E-ISSN: 1308-5735 ISSN: 1308-5727
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Volume 7, Issue 1

March 2015

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CONGRESS CALENDAR
Other
The Evolution of Body Size
Ron Rosenfeld
Idiopathic Short Stature
Jan M. Wit
Insulin-Like Growth Factor Treatment of Growth Disorders
Ron Rosenfeld
Management of Growth Hormone Deficiency in Children Irradiated for Brain Tumours
Stephen M. Shalet
Clinical and Molecular Characterisation of Patients with Congenital Hyperinsulinism
Sian Ellard
Aromatase Inhibitors in Paediatric Endocrinology
Jan M. Wit
Genetics and Clinical Characteristics of Neonatal Diabetes
Sian Ellard
Growth Hormone Treatment in Childhood Intracranial Tumors - Hacettepe Experience
Z. Alev Özön
E. Nazlı Gönç
Ayfer Alikaşifoğlu
Nurgün Kandemir
Growth Hormone Therapy in Five Patients with Malignant Intracranial Tumors
Z. Alev Özön
Betül Yaman
E. Nazlı Gönç
Ayfer Alikaşifoğlu
Nurgün Kandemir
Mutant Neurogenin-3 in Permanent Neonatal Diabetes and Congenital Malabsorptive Diarrhea
Suna Hancılı
Ayla Güven
Martine Vaxillaire
Premature Menarche Associated with McCune-Albright Syndrome in an Infant
Enver Şimşek
Çiğdem Binay
HADH Mutation is a Rare Cause of Hyperinsulinaemic Hypoglycaemia
Elif Özsu
Gül Yeşiltepe Mutlu
Filiz Mine Çizmecioğlu
Şükrü Hatun
A Novel GH1 Functional Mutation in a Family with Isolated Growth Hormone Deficiency
Fatih Gürbüz
Bilgin Yüksel
Atıl Bişgin
Eda Mengen
Ali Kemal Topaloğlu
Persistent Hyperinsulinemic Hypoglycemia Due to SUR1 (ABCC8) Mutation in Newborn Twins: An Eight-Year Follow-Up
Betül Ersoy
Nermin Tansuğ
Abdülkadir Genç
Deniz Kızılay
Seniha Kiremitçi
Pascale De Lonlay
Primary Melanocytic Suprasellar Tumor Presenting with Growth Hormone Deficiency
Ayfer Alikaşifoğlu
Doğuş Vurallı
Figen Söylemezoğlu
E. Nazlı Gönç
Z. Alev Özön
Nurgün Kandemir
A Rare Case of Neonatal Diabetes due to COQ2 Gene Mutation
E. Nazlı Gönç
Meltem Çakır
Ali Düzova
Fatih Özaltın
Ayfer Alikaşifoğlu
Z. Alev Özön
Nurgün Kandemir
Follow-up of Two Cases of Medulloblastoma with/without Growth Hormone Therapy
Saygın Abalı
Serap Turan
Zeynep Atay
Belma Haliloğlu
Serpil Baş
Tülay Güran
Abdullah Bereket
Growth without Growth Hormone Syndrome in a Patient with Craniopharyngioma
Zeynep Atay
Serap Turan
Belma Haliloğlu
Saygın Abalı
Serpil Baş
Tülay Güran
Abdullah Bereket
ABCC8 Frameshift Mutation in Exon 28 (c.3512delT) is a Founder Mutation for Autosomal Recessive Hyperinsulinemic Hypoglycemia in Eastern Anatolia
Özlem Sangün
Bilin Çetinkaya
Birgin Törer
Hande Gülcan
Khalid Hussein
Treatment of Growth Hormone Deficiency in Langerhans Cell Histiocytosis
Z. Alev Özön
Gönül Büyükyılmaz
E. Nazlı Gönç
Ayfer Alikaşifoğlu
Nurgün Kandemir
Long-term Endocrine Evaluation of Childhood Brain Tumors
Zehra Yavaş Abalı
Firdevs Baş
Şükran Poyrazoğlu
Neşe Akcan
Mikayir Genens
Rüveyde Bundak
Feyza Darendeliler