| 1. | Cover
Page I
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| 2. | Editörden
Nurgün Kandemir, Ayfer Alikaşifoğlu, Alev Özön, Nazlı Gönç
Page II
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| 3. | The Evolution of Body Size
Ron Rosenfeld
Page 1
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| 4. | Idiopathic Short Stature
Jan M. Wit
Page 2
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| 5. | Insulin-Like Growth Factor Treatment of Growth Disorders
Ron Rosenfeld
Page 3
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| 6. | Management of Growth Hormone Deficiency in Children Irradiated for Brain Tumours
Stephen M. Shalet
Page 4
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| 7. | Clinical and Molecular Characterisation of Patients with Congenital Hyperinsulinism
Sian Ellard
Page 5
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| 8. | Aromatase Inhibitors in Paediatric Endocrinology
Jan M. Wit
Page 6
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| 9. | Genetics and Clinical Characteristics of Neonatal Diabetes
Sian Ellard
Page 7
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| 10. | Growth Hormone Treatment in Childhood Intracranial Tumors - Hacettepe Experience
Z. Alev Özön, E. Nazlı Gönç, Ayfer Alikaşifoğlu, Nurgün Kandemir
Page 8
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| 11. | Growth Hormone Therapy in Five Patients with Malignant Intracranial Tumors
Z. Alev Özön, Betül Yaman, E. Nazlı Gönç, Ayfer Alikaşifoğlu, Nurgün Kandemir
Page 9
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| 12. | Mutant Neurogenin-3 in Permanent Neonatal Diabetes and Congenital Malabsorptive Diarrhea
Suna Hancılı, Ayla Güven, Martine Vaxillaire
Page 10
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| 13. | Premature Menarche Associated with McCune-Albright Syndrome in an Infant
Centre National De La Recherche Scientifique Umr, Genomics And Metabolic Diseases, Lille Pasteur Institute, Lille Nord De France University, France
Enver Şimşek, Çiğdem Binay
Page 11
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| 14. | HADH Mutation is a Rare Cause of Hyperinsulinaemic Hypoglycaemia
Eskisehir Osmangazi University Faculty Of Medicine, Department Of Pediatrics Endocrinology, Eskisehir, Turkey\R\N
Elif Özsu, Gül Yeşiltepe Mutlu, Filiz Mine Çizmecioğlu, Şükrü Hatun
Page 12
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| 15. | A Novel GH1 Functional Mutation in a Family with Isolated Growth Hormone Deficiency
Fatih Gürbüz, Bilgin Yüksel, Atıl Bişgin
Page 13
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| 16. | Persistent Hyperinsulinemic Hypoglycemia Due to SUR1 (ABCC8) Mutation in Newborn Twins: An Eight-Year Follow-Up
Betül Ersoy, Nermin Tansuğ, Abdülkadir Genç, Pascale De Lonlay
Page 14
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| 17. | Primary Melanocytic Suprasellar Tumor Presenting with Growth Hormone Deficiency
Ayfer Alikaşifoğlu, Doğuş Vurallı, Figen Söylemezoğlu
Page 15
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| 18. | A Rare Case of Neonatal Diabetes due to COQ2 Gene Mutation
E. Nazlı Gönç, Meltem Çakır
Page 16
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| 19. | Hacettepe University Faculty Of Medicine Department Of Pediatric Endocrinology, Ankara, Turkey
Saygın Abalı, Serap Turan, Zeynep Atay, Serpil Baş, Tülay Güran
Pages 17 - 18
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| 20. | Marmara University Faculty Of Medicine, Department Of Pediatric Endocrinology, Istanbul, Turkey
Zeynep Atay, Serap Turan, Belma Haliloğlu, Saygın Abalı, Serpil Baş, Tülay Güran, Abdullah Bereket
Page 19
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| 21. | ABCC8 Frameshift Mutation in Exon 28 (c.3512delT) is a Founder Mutation for Autosomal Recessive Hyperinsulinemic Hypoglycemia in Eastern Anatolia
Özlem Sangün, Bilin Çetinkaya, Khalid Hussein
Page 20
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| 22. | Ucl Institute Of Child Health, Clinical And Molecular Genetics Unit, Developmental Endocrinology Research Group, Uk
Z. Alev Özön, Gönül Büyükyılmaz, E. Nazlı Gönç, Ayfer Alikaşifoğlu, Nurgün Kandemir
Page 21
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| 23. | Long-term Endocrine Evaluation of Childhood Brain Tumors
Zehra Yavaş Abalı, Firdevs Baş, Şükran Poyrazoğlu, Neşe Akcan
Page 22
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| 24. | CONGRESS CALENDAR
Page 23
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