Sibylle Junge

Hannover, NI, Germany

Last Updated: 09/26/2026

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Found 18 publications

UCCL-IKF-AIO-STO-0124 NeoART-an international phase Ib/II platform trial investigating trastuzumab deruxtecan (T-DXd) combined with neoadjuvant chemotherapy for HER2-positive, resectable esophagogastric adenocarcinoma (EGA).

UCCL-IKF-AIO-STO-0124 NeoART-an international phase Ib/II platform trial investigating trastuzumab deruxtecan (T-DXd) combined with neoadjuvant chemotherapy for HER2-positive, resectable esophagogastric adenocarcinoma (EGA).

Journal: ESMO gastrointestinal oncology

Published: April 30, 2026

Mucoid Staphylococcus aureus: A Clinical Trial of Its Prevalence and Association with Lung Function in People with Cystic Fibrosis.

Mucoid Staphylococcus aureus: A Clinical Trial of Its Prevalence and Association with Lung Function in People with Cystic Fibrosis.

Journal: American journal of respiratory and critical care medicine

Published: February 07, 2025

SAGA-a phase Ib/II single-arm, multicenter study of sacituzumab govitecan for patients with metastatic esophagogastric adenocarcinoma.

SAGA-a phase Ib/II single-arm, multicenter study of sacituzumab govitecan for patients with metastatic esophagogastric adenocarcinoma.

Journal: ESMO gastrointestinal oncology

Published: April 12, 2024

Spirometric and anthropometric improvements in response to elexacaftor/tezacaftor/ivacaftor depending on age and lung disease severity.

Spirometric and anthropometric improvements in response to elexacaftor/tezacaftor/ivacaftor depending on age and lung disease severity.

Journal: Frontiers in pharmacology

Published: February 22, 2023

Comparison of Three Eradication Treatment Protocols for Pseudomonas Aeruginosa in Children and Adolescents with Cystic Fibrosis.

Comparison of Three Eradication Treatment Protocols for Pseudomonas Aeruginosa in Children and Adolescents with Cystic Fibrosis.

Journal: Klinische Padiatrie

Published: February 09, 2023

Changes in cystic fibrosis transmembrane conductance regulator protein expression prior to and during elexacaftor-tezacaftor-ivacaftor therapy.

Changes in cystic fibrosis transmembrane conductance regulator protein expression prior to and during elexacaftor-tezacaftor-ivacaftor therapy.

Journal: Frontiers in pharmacology

Published: December 02, 2022

The First 4 Years - Outcome of Children Identified by Newborn Screening for CF in Germany.

The First 4 Years - Outcome of Children Identified by Newborn Screening for CF in Germany.

Journal: Klinische Padiatrie

Published: January 31, 2022

CFTR modulation with elexacaftor-tezacaftor-ivacaftor in people with cystic fibrosis assessed by the β-adrenergic sweat rate assay.

CFTR modulation with elexacaftor-tezacaftor-ivacaftor in people with cystic fibrosis assessed by the β-adrenergic sweat rate assay.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: June 01, 2021

Intestinal current measurement and nasal potential difference to make a diagnosis of cases with inconclusive CFTR genetics and sweat test.

Intestinal current measurement and nasal potential difference to make a diagnosis of cases with inconclusive CFTR genetics and sweat test.

Journal: BMJ open respiratory research

Published: August 04, 2020

Assessment of a Mobile App by Adolescents and Young Adults With Cystic Fibrosis: Pilot Evaluation.

Assessment of a Mobile App by Adolescents and Young Adults With Cystic Fibrosis: Pilot Evaluation.

Journal: JMIR mHealth and uHealth

Published: October 07, 2018

Factors Associated with Worse Lung Function in Cystic Fibrosis Patients with Persistent Staphylococcus aureus.

Factors Associated with Worse Lung Function in Cystic Fibrosis Patients with Persistent Staphylococcus aureus.

Journal: PloS one

Published: June 25, 2016

Skeletal Muscle Function in Young Patients With Cystic Fibrosis.

Skeletal Muscle Function in Young Patients With Cystic Fibrosis.

Journal: Pediatric exercise science

Published: April 06, 2016

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Last Updated: 09/26/2026