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Wilms Tümörü Hastalarında Uzun Dönemli Böbrek Fonksiyonları
(Tıp Fakültesi, 2014)BACKGROUND: Wilms tumor is the most common renal malignancy of childhood. Following the development in chemotherapy, the survival rates have increased up to 90%. Due to the improvement in prognosis and increase in survival ... -
Wilms tümörü vakalarına eşlik eden konjenital anomali, malformasyon ve genetik sendromlar
(Tıp Fakültesi, 2023-03-28)Aim: To evaluate the clinical abnormalities with a tendency to develop Wilms tumor, under genetic syndromes, anomalies and malformations. Patients and Methods: Between 1971 and 2023, 68 patients were diagnosed with Wilms ... -
Wilms tümörü vakalarına eşlik eden konjenital anomali, malformasyon ve genetik sendromlar
(Tıp Fakültesi, 2023-03-28)Aim: To evaluate the clinical abnormalities with a tendency to develop Wilms tumor, under genetic syndromes, anomalies and malformations. Patients and Methods: Between 1971 and 2023, 68 patients were diagnosed with Wilms ... -
Wilms' Tumor In Children: An Overview
(Karger, 2008)Wilms' tumor is the most frequently occurring renal tumor in children and is one of the most treatment-responsive tumors. A tumor-suppressor gene and other genetic abnormalities have been implicated in its etiology. In ... -
Wilms' Tumour-Associated Late Nephrotic Syndrome Responsive To Treatment
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Wilson Hastalarında Serum Değişken Ve Göreceli Değişken Bakır Düzeylerinin Klinik Parametreler ve Multiparametrik Karaciğer Mrı Bulgularıyla Karşılaştırılması
(Tıp Fakültesi, 2022)Durukan BM. The Evaluation of Exchangeable and Relative Exchangeable Copper with Clinical Parameters and Multiparametric Liver MRI Findings in Patients with Wilson Disease. Hacettepe University Faculty of Medicine, Thesis ... -
Wilson Hastalarının Klinik Izlemi ve Uzun Dönem Tedavi Sonuçlarının Değerlendirilmesi
(Tıp Fakültesi, 2014)Wilson's disease (WD) is characterized by degenerative changes in the brain, liver and cornea as a result of excessive accumulation of copper in tissues. While it is known as a chronic liver disease, early diagnosis and ... -
Wiskott Aldrich Sendromu ve X E Bağlı Geçişli Trombositopeni Tanılarıyla Izlenen 23 Vakanın Demografik Özellikleri, Klinik, Laboratuvar Bulguları ve Klinik Seyirleri
(Tıp Fakültesi, 2014)Wiskott Aldrich syndrome (WAS) is an X linked inherited immune deficiency caused by mutations occuring at WASp gene, characterized by microthrombocytopenia (microplatelet and low count of platelet), eczema and recurrent ... -
Work-Related Asthma In Montreal, Quebec: Population Attributable Risk In A Community-Based Study
(Pulsus Group Inc, 2008)BACKGROUND: Occupational exposures are an important cause of adult-onset asthma but the population attributable risk percentage (PAR%) has been less frequently studied. OBJECTIVES: To examine the distribution and determinants ... -
Worldwide Distribution And Broader Clinical Spectrum Of Muscle-Eye-Brain Disease
(Oxford Univ Press, 2003)Muscle-eye-brain disease (MEB), an autosomal recessive disorder prevalent in Finland, is characterized by congenital muscular dystrophy, brain malformation and ocular abnormalities. Since the MEB phenotype overlaps ... -
Wses Guidelines For Management Of Clostridium Difficile Infection In Surgical Patients
(2015)In the last two decades there have been dramatic changes in the epidemiology of Clostridium difficile infection (CDI), with increases in incidence and severity of disease in many countries worldwide. The incidence of CDI ... -
Wwox And Ap2 Gamma Expression Levels Predict Tamoxifen Response
(Amer Assoc Cancer Research, 2007)Purpose: Assessment of expression levels of Wwox, Wwox- interacting proteins Ap2 alpha, Ap2 gamma, and ErbB4, the Ap2 gamma transcriptional target protein Her2, and the possible Ap2 alpha transcriptional target Prka Rl ... -
X-Linked Recessive Inheritance Of Radial Ray Deficiencies In A Family With Four Affected Males
(Nature Publishing Group, 2001)Radial ray deficiencies are frequently associated with additional clinical anomalies and have a heterogeneous aetiology. X-linked forms are extremely rare. We report a family in which four male relatives show bilateral ... -
Xanthogranulomatous Cystitis: A Challenging Imitator Of Bladder Cancer
(2010)Xanthogranulomatous cystitis is a rare, benign, chronic inflammatory disease of the bladder, mimicking malignancy with unknown etiology. Herein, we report a 57-year-old man who presented with pollakiuria, nocturia, dysuria, ... -
Xanthogranulomatous Endometritis: A Challenging Imitator Of Endometrial Carcinoma
(2007)Xanthogranulomatous inflammation is a distinguished histopathological entity affecting several organs, predominantly the kidney and gallbladder. So far, only a small number of cases of xanthogranulomatous inflammation ...