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Semra Kurul

Showing results (21-30 of 25) with videos related to

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Journal of Paediatrics and Child Health|August 11, 2006
Aorta coarctation presenting with intracranial aneurysm ruptureOrkide Hüdaoğlu, Semra Kurul, Handan Cakmakci, et al.
Journal of Child Neurology|July 11, 2007
Basilar artery thrombosis in a child heterozygous for prothrombin gene G20210A mutationOrkide Hüdaoglu, Semra Kurul, Uluç Yis, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 13, 2006
A case of Walker-Warburg syndrome resulting from a homozygous POMT1 mutationUluç Yis, Gökhan Uyanik, Semra Kurul, et al.
Pediatric Nephrology (Berlin, Germany)|March 26, 2004
Frequent vaccination and immune complex deposition in unilateral nephrectomized miceSemra Kurul, Salih Kavukcu, Banu Sis, et al.
The Turkish Journal of Pediatrics|January 12, 2005
Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophyAyfer Ulgenalp, Ozlem Giray, Elçin Bora, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Journal of Paediatrics and Child Health|August 11, 2006
Aorta coarctation presenting with intracranial aneurysm ruptureOrkide Hüdaoğlu, Semra Kurul, Handan Cakmakci, et al.
Journal of Child Neurology|July 11, 2007
Basilar artery thrombosis in a child heterozygous for prothrombin gene G20210A mutationOrkide Hüdaoglu, Semra Kurul, Uluç Yis, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 13, 2006
A case of Walker-Warburg syndrome resulting from a homozygous POMT1 mutationUluç Yis, Gökhan Uyanik, Semra Kurul, et al.
Pediatric Nephrology (Berlin, Germany)|March 26, 2004
Frequent vaccination and immune complex deposition in unilateral nephrectomized miceSemra Kurul, Salih Kavukcu, Banu Sis, et al.
The Turkish Journal of Pediatrics|January 12, 2005
Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophyAyfer Ulgenalp, Ozlem Giray, Elçin Bora, et al.
Pageof 3