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Toplam kayıt 241, listelenen: 71-80
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 ...