Results 201 to 210 of about 6,576 (240)

A case of congenital hyperinsulinism presenting with diabetes after long-term diazoxide therapy. [PDF]

Diabetol Int
Furuzono M, Makimura M, Miyako K.
europepmc   +1 more source

Opposite kinetics of L-leucine and L-phenylalanine induced insulin release studies with the perfused rat pancreas [PDF]

, 1972
Landgraf, R., Landgraf-Leurs, M. M. C., Schwarz, K., Scriba, Peter Christian   +3 more
core  

Characterization of Congenital Hyperinsulinism in Argentina: Clinical Features, Genetic Findings, and Treatment Outcomes

Pacheco G, Bastida MG, Cáceres J, Alonso G, Aziz M, Suarez M, Flores A, Femenia V, Forclaz MV, Houghton JA, Bennett JJ, Martin S, Flanagan SE, Tangari-Saredo A.   +13 more
europepmc   +1 more source

Clinical, genetic, and radionuclide characteristics of the focal form of congenital hyperinsulinism

, 2019
Diliara Gubaeva, Maria Melikyan, Д. В. Рыжкова, Mikhail D. Poyda, Vladimir G. Bairov, Anna A. Sukhotskaya, Yu. Yu. Sokolov, А. М. Ефременков, Л. Б. Митрофанова, Henrik Thybo Christesen, И. Л. Никитина   +10 more
openalex   +2 more sources

Clinical and Genetic Characteristics of Congenital Hyperinsulinism in Norway: A Nationwide Cohort Study.

J Clin Endocrinol Metab
Velde CD, Molnes J, Berland S, Njølstad PR, Molven A.   +4 more
europepmc   +1 more source

Congenital hyperinsulinism and surgical outcome in a single tertiary center in Brazil. [PDF]

J Pediatr (Rio J)
Liberatore RDR, Monteiro ICM, Pileggi FO, Canesin WC, Sbragia L.   +4 more
europepmc   +1 more source

Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the likely disruption ofFOXA2

, 2023
Laver TW, Wakeling MN, Caswell RC, Bunce B, Yau D, Houghton JA, Hopkins JJ, Weedon MN, Saraff V, Kershaw M, Honey EM, Murphy N, Giri D, Nath S, Saredo AT, Banerjee I, Hussain K, Owens ND, Flanagan SE.   +18 more
europepmc   +1 more source

SAT-272 A Phase 2 Comparison of a Stable Liquid Glucagon to Placebo for the Treatment of Congenital Hyperinsulinism

, 2019
Paul Thornton, Martin J. Cummins, Khaled Junaidi, Kenneth E. Johnson   +3 more
openalex   +1 more source

Congenital Hyperinsulinism in Humans and Insulin Secretory Dysfunction in Mice Caused by Biallelic DNAJC3 Variants. [PDF]

Int J Mol Sci
Welters A, Nortmann O, Wörmeyer L, Freiberg C, Eberhard D, Bachmann N, Bergmann C, Mayatepek E, Meissner T, Kummer S.   +9 more
europepmc   +1 more source

Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. [PDF]

Eur J Hum Genet
Laver TW, Wakeling MN, Caswell RC, Bunce B, Yau D, Männistö JME, Houghton JAL, Hopkins JJ, Weedon MN, Saraff V, Kershaw M, Honey EM, Murphy N, Giri D, Nath S, Tangari Saredo A, Banerjee I, Hussain K, Owens NDL, Flanagan SE.   +19 more
europepmc   +1 more source