Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Z Yapici

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
Acta Paediatrica (Oslo, Norway : 1992)|June 29, 2005
Non-progressive congenital ataxia with cerebellar hypoplasia in three familiesZ Yapici, M Eraksoy
Annals of Tropical Paediatrics|June 5, 2010
Analgesic effects of skin-to-skin contact and breastfeeding in procedural pain in healthy term neonatesF Okan, A Ozdil, A Bulbul, et al.
The International Journal of Neuroscience|October 6, 2007
High interleukin-10 production is associated with anti-acetylcholine receptor antibody production and treatment response in juvenile myasthenia gravisZ Yapici, E Tüzün, V Altunayoğlu, et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology|October 7, 2011
Five recurrent ectopic pregnancies in a patient with MUC1 expression deficiencyG Bozdag, Z G Atak, Z Yapici, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 14, 2016
Fibromatous lesion of the scalp: is it an underestimated sign of tuberous sclerosis?C Baykal, P Tekturk, A Polat Ekinci, et al.
Neuropediatrics|July 30, 2009
Two cases with progressive cystic leukoencephalopathyZ Yapici, G Benbir, S Saltik, et al.
Clinical Genetics|January 31, 2012
High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher diseaseB Bilir, Z Yapici, C Yalcinkaya, et al.
Molecular Genetics and Metabolism|December 4, 2014
Cerebrospinal fluid synaptic proteins as useful biomarkers in tyrosine hydroxylase deficiencyC Ortez, S T Duarte, A Ormazábal, et al.
Neuromuscular Disorders : NMD|August 25, 2019
Mutation spectrum of 260 dystrophinopathy patients from Turkey and important highlights for genetic counselingG Toksoy, H Durmus, A Aghayev, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Acta Paediatrica (Oslo, Norway : 1992)|June 29, 2005
Non-progressive congenital ataxia with cerebellar hypoplasia in three familiesZ Yapici, M Eraksoy
Annals of Tropical Paediatrics|June 5, 2010
Analgesic effects of skin-to-skin contact and breastfeeding in procedural pain in healthy term neonatesF Okan, A Ozdil, A Bulbul, et al.
The International Journal of Neuroscience|October 6, 2007
High interleukin-10 production is associated with anti-acetylcholine receptor antibody production and treatment response in juvenile myasthenia gravisZ Yapici, E Tüzün, V Altunayoğlu, et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology|October 7, 2011
Five recurrent ectopic pregnancies in a patient with MUC1 expression deficiencyG Bozdag, Z G Atak, Z Yapici, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 14, 2016
Fibromatous lesion of the scalp: is it an underestimated sign of tuberous sclerosis?C Baykal, P Tekturk, A Polat Ekinci, et al.
Neuropediatrics|July 30, 2009
Two cases with progressive cystic leukoencephalopathyZ Yapici, G Benbir, S Saltik, et al.
Clinical Genetics|January 31, 2012
High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher diseaseB Bilir, Z Yapici, C Yalcinkaya, et al.
Molecular Genetics and Metabolism|December 4, 2014
Cerebrospinal fluid synaptic proteins as useful biomarkers in tyrosine hydroxylase deficiencyC Ortez, S T Duarte, A Ormazábal, et al.
Neuromuscular Disorders : NMD|August 25, 2019
Mutation spectrum of 260 dystrophinopathy patients from Turkey and important highlights for genetic counselingG Toksoy, H Durmus, A Aghayev, et al.
Pageof 1