Case Report

A Novel Homozygous Mutation in the Transient Receptor Potential Melastatin 6 Gene: A Case Report
  • Ayça Altıncık
  • Karl Peter Schlingmann
  • Mahya Sultan Tosun
J Clin Res Pediatr Endocrinol 2016; 8: 101-104 DOI: 10.4274/jcrpe.2254 PMID:26759217
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

Case Reports

A Patient with 22q11.2 Deletion Syndrome: Case Report
  • Sema Kabataş Eryılmaz
  • Firdevs Baş
  • Ali Satan
  • Feyza Darendeliler
  • Rüveyde Bundak
  • Hülya Günöz
  • Nurçin Saka
J Clin Res Pediatr Endocrinol 2009; 1: 151-154 DOI: 10.4008/jcrpe.v1i3.46 PMID:21274400

Original Article

Under-recognized Hypoparathyroidism in Thalassemia
  • Hataitip Tangngam
  • Pat Mahachoklertwattana
  • Preamrudee Poomthavorn
  • Ampaiwan Chuansumrit
  • Nongnuch Sirachainan
  • La-or Chailurkit
  • Patcharin Khlairit
J Clin Res Pediatr Endocrinol 2018; 10: 324-330 DOI: 10.4274/jcrpe.0020 PMID:29726397

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