Archives - Journal of Clinical Research ın Pediatric Endocrinology

Congress Calendar 1

Editorial

Nurgün Kandemir

Ayfer Alikaşifoğlu

Congress Calendar

CONGRESS CALENDAR

Other

The Evolution of Body SizePDF Article

Idiopathic Short StaturePDF Article

Insulin-Like Growth Factor Treatment of Growth DisordersPDF Article

Management of Growth Hormone Deficiency in Children Irradiated for Brain TumoursPDF Article

Stephen M. Shalet

Clinical and Molecular Characterisation of Patients with Congenital HyperinsulinismPDF Article

Aromatase Inhibitors in Paediatric EndocrinologyPDF Article

Genetics and Clinical Characteristics of Neonatal DiabetesPDF Article

Growth Hormone Treatment in Childhood Intracranial Tumors - Hacettepe ExperiencePDF Article

E. Nazlı Gönç

Ayfer Alikaşifoğlu

Nurgün Kandemir

Growth Hormone Therapy in Five Patients with Malignant Intracranial TumorsPDF Article

E. Nazlı Gönç

Ayfer Alikaşifoğlu

Nurgün Kandemir

Mutant Neurogenin-3 in Permanent Neonatal Diabetes and Congenital Malabsorptive DiarrheaPDF Article

Martine Vaxillaire

Premature Menarche Associated with McCune-Albright Syndrome in an InfantPDF Article

HADH Mutation is a Rare Cause of Hyperinsulinaemic HypoglycaemiaPDF Article

Gül Yeşiltepe Mutlu

Filiz Mine Çizmecioğlu

A Novel GH1 Functional Mutation in a Family with Isolated Growth Hormone DeficiencyPDF Article

Ali Kemal Topaloğlu

Persistent Hyperinsulinemic Hypoglycemia Due to SUR1 (ABCC8) Mutation in Newborn Twins: An Eight-Year Follow-UpPDF Article

Abdülkadir Genç

Deniz Kızılay

Seniha Kiremitçi

Pascale De Lonlay

Primary Melanocytic Suprasellar Tumor Presenting with Growth Hormone DeficiencyPDF Article

Ayfer Alikaşifoğlu

Doğuş Vurallı

Figen Söylemezoğlu

E. Nazlı Gönç

Nurgün Kandemir

A Rare Case of Neonatal Diabetes due to COQ2 Gene MutationPDF Article

E. Nazlı Gönç

Fatih Özaltın

Ayfer Alikaşifoğlu

Nurgün Kandemir

Follow-up of Two Cases of Medulloblastoma with/without Growth Hormone TherapyPDF Article

Belma Haliloğlu

Abdullah Bereket

Growth without Growth Hormone Syndrome in a Patient with CraniopharyngiomaPDF Article

Belma Haliloğlu

Abdullah Bereket

ABCC8 Frameshift Mutation in Exon 28 (c.3512delT) is a Founder Mutation for Autosomal Recessive Hyperinsulinemic Hypoglycemia in Eastern AnatoliaPDF Article

Bilin Çetinkaya

Treatment of Growth Hormone Deficiency in Langerhans Cell HistiocytosisPDF Article

Gönül Büyükyılmaz

E. Nazlı Gönç

Ayfer Alikaşifoğlu

Nurgün Kandemir

Long-term Endocrine Evaluation of Childhood Brain TumorsPDF Article

Zehra Yavaş Abalı

Şükran Poyrazoğlu

Rüveyde Bundak

Feyza Darendeliler