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Toplam kayıt 377, listelenen: 11-20
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism
(American Society for Clinical Investigation Inc, 2018)
Defects in genes mediating thyroid hormone biosynthesis result in dyshormonogenic congenital hypothyroidism (CH). Here, we report homozygous truncating mutations in SLC26A7 in 6 unrelated families with goitrous CH and show ...
Robotic transoral vestibular parathyroidectomy: Two case reports and review of literature
(Baishideng Publishing Group Inc, 2018)
Advances in preoperative localization studies and demands for scarless surgery have promoted the investigation for remote techniques in parathyroid surgery. Transoral vestibular approach seems to provide the most comfortable ...
Effects of systemic erythropoietin treatment and heterogeneous xenograft in combination on bone regeneration of a critical-size defect in an experimental model
(Churchill Livingstone, 2018)
The aim of the present study was to evaluate the effects of systemic EPO treatment alone or in combination with xenogenic bone graft augmentation on bone regeneration. Eleven adult male Sprague-Dawley rats were used in the ...
Impact of sorafenib on epidural fibrosis: An immunohistochemical study
(Baishideng Publishing Group Inc, 2018)
AIM To determine if sorafenib, an antineoplastic agent, could prevent the development of spinal epidural fibrosis (EF). METHODS The study used CD105 and osteopontin antibodies in an immunohistochemical approach to quantify ...
The determination of tenofovir level in breast milk of nursing mothers under tenofovir therapy
(Wiley, 2018)
In this study, we aimed to determine of tenofovir concentration in maternal plasma, breast milk and plasma of infants and factors affecting drug levels in chronic hepatitis B (CHB) patients using tenofovir disoproxil ...
Atypical fibroxanthoma arising on chronic burn scar: A rare case report and the review of the literature
(Springer, 2018)
Atypical Fibroxanthoma (AFX) is a rare cutaneous mesenchymal neoplasm, predominantly found on sundamaged skin of the head and neck in elderly patients. But uncommonly it can develop on a burn scar with or without actinic ...
Assessment of auditory brainstem responses in hypothyroidism and hyperthyroidism
(Derman Medical Publishing, 2018)
Aim: This study aimed to determine the effect of thyroid hormone changes on hearing pathways by assessing audiometry and auditory brainstem responses of hypothyroid and hyperthyroid patients and to determine whether ...
Mi196a2 T/C variant as possible predisposal factor for ankylosing spondylitis in a Turkish population
(Elsevier Science Bv, 2018)
Ankylosing spondylitis (AS) is a chronic inflammatory disorder. Micro RNAs (miRNAs), small noncoding RNA molecules, can function as either oncogenes or tumor suppressor genes. Altered miRNA expression has been implicated ...
Do UCP2, IL-17, mi196a2, and NR3C1 gene variants contribute to the risk of microtia? A preliminary study in Turkish population
(Elsevier Science Bv, 2018)
Microtia is a congenital malformation of variable severity of theexternal and middle ear. Although many genetic and environmen-tal factors are investigated the etiopathogenesis of microtia, it isstill uncertain. We performed ...
Confocal laser endomicroscopy and optical coherence tomography for the diagnosis of prostate cancer: A needle-based, in vivo feasibility study protocol (Ideal phase 2a)
(JMIR Publications, Inc, 2018)
Background: Focal therapy for prostate cancer has been proposed as an alternative treatment to whole-gland therapies in selected men to diminish side effects in localized prostate cancer. As nowadays imaging cannot offer ...