Ara
Toplam kayıt 177, listelenen: 121-130
Prenatal diagnosis of Comel-Netherton syndrome with PGD, case report and review article
(SPRINGER/PLENUM PUBLISHERS, 2011)
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Missing atrioventricular echogenic mass during paediatric HeartWare (R) implantation
(VIA MEDICA, 2017)
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The rate and significance of type 1/type 2 serum amyloid A protein gene polymorphisms in patients with ankylosing spondylitis and amyloidosis
(TAYLOR & FRANCIS LTD, 2015)
A relationship between the presence of amyloidosis and SAA1 genotype has been shown in recent studies of (principally) familial Mediterranean fever patients. We found that the SAA1 rs12218 polymorphism was significantly ...
Air leak without subcutaneous emphysema in an adult patient due to thyroidectomy
(VIA MEDICA, 2017)
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Aquaporin-4 antibody seropositivity in myasthenia gravis patients with thymoma
(WILEY-BLACKWELL, 2013)
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Does resolved HBV or anti-HBc-only carry the same risk of HBV reactivation?
(SAGE PUBLICATIONS LTD, 2018)
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Nerve-sparing techniques and results in robot-assisted radical prostatectomy
(KOREAN UROLOGICAL ASSOC, 2016)
Nerve-sparing techniques in robot-assisted radical prostatectomy (RARP) have advanced with the developments defining the prostate anatomy and robotic surgery in recent years. In this review we discussed the surgical anatomy, ...
Foramina parietalia permagna: familial and radiological evaluation of two cases and review of literature
(SPRINGER, 2017)
Purpose Foramina parietalia permagna is a variable intramembranous ossification defect of the parietal bones. Foramina parietalia permagna have an autosomal dominant inheritance, and it is showed that mutations in chromosome ...
Intradiploic Hematoma in a Hemophilic Patient: Hemophilic Pseudotumor of Calvarium
(GALENOS YAYINCILIK, 2017)
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