ISSN:1308-5727
E-ISSN:1308-5735
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ISSN:1308-5727
E-ISSN:1308-5735
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Case Report
Inherited Deletion of 1q, Hyperparathyroidism and Signs of Y-chromosomal Influence in a Patient with Turner Syndrome
Alejandro F. Siller
Alex Shimony
Marwan Shinawi
Ina Amarillo
Louis P. Dehner
Katherine Semenkovich
Ana María Arbeláez
J Clin Res Pediatr Endocrinol 2019; 11: 88-93
DOI: 10.4274/jcrpe.galenos.2018.2018.0005
PMID:29739732
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Primary Hyperparathyroidism Presenting as Posterior Reversible Encephalopathy Syndrome: A Report of Two Cases
Rimesh Pal
Aditya Dutta
Kanhaiya Agrawal
Nimisha Jain
Pinaki Dutta
Anil Bhansali
Arunanshu Behera
Sanjay Kumar Bhadada
J Clin Res Pediatr Endocrinol 2020; 12: 432-438
DOI: 10.4274/jcrpe.galenos.2020.2019.0181
PMID:32129057
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Original Article
Intraoperative Parathyroid Hormone Monitoring Corroborates the Success of Parathyroidectomy in Children
Ahmet Çelik
Emre Divarcı
Zafer Dökümcü
Orkan Ergün
Samim Özen
Damla Gökşen
Şükran Darcan
Yeşim Ertan
J Clin Res Pediatr Endocrinol 2014; 6: 158-162
DOI: 10.4274/jcrpe.1401
PMID:25241609
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Case Report
The Effectiveness of Cinacalcet as an Adjunctive Therapy for Hereditary 1,25 Dihydroxyvitamin D3-Resistant Rickets
Ayşehan Akıncı
İsmail Dündar
Meltem Kıvılcım
J Clin Res Pediatr Endocrinol 2017; 9: 172-178
DOI: 10.4274/jcrpe.3486
PMID:27796266
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Case Report
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
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Primary Hyperparathyroidism Masquerading as Rickets: Diagnostic Challenge and Treatment Outcomes
Deep Dutta
Manoj Kumar
Ram Narayan Das
Saumik Datta
Dibakar Biswas
Sujoy Ghosh
Satinath Mukhopadhyay
Subhankar Chowdhury
J Clin Res Pediatr Endocrinol 2013; 5: 266-269
DOI: 10.4274/Jcrpe.1060
PMID:24379038
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An Unusual Presentation of Parathyroid Adenoma in an Adolescent: Calcific Achilles Tendinitis
Selim Kurtoğlu
Leyla Akın
Mustafa Kendirci
Sedat Çağlı
Salih Özgöçmen
J Clin Res Pediatr Endocrinol 2015; 7: 333-335
DOI: 10.4274/jcrpe.2193
PMID:26777046
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Identification and Functional Characterization of a Calcium-Sensing Receptor Mutation in an Infant with Familial Hypocalciuric Hypercalcemia
Anna Papadopoulou
Evangelia Gole
Katerina Melachroinou
Christos Meristoudis
Tania Siahanidou
Anastasios Papadimitriou
J Clin Res Pediatr Endocrinol 2016; 8: 341-346
DOI: 10.4274/jcrpe.2800
PMID:27087013
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Original Article
Childhood Sustained Hypercalcemia: A Diagnostic Challenge
Nisa Eda Çullas İlarslan
Zeynep Şıklar
Merih Berberoğlu
J Clin Res Pediatr Endocrinol 2017; 9: 315-322
DOI: 10.4274/jcrpe.4247
PMID:28443817
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