Atıf İçin Kopyala
ERBAŞ İ. M., Catli G., Paketci A., ANIK A., DEMİR K., BÖBER E., ...Daha Fazla
GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS, cilt.18, sa.3, ss.317-335, 2020 (ESCI)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
18
Sayı:
3
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Basım Tarihi:
2020
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Dergi Adı:
GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS
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Derginin Tarandığı İndeksler:
Emerging Sources Citation Index (ESCI), Scopus, Academic Search Premier, CAB Abstracts, CINAHL, EMBASE, Veterinary Science Database
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Sayfa Sayıları:
ss.317-335
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Anahtar Kelimeler:
diazoxide, hyperinsulinism, hypoglycaemia, neuroglycopenic symptom, KATP channel, 11P15 IMPRINTED GENES, TERM-FOLLOW-UP, LONG-TERM, SURGICAL-MANAGEMENT, TURKISH PATIENTS, MUTATIONS, CHILDREN, ABCC8, DIAGNOSIS, INFANCY
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Dokuz Eylül Üniversitesi Adresli:
Evet
Özet
INTRODUCTION: Congenital hyperinsulinemic hypoglycemia is a rare disease caused by uncontrolled release of insulin from the pancreas. In this study, we aimed to evaluate the clinical and genetic characteristics and prognosis of the patients with congenital hyperinsulinemic hypoglycemia.