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

Risultato della ricerca: Contributo in rivista › Articolo in rivista

17 Citazioni (Scopus)

Lingua originale	English
pagine (da-a)	209-217
Numero di pagine	9
Rivista	Diabetes
Volume	2011
Stato di pubblicazione	Pubblicato - 2011

Keywords

18F-DOPA
hyperinsulinism
mutation

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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:National Service Center, 1701 North Beaureguard Street:Alexandria, VA 22311:(800)232-3472, (703)549-1500, INTERNET: http://www.diabetes.org/diabetscare, Fax: (703)549-6995",

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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, pagg. 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 -