Case Report

Pseudohypoparathyroidism Presenting with Ventricular Arrhythmia: A Case Report
  • Sedat Işıkay
  • İlyas Akdemir
  • Kutluhan Yılmaz
J Clin Res Pediatr Endocrinol 2012; 4: 42-44 DOI: 10.4274/Jcrpe.476 PMID:22394705
Long-Term Follow-Up of a Pseudohypoparathyroidism Type 1A Patient with Missense Mutation (Pro115Ser) in Exon 5
  • Şenay Savaş Erdeve
  • Merih Berberoğlu
  • Zeynep Şıklar
  • Olcay Evliyaoğlu
  • Olaf Hiort
  • Gönül Öcal
J Clin Res Pediatr Endocrinol 2010; 2: 85-88 DOI: 10.4274/jcrpe.v2i2.85 PMID:21274345
The First Turkish Case of Hypoparathyroidism, Deafness and Renal Dysplasia (HDR) Syndrome
  • Hakan Döneray
  • Takeshi Usui
  • Avni Kaya
  • Ayşe Sena Dönmez
J Clin Res Pediatr Endocrinol 2015; 7: 140-143 DOI: 10.4274/jcrpe.1874 PMID:26316437
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
A Novel De Novo GATA Binding Protein 3 Mutation in a Turkish Boy with Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome
  • Gül Yeşiltepe Mutlu
  • Heves Kırmızıbekmez
  • Akie Nakamura
  • Maki Fukami
  • Şükrü Hatun
J Clin Res Pediatr Endocrinol 2015; 7: 344-348 DOI: 10.4274/jcrpe.2249 PMID:26777049

Case Report

Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene
  • Sezgin Sahin
  • Olaf Hiort
  • Susanne Thiele
  • Olcay Evliyaoglu
  • Beyhan Tüysüz
J Clin Res Pediatr Endocrinol 2017; 9: 74-79 DOI: 10.4274/jcrpe.3191 PMID:27425121

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
Vitamin D Deficiency Rickets Mimicking Pseudohypoparathyroidism
  • Leyla Akın
  • Selim Kurtoğlu
  • Aysel Yıldız
  • Mustafa Ali Akın
  • Mustafa Kendirici
J Clin Res Pediatr Endocrinol 2010; 2: 173-175 DOI: 10.4274/jcrpe.v2i4.173 PMID:21274319
A Novel Mutation Causing Pseudohypoparathyroidism 1A with Congenital Hypothyroidism and Osteoma Cutis
  • Tamar Lubell
  • Maria Garzon
  • Kwame Anyane-Yeboa
  • Bina Shah
J Clin Res Pediatr Endocrinol 2009; 1: 244-247 DOI: 10.4274/jcrpe.v1i5.244 PMID:21274302

Original Research

Pseudohypoparathyroidism Type 1A-Subclinical Hypothyroidism and Rapid Weight Gain as Early Clinical Signs: A Clinical Review of 10 Cases
  • Simon Kayemba-Kay’s
  • Cedric Tripon
  • Anne Heron
  • Peter Hindmarsh
J Clin Res Pediatr Endocrinol 2016; 8: 432-438 DOI: 10.4274/jcrpe.2743 PMID:27467896

Other

Current Perspectives on Pseudohypoparathyroidism-New Classification
  • Serap Turan
J Clin Res Pediatr Endocrinol 2016; 8: 1-2
A Case of Polyglandular Autoimmune Syndrome Type One with Hypercalcemia and Hypotension
  • Nilüfer Özdemir Kutbay
  • Banu Sarer Yürekli
  • Miray Yaman
  • Mehmet Erdoğan
  • Şevki Çetinkalp
  • L. Füsun Saygılı
  • Şükran Darcan
  • A. Gökhan Özgen
J Clin Res Pediatr Endocrinol 2015; 7: 51-51
A Rare GCMB Gene Mutation in an Isolated Hypoparathyroidism Case
  • Biray Ertürk
  • Emin Karaca
  • Caroline Silce
  • Ferda Özkınay
J Clin Res Pediatr Endocrinol 2015; 7: 59-59
Hypoparathyroidism-Deafness-Renal Disease Syndrome: The First Case Report from Turkey
  • Hakan Döneray
  • Takeshi Usui
  • Avni Kaya
  • Ayşe Sena Dönmez
J Clin Res Pediatr Endocrinol 2015; 7: 73-73
A Case with Acrodysostosis and Hormone Resistance
  • Selma Tunç
  • Korcan Demircan Sezer
  • Filiz Hazan
  • Özgür Kırbıyık
  • Eren Soyaltın
  • Özlem Nalbantoğlu Elmas
  • Melek Yıldız
  • Hüseyin Anıl Korkmaz
  • Behzat Özkan
J Clin Res Pediatr Endocrinol 2015; 7: 75-75

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