Original Article

The Evaluation of Etiological Distribution and the Rate of Congenital Hypothyroidism among the Cases Referred from National Screening Program
  • Zeynep Donbaloglu
  • Şenay Savaş Erdeve
  • Semra Çetinkaya
  • Zehra Aycan
J Clin Res Pediatr Endocrinol 0; 0: 0-0 [e-Pub] DOI: 10.4274/jcrpe.0255 PMID:30630811
Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants
  • Tülay Güran
  • Başak Tezel
  • Fatih Gürbüz
  • Beray Selver Eklioğlu
  • Nihal Hatipoğlu
  • Cengiz Kara
  • Enver Şimşek
  • Filiz Mine Çizmecioğlu
  • Alev Ozon
  • Firdevs Baş
  • Murat Aydın
  • Feyza Darendeliler
J Clin Res Pediatr Endocrinol 2019; 11: 13-23 DOI: 10.4274/jcrpe.galenos.2018.2018.0117 PMID:30111524
The Role of Interleukin-6 and C-Reactive Protein in Non-Thyroidal Illness in Premature Infants Followed in Neonatal Intensive Care Unit
  • Dilek Dilli
  • Uğur Dilmen
J Clin Res Pediatr Endocrinol 2012; 4: 66-71 DOI: 10.4274/jcrpe.625 PMID:22672862
Epidemiology of Congenital Hypothyroidism in Markazi Province, Iran
  • Fatemeh Dorreh
  • Parsa Y. Chaijan
  • Javad Javaheri
  • Ali Hossein Zeinalzadeh
J Clin Res Pediatr Endocrinol 2014; 6: 105-110 DOI: 10.4274/jcrpe.1287 PMID:24932604
Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life
  • Filiz Mine Çizmecioğlu
  • Jeremy Huw Jones
  • Wendy Forsyth Paterson
  • Sakina Kherra
  • Mariam Kourime
  • Ruth McGowan
  • M. Guftar Shaikh
  • Malcolm Donaldson
J Clin Res Pediatr Endocrinol 2018; 10: 264-273 DOI: 10.4274/jcrpe.0029 PMID:29553044

Review

Neonatal Hypopituitarism: Approaches to Diagnosis and Treatment
  • Selim Kurtoğlu
  • Ahmet Özdemir
  • Nihal Hatipoğlu
J Clin Res Pediatr Endocrinol 2019; 11: 4-12 DOI: 10.4274/jcrpe.galenos.2018.2018.0036 PMID:29739730
Fetal and Neonatal Endocrine Disruptors
  • Tolga Ünüvar
  • Atilla Büyükgebiz
J Clin Res Pediatr Endocrinol 2012; 4: 51-60 DOI: 10.4274/Jcrpe.569 PMID:22672860
Update on Some Aspects of Neonatal Thyroid Disease
  • Tamar Simpser
  • Robert Rapaport
J Clin Res Pediatr Endocrinol 2010; 2: 95-99 DOI: 10.4274/jcrpe.v2i3.95 PMID:21274321
Maternal Obesity and its Short- and Long-Term Maternal and Infantile Effects
  • Levent Korkmaz
  • Osman Baştuğ
  • Selim Kurtoğlu
J Clin Res Pediatr Endocrinol 2016; 8: 114-124 DOI: 10.4274/jcrpe.2127 PMID:26758575

Original Research

Fetal-Neonatal Ovarian Cysts-Their Monitoring and Management: Retrospective Evaluation of 20 Cases and Review of the Literature
  • Mustafa Ali Akın
  • Leyla Akın
  • Sibel Özbek
  • Gülay Tireli
  • Sultan Kavuncuoğlu
  • Serdar Sander
  • Mustafa Akçakuş
  • Tamer Güneş
  • M. Adnan Öztürk
  • Selim Kurtoğlu
J Clin Res Pediatr Endocrinol 2010; 2: 28-33 DOI: 10.4274/jcrpe.v2i1.28 PMID:21274333
Transient Congenital Hypothyroidism in Turkey: An Analysis on Frequency and Natural Course
  • Cengiz Kara
  • Figen Günindi
  • Gülay Can Yılmaz
  • Murat Aydın
J Clin Res Pediatr Endocrinol 2016; 8: 170-179 DOI: 10.4274/jcrpe.2345 PMID:27086592
Neonatal Thyroid-Stimulating Hormone Screening as a Monitoring Tool for Iodine Deficiency in Turkey
  • Nilgün Çaylan
  • Başak Tezel
  • Sema Özbaş
  • Nuran Şahin
  • Şirin Aydın
  • Deniz Acıcan
  • Bekir Keskinkılıç
J Clin Res Pediatr Endocrinol 2016; 8: 187-191 DOI: 10.4274/jcrpe.2526 PMID:27086874
Hidden Toxicity in Neonatal Intensive Care Units: Phthalate Exposure in Very Low Birth Weight Infants
  • Atalay Demirel
  • Asuman Çoban
  • Şükran Yıldırım
  • Canan Doğan
  • Rukiye Sancı
  • Zeynep İnce
J Clin Res Pediatr Endocrinol 2016; 8: 298-304 DOI: 10.4274/jcrpe.3027 PMID:27097850

Case Reports

Neonatal Hyperthyroidism Associated with Isolated Submandibular Sialadenitis: Is it Just a Coincidence?
  • Ayşın Uçkun Kitapçı
  • Ali Süha Çalıkoğlu
J Clin Res Pediatr Endocrinol 2010; 2: 43-45 DOI: 10.4274/jcrpe.v2i1.43 PMID:21274336
Neonatal Diabetes Mellitus Accompanied by Diabetic Ketoacidosis and Mimicking Neonatal Sepsis: A Case Report
  • Ayhan Abacı
  • Cem Hasan Razi
  • Osman Özdemir
  • Samil Hızlı
  • Fatih Kıslal
  • Pınar Işık Argas
  • Nimet Kabakuş
J Clin Res Pediatr Endocrinol 2010; 2: 131-133 DOI: 10.4274/jcrpe.v2i3.131 PMID:21274328
Sporadic Nonautoimmune Neonatal Hyperthyroidism Due to A623V Germline Mutation in the Thyrotropin Receptor Gene
  • Zehra Aycan
  • Sebahat Yılmaz Ağladıoğlu
  • Serdar Ceylaner
  • Semra Çetinkaya
  • Veysel Nijat Baş
  • Havva Nur Peltek Kendirici
J Clin Res Pediatr Endocrinol 2010; 2: 168-172 DOI: 10.4274/jcrpe.v2i4.168 PMID:21274318
Neonatal Sludge: A finding of congenital hypothyroidism
  • Selim Kurtoğlu
  • Dilek Çoban
  • Mustafa Ali Akın
  • Leyla Akın
  • Ali Yıkılmaz
J Clin Res Pediatr Endocrinol 2009; 1: 197-200 DOI: 10.4274/jcrpe.v1i4.54 PMID:21274296

Case Report

Transient Neonatal Diabetes due to a Mutation in KCNJ11 in a Child with Klinefelter Syndrome
  • Amanda R. Dahl
  • Radhika Dhamija
  • Alaa Al Nofal
  • Siobhan T. Pittock
  • W. Frederick Schwenk
  • Seema Kumar
J Clin Res Pediatr Endocrinol 2018; 10: 79-82 DOI: 10.4274/jcrpe.4807 PMID:28766502
Neonatal Episodic Hypoglycemia: A Finding of Valproic Acid Withdrawal
  • Dilek Çoban
  • Selim Kurtoğlu
  • Mustafa Ali Akın
  • Mustafa Akçakuş
  • Tamer Güneş
J Clin Res Pediatr Endocrinol 2010; 2: 92-94 DOI: 10.4274/jcrpe.v2i2.92 PMID:21274347
Wolcott-Rallison Syndrome Due to a Novel Mutation (R491X) in EIF2AK3 Gene
  • Ercan Mıhçı
  • Doğa Tu¨rkkahraman
  • Sian Ellard
  • Sema Akçurin
  • İffet Bircan
J Clin Res Pediatr Endocrinol 2012; 4: 101-103 DOI: 10.4274/Jcrpe.619 PMID:22672868
Permanent Neonatal Diabetes Mellitus: Same Mutation, Different Glycemic Control with Sulfonylurea Therapy on Long-Term Follow-up
  • Banu Küçükemre Ay
  • Rüveyde Bundak
  • Firdevs Baş
  • Hülya Maraş
  • Nurçin Saka
  • Hülya Günöz
  • Feyza Darendeliler
J Clin Res Pediatr Endocrinol 2012; 4: 107-110 DOI: 10.4274/Jcrpe.524 PMID:22672870
Neonatal Seizure as a Manifestation of Unrecognized Maternal Hyperparathyroidism
  • Hüseyin Anıl Korkmaz
  • Behzat Özkan
  • Demet Terek
  • Ceyhun Dizdarer
  • Sertaç Arslanoğlu
J Clin Res Pediatr Endocrinol 2013; 5: 206-208 DOI: 10.4274/Jcrpe.1037 PMID:24072092
Pancreatic Agenesis due to Compound Heterozygosity for a Novel Enhancer and Truncating Mutation in the PTF1A Gene
  • Monica Gabbay
  • Sian Ellard
  • Elisa De Franco
  • Regina S. Moisés
J Clin Res Pediatr Endocrinol 2017; 9: 274-277 DOI: 10.4274/jcrpe.4494 PMID:28663161

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