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Journal of Clinical Research in Pediatric Endocrinology
|
August 28, 2025
Real-World Experience from Türkiye: Genetic and Therapeutic Insights in Pediatric Heterozygous Familial Hypercholesterolemia
Havva Yazıcı, Esra Er, Fehime Erdem, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
October 9, 2025
Mucolipidosis type II and III: clinical spectrum, genetic landscape, and longitudinal outcomes in a pediatric cohort with six novel mutations
Fehime Erdem, Ebru Canda, Havva Yazıcı, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
November 5, 2023
Experience with carnitine palmitoyltransferase II deficiency: diagnostic challenges in the myopathic form
Havva Yazıcı, Gunes Ak, Merve Yoldas Çelik, et al.
Journal of Clinical Lipidology
|
January 20, 2026
Severe hypercholesterolemia in a pediatric cohort: Familial homozygous and autosomal recessive hypercholesterolemia
Havva Yazıcı, Ebru Canda, Fehime Erdem, et al.
Neuropediatrics
|
December 26, 2025
EVALUATION OF EXPERIENCED CLINICAL EVENTS IN POMPE DISEASE BASED ON REAL-LIFE DATA
Fehime Erdem Karapınar, Havva Yazıcı, Merve Yoldaş Çelik, et al.
Metabolic Brain Disease
|
June 22, 2026
Treatment strategies, radiological recovery, and neurodevelopmental outcomes in paediatric Maple Syrup Urine Disease: a 20-year single-centre experience from Türkiye
Kemal Uylaş, Havva Yazıcı, Yasemin Atik Altınok, et al.
Pediatric Blood & Cancer
|
April 13, 2023
Hematopoietic stem cell transplantation with reduced toxicity conditioning regimen in mitochondrial neurogastrointestinal encephalopathy syndrome
Gülcihan Ozek, Serap Aksoylar, Sema Kalkan Uçar, et al.
Lipids in Health and Disease
|
November 13, 2024
Determination of selected oxysterol levels, oxidative stress, and macrophage activation indicators in children and adolescents with familial hypercholesterolemia
Erhan Canbay, Ebru Canda, Havva Yazıcı, et al.
Diagnostics (Basel, Switzerland)
|
November 13, 2025
Genotype-Phenotype Correlations and Shifting Diagnosis Age in Turkish Mucopolysaccharidosis Type II Patients: A Multicenter Retrospective Study
Havva Yazıcı, Esra Kara, Fatma Derya Bulut, et al.
Molecular Genetics and Metabolism Reports
|
November 2, 2020
<i>SURF1</i> related Leigh syndrome: Clinical and molecular findings of 16 patients from Turkey
Melis Kose, Ebru Canda, Mehtap Kagnici, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 55) with videos related to
Sort By:
Page
of 6
Journal of Clinical Research in Pediatric Endocrinology
|
August 28, 2025
Real-World Experience from Türkiye: Genetic and Therapeutic Insights in Pediatric Heterozygous Familial Hypercholesterolemia
Havva Yazıcı, Esra Er, Fehime Erdem, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
October 9, 2025
Mucolipidosis type II and III: clinical spectrum, genetic landscape, and longitudinal outcomes in a pediatric cohort with six novel mutations
Fehime Erdem, Ebru Canda, Havva Yazıcı, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
November 5, 2023
Experience with carnitine palmitoyltransferase II deficiency: diagnostic challenges in the myopathic form
Havva Yazıcı, Gunes Ak, Merve Yoldas Çelik, et al.
Journal of Clinical Lipidology
|
January 20, 2026
Severe hypercholesterolemia in a pediatric cohort: Familial homozygous and autosomal recessive hypercholesterolemia
Havva Yazıcı, Ebru Canda, Fehime Erdem, et al.
Neuropediatrics
|
December 26, 2025
EVALUATION OF EXPERIENCED CLINICAL EVENTS IN POMPE DISEASE BASED ON REAL-LIFE DATA
Fehime Erdem Karapınar, Havva Yazıcı, Merve Yoldaş Çelik, et al.
Metabolic Brain Disease
|
June 22, 2026
Treatment strategies, radiological recovery, and neurodevelopmental outcomes in paediatric Maple Syrup Urine Disease: a 20-year single-centre experience from Türkiye
Kemal Uylaş, Havva Yazıcı, Yasemin Atik Altınok, et al.
Pediatric Blood & Cancer
|
April 13, 2023
Hematopoietic stem cell transplantation with reduced toxicity conditioning regimen in mitochondrial neurogastrointestinal encephalopathy syndrome
Gülcihan Ozek, Serap Aksoylar, Sema Kalkan Uçar, et al.
Lipids in Health and Disease
|
November 13, 2024
Determination of selected oxysterol levels, oxidative stress, and macrophage activation indicators in children and adolescents with familial hypercholesterolemia
Erhan Canbay, Ebru Canda, Havva Yazıcı, et al.
Diagnostics (Basel, Switzerland)
|
November 13, 2025
Genotype-Phenotype Correlations and Shifting Diagnosis Age in Turkish Mucopolysaccharidosis Type II Patients: A Multicenter Retrospective Study
Havva Yazıcı, Esra Kara, Fatma Derya Bulut, et al.
Molecular Genetics and Metabolism Reports
|
November 2, 2020
<i>SURF1</i> related Leigh syndrome: Clinical and molecular findings of 16 patients from Turkey
Melis Kose, Ebru Canda, Mehtap Kagnici, et al.
Page
of 6