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Ozlem Engiz

Showing results (11-20 of 16) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|January 19, 2013
Infantile malignant osteopetrosis: a rare cause of neonatal hypocalcemiaOzlem Engiz, Semra Kara, Denizhan Bagrul, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 14, 2009
Early prophylactic thyroidectomy for RET mutation-positive MEN 2BOzlem Engiz, Gonul Ocal, Zeynep Siklar, et al.
Developmental Medicine and Child Neurology|March 16, 2007
Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1-11.2;p13.3)Sevim Balci, Aysun Unal, Ozlem Engiz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 3, 2011
Two pediatric patients with Von Hippel-Lindau disease type 2b: from patient to screening, from screening to patientNazli Gonc, Ozlem Engiz, Hartmut P H Neumann, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Ring chromosome 4 and Wolf-Hirschhorn syndrome (WHS) in a child with multiple anomaliesSevim Balci, Ozlem Engiz, Dilek Aktaş, et al.
Pediatric Hematology and Oncology|October 14, 2008
Evaluation of glucose homeostasis in transfusion-dependent thalassemic patientsZeynep Siklar, Funda Erkasar Citak, Zümrüt Uysal, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 19, 2013
Infantile malignant osteopetrosis: a rare cause of neonatal hypocalcemiaOzlem Engiz, Semra Kara, Denizhan Bagrul, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 14, 2009
Early prophylactic thyroidectomy for RET mutation-positive MEN 2BOzlem Engiz, Gonul Ocal, Zeynep Siklar, et al.
Developmental Medicine and Child Neurology|March 16, 2007
Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1-11.2;p13.3)Sevim Balci, Aysun Unal, Ozlem Engiz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 3, 2011
Two pediatric patients with Von Hippel-Lindau disease type 2b: from patient to screening, from screening to patientNazli Gonc, Ozlem Engiz, Hartmut P H Neumann, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Ring chromosome 4 and Wolf-Hirschhorn syndrome (WHS) in a child with multiple anomaliesSevim Balci, Ozlem Engiz, Dilek Aktaş, et al.
Pediatric Hematology and Oncology|October 14, 2008
Evaluation of glucose homeostasis in transfusion-dependent thalassemic patientsZeynep Siklar, Funda Erkasar Citak, Zümrüt Uysal, et al.
Pageof 2