Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management.

Kj Loechner; A Akrouh; Ht Kurata; C Dionisi Vici; Arianna Maiorana; Milena Pizzoferro; Vittoria Rufini; J De Ville De Goyet; C Colombo; F Barbetti; Jc Koster; Cg Nichols

Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management.

Kj Loechner, A Akrouh, Ht Kurata, C Dionisi Vici, Arianna Maiorana, Milena Pizzoferro, Vittoria Rufini, J De Ville De Goyet, C Colombo, F Barbetti, Jc Koster, Cg Nichols

Research output: Contribution to journal › Article

17 Citations (Scopus)

Original language	English
Pages (from-to)	209-217
Number of pages	9
Journal	Diabetes
Volume	2011
Publication status	Published - 2011

Keywords

18F-DOPA
hyperinsulinism
mutation

Cite this

Loechner, K., Akrouh, A., Kurata, H., Dionisi Vici, C., Maiorana, A., Pizzoferro, M., Rufini, V., De Ville De Goyet, J., Colombo, C., Barbetti, F., Koster, J., & Nichols, C. (2011). Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management. Diabetes, 2011, 209-217.

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title = "Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management.",

keywords = "18F-DOPA, hyperinsulinism, mutation, 18F-DOPA, hyperinsulinism, mutation",

author = "Kj Loechner and A Akrouh and Ht Kurata and {Dionisi Vici}, C and Arianna Maiorana and Milena Pizzoferro and Vittoria Rufini and {De Ville De Goyet}, J and C Colombo and F Barbetti and Jc Koster and Cg Nichols",

year = "2011",

language = "English",

volume = "2011",

pages = "209--217",

journal = "Diabetes",

issn = "0012-1797",

publisher = "American Diabetes Association Inc.",

}

Loechner, K, Akrouh, A, Kurata, H, Dionisi Vici, C, Maiorana, A, Pizzoferro, M, Rufini, V, De Ville De Goyet, J, Colombo, C, Barbetti, F, Koster, J & Nichols, C 2011, 'Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management.', Diabetes, vol. 2011, pp. 209-217.

TY - JOUR

T1 - Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management.

AU - Loechner, Kj

AU - Akrouh, A

AU - Kurata, Ht

AU - Dionisi Vici, C

AU - Maiorana, Arianna

AU - Pizzoferro, Milena

AU - Rufini, Vittoria

AU - De Ville De Goyet, J

AU - Colombo, C

AU - Barbetti, F

AU - Koster, Jc

AU - Nichols, Cg

PY - 2011

Y1 - 2011

KW - 18F-DOPA

KW - hyperinsulinism

KW - mutation

KW - 18F-DOPA

KW - hyperinsulinism

KW - mutation

UR - http://hdl.handle.net/10807/12267

M3 - Article

SN - 0012-1797

VL - 2011

SP - 209

EP - 217

JO - Diabetes

JF - Diabetes

ER -

Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management.

Keywords

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