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Diabetologia
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October 23, 2021
Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics
Kashyap A Patel, Mehmet N Ozbek, Melek Yildiz, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 14, 2022
Steroid Hormone Profiles and Molecular Diagnostic Tools in Pediatric Patients With non-CAH Primary Adrenal Insufficiency
Tuba Seven Menevse, Yasemin Kendir Demirkol, Busra Gurpinar Tosun, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
October 8, 2024
Evaluation of Growth Characteristics and Final Height of Cases Diagnosed with Noonan Syndrome on Growth Hormone Treatment
Zeynep Şıklar, Merih Berberoğlu, Sirmen Kızılcan Çetin, et al.
Hormone Research in Paediatrics
|
March 30, 2012
The exon 3-deleted/full-length growth hormone receptor polymorphism and response to growth hormone therapy in growth hormone deficiency and Turner syndrome: a multicenter study
Firdevs Baş, Feyza Darendeliler, Zehra Aycan, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
May 29, 2025
Comparison of the clinical characteristics of children with Silver-Russell syndrome genetically confirmed or not and their response to growth hormone therapy: a national multicenter study
İlker Tolga Özgen, Tuğçe Kandemir, Melek Yıldız, et al.
Diabetologia
|
June 25, 2026
Autoantibody screening in children who are first-degree relatives of individuals with type 1 diabetes in a sibling-dominant cohort in Turkey: a multicentre study on prevalence, determinants and post-screening parent-child anxiety
Uğur C Yılmaz, Deniz Ö Kızılay, Özlem K Kurt, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
March 25, 2015
Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey
Şükran Poyrazoğlu, Teoman Akçay, İlknur Arslanoğlu, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 3, 2015
Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort
Tulay Guran, Federica Buonocore, Nurcin Saka, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
September 14, 2019
Nationwide Turkish Cohort Study of Hypophosphatemic Rickets
Zeynep Şıklar, Serap Turan, Abdullah Bereket, et al.
Hormone Research in Paediatrics
|
July 2, 2025
Genotype, Phenotype Characteristics and Long-Term Follow-Up of Patients with Vitamin D-Dependent Rickets Type IA: A Nationwide Multi-Centre Retrospective Cross-Sectional Study
Atilla Cayir, Huseyin Demirbilek, Ayberk Türkyılmaz, et al.
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of 14
Search research articles
Search
Showing results (121-130 of 136) with videos related to
Sort By:
Page
of 14
Diabetologia
|
October 23, 2021
Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics
Kashyap A Patel, Mehmet N Ozbek, Melek Yildiz, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 14, 2022
Steroid Hormone Profiles and Molecular Diagnostic Tools in Pediatric Patients With non-CAH Primary Adrenal Insufficiency
Tuba Seven Menevse, Yasemin Kendir Demirkol, Busra Gurpinar Tosun, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
October 8, 2024
Evaluation of Growth Characteristics and Final Height of Cases Diagnosed with Noonan Syndrome on Growth Hormone Treatment
Zeynep Şıklar, Merih Berberoğlu, Sirmen Kızılcan Çetin, et al.
Hormone Research in Paediatrics
|
March 30, 2012
The exon 3-deleted/full-length growth hormone receptor polymorphism and response to growth hormone therapy in growth hormone deficiency and Turner syndrome: a multicenter study
Firdevs Baş, Feyza Darendeliler, Zehra Aycan, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
May 29, 2025
Comparison of the clinical characteristics of children with Silver-Russell syndrome genetically confirmed or not and their response to growth hormone therapy: a national multicenter study
İlker Tolga Özgen, Tuğçe Kandemir, Melek Yıldız, et al.
Diabetologia
|
June 25, 2026
Autoantibody screening in children who are first-degree relatives of individuals with type 1 diabetes in a sibling-dominant cohort in Turkey: a multicentre study on prevalence, determinants and post-screening parent-child anxiety
Uğur C Yılmaz, Deniz Ö Kızılay, Özlem K Kurt, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
March 25, 2015
Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey
Şükran Poyrazoğlu, Teoman Akçay, İlknur Arslanoğlu, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 3, 2015
Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort
Tulay Guran, Federica Buonocore, Nurcin Saka, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
September 14, 2019
Nationwide Turkish Cohort Study of Hypophosphatemic Rickets
Zeynep Şıklar, Serap Turan, Abdullah Bereket, et al.
Hormone Research in Paediatrics
|
July 2, 2025
Genotype, Phenotype Characteristics and Long-Term Follow-Up of Patients with Vitamin D-Dependent Rickets Type IA: A Nationwide Multi-Centre Retrospective Cross-Sectional Study
Atilla Cayir, Huseyin Demirbilek, Ayberk Türkyılmaz, et al.
Page
of 14