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.

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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.
Authors: Loechner KJ; Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill, USA., Akrouh A, Kurata HT, Dionisi-Vici C, Maiorana A, Pizzoferro M, Rufini V, de Ville de Goyet J, Colombo C, Barbetti F, Koster JC, Nichols CG
Source: Diabetes [Diabetes] 2011 Jan; Vol. 60 (1), pp. 209-17. Date of Electronic Publication: 2010 Oct 27.
Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural
Journal Info: Publisher: American Diabetes Association Country of Publication: United States NLM ID: 0372763 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1939-327X (Electronic) Linking ISSN: 00121797 NLM ISO Abbreviation: Diabetes Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: 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.
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  Data: <searchLink fieldCode="AU" term="%22Loechner+KJ%22">Loechner KJ</searchLink>; Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill, USA.<br /><searchLink fieldCode="AU" term="%22Akrouh+A%22">Akrouh A</searchLink><br /><searchLink fieldCode="AU" term="%22Kurata+HT%22">Kurata HT</searchLink><br /><searchLink fieldCode="AU" term="%22Dionisi-Vici+C%22">Dionisi-Vici C</searchLink><br /><searchLink fieldCode="AU" term="%22Maiorana+A%22">Maiorana A</searchLink><br /><searchLink fieldCode="AU" term="%22Pizzoferro+M%22">Pizzoferro M</searchLink><br /><searchLink fieldCode="AU" term="%22Rufini+V%22">Rufini V</searchLink><br /><searchLink fieldCode="AU" term="%22de+Ville+de+Goyet+J%22">de Ville de Goyet J</searchLink><br /><searchLink fieldCode="AU" term="%22Colombo+C%22">Colombo C</searchLink><br /><searchLink fieldCode="AU" term="%22Barbetti+F%22">Barbetti F</searchLink><br /><searchLink fieldCode="AU" term="%22Koster+JC%22">Koster JC</searchLink><br /><searchLink fieldCode="AU" term="%22Nichols+CG%22">Nichols CG</searchLink>
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  Data: <searchLink fieldCode="JN" term="%220372763%22">Diabetes</searchLink> [Diabetes] 2011 Jan; Vol. 60 (1), pp. 209-17. <i>Date of Electronic Publication: </i>2010 Oct 27.
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  Data: Case Reports; Journal Article; Research Support, N.I.H., Extramural
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22American+Diabetes+Association%22">American Diabetes Association </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>0372763 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1939-327X (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200121797%22">00121797 </searchLink><i>NLM ISO Abbreviation: </i>Diabetes <i>Subsets: </i>MEDLINE
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        Value: 10.2337/db10-0731
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      – TitleFull: 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.
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              Text: 2011 Jan
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