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The Turkish Journal of Pediatrics|June 25, 2004
Fucosidosis with hypothyroidism: a case reportNeslihan Onenli-Mungan, Güler Ozer, Sakir Altunbaşak, et al.
The Turkish Journal of Pediatrics|September 22, 2015
X-linked adrenoleukodystrophy in a 6-year-old boy initially presenting with psychiatric symptomsFaruk İncecik, M Özlem Hergüner, Gülen Mert, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 22, 2018
Twenty-seven mutations with three novel pathologenic variants causing biotinidase deficiency: a report of 203 patients from the southeastern part of TurkeyBerna Seker Yilmaz, Neslihan Onenli Mungan, Deniz Kor, et al.
International Journal of Pharmaceutics|January 13, 2009
Intravesical cationic nanoparticles of chitosan and polycaprolactone for the delivery of Mitomycin C to bladder tumorsErem Bilensoy, Can Sarisozen, Güneş Esendağli, et al.
Journal of Inherited Metabolic Disease|May 30, 2025
Audiovestibular Findings in Gaucher Disease Types I and III: Evidence of Vestibular Involvement in GD1Elvan Onan, Fatma Derya Bulut, Deniz Kor, et al.
Digestive Diseases and Sciences|April 6, 2007
HFE gene mutation, chronic liver disease, and iron overload In TurkeyOya Yönal, Ozden Hatirnaz, Filiz Akyüz, et al.
Oncology Letters|January 21, 2016
Olfactory neuroblastoma: A case reportGonca Hanedan Uslu, Emine Canyilmaz, Ahmet Yasar Zengin, et al.
Urology|May 11, 2010
Fournier's gangrene: overview of prognostic factors and definition of new prognostic parameterBulent Erol, Altug Tuncel, Volkan Hanci, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 28, 2010
Thyroid peroxidase gene mutations causing congenital hypothyroidism in three Turkish familiesMehmet Nuri Ozbek, Abdi Burak Uslu, Neslihan Onenli-Mungan, et al.
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