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There are 12201 results for: content related to: Hyperinsulinemic hypoglycemia evolving to gestational diabetes and diabetes mellitus in a family carrying the inactivating ABCC8 E1506K mutation

  1. Diagnosis and treatment of neonatal diabetes: an United States experience

    Pediatric Diabetes

    Volume 9, Issue 5, October 2008, Pages: 450–459, Julie Støy, Siri Atma W Greeley, Veronica P Paz, Honggang Ye, Ashley N Pastore, Kinga B Skowron, Rebecca B Lipton, Fran R Cogen, Graeme I Bell, Louis H Philipson and United States Neonatal Diabetes Working Group

    Article first published online : 25 JUL 2008, DOI: 10.1111/j.1399-5448.2008.00433.x

  2. The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy

    Clinical Genetics

    Volume 75, Issue 5, May 2009, Pages: 440–448, T Sandal, LB Laborie, K Brusgaard, SÅ Eide, HBT Christesen, O Søvik, PR Njølstad and A Molven

    Article first published online : 21 APR 2009, DOI: 10.1111/j.1399-0004.2009.01152.x

  3. You have full text access to this OnlineOpen article
    Dominantly acting ABCC8 mutations in patients with medically unresponsive hyperinsulinaemic hypoglycaemia

    Clinical Genetics

    Volume 79, Issue 6, June 2011, Pages: 582–587, SE Flanagan, RR Kapoor, I Banerjee, C Hall, VV Smith, K Hussain and S Ellard

    Article first published online : 22 MAY 2010, DOI: 10.1111/j.1399-0004.2010.01476.x

  4. You have free access to this content
    Mutations in the ABCC8 gene encoding the SUR1 subunit of the KATP channel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal period

    Diabetes, Obesity and Metabolism

    Volume 9, Issue s2, November 2007, Pages: 28–39, A. M. Patch, S. E. Flanagan, C. Boustred, A. T. Hattersley and S. Ellard

    Article first published online : 4 OCT 2007, DOI: 10.1111/j.1463-1326.2007.00772.x

  5. You have free access to this content
    Permanent neonatal diabetes mellitus – the importance of diabetes differential diagnosis in neonates and infants

    European Journal of Clinical Investigation

    Volume 41, Issue 3, March 2011, Pages: 323–333, Oscar Rubio-Cabezas, Tomasz Klupa, Maciej T. Malecki and CEED3 Consortium

    Article first published online : 4 NOV 2010, DOI: 10.1111/j.1365-2362.2010.02409.x

  6. Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children

    Clinical Genetics

    Volume 83, Issue 5, May 2013, Pages: 439–445, S Jahnavi, V Poovazhagi, V Mohan, D Bodhini, P Raghupathy, A Amutha, P Suresh Kumar, P Adhikari, M Shriraam, T Kaur, AK Das, J Molnes, PR Njolstad, R Unnikrishnan and V Radha

    Article first published online : 20 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01939.x

  7. You have full text access to this Open Access content
    Genetics and pathophysiology of neonatal diabetes mellitus

    Journal of Diabetes Investigation

    Volume 2, Issue 3, June 2011, Pages: 158–169, Rochelle N Naylor, Siri Atma W Greeley, Graeme I Bell and Louis H Philipson

    Article first published online : 2 MAR 2011, DOI: 10.1111/j.2040-1124.2011.00106.x

  8. Partial ABCC8 gene deletion mutations causing diazoxide-unresponsive hyperinsulinaemic hypoglycaemia

    Pediatric Diabetes

    Volume 13, Issue 3, May 2012, Pages: 285–289, SE Flanagan, A Damhuis, I Banerjee, D Rokicki, C Jefferies, RR Kapoor, K Hussain and S Ellard

    Article first published online : 7 OCT 2011, DOI: 10.1111/j.1399-5448.2011.00821.x

  9. You have free access to this content
    Mutation spectra of ABCC8 gene in Spanish patients with hyperinsulinism of infancy (HI)

    Human Mutation

    Volume 27, Issue 2, February 2006, Page: 214, Ana Fernández–Marmiesse, Antonio Salas, Ana Vega, José Ramón Fernández–Lorenzo, Jesús Barreiro and Ángel Carracedo

    Article first published online : 20 JAN 2006, DOI: 10.1002/humu.9401

  10. You have free access to this content
    Mutations in the genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) in diabetes mellitus and hyperinsulinism

    Human Mutation

    Volume 27, Issue 3, March 2006, Pages: 220–231, Anna L. Gloyn, Juveria Siddiqui and Sian Ellard

    Article first published online : 13 JAN 2006, DOI: 10.1002/humu.20292

  11. Novel ABCC8 (SUR1) Gene Mutations in Asian Indian Children with Congenital Hyperinsulinemic Hypoglycemia

    Annals of Human Genetics

    Volume 78, Issue 5, September 2014, Pages: 311–319, Suresh Jahnavi, Varadarajan Poovazhagi, Sekar Kanthimathi, Kandasamy Balamurugan, Dhanasekaran Bodhini, Jaivinder Yadav, Vandana Jain, Rajesh Khadgawat, Mahuya Sikdar, Ayurchelvan Bhavatharini, Ashok Kumar Das, Tanvir Kaur, Viswanathan Mohan and Venkatesan Radha

    Article first published online : 12 AUG 2014, DOI: 10.1111/ahg.12070

  12. Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinism

    Clinical Genetics

    C. Saint-Martin, Q. Zhou, G.M. Martin, C. Vaury, G. Leroy, J.-B. Arnoux, P. de Lonlay, S.-L. Shyng and C. Bellanné-Chantelot

    Article first published online : 6 JUN 2014, DOI: 10.1111/cge.12428

  13. Common variants in the ATP-sensitive K+ channel genes KCNJ11 (Kir6.2) and ABCC8 (SUR1) in relation to glucose intolerance: population-based studies and meta-analyses

    Diabetic Medicine

    Volume 22, Issue 5, May 2005, Pages: 590–598, R. M. Van Dam, B. Hoebee, J. C. Seidell, M. M. Schaap, T. W. A. De Bruin and E. J. M. Feskens

    Article first published online : 18 APR 2005, DOI: 10.1111/j.1464-5491.2005.01465.x

  14. Genetic variants in potassium channels are associated with type 2 diabetes in a Mongolian population

    Journal of Diabetes

    Volume 4, Issue 3, September 2012, Pages: 238–242, Zagaa ODGEREL, Hee S. LEE, Narnygerel ERDENEBILEG, Suren GANDBOLD, Munkhjargal LUVSANJAMBA, Nyamkhishig SAMBUUGHIN, Sainbileg SONOMTSEREN, Purevdulam SHARAVDORJ, Erdenezul JODOV, Khasag ALTAISAIKHAN and Lev G. GOLDFARB

    Article first published online : 17 AUG 2012, DOI: 10.1111/j.1753-0407.2011.00177.x

  15. Permanent neonatal diabetes mellitus: prevalence and genetic diagnosis in the SEARCH for Diabetes in Youth Study

    Pediatric Diabetes

    Volume 14, Issue 3, May 2013, Pages: 174–180, Roopa Kanakatti Shankar, Catherine Pihoker, Lawrence M. Dolan, Debra Standiford, Angela Badaru, Dana Dabelea, Beatriz Rodriguez, Mary Helen Black, Giuseppina Imperatore, Andrew Hattersley, Sian Ellard, Lisa K. Gilliam and for the SEARCH for Diabetes in Youth Study Group

    Article first published online : 10 OCT 2012, DOI: 10.1111/pedi.12003

  16. Focal congenital hyperinsulinism managed by medical treatment: a diagnostic algorithm based on molecular genetic screening

    Clinical Endocrinology

    Volume 81, Issue 5, November 2014, Pages: 679–688, Arianna Maiorana, Fabrizio Barbetti, Arianna Boiani, Vittoria Rufini, Milena Pizzoferro, Paola Francalanci, Flavio Faletra, Colin G. Nichols, Chiara Grimaldi, Jean de Ville de Goyet, Jacques Rahier, Jean-Claude Henquin and Carlo Dionisi-Vici

    Article first published online : 30 JAN 2014, DOI: 10.1111/cen.12400

  17. Familial mild hyperglycemia associated with a novel ABCC8-V84I mutation within three generations

    Pediatric Diabetes

    Volume 12, Issue 3pt2, May 2011, Pages: 266–269, Lucie Gonsorcikova, Martine Vaxillaire, Stepanka Pruhova, Aurélie Dechaume, Petra Dusatkova, Ondrej Cinek, Oluf Pedersen, Philippe Froguel, Torben Hansen and Jan Lebl

    Article first published online : 9 JAN 2011, DOI: 10.1111/j.1399-5448.2010.00719.x

  18. Incidence, genetics, and clinical phenotype of permanent neonatal diabetes mellitus in northwest Saudi Arabia

    Pediatric Diabetes

    Volume 13, Issue 6, September 2012, Pages: 499–505, Abdelhadi M Habeb, Mohamed SF Al-Magamsi, Ihsan M Eid, Mohamed I Ali, Andrew T Hattersley, Khalid Hussain and Sian Ellard

    Article first published online : 8 NOV 2011, DOI: 10.1111/j.1399-5448.2011.00828.x

  19. KATP channel mutations in infants with permanent diabetes diagnosed after 6 months of life

    Pediatric Diabetes

    Volume 13, Issue 4, June 2012, Pages: 322–325, Oscar Rubio-Cabezas, Sarah E Flanagan, Annet Damhuis, Andrew T Hattersley and Sian Ellard

    Article first published online : 10 OCT 2011, DOI: 10.1111/j.1399-5448.2011.00824.x

  20. Incidence of neonatal diabetes in Austria–calculation based on the Austrian Diabetes Register

    Pediatric Diabetes

    Volume 11, Issue 1, February 2010, Pages: 18–23, Barbara Wiedemann, Edith Schober, Thomas Waldhoer, Julia Koehle, Sarah E Flanagan, Deborah JG Mackay, Elisabeth Steichen, Dagmar Meraner, Lothar-Bernd Zimmerhackl, Andrew T Hattersley, Sian Ellard and Sabine Hofer

    Article first published online : 3 JUN 2009, DOI: 10.1111/j.1399-5448.2009.00530.x