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

Case Report

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

Original Article

Long-term Clinical Follow-up of Patients with Familial Hypomagnesemia with Secondary Hypocalcemia
  • Elvan Bayramoğlu
  • Melikşah Keskin
  • Zehra Aycan
  • Şenay Savaş-Erdeve
  • Semra Çetinkaya
J Clin Res Pediatr Endocrinol 2021; 13: 300-307 DOI: 10.4274/jcrpe.galenos.2021.2020.0192 PMID:33565749