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Toplam kayıt 455, listelenen: 421-430
The Utility of Transrectal Ultrasound in Adolescents When Transabdominal or Transvaginal Ultrasound Is Not Feasible
(ELSEVIER SCIENCE INC, 2013)
Study Objective: To present the indications and diagnosis in adolescents undergoing transrectal ultrasound (RU). Design: Retrospective chart review. Participants: Adolescents presenting to gynecology clinic between January ...
The long pentraxin-3 is a useful marker for diagnosis of ovarian torsion: An experimental rat model
(TAYLOR & FRANCIS INC, 2016)
Pentraxin-3 (PTX3) plays an important role in the primary inflammatory response. We aim to evaluate PTX3 as a diagnostic marker of ovarian torsion in an experimental rat model. In this study, 16 female Sprague Dawley albino ...
Success of Ranibizumab in Central Serous Chorioretinopathy Resistant to Bevacizumab
(MARY ANN LIEBERT, INC, 2014)
Purpose: To present effectiveness of intravitreal ranibizumab (IVR) injection for central serous chorioretinopathy (CSC), resistant to intravitreal bevacizumab (IVB) injection. Methods: Files of the patients who had the ...
Spontaneously rapid and complete resolution of acute subdural hemorrhage in a 1-year-old patient
(W B SAUNDERS CO-ELSEVIER INC, 2016)
Acute subdural hematoma is one of the neurosurgical emergencies that could lead to mortality, thus needing urgent surgical intervention in most of the cases. A 1-year-old female patient was admitted to the emergency ...
Superovulation alters embryonic poly(A)-binding protein (Epab) and poly(A)-binding protein, cytoplasmic 1 (Pabpc1) gene expression in mouse oocytes and early embryos
(CSIRO PUBLISHING, 2016)
Embryonic poly(A)-binding protein (EPAB) and poly(A)-binding protein, cytoplasmic 1 (PABPC1) play critical roles in translational regulation of stored maternal mRNAs required for proper oocyte maturation and early embryo ...
Mandibuloacral dysplasia and LMNA A529V mutation in Turkish patients with severe skeletal changes and absent breast development
(LIPPINCOTT WILLIAMS & WILKINS, 2016)
Mandibuloacral dysplasia (MAD) is an autosomal recessive disorder characterized by acroosteolysis (resorption of terminal phalanges), skin changes (hyperpigmentation), clavicular hypoplasia, craniofascial anomalies, a hook ...
Overexpression of Fc mu receptor (FCMR, TOSO) gene in chronic lymphocytic leukemia patients
(HUMANA PRESS INC, 2012)
Rai and Binet staging systems that have been used as a standard method for evaluating the prognosis of chronic lymphocytic leukemia (CLL) have some restrictions in distinguishing the early stage CLL patients that will ...
Toll-Like Receptors in the Progression of Autosomal Dominant Polycystic Kidney Disease
(WILEY, 2016)
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary cause of chronic kidney disease. The intriguing role of innate immune system and inflammation become a target for potential therapeutic ...
Evaluation of Normal Appearing White Matter in Multiple Sclerosis Comparison of Diffusion Magnetic Resonance, Magnetization Transfer Imaging and Multivoxel Magnetic Resonance Spectroscopy Findings with Expanded Disability Status Scale
(SPRINGER HEIDELBERG, 2011)
Purpose The aim of this study was to determine diffusion magnetic resonance imaging (MRI), magnetization transfer (MT) imaging and multivoxel MR spectroscopy findings in plaques, periplaque white matter and normal appearing ...
Counteraction of Apoptotic and Inflammatory Effects of Adriamycin in the Liver Cell Culture by Clinopitolite
(HUMANA PRESS INC, 2016)
Growing evidence has been reported on adriamycin (ADR) hepatotoxicity in literature. Hepatotoxicity caused by the use of drugs has a serious undesirable effect in the cure of cancer patients that needs to be eliminated. ...