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Havva Yazici

Showing results (1-10 of 11) with videos related to

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Archivos Argentinos De Pediatria|January 24, 2022
Severe perinatal hypophosphatasia case with a novel mutationHavva Yazici, Ebru Canda, Sema Kalkan Ucar, et al.
JIMD Reports|January 14, 2022
Two siblings with galactose mutarotase deficiency: Clinical differencesHavva Yazici, Ebru Canda, Yasemin Atik Altınok, et al.
Journal of Child Neurology|July 31, 2025
Distinct Brain Magnetic Resonance Imaging (MRI) Findings Across Mucopolysaccharidosis Types: Novel InsightsNisa Baspinar, Havva Yazici, Cenk Eraslan, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 7, 2022
Long-term follow-up of alkaptonuria patients: single center experienceAyse Ergul Bozaci, Havva Yazici, Ebru Canda, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 12, 2018
Single center experience of biotinidase deficiency: 259 patients and six novel mutationsEbru Canda, Havva Yazici, Esra Er, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 12, 2023
Unique clinical presentations and follow-up outcomes from experience with congenital disorders of glycosylation: PMM2-PGM1-DPAGT1-MPI-POMT2-B3GALNT2-DPM1-SRD5A3-CDGMerve Yoldas Celik, Havva Yazici, Fehime Erdem, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|March 19, 2024
Long-term clinical outcomes and management of hypertriglyceridemia in children with Apo-CII deficiencyMerve Yoldas Celik, Ebru Canda, Havva Yazici, et al.
JIMD Reports|May 12, 2021
Tetrahydrobiopterin deficiencies: Lesson from clinical experienceAyse Ergul Bozaci, Esra Er, Havva Yazici, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 19, 2024
Splenomegaly and progressive neurologic involvement: Think about Niemann-Pick type C diseaseMerve Yoldas Celik, Havva Yazici, Fehime Erdem, et al.
European Journal of Pediatrics|December 10, 2024
Glutaric aciduria type 1: Insights into diagnosis and neurogenetic outcomesMerve Yoldas Celik, Ebru Canda, Havva Yazici, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Archivos Argentinos De Pediatria|January 24, 2022
Severe perinatal hypophosphatasia case with a novel mutationHavva Yazici, Ebru Canda, Sema Kalkan Ucar, et al.
JIMD Reports|January 14, 2022
Two siblings with galactose mutarotase deficiency: Clinical differencesHavva Yazici, Ebru Canda, Yasemin Atik Altınok, et al.
Journal of Child Neurology|July 31, 2025
Distinct Brain Magnetic Resonance Imaging (MRI) Findings Across Mucopolysaccharidosis Types: Novel InsightsNisa Baspinar, Havva Yazici, Cenk Eraslan, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 7, 2022
Long-term follow-up of alkaptonuria patients: single center experienceAyse Ergul Bozaci, Havva Yazici, Ebru Canda, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 12, 2018
Single center experience of biotinidase deficiency: 259 patients and six novel mutationsEbru Canda, Havva Yazici, Esra Er, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 12, 2023
Unique clinical presentations and follow-up outcomes from experience with congenital disorders of glycosylation: PMM2-PGM1-DPAGT1-MPI-POMT2-B3GALNT2-DPM1-SRD5A3-CDGMerve Yoldas Celik, Havva Yazici, Fehime Erdem, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|March 19, 2024
Long-term clinical outcomes and management of hypertriglyceridemia in children with Apo-CII deficiencyMerve Yoldas Celik, Ebru Canda, Havva Yazici, et al.
JIMD Reports|May 12, 2021
Tetrahydrobiopterin deficiencies: Lesson from clinical experienceAyse Ergul Bozaci, Esra Er, Havva Yazici, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 19, 2024
Splenomegaly and progressive neurologic involvement: Think about Niemann-Pick type C diseaseMerve Yoldas Celik, Havva Yazici, Fehime Erdem, et al.
European Journal of Pediatrics|December 10, 2024
Glutaric aciduria type 1: Insights into diagnosis and neurogenetic outcomesMerve Yoldas Celik, Ebru Canda, Havva Yazici, et al.
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