Review

The Clinical Spectrum of Resistance to Thyroid Hormone Alpha in Children and Adults
  • İbrahim Mert Erbaş
  • Korcan Demir
J Clin Res Pediatr Endocrinol 2021; 13: 1-14 DOI: 10.4274/jcrpe.galenos.2020.2019.0190 PMID:32349464

Original Article

Catch-up Growth in Prepubertal Children Treated for Juvenile Hypothyroidism and Growth Hormone Deficiency can be Modelled with a Monomolecular Function
  • Jan M. Wit
  • Theo C. J. Sas
  • Michael B. Rank
  • Paula van Dommelen
J Clin Res Pediatr Endocrinol 2021; 13: 15-22 DOI: 10.4274/jcrpe.galenos.2020.2020.0130 PMID:32936765
Quality of Life and Psychological Well-being in Children and Adolescents with Disorders of Sex Development
  • Birsen Şentürk Pilan
  • Burcu Özbaran
  • Didem Çelik
  • Tuğçe Özcan
  • Samim Özen
  • Damla Gökşen
  • İbrahim Ulman
  • Ali Avanoğlu
  • Sibel Tiryaki
  • Hüseyin Onay
  • Özgür Çoğulu
  • Ferda Özkınay
  • Şükran Darcan
J Clin Res Pediatr Endocrinol 2021; 13: 23-33 DOI: 10.4274/jcrpe.galenos.2020.2020.0141 PMID:32938579
Identification of Three Novel and One Known Mutation in the Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis
  • Maha Sherif
  • Hüseyin Demirbilek
  • Atilla Çayır
  • Sophia Tahir
  • Büşra Çavdarlı
  • Meliha Demiral
  • Ayşe Nurcan Cebeci
  • Doğuş Vurallı
  • Sofia Asim Rahman
  • Edip Unal
  • Gönül Büyükyılmaz
  • Riza Taner Baran
  • Mehmet Nuri Özbek
  • Khalid Hussain
J Clin Res Pediatr Endocrinol 2021; 13: 34-43 DOI: 10.4274/jcrpe.galenos.2020.2020.0152 PMID:32938580
Very High Incidence of Type 1 Diabetes Among Children Aged Under 15 Years in Tlemcen, Northwest Algeria (2015-2018)
  • Sarra Khater
  • Ammaria Aouar
  • Nawel Bensmain
  • Salih Bendedouche
  • Nafissa Chabni
  • Houari Hamdaoui
  • Abdellatif Moussouni
  • Zakarya Moqaddem
J Clin Res Pediatr Endocrinol 2021; 13: 44-51 DOI: 10.4274/jcrpe.galenos.2020.2020.0073 PMID:32938578
A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogonadism
  • Asude Durmaz
  • Ayça Aykut
  • Tahir Atik
  • Samim Özen
  • Durdugül Ayyıldız Emecen
  • Aysun Ata
  • Esra Işık
  • Damla Gökşen
  • Özgür Çoğulu
  • Ferda Özkınay
J Clin Res Pediatr Endocrinol 2021; 13: 52-60 DOI: 10.4274/jcrpe.galenos.2020.2020.0101 PMID:32936766
Transforming Growth Factor-β1 and Receptor for Advanced Glycation End Products Gene Expression and Protein Levels in Adolescents with Type 1 Diabetes Mellitus
  • Ana Ninić
  • Dragana Bojanin
  • Miron Sopić
  • Marija Mihajlović
  • Jelena Munjas
  • Tatjana Milenković
  • Aleksandra Stefanović
  • Jelena Vekić
  • Vesna Spasojević-Kalimanovska
J Clin Res Pediatr Endocrinol 2021; 13: 61-71 DOI: 10.4274/jcrpe.galenos.2020.2020.0155 PMID:32936764
Frequency of Celiac Disease and Spontaneous Normalization Rate of Celiac Serology in Children and Adolescent Patients with Type 1 Diabetes
  • Edip Unal
  • Meliha Demiral
  • Birsen Baysal
  • Mehmet Ağın
  • Elif Gökçe Devecioğlu
  • Hüseyin Demirbilek
  • Mehmet Nuri Özbek
J Clin Res Pediatr Endocrinol 2021; 13: 72-79 DOI: 10.4274/jcrpe.galenos.2020.2020.0108 PMID:32820875
Genotype and Phenotype Heterogeneity in Neonatal Diabetes: A Single Centre Experience in Turkey
  • Yasemin Denkboy Öngen
  • Erdal Eren
  • Özgecan Demirbaş
  • Elif Sobu
  • Sian Ellard
  • Elisa De Franco
  • Ömer Tarım
J Clin Res Pediatr Endocrinol 2021; 13: 80-87 DOI: 10.4274/jcrpe.galenos.2020.2020.0093 PMID:32820876
Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience
  • Emine Çamtosun
  • İsmail Dündar
  • Ayşehan Akıncı
  • Leman Kayaş
  • Nurdan Çiftçi
J Clin Res Pediatr Endocrinol 2021; 13: 88-99 DOI: 10.4274/jcrpe.galenos.2020.2020.0132 PMID:32938577

Case Report

Homozygous Mutation in the Insulin Receptor Gene Associated with Mild Type A Insulin Resistance Syndrome: A Case Report
  • Bülent Hacihamdioğlu
  • Elif Gülşah Baş
  • Kenan Delil
J Clin Res Pediatr Endocrinol 2021; 13: 100-103 DOI: 10.4274/jcrpe.galenos.2020.2019.0213 PMID:32018348
The Unusual Case of Fibroma of Tendon Sheath in a Young Girl with Turner Syndrome Undergoing Growth Hormone Treatment
  • Yong Hee Hong
  • Dong Gyu Kim
  • Jong Hyun Lee
  • Min Jung Jung
  • Chang Yong Choi
J Clin Res Pediatr Endocrinol 2021; 13: 104-108 DOI: 10.4274/jcrpe.galenos.2020.2019.0223 PMID:32349463
6q25.1-q25.3 Microdeletion in a Chinese Girl
  • Mian-Ling Zhong
  • Ye-Mei Song
  • Chao-Chun Zou
J Clin Res Pediatr Endocrinol 2021; 13: 109-113 DOI: 10.4274/jcrpe.galenos.2020.2020.0008 PMID:32380822
Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation
  • Hüsniye Yücel
  • Çiğdem Genç Sel
  • Çiğdem Seher Kasapkara
  • Gülin Karacan Küçükali
  • Senay Savas-Erdeve
  • Ülkühan Öztoprak
  • Serdar Ceylaner
  • Saliha Şenel
  • Meltem Akçaboy
J Clin Res Pediatr Endocrinol 2021; 13: 114-118 DOI: 10.4274/jcrpe.galenos.2020.2020.0004 PMID:32302086
Sirolimus Therapy and Follow-up in a Patient with Severe Congenital Hyperinsulinism Following Subtotal Pancreatectomy
  • Qiong Chen
  • Yongxing Chen
  • Xiaohong Wang
  • Haihua Yang
  • Yingxian Zhang
  • Xiaojing Liu
  • Yun Yan
  • Haiyan Wei
J Clin Res Pediatr Endocrinol 2021; 13: 119-123 DOI: 10.4274/jcrpe.galenos.2020.2020.0033 PMID:32482020

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