Başlık için Dahili Tıp Bilimleri Bölümü listeleme
Toplam kayıt 3839, listelenen: 505-524
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Behçet Hastalarında Eritema Nodozum Varlığının Klinik Bulgularla İlişkisi
(Tıp Fakültesi, 2018)Introduction and Purpose Behçet's disease is a heterogeneous vasculitis with predominantly mucocutaneous findings characterized by unexplained neutrophilic hyperfunction and autoinflammatory responses. Eritema nodosum ... -
Behçet Hastalarında Hedef Doku ve Organ Tutulumuna Göre Nötrofil/Lenfosit Oranı, Sedimentasyon, C-Reaktif Protein Düzeylerinin İncelenmesi
(Tıp Fakültesi, 2018)Behçet’s disease is a multisystemic and inflammatory disease which is characterized by oral, genital ulcers, vasculitis involving vessels of all sizes and cutaneous, ocular, vascular, articular, neurological and gastrointestinal ... -
Behçet hastalığı; organ tehdit eden bulgular ve tedavi yaklaşımı
(Hacettepe Üniversitesi Tıp Fakültesi, 2020) -
Behçet’S Disease In Children: Single-Center Experience
(2019)Aim: In this study, it was aimed to summarize the demographics, and clinical and laboratory findings of children who were diagnosed as having Behçet’s disease, and also to determine the efficacy, duration, and adverse ... -
Beneficial Effect of Methylprednisolone on Cardiac Myocytes in a Rat Model of Severe Brain Injury
(Tohoku Univ Medical Press, 2005)Cardiac injury, occurred after traumatic brain injury (TBI), has been recognized for more than a century. Bcl-2 is a key regulatory component of the mitochondrial cell death pathway, and its overexpression is cytoprotective ... -
Benefit Of High-Dose Methylprednisolone In Comparison With Conventional-Dose Prednisolone During Remission Induction Therapy In Childhood Acute Lymphoblastic Leukemia For Long-Term Follow-Up
(Nature Publishing Group, 2003)Eight-year event-free survival (EFS) was evaluated in 205 patients with acute lymphoblastic leukemia (ALL), to consider the efficacy of high-dose methylprednisolone (HDMP) given during remission induction chemotherapy ... -
Benign Mesenchymoma of the Esophagus
(Elsevier Science Bv, 1997)Benign mesenchymoma is an extremely rare neoplasm mostly located in or about the kidney and is composed of a haphazard mixture of adult fat, fibrous tissue and tangled blood vessels, scattered nests or masses of smooth ... -
Benign Mixed Epithelial and Stromal Tumor of the Kidney
(2006)A 51-year-old, perimenopausal, female patient with 1-month history of right flank pain who was diagnosed with a renal mass and underwent nephron-sparing partial nephrectomy is presented. The renal mass was found to be a ... -
Benign ve malign kas-iskelet sistemi tümörlerinin ayrımında monoeksponansiyel difüzyon ağırlıklı görüntüleme, intravoxel incoherent motion ve difüzyon kurtozis modellerinin kullanıldığı multiparametrik yaklaşım
(Tıp Fakültesi, 2021)The aim of our study was to evaluate the value of multiparametric analysis of monoexponential DWI, IVIM and DK models for differentiating benign and malignant musculoskeletal tumors. Between Aug 2019 to Nov 2020, a total ... -
Bernard Lerer: Recipient of the 2014 Inaugural Werner Kalow Responsible Innovation Prize in Global Omics and Personalized Medicine (Pacific Rim Association For Clinical Pharmacogenetics)
(Mary Ann Liebert, Inc, 2014)This article announces the recipient of the 2014 inaugural Werner Kalow Responsible Innovation Prize in Global Omics and Personalized Medicine by the Pacific Rim Association for Clinical Pharmacogenetics (PRACP): Bernard ... -
Besin Alerjisi Olan Çocukların Beslenme Durumunun Değerlendirilmesi
(Tıp Fakültesi, 2018)The only treatment of food allergy is the removal of causative food from diet. Foods that cause allergy in childhood include the essential nutrients necessary for the growth of the child. The aim of this study is to assess ... -
Beslenme Anketi Yöntemi ile Hemodiyaliz Hastalarının Günlük Tuz Alımı Hesaplanabilir mi?
(Tıp Fakültesi, 2013)Dietary salt intake is the primary reason of weight gain between two dialysis for the hemodialysed patient population. Osmotic polydipsia which develops secondarily to salt intake, is accompanied by fluid intake. Increase ... -
Beta Talasemi Major Hastalarinda Oral Deferasirox ve Diğer Demir Şelasyon Tedavilerinin Kardiak, Hepatik ve Endokrin Organlardaki Demir Birikimi Üzerine Etkisinin T2* Mrg ile Değerlendirilmesi
(Tıp Fakültesi, 2014)Thirtyseven patients with β thalassemia major who were being followed up in Hacettepe University, İhsan Doğramacı Children’s Hospital, Division of Pediatric Hematology and on the same study drugs for at least 1 year were ... -
Beta-Globin Haplotype And Xmni Polymorphism At Position G-Gamma-158 And Hbf Production In Fanconis Anemia
(Ferrata Storti Foundation, 1992)Background. Patients with aplastic anemia show to a variable degree an increase of the red blood cell volume and percentage of HbF. The extent of HbF reactivation in sickle cell anemia and thalassemia major is related to ... -
Bevacizumab + Capecitabine As Maintenance Therapy After Initial Bevacizumab + Xelox Treatment In Previously Untreated Patients with Metastatic Colorectal Cancer: Phase Ill 'Stop And Go' Study Results - A Turkish Oncology Group Trial
(Karger, 2013)Objective: It was the aim of this study to evaluate maintenance therapy with bevacizumab + capecitabine following induction with bevacizumab + capecitabine + oxaliplatin (XELOX) versus bevacizumab + XELOX until progression ... -
Bi-Allelic Csf1R Mutations Cause Skeletal Dysplasia Of Dysosteosclerosis-Pyle Disease Spectrum And Degenerative Encephalopathy With Brain Malformation
(2019)Colony stimulating factor 1 receptor (CSF1R) plays key roles in regulating development and function of the monocyte/macrophage lineage, including microglia and osteoclasts. Mono-allelic mutations of CSF1R are known to cause ... -
Biallelic Hypomorphic Mutations In A Linear Deubiquitinase Define Otulipenia, An Early-Onset Autoinflammatory Disease
(Natl Acad Sciences, 2016)Systemic autoinflammatory diseases are caused by mutations in genes that function in innate immunity. Here, we report an autoinflammatory disease caused by loss-of-function mutations in OTULIN (FAM105B), encoding a ... -
Biallelic Mutations in Snx14 Cause A Syndromic Form of Cerebellar Atrophy and Lysosome-Autophagosome Dysfunction
(2015)Pediatric-onset ataxias often present clinically with developmental delay and intellectual disability, with prominent cerebellar atrophy as a key neuroradiographic finding. Here we describe a novel clinically distinguishable ... -
Bilateral Additional Renal Arteries And An Additional Right Renal Vein Associated With Unrotated Kidneys
(Saudi Med J, 2003)We report a rare anomaly of the kidneys and its vessels, which were found during the routine dissection of a 68-year-old male cadaver. The anomaly consisted of bilateral additional renal arteries originating from the ...