3.9 Article

Glibenclamide Unresponsiveness in a Brazilian Child with Permanent Neonatal Diabetes Mellitus and DEND Syndrome Due to a C166Y Mutation in KCNJ11 (Kir6.2) Gene

Related references

Note: Only part of the references are listed.
Article Endocrinology & Metabolism

Sulphonylurea therapy improves cognition in a patient with the V59M KCNJ11 mutation

A. S. Slingerland et al.

DIABETIC MEDICINE (2008)

Review Endocrinology & Metabolism

Neonatal diabetes mellitus

Lydia Aguilar-Bryan et al.

ENDOCRINE REVIEWS (2008)

Article Endocrinology & Metabolism

The G53D mutation in Kir6.2 (KCNJ11) is associated with neonatal diabetes and motor dysfunction in adulthood that is improved with sulfonylurea therapy

Joseph C. Koster et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2008)

Article Clinical Neurology

Sulfonylurea improves CNS function in a case of intermediate DEND syndrome caused by a mutation in KCNJ11

Woj Ciech Mlynarski et al.

NATURE CLINICAL PRACTICE NEUROLOGY (2007)

Article Endocrinology & Metabolism

Molecular basis of neonatal diabetes in Japanese patients

Shigeru Suzuki et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2007)

Article Medicine, General & Internal

Activating mutations in the ABCC8 gene in neonatal diabetes mellitus

Andrey P. Babenko et al.

NEW ENGLAND JOURNAL OF MEDICINE (2006)

Article Medicine, General & Internal

Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations

Ewan R. Pearson et al.

NEW ENGLAND JOURNAL OF MEDICINE (2006)

Review Pediatrics

Neonatal diabetes mellitus: from understudy to center stage

MA Sperling

CURRENT OPINION IN PEDIATRICS (2005)

Article Multidisciplinary Sciences

Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features

P Proks et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)

Article Endocrinology & Metabolism

Glibenclamide treatment in permanent neonatal diabetes mellitus due to an activating mutation in Kir6.2

A Zung et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2004)