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

Ali Dursun

Showing results (21-30 of 88) with videos related to

Pageof 9
Sort By:
European Journal of Pediatrics|February 13, 2020
Predictors of acute metabolic decompensation in children with maple syrup urine disease at the emergency departmentYılmaz Yıldız, Leman Akcan Yıldız, Ali Dursun, et al.
The Journal of Steroid Biochemistry and Molecular Biology|March 10, 2016
Novel and prevalent CYP11B1 gene mutations in Turkish patients with 11-β hydroxylase deficiencyNurgun Kandemir, Didem Yucel Yilmaz, E Nazli Gonc, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 21, 2022
Hyperinsulinism May Be Underreported in Hypoglycemic Patients with Phosphomannomutase 2 DeficiencyDoğuş Vurallı, Yılmaz Yıldız, Alev Ozon, et al.
Molecular Genetics and Metabolism|June 26, 2012
Microarray based mutational analysis of patients with methylmalonic acidemia: identification of 10 novel mutationsHalil Dündar, Riza Köksal Özgül, Ayşegül Güzel-Ozantürk, et al.
Free Radical Biology & Medicine|January 2, 2022
An investigation of different intracellular parameters for Inborn Errors of Metabolism: Cellular stress, antioxidant response and autophagyNeşe Vardar Acar, Ali Dursun, Damla Aygün, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 13, 2020
Oral health status of children with phenylketonuriaElif Ballikaya, Yilmaz Yildiz, Hatice Serap Sivri, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 6, 2022
Organic acidemias in the neonatal period: 30 years of experience in a referral center for inborn errors of metabolismYagmur Unsal, Murat Yurdakok, Sule Yigit, et al.
Molecular Genetics and Metabolism|May 18, 2023
COVID-19 in inherited metabolic disorders: Clinical features and risk factors for disease severityAyca Burcu Kahraman, Yılmaz Yıldız, Kısmet Çıkı, et al.
Molecular Genetics and Metabolism|October 14, 2023
Predictors of eventual requirement of phenylalanine-restricted diet in young infants with phenylalanine hydroxylase deficiency initially managed with sapropterin monotherapyKısmet Çıkı, Yılmaz Yıldız, Ayça Burcu Kahraman, et al.
Arthritis and Rheumatism|October 31, 2009
Increased frequency of extremely skewed X chromosome inactivation in juvenile idiopathic arthritisElif Uz, Chigdem Mustafa, Rezan Topaloglu, et al.
Pageof 9

Showing results (21-30 of 88) with videos related to

Sort By:
Pageof 9
European Journal of Pediatrics|February 13, 2020
Predictors of acute metabolic decompensation in children with maple syrup urine disease at the emergency departmentYılmaz Yıldız, Leman Akcan Yıldız, Ali Dursun, et al.
The Journal of Steroid Biochemistry and Molecular Biology|March 10, 2016
Novel and prevalent CYP11B1 gene mutations in Turkish patients with 11-β hydroxylase deficiencyNurgun Kandemir, Didem Yucel Yilmaz, E Nazli Gonc, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 21, 2022
Hyperinsulinism May Be Underreported in Hypoglycemic Patients with Phosphomannomutase 2 DeficiencyDoğuş Vurallı, Yılmaz Yıldız, Alev Ozon, et al.
Molecular Genetics and Metabolism|June 26, 2012
Microarray based mutational analysis of patients with methylmalonic acidemia: identification of 10 novel mutationsHalil Dündar, Riza Köksal Özgül, Ayşegül Güzel-Ozantürk, et al.
Free Radical Biology & Medicine|January 2, 2022
An investigation of different intracellular parameters for Inborn Errors of Metabolism: Cellular stress, antioxidant response and autophagyNeşe Vardar Acar, Ali Dursun, Damla Aygün, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 13, 2020
Oral health status of children with phenylketonuriaElif Ballikaya, Yilmaz Yildiz, Hatice Serap Sivri, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 6, 2022
Organic acidemias in the neonatal period: 30 years of experience in a referral center for inborn errors of metabolismYagmur Unsal, Murat Yurdakok, Sule Yigit, et al.
Molecular Genetics and Metabolism|May 18, 2023
COVID-19 in inherited metabolic disorders: Clinical features and risk factors for disease severityAyca Burcu Kahraman, Yılmaz Yıldız, Kısmet Çıkı, et al.
Molecular Genetics and Metabolism|October 14, 2023
Predictors of eventual requirement of phenylalanine-restricted diet in young infants with phenylalanine hydroxylase deficiency initially managed with sapropterin monotherapyKısmet Çıkı, Yılmaz Yıldız, Ayça Burcu Kahraman, et al.
Arthritis and Rheumatism|October 31, 2009
Increased frequency of extremely skewed X chromosome inactivation in juvenile idiopathic arthritisElif Uz, Chigdem Mustafa, Rezan Topaloglu, et al.
Pageof 9