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Journal Articles

Is the Gut the “Sweet Spot” for the Treatment of Diabetes?

Francesco Rubino, Stephanie A. Amiel

Diabetes 2014;63(7):2225–2228

DOI: https://doi.org/10.2337/db14-0402

Published: 14 June 2014

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Journal Articles

Severe Persistent Hyperinsulinemic Hypoglycemia due to a De Novo Glucokinase Mutation

Antonio L. Cuesta-Muñoz, Hanna Huopio, Timo Otonkoski, Juan M. Gomez-Zumaquero, Kirsti Näntö-Salonen, Jacques Rahier, Soledad López-Enriquez, Maria A. García-Gimeno, Pascual Sanz, Federico C. Soriguer, Markku Laakso

Diabetes 2004;53(8):2164–2168

DOI: https://doi.org/10.2337/diabetes.53.8.2164

Published: 01 August 2004

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Journal Articles

Familial Hyperinsulinemic Hypoglycemia Caused by a Defect in the SCHAD Enzyme of Mitochondrial Fatty Acid Oxidation

Anders Molven, Guri E. Matre, Marinus Duran, Ronald J. Wanders, Unni Rishaug, Pål R. Njølstad, Egil Jellum, Oddmund Søvik

Diabetes 2004;53(1):221–227

DOI: https://doi.org/10.2337/diabetes.53.1.221

Published: 01 January 2004

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Journal Articles

The Focal Form of Persistent Hyperinsulinemic Hypoglycemia of Infancy: Morphological and Molecular Studies Show Structural and Functional Differences With Insulinoma

Christine Sempoux, Yves Guiot, Karin Dahan, Pierre Moulin, Martine Stevens, Virginie Lambot, Pascale de Lonlay, Jean-Christophe Fournet, Claudine Junien, Francis Jaubert, Claire Nihoul-Fekete, Jean-Marie Saudubray, Jacques Rahier

Diabetes 2003;52(3):784–794

DOI: https://doi.org/10.2337/diabetes.52.3.784

Published: 01 March 2003

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Journal Articles

The Second Activating Glucokinase Mutation (A456V): Implications for Glucose Homeostasis and Diabetes Therapy

Henrik B.T. Christesen, Bendt B. Jacobsen, Stella Odili, Carol Buettger, Antonio Cuesta-Munoz, Torben Hansen, Klaus Brusgaard, Ornella Massa, Mark A. Magnuson, Chiyo Shiota, Franz M. Matschinsky, Fabrizio Barbetti

Diabetes 2002;51(4):1240–1246

DOI: https://doi.org/10.2337/diabetes.51.4.1240

Published: 01 April 2002

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Meeting Abstracts

The focal form of persistent hyperinsulinemic hypoglycemia of infancy.

C Sempoux, Y Guiot, J Rahier

Diabetes 2001;50(suppl_1):S182

DOI: https://doi.org/10.2337/diabetes.50.2007.S182

Published: 01 February 2001

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Meeting Abstracts

Genetic analysis of Japanese patients with persistent hyperinsulinemic hypoglycemia of infancy: nucleotide-binding fold-2 mutation impairs cooperative binding of adenine nucleotides to sulfonylurea receptor 1.

Y Tanizawa, K Matsuda, M Matsuo, Y Ohta, N Ochi, M Adachi, M Koga, S Mizuno, M Kajita, Y Tanaka, K Tachibana, H Inoue, S Furukawa, T Amachi, K Ueda, Y Oka

Diabetes 2000;49(1):114–120

DOI: https://doi.org/10.2337/diabetes.49.1.114

Published: 01 January 2000

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Meeting Abstracts

Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.

B Glaser, F Ryan, M Donath, H Landau, C A Stanley, L Baker, D E Barton, P S Thornton

Diabetes 1999;48(8):1652–1657

DOI: https://doi.org/10.2337/diabetes.48.8.1652

Published: 01 August 1999

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Meeting Abstracts

A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland.

T Otonkoski, C Ammälä, H Huopio, G J Cote, J Chapman, K Cosgrove, R Ashfield, E Huang, J Komulainen, F M Ashcroft, M J Dunne, J Kere, P M Thomas

Diabetes 1999;48(2):408–415

DOI: https://doi.org/10.2337/diabetes.48.2.408

Published: 01 February 1999

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Meeting Abstracts

Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy.

S L Shyng, T Ferrigni, J B Shepard, A Nestorowicz, B Glaser, M A Permutt, C G Nichols

Diabetes 1998;47(7):1145–1151

DOI: https://doi.org/10.2337/diabetes.47.7.1145

Published: 01 July 1998

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Journal Articles

Ductal Cyst Formation in Collagen-Embedded Adult Human Islet Preparations: A Means to the Reproduction of Nesidioblastosis In Vitro

Julie Kerr-Conte, François Pattou, Martine Lecomte-Houcke, YingJian Xia, Benoni Boilly, Charles Proye, Jean Lefebvre

Diabetes 1996;45(8):1108–1114

DOI: https://doi.org/10.2337/diab.45.8.1108

Published: 01 August 1996

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Journal Articles

Induction of Nesidioblastosis Will Reverse Diabetes in Syrian Golden Hamster

Lawrence Rosenberg, William P Duguid, Rea A Brown, Aaron I Vinik

Diabetes 1988;37(3):334–341

DOI: https://doi.org/10.2337/diab.37.3.334

Published: 01 March 1988

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Journal Articles

Developmental Changes in Immunoreactive Content of Novel Pituitary Protein 7B2 in Human Pancreas and Its Identification in Pancreatic Tumors

Hitoshi Suzuki, Nicos D Christofides, Michel Chretien, Nabil G Seidah, Julia M Polak, Stephen R Bloom

Diabetes 1987;36(11):1276–1279

DOI: https://doi.org/10.2337/diab.36.11.1276

Published: 01 November 1987

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Journal Articles

Nesidioblastosis: The Pathologic Basis of Persistent Hyperinsulinemic Hypoglycemia in Infants: Morphologic and Quantitative Analysis of Seven Cases Based on Specific Immunostaining and Electron Microscopy

Philipp U Heitz, MD, Günter Klöppel, MD, Walter H Häcki, MD, Julia M Polak, MD, A G Everson Pearse, MD

Diabetes 1977;26(7):632–642

DOI: https://doi.org/10.2337/diab.26.7.632

Published: 01 July 1977

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NARROW

Is the Gut the “Sweet Spot” for the Treatment of Diabetes?

Severe Persistent Hyperinsulinemic Hypoglycemia due to a De Novo Glucokinase Mutation

Familial Hyperinsulinemic Hypoglycemia Caused by a Defect in the SCHAD Enzyme of Mitochondrial Fatty Acid Oxidation

The Focal Form of Persistent Hyperinsulinemic Hypoglycemia of Infancy: Morphological and Molecular Studies Show Structural and Functional Differences With Insulinoma

The Second Activating Glucokinase Mutation (A456V): Implications for Glucose Homeostasis and Diabetes Therapy

The focal form of persistent hyperinsulinemic hypoglycemia of infancy.

Genetic analysis of Japanese patients with persistent hyperinsulinemic hypoglycemia of infancy: nucleotide-binding fold-2 mutation impairs cooperative binding of adenine nucleotides to sulfonylurea receptor 1.

Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.

A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland.

Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy.

Ductal Cyst Formation in Collagen-Embedded Adult Human Islet Preparations: A Means to the Reproduction of Nesidioblastosis In Vitro

Induction of Nesidioblastosis Will Reverse Diabetes in Syrian Golden Hamster

Developmental Changes in Immunoreactive Content of Novel Pituitary Protein 7B2 in Human Pancreas and Its Identification in Pancreatic Tumors

Nesidioblastosis: The Pathologic Basis of Persistent Hyperinsulinemic Hypoglycemia in Infants: Morphologic and Quantitative Analysis of Seven Cases Based on Specific Immunostaining and Electron Microscopy

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