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

Talim

Showing results (11-20 of 159) with videos related to

Pageof 16
Sort By:
Current Eye Research|January 2, 2024
Mimicking TGFBI Hot-Spot Mutation Did Not Result in Any Deposit Formation in the Zebrafish CorneaFulya Yaylacıoğlu Tuncay, Beril Talim, Pervin Rukiye Dinçer
Rheumatology International|March 28, 2009
Sarcoid-like granulomas in common variable immunodeficiencyHasibe Artac, Banu Bozkurt, Beril Talim, et al.
Urologia Internationalis|August 21, 2002
A reevaluation of the structures accepted to represent the postnatal gubernaculumF Cahit Tanyel, Beril Talim, Gülsev Kale, et al.
Surgery Today|September 22, 2005
Aneurysmal bone cyst of the rib in a child: report of a caseTutku Soyer, Ibrahim Karnak, Beril Talim, et al.
Clinical Neurology and Neurosurgery|November 28, 2021
A novel bi-allelic variant in the SDHB gene causes a severe mitochondrial complex II deficiency: a case reportAsli Ece Solmaz, Erhan Pariltay, Beril Talim, et al.
Pathology, Research and Practice|February 24, 2001
Differences in the morphology of the processus vaginalis with sex and underlying disease conditionF C Tanyel, B Talim, G Kale, et al.
BMC Neurology|December 17, 2018
LARGE expression in different types of muscular dystrophies other than dystroglycanopathyBurcu Balci-Hayta, Beril Talim, Gulsev Kale, et al.
Journal of Inherited Metabolic Disease|June 13, 2015
Clinical characteristics of megaconial congenital muscular dystrophy due to choline kinase beta gene defects in a series of 15 patientsGoknur Haliloglu, Beril Talim, Cigdem Genc Sel, et al.
Neuromuscular Disorders : NMD|September 19, 2012
Coexistence of two distinct intragenic dystrophin deletions in two maternal cousins with Duchenne Muscular DystrophyBurcu Balci-Hayta, Beril Talim, Pervin Dinçer, et al.
Neuromuscular Disorders : NMD|March 10, 2009
Demyelinating disease of central and peripheral nervous systems associated with a A8344G mutation in tRNALysI Erol, F Alehan, R Horvath, et al.
Pageof 16

Showing results (11-20 of 159) with videos related to

Sort By:
Pageof 16
Current Eye Research|January 2, 2024
Mimicking TGFBI Hot-Spot Mutation Did Not Result in Any Deposit Formation in the Zebrafish CorneaFulya Yaylacıoğlu Tuncay, Beril Talim, Pervin Rukiye Dinçer
Rheumatology International|March 28, 2009
Sarcoid-like granulomas in common variable immunodeficiencyHasibe Artac, Banu Bozkurt, Beril Talim, et al.
Urologia Internationalis|August 21, 2002
A reevaluation of the structures accepted to represent the postnatal gubernaculumF Cahit Tanyel, Beril Talim, Gülsev Kale, et al.
Surgery Today|September 22, 2005
Aneurysmal bone cyst of the rib in a child: report of a caseTutku Soyer, Ibrahim Karnak, Beril Talim, et al.
Clinical Neurology and Neurosurgery|November 28, 2021
A novel bi-allelic variant in the SDHB gene causes a severe mitochondrial complex II deficiency: a case reportAsli Ece Solmaz, Erhan Pariltay, Beril Talim, et al.
Pathology, Research and Practice|February 24, 2001
Differences in the morphology of the processus vaginalis with sex and underlying disease conditionF C Tanyel, B Talim, G Kale, et al.
BMC Neurology|December 17, 2018
LARGE expression in different types of muscular dystrophies other than dystroglycanopathyBurcu Balci-Hayta, Beril Talim, Gulsev Kale, et al.
Journal of Inherited Metabolic Disease|June 13, 2015
Clinical characteristics of megaconial congenital muscular dystrophy due to choline kinase beta gene defects in a series of 15 patientsGoknur Haliloglu, Beril Talim, Cigdem Genc Sel, et al.
Neuromuscular Disorders : NMD|September 19, 2012
Coexistence of two distinct intragenic dystrophin deletions in two maternal cousins with Duchenne Muscular DystrophyBurcu Balci-Hayta, Beril Talim, Pervin Dinçer, et al.
Neuromuscular Disorders : NMD|March 10, 2009
Demyelinating disease of central and peripheral nervous systems associated with a A8344G mutation in tRNALysI Erol, F Alehan, R Horvath, et al.
Pageof 16