ, Veteriner Fakultesi Dergisi, 2013)
This study was performed in ticks collected with the flagging method from localities situated along Anatolian side of Istanbul to the Bulgarian border of Turkey which is under the effect of Black Sea climate. All ticks ...
Effects of idiopathic erythrocytosis on the left ventricular diastolic functions and the spectrum of genetic mutations: A case control study
(Lippincott Williams & Wilkins, 2022)
Background: We have aimed at exposing left ventricular diastolic functions and the presence of known genetic mutations for familial erythrocytosis, in patients who exhibit idiopathic erythrocytosis. Methods: Sixty-four ...
TSHRV656F Activating Variant of the Thyroid Stimulating Hormone Receptor Gene in Neonatal Onset Hyperthyroidism: A Case Review
(Galenos Yayincilik, 2022)
An activating variant of the thyroid stimulating hormone receptor (TSHR) gene is one of the rare causes of neonatal hyperthyroidism. This disorder may occur as a result of an autosomal dominant inheritance or sporadically ...