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European Journal of Pediatrics
|
February 13, 2020
Predictors of acute metabolic decompensation in children with maple syrup urine disease at the emergency department
Yılmaz 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 deficiency
Nurgun 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 Deficiency
Doğuş 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 mutations
Halil 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 autophagy
Neşe Vardar Acar, Ali Dursun, Damla Aygün, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 13, 2020
Oral health status of children with phenylketonuria
Elif 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 metabolism
Yagmur 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 severity
Ayca 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 monotherapy
Kısmet 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 arthritis
Elif Uz, Chigdem Mustafa, Rezan Topaloglu, et al.
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Search research articles
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Showing results (21-30 of 88) with videos related to
Sort By:
Page
of 9
European Journal of Pediatrics
|
February 13, 2020
Predictors of acute metabolic decompensation in children with maple syrup urine disease at the emergency department
Yılmaz 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 deficiency
Nurgun 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 Deficiency
Doğuş 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 mutations
Halil 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 autophagy
Neşe Vardar Acar, Ali Dursun, Damla Aygün, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 13, 2020
Oral health status of children with phenylketonuria
Elif 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 metabolism
Yagmur 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 severity
Ayca 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 monotherapy
Kısmet 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 arthritis
Elif Uz, Chigdem Mustafa, Rezan Topaloglu, et al.
Page
of 9