Ara
Toplam kayıt 59, listelenen: 51-59
Biyokimyasal Olarak Düşük Alkalen Fosfataz Düzeyi Saptanan Bireylerin Hipofosfatazya Açısından Değerlendirilmesi
(Tıp Fakültesi, 2023)
Hypophosphatasia (HPP) (OMIM 146300, 241500, 241510) is a rare, inherited disease characterized by bone and tooth mineralization disorder resulting from decreased non-tissue-specific alkaline phosphatase activity. There ...
Puberte Gecikmesi Nedeniyle Başvuran Yapisal Büyüme Puberte Gecikmesi Ve İzole Hipogonadotropik Hipogonadizm Tanili Erkek Çocuklarinin Uzun Dönem Boy Ve Puberte Gelişimi Durumlarinin Değerlendirilmesi
(Tıp Fakültesi, 2023-01)
Dogan O, Evaluation of Long-Term Height and Puberty Development in Boys with Constitutional Growth Delay in Puberty and Isolated Hypogonadotropic Hypogonadism Presenting Due to Delayed Puberty, Hacettepe University Faculty ...
Pediatrik Romatolojik Hastalıklarda Kullanılan Siklofosfamid Tedavisi Gonad Yetmezliğine Neden Olur Mu?
(Tıp Fakültesi, 2023)
Introduction: Cyclophosphamide (CYC) with its immunosuppressive properties continues to be the drug of choice in patients with severe rheumatic disease, such as vasculitis and systemic lupus erythematosus (SLE). However, ...
Çocukluk Çağında Pnömotoraks
(Tıp Fakültesi, 2023)
Aka, M. Pneumothorax in childhood. Hacettepe University Faculty of Medicine, Department of Pediatrics, Thesis in Pediatrics, Ankara 2023. Pneumothorax is the presence of air in the pleural space due to alveolar damage. ...
Pediatrik Nöroloji Bilim Dalı İzleminde Olan ve Polisomnografi İncelemesi Yapılan Hastaların Retrospektif Olarak Değerlendirilmesi
(Tıp Fakültesi, 2020-02)
Cebeci K., Retrospective Evaluation of Polysomnographic Features in Children with Chronic Neurological Disorders and Multiple Disabilities. Hacettepe University Faculty of Medicine, Thesis in Pediatrics, Ankara-2020. ...
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 ...
DİYET UYGULAYAN VEYA SAPROPTERİN HİDROKLORİD ALAN FENİLKETONÜRİ HASTALARI VE AİLELERİNİN STRES DÜZEYLERİ VE YAŞAM KALİTELERİNİN DEĞERLENDİRİLMESİ
(Tıp Fakültesi, 2020)
Demirel D. Evaluation of stress levels and quality of life of phenylketonuria patients on diet and/or sapropterin hydrocloride therapy and their parents, Hacettepe University Faculty of Medicine, Department of Pediatrics, ...
Genetik ve Metabolik Epilepsilerin Pediatrik Epilepsideki Yeri, Klinik ve Tanısal Değerlendirmesi
(Tıp Fakültesi, 2023-09-11)
Epilepsy is a common neurological disorder affecting patients of all ages. The etiology of epilepsy constitutes a heterogeneous group of entities. Information on genetic and metabolic etiologies of epilepsy has been ...