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Molecular Basis of Hirschsprung’s Disease and Other Congenital Enteric Neuropathies

✍ Scribed by Goldstein, Allan M.

Book ID
123068885
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
236 KB
Volume
17
Category
Article
ISSN
1043-1489

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Congenital hyperinsulinism: Molecular ba
Congenital hyperinsulinism: Molecular basis of a heterogeneous disease
✍ Thomas Meissner; Beatrice Beinbrech; Ertan Mayatepek 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 274 KB 👁 1 views

## Communicated by Johannes Zschocke Congenital hyperinsulinism (CHI) is a disease phenotype characterized by increased, usually irregular, insulin secretion leading to hypoglycemia, coma, and severe brain damage, left untreated. Hyperinsulinism may be caused by a range of biochemical disturbances