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

Huseyin Per

Showing results (41-50 of 61) with videos related to

Pageof 7
Sort By:
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|December 7, 2017
The relationship between hematological parameters and prognosis of children with acute ischemic strokeEbru Yilmaz, Ayse Bayram Kacar, Adil Bozpolat, et al.
Neuropediatrics|August 25, 2017
Erratum: Neurological Manifestations in Familial Mediterranean Fever: Results of 22 Children from a Reference Center in Kayseri, an Urban Area in Central Anatolia, TurkeyMehmet Canpolat, Hakan Gumus, Zubeyde Gunduz, et al.
Neuropediatrics|September 23, 2016
Neurological Manifestations in Familial Mediterranean Fever: Results of 22 Children from a Reference Center in Kayseri, an Urban Area in Central Anatolia, TurkeyMehmet Canpolat, Hakan Gumus, Zubeyde Gunduz, et al.
Journal of Child Neurology|September 17, 2014
Brain abscesses in children: results of 24 children from a reference center in Central Anatolia, TurkeyMehmet Canpolat, Ozgur Ceylan, Huseyin Per, et al.
Neurogenetics|May 31, 2025
A case series of joubert syndrome evaluated with whole exome sequencing and the utility of optical genome mapping in the diagnosisAslihan Kiraz, Murat Erdogan, Burhan Balta, et al.
Turkish Neurosurgery|March 24, 2021
The Spectrum of Underlying Diseases in Children with TorticollisAbdulfettah Tumturk, Sureyya Burcu Gorkem, Elif Nurdan Ozmansur, et al.
Iscience|March 9, 2026
Distinct mutational signature and clonal evolution in constitutional mismatch repair deficiency-associated high-grade gliomasChang Li, E Zeynep Erson-Omay, Yavuz Koksal, et al.
Journal of Neurogenetics|September 25, 2024
Molecular analysis of <i>SMN2, NAIP,</i> and <i>GTF2H2</i> gene deletions and relationships with clinical subtypes of spinal muscular atrophyNilgun Karasu, Hamit Acer, Hilal Akalin, et al.
Journal of Human Genetics|October 2, 2015
Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 geneFatih Bayrakli, Hatice Gamze Poyrazoglu, Sirin Yuksel, et al.
Journal of Clinical Laboratory Analysis|December 20, 2023
Evaluation of chromosomal abnormalities in the postnatal cohort: A single-center study on 14,242 patientsHilal Akalin, Izem Olcay Sahin, Seyma Aktas Paskal, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|December 7, 2017
The relationship between hematological parameters and prognosis of children with acute ischemic strokeEbru Yilmaz, Ayse Bayram Kacar, Adil Bozpolat, et al.
Neuropediatrics|August 25, 2017
Erratum: Neurological Manifestations in Familial Mediterranean Fever: Results of 22 Children from a Reference Center in Kayseri, an Urban Area in Central Anatolia, TurkeyMehmet Canpolat, Hakan Gumus, Zubeyde Gunduz, et al.
Neuropediatrics|September 23, 2016
Neurological Manifestations in Familial Mediterranean Fever: Results of 22 Children from a Reference Center in Kayseri, an Urban Area in Central Anatolia, TurkeyMehmet Canpolat, Hakan Gumus, Zubeyde Gunduz, et al.
Journal of Child Neurology|September 17, 2014
Brain abscesses in children: results of 24 children from a reference center in Central Anatolia, TurkeyMehmet Canpolat, Ozgur Ceylan, Huseyin Per, et al.
Neurogenetics|May 31, 2025
A case series of joubert syndrome evaluated with whole exome sequencing and the utility of optical genome mapping in the diagnosisAslihan Kiraz, Murat Erdogan, Burhan Balta, et al.
Turkish Neurosurgery|March 24, 2021
The Spectrum of Underlying Diseases in Children with TorticollisAbdulfettah Tumturk, Sureyya Burcu Gorkem, Elif Nurdan Ozmansur, et al.
Iscience|March 9, 2026
Distinct mutational signature and clonal evolution in constitutional mismatch repair deficiency-associated high-grade gliomasChang Li, E Zeynep Erson-Omay, Yavuz Koksal, et al.
Journal of Neurogenetics|September 25, 2024
Molecular analysis of <i>SMN2, NAIP,</i> and <i>GTF2H2</i> gene deletions and relationships with clinical subtypes of spinal muscular atrophyNilgun Karasu, Hamit Acer, Hilal Akalin, et al.
Journal of Human Genetics|October 2, 2015
Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 geneFatih Bayrakli, Hatice Gamze Poyrazoglu, Sirin Yuksel, et al.
Journal of Clinical Laboratory Analysis|December 20, 2023
Evaluation of chromosomal abnormalities in the postnatal cohort: A single-center study on 14,242 patientsHilal Akalin, Izem Olcay Sahin, Seyma Aktas Paskal, et al.
Pageof 7