Gesche Duker

Bonn, NW, Germany

Last Updated: 09/26/2026

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Found 9 publications

Anti-TNF therapy for inflammatory bowel disease in patients with neurodegenerative Niemann-Pick disease Type C.

Anti-TNF therapy for inflammatory bowel disease in patients with neurodegenerative Niemann-Pick disease Type C.

Journal: Wellcome open research
Published: December 23, 2021

Management of esophageal perforations in infants by endoscopic vacuum therapy: a single center case series.

Management of esophageal perforations in infants by endoscopic vacuum therapy: a single center case series.

Journal: BMC gastroenterology
Published: December 18, 2021

Case Report: Extended Clinical Spectrum of the Neonatal Diabetes With Congenital Hypothyroidism Syndrome.

Case Report: Extended Clinical Spectrum of the Neonatal Diabetes With Congenital Hypothyroidism Syndrome.

Journal: Frontiers in endocrinology
Published: February 07, 2021

Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations.

Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations.

Journal: Journal of clinical medicine
Published: December 31, 2020

Novel variants and clinical symptoms in four new ALG3-CDG patients, review of the literature, and identification of AAGRP-ALG3 as a novel ALG3 variant with alanine and glycine-rich N-terminus.

Novel variants and clinical symptoms in four new ALG3-CDG patients, review of the literature, and identification of AAGRP-ALG3 as a novel ALG3 variant with alanine and glycine-rich N-terminus.

Journal: Human mutation
Published: January 22, 2019

Infancy-Onset T1DM, Short Stature, and Severe Immunodysregulation in Two Siblings With a Homozygous LRBA Mutation.

Infancy-Onset T1DM, Short Stature, and Severe Immunodysregulation in Two Siblings With a Homozygous LRBA Mutation.

Journal: The Journal of clinical endocrinology and metabolism
Published: January 09, 2016

Impaired antibacterial autophagy links granulomatous intestinal inflammation in Niemann-Pick disease type C1 and XIAP deficiency with NOD2 variants in Crohn's disease.

Impaired antibacterial autophagy links granulomatous intestinal inflammation in Niemann-Pick disease type C1 and XIAP deficiency with NOD2 variants in Crohn's disease.

Journal: Gut
Published: July 16, 2015

Rapunzel's Syndrome--a rare phenomenon.

Rapunzel's Syndrome--a rare phenomenon.

Journal: Klinische Padiatrie
Published: August 26, 2014

Mutations in the human UBR1 gene and the associated phenotypic spectrum.

Mutations in the human UBR1 gene and the associated phenotypic spectrum.

Journal: Human mutation
Published: November 08, 2013
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Last Updated: 09/26/2026