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Annette Rønholt Larsen

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Frontiers in Endocrinology|March 8, 2021
A Sensitive Plasma Insulin Immunoassay to Establish the Diagnosis of Congenital HyperinsulinismJulie Siersbæk, Annette Rønholt Larsen, Mads Nybo, et al.
Histology and Histopathology|February 2, 2024
Genotype-histotype-phenotype correlations in hyperinsulinemic hypoglycemiaAnnette Rønholt Larsen, Klaus Brusgaard, Henrik Thybo Christesen, et al.
Frontiers in Endocrinology|January 21, 2026
Germline and somatic mutations in histologically atypical congenital hyperinsulinismAnnette Rønholt Larsen, Evgenia Globa, Ditte Caroline Andersen, et al.
European Journal of Medical Genetics|February 24, 2019
Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinismHenrik Thybo Christesen, Lene Gaarsmand Christensen, Åsa Mattsson Löfgren, et al.
Human Mutation|February 7, 2020
Update of variants identified in the pancreatic β-cell K<sub>ATP</sub> channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetesElisa De Franco, Cécile Saint-Martin, Klaus Brusgaard, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Frontiers in Endocrinology|March 8, 2021
A Sensitive Plasma Insulin Immunoassay to Establish the Diagnosis of Congenital HyperinsulinismJulie Siersbæk, Annette Rønholt Larsen, Mads Nybo, et al.
Histology and Histopathology|February 2, 2024
Genotype-histotype-phenotype correlations in hyperinsulinemic hypoglycemiaAnnette Rønholt Larsen, Klaus Brusgaard, Henrik Thybo Christesen, et al.
Frontiers in Endocrinology|January 21, 2026
Germline and somatic mutations in histologically atypical congenital hyperinsulinismAnnette Rønholt Larsen, Evgenia Globa, Ditte Caroline Andersen, et al.
European Journal of Medical Genetics|February 24, 2019
Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinismHenrik Thybo Christesen, Lene Gaarsmand Christensen, Åsa Mattsson Löfgren, et al.
Human Mutation|February 7, 2020
Update of variants identified in the pancreatic β-cell K<sub>ATP</sub> channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetesElisa De Franco, Cécile Saint-Martin, Klaus Brusgaard, et al.
Pageof 1