Ara
Toplam kayıt 241, listelenen: 61-80
Childhood Onset Analgesic Intolerance: A Marker For Bronchial-Asthma In Adulthood?
(W B Saunders Co Ltd, 2008)
Analgesic intolerance (AI) which is classically known as a disease of the middle-aged adults, not uncommonly starts in childhood. In this study we sought to identify the characteristics of childhood onset Al and evaluated ...
Corticotropin Tests For Hypothalamic-Pituitary-Adrenal Insufficiency: A Metaanalysis
(Endocrine Soc, 2008)
Context: The diagnostic value of tests for detecting hypothalamic-pituitary adrenal insufficiency (HPAI) is controversial. Objective: Our objective was to compare standard-dose and low-dose corticotropin tests for diagnosing ...
Evaluation Of Prenatal-Onset Osteochondrodysplasias By Ultrasonography: A Retrospective And Prospective Analysis
(Wiley-Liss, 2008)
The osteochondrodysplasia or skeletal dysplasias are a heterogenous group of over 350 distinct disorders of skeletogenesis. Many manifest in the prenatal diagnosis. A retrospective analysis evaluated 1,500 cases referred ...
An Unusual Association Between Familial Mediterranean Fever and Igm Nephropathy
(Karger, 2008)
Objective: To report a case with the diagnosis of IgM nephropathy and familial Mediterranean fever (FMF). Clinical Presentation and Intervention: A 9-year-old boy was admitted to our hospital with recurrent abdominal pain ...
Gross Deletions Involving Ighm, Btk, Or Artemis: A Model For Genomic Lesions Mediated By Transposable Elements
(Cell Press, 2008)
Most genetic disruptions underlying human disease are microlesions, whereas gross lesions are rare with gross deletions being most frequently found (6%). Similar observations have been made in primary immunodeficiency ...
Human Osteoclast-Poor Osteopetrosis With Hypogammaglobulinemia Due To Tnfrsf11A (Rank) Mutations
(Cell Press, 2008)
Autosomal-Recessive Osteopetrosis (ARO) comprises a heterogeneous group of bone diseases for which mutations in five genes are known as causative. Most ARO are classified as osteoclast-rich, but recently a subset of ...
Identification Of A Founder Mutation In Tpm3 In Nemaline Myopathy Patients Of Turkish Origin
(Nature Publishing Group, 2008)
To date, six genes are known to cause nemaline (rod) myopathy (NM), a rare congenital neuromuscular disorder. In an attempt to find a seventh gene, we performed linkage and subsequent sequence analyses in 12 Turkish families ...
Türkiye Nüfus ve Sağlık Araştırması Özet Rapor 2008
(Hacettepe Üniversitesi Nüfus Etütleri Enstitüsü, 2008)
Bu yayında yer alan bilgilerden Hacettepe Üniversitesi Nüfus Etütleri Enstitüsü sorumludur ve hiç bir şekilde Türkiye Bilimsel ve Teknolojik Araştırma Kurumu’nun (TÜBİTAK) görüşünü yansıtmamaktadır. 2008 Türkiye Nüfus ve ...
Dysplasia and Disorder of cell Membrane Entirety in Iron-Deficiency Anemia
(Taylor and Francis, 2008)
Peripheral blood smears of 43 patients (26 males, median age 18 months, range: 6-180 months) with nutritional iron-deficiency anemia (IDA) were examined for the presence of trilineage hematological dysplasia. Twelve patients ...
Intravenous Immunoglobulin in The Treatment of Severe MethotrexateInduced Acral Erythema
(Wolters Kluwer, 2008)
Two New Cases with Pearson Syndrome and Review of Hacettepe Experience
(2008)
SUMMARY: Topaloğlu R, Lebre AS, Demirkaya E, Kuşkonmaz B, Coşkun T,
Orhan D, Gürgey A, Gümrük F. Two new cases with Pearson syndrome and
review of Hacettepe experience. Turk J Pediatr 2008; 50: 572-576.
Pearson syndrome ...
Icone: An International Consortium Of Neuro Endovascular Centres
(Edizioni Centauro, 2008)
The proliferation of new endovascular devices and therapeutic strategies calls for a prudent and rational evaluation of their clinical benefit. This evaluation must be done in an effective manner and in collaboration with ...