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Eray Dirik

Showing results (31-40 of 57) with videos related to

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Pediatric Neurology|May 4, 2005
Diagnostic value of diffusion-weighted magnetic resonance imaging in pediatric cerebral diseasesYasemin Fatma Oksuzler, Handan Cakmakci, Semra Kurul, et al.
Journal of Child Neurology|July 1, 2004
Assessment of child neurology outpatients with headache, dizziness, and faintingFatma Neslihan Inal Emiroğlu, Semra Kurul, Aynur Akay, et al.
Pediatric Neurology|November 26, 2009
Metabolic alterations during valproic acid treatment: a prospective studyAyhan Abaci, Murat Saygi, Uluc Yis, 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.
Journal of Child Neurology|August 24, 2007
Spinocerebellar ataxia type 2 in a Turkish familyEray Dirik, Uluç Yiş, Nazli Başak, et al.
Journal of Paediatrics and Child Health|August 11, 2006
Aorta coarctation presenting with intracranial aneurysm ruptureOrkide Hüdaoğlu, Semra Kurul, Handan Cakmakci, et al.
Acta Neurologica Belgica|November 9, 2012
Polysomnographic and long-term video electroencephalographic evaluation of cases presenting with parasomniasUluç Yiş, Semra Hiz Kurul, Ibrahim Öztura, et al.
Cerebellum (London, England)|November 22, 2008
Two young sisters with spinocerebellar ataxia type 2 showing different clinical progression of diseaseUluç Yiş, Eray Dirik, Semra Hiz Kurul, et al.
Journal of Child Neurology|March 18, 2009
Temporary diazepam responsive apneic attacks and congenital myasthenic syndromeUluç Yis, Semra Hiz Kurul, Ibrahim Oztura, et al.
American Journal of Medical Genetics. Part A|August 5, 2010
Congenital generalized lipodystrophy, type 4 (CGL4) associated with myopathy due to novel PTRF mutationsSavitha Shastry, Mauricio R Delgado, Eray Dirik, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
Pediatric Neurology|May 4, 2005
Diagnostic value of diffusion-weighted magnetic resonance imaging in pediatric cerebral diseasesYasemin Fatma Oksuzler, Handan Cakmakci, Semra Kurul, et al.
Journal of Child Neurology|July 1, 2004
Assessment of child neurology outpatients with headache, dizziness, and faintingFatma Neslihan Inal Emiroğlu, Semra Kurul, Aynur Akay, et al.
Pediatric Neurology|November 26, 2009
Metabolic alterations during valproic acid treatment: a prospective studyAyhan Abaci, Murat Saygi, Uluc Yis, 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.
Journal of Child Neurology|August 24, 2007
Spinocerebellar ataxia type 2 in a Turkish familyEray Dirik, Uluç Yiş, Nazli Başak, et al.
Journal of Paediatrics and Child Health|August 11, 2006
Aorta coarctation presenting with intracranial aneurysm ruptureOrkide Hüdaoğlu, Semra Kurul, Handan Cakmakci, et al.
Acta Neurologica Belgica|November 9, 2012
Polysomnographic and long-term video electroencephalographic evaluation of cases presenting with parasomniasUluç Yiş, Semra Hiz Kurul, Ibrahim Öztura, et al.
Cerebellum (London, England)|November 22, 2008
Two young sisters with spinocerebellar ataxia type 2 showing different clinical progression of diseaseUluç Yiş, Eray Dirik, Semra Hiz Kurul, et al.
Journal of Child Neurology|March 18, 2009
Temporary diazepam responsive apneic attacks and congenital myasthenic syndromeUluç Yis, Semra Hiz Kurul, Ibrahim Oztura, et al.
American Journal of Medical Genetics. Part A|August 5, 2010
Congenital generalized lipodystrophy, type 4 (CGL4) associated with myopathy due to novel PTRF mutationsSavitha Shastry, Mauricio R Delgado, Eray Dirik, et al.
Pageof 6