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Vici syndrome in siblings born to consanguineous parents.
Tasdemir S, Sahin I, Cayır A, Yuce I, Ceylaner S, Tatar A. Tasdemir S, et al. Among authors: sahin i. Am J Med Genet A. 2016 Jan;170A(1):220-5. doi: 10.1002/ajmg.a.37398. Epub 2015 Sep 23. Am J Med Genet A. 2016. PMID: 26395118 Review.
RECURRENT RAB3GAP1 MUTATIONS IN THE TURKISH POPULATION.
Tasdemir S, Sahin I, Morris-Rosendahl DJ, Marzioglu E, Cayir A, Yuce I, Tatar A. Tasdemir S, et al. Among authors: sahin i. Genet Couns. 2015;26(4):415-23. Genet Couns. 2015. PMID: 26852512
A rare cause of dyspnea in emergency medicine: Keutel syndrome.
Bayramoğlu A, Saritemur M, Tasdemir S, Omeroglu M, Erdem HB, Sahin I. Bayramoğlu A, et al. Among authors: sahin i. Am J Emerg Med. 2016 May;34(5):935.e3-5. doi: 10.1016/j.ajem.2015.09.020. Epub 2015 Sep 21. Am J Emerg Med. 2016. PMID: 26462901 No abstract available.
Correlation with Platelet Parameters and Genetic Markers of Thrombophilia Panel (Factor II g.20210G>A, Factor V Leiden, MTHFR (C677T, A1298C), PAI-1, β-Fibrinogen, Factor XIIIA (V34L), Glycoprotein IIIa (L33P)) in Ischemic Strokes.
Tasdemir S, Erdem HB, Sahin I, Ozel L, Ozdemir G, Eroz R, Tatar A. Tasdemir S, et al. Among authors: sahin i. Neuromolecular Med. 2016 Jun;18(2):170-6. doi: 10.1007/s12017-016-8386-x. Epub 2016 Mar 7. Neuromolecular Med. 2016. PMID: 26951304
Holoprosencephaly: ZIC2 mutation in a case with panhypopituitarism.
Tasdemir S, Sahin I, Cayır A, Doneray H, Solomon BD, Muenke M, Yuce I, Tatar A. Tasdemir S, et al. Among authors: sahin i. J Pediatr Endocrinol Metab. 2014 Jul;27(7-8):777-81. doi: 10.1515/jpem-2013-0449. J Pediatr Endocrinol Metab. 2014. PMID: 24706429
744 results