Browsing Dahili Tıp Bilimleri Bölümü Makale Koleksiyonu by Title
Now showing items 1086-1105 of 2912
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Factor V Q 506 Mutation In Children With Thrombosis
(Wiley-Liss, 1996)The factor V Leiden mutation in 12-children with thrombosis and in 20 controls was investigated, Five heterozygous individuals and 1 homozygous individual among the cases with thrombosis and 1 heterozygous individual among ... -
Factors Affecting Development Of Pneumothorax In Critically Ill Children: A 3-Year Study
(2019)Background: To determine the factors affecting the development of pneumothorax in critically ill children admitted to pediatric intensive care unit (PICU). Methods: This was a single-centered retrospective case control ... -
Factors Affecting Food Allergy-Related Quality Of Life From Parents' Perception In Turkish Children
(2018)Purpose Food allergy (FA) affects the daily lives of children and parents in varying degrees. The Food Allergy Quality of Life Questionnaire-Parent Form (FAQLQ-PF) is a valid and reliable instrument to assess the quality ... -
Factors Associated With Pulmonary Hypertension And Long-Term Survival In Bronchiectasis Subjects
(W B Saunders Co Ltd, 2016)Background: The development of pulmonary hypertension (PH) and its effect on long-term survival in bronchiectasis subjects has not been explored. The present study aims to analyze the factors associated with PH and its ... -
Familial Adult Onset Myoclonic Epilepsy Associated With Migraine
(W B Saunders Co Ltd, 2000)We report a new type of migraine associated epileptic syndrome in a family. adult onset myoclonic epilepsy with benign course and migraine. Affected members of the family had myoclonic and rare generalised tonic-clonic ... -
Familial Mediterranean Fever In The 'Chuetas' Of Mallorca: A Question Of Jewish Origin Or Genetic Heterogeneity
(Nature Publishing Group, 2000)Familial Mediterranean fever (FMF) is a hereditary disease commonly found among Jews, Armenians, Turks and Arabs. Recently, FMF was found in the 'Chuetas', a unique community on the island of Mallorca (Spain). To address ... -
Familial Mediterranean Fever: Current Perspectives
(2016)Familial Mediterranean fever (FMF) is the most frequent monogenic autoinflammatory disease, and it is characterized by recurrent attacks of fever and polyserositis. The disease is associated with mutations in the MEFV gene ... -
Familial Mediterranean Fever: Recent Developments In Pathogenesis And New Recommendations For Management
(2017)Familial Mediterranean fever (FMF) is the most common monogenic autoinflammatory disease (AID) affecting mainly the ethnic groups originating from Mediterranean basin. The disease is characterized by self-limited inflammatory ... -
Familial Peripheric Polyneuropathy Plus Camptodactyly; Three Sisters
(Galenos Yayıncılık, 2012)Camptodactyly, the flexion contracture of the proximal interphalangeal joint usually involves the small finger and may be a component of some autosomal dominant diseases, such as Marfan's syndrome, cranio-carpo-tarsal ... -
Fanconi Anemia: A Single Center Experience Of A Large Cohort
(2019)Fanconi anemia (FA) is an inherited disease, characterized by congenital malformations, short stature, progressive bone marrow failure and predisposition to leukemia and solid tumors. The aim of this study was to evaluate ... -
Fanconi Anemia: A Single Center Experience of a Large Cohort
(Hacettepe Medical Center, 2019) -
Fast Track Algorithm: How To Differentiate A “Scleroderma Pattern” From A “Non-Scleroderma Pattern”
(2019)Objectives: This study was designed to propose a simple “Fast Track algorithm” for capillaroscopists of any level of experience to differentiate “scleroderma patterns” from “non-scleroderma patterns” on capillaroscopy and ... -
Features Of Asthma Which Provide Meaningful Insights For Understanding The Disease Heterogeneity
(2018)Background Data‐driven methods such as hierarchical clustering (HC) and principal component analysis (PCA) have been used to identify asthma subtypes, with inconsistent results. Objective To develop a framework for the ... -
Fever, Hepatosplenomegaly And Pancytopenia In A Patient Living In The Mediterranean Region
(British Med Journal Publ Group, 1998)