Sabina Grohe-Schmitt

Erlangen, BY 91054, Germany

Last Updated: 09/26/2026

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Found 12 publications

Decoding the diagnostic and therapeutic potential of microbiota using pan-body pan-disease microbiomics.

Decoding the diagnostic and therapeutic potential of microbiota using pan-body pan-disease microbiomics.

Journal: Nature communications

Published: December 18, 2023

Evaluating the Use of Neonatal Colonization Screening for Empiric Antibiotic Therapy of Sepsis and Pneumonia.

Evaluating the Use of Neonatal Colonization Screening for Empiric Antibiotic Therapy of Sepsis and Pneumonia.

Journal: Antibiotics (Basel, Switzerland)

Published: December 25, 2022

Increase of liver stiffness and altered bile acid metabolism after triple CFTR modulator initiation in children and young adults with cystic fibrosis.

Increase of liver stiffness and altered bile acid metabolism after triple CFTR modulator initiation in children and young adults with cystic fibrosis.

Journal: Liver international : official journal of the International Association for the Study of the Liver

Published: December 09, 2022

Transforming Growth Factor ß1 and Gap Junction Protein Alpha 4 Gene Heterogeneity in Relation to the Severity of Clinical Disease in Cystic Fibrosis.

Transforming Growth Factor ß1 and Gap Junction Protein Alpha 4 Gene Heterogeneity in Relation to the Severity of Clinical Disease in Cystic Fibrosis.

Journal: Frontiers in bioscience (Landmark edition)

Published: October 18, 2022

Mannose-Binding Lectin (MBL) and Gap Junction Protein Alpha 4 (GJA4) Gene Heterogeneity in Relation to Severity of Clinical Disease in Cystic Fibrosis.

Mannose-Binding Lectin (MBL) and Gap Junction Protein Alpha 4 (GJA4) Gene Heterogeneity in Relation to Severity of Clinical Disease in Cystic Fibrosis.

Journal: Frontiers in bioscience (Landmark edition)

Published: December 30, 2021

Impact of a Gap Junction Protein Alpha 4 Variant on Clinical Disease Phenotype in F508del Homozygous Patients With Cystic Fibrosis.

Impact of a Gap Junction Protein Alpha 4 Variant on Clinical Disease Phenotype in F508del Homozygous Patients With Cystic Fibrosis.

Journal: Frontiers in genetics

Published: June 07, 2020

Clinical relevance of Aspergillus fumigatus sensitization in cystic fibrosis.

Clinical relevance of Aspergillus fumigatus sensitization in cystic fibrosis.

Journal: Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology

Published: September 02, 2019

Lymphocytic interstitial pneumonia and follicular bronchiolitis in children: A registry-based case series.

Lymphocytic interstitial pneumonia and follicular bronchiolitis in children: A registry-based case series.

Journal: Pediatric pulmonology

Published: July 19, 2019

Prospective multicenter German study on pulmonary colonization with Scedosporium /Lomentospora species in cystic fibrosis: Epidemiology and new association factors.

Prospective multicenter German study on pulmonary colonization with Scedosporium /Lomentospora species in cystic fibrosis: Epidemiology and new association factors.

Journal: PloS one

Published: September 18, 2016

Airway inflammation in mild cystic fibrosis.

Airway inflammation in mild cystic fibrosis.

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

Published: October 25, 2015

Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia.

Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia.

Journal: Nature genetics

Published: December 06, 2013

Transforming growth factor β1 genotypes in relation to TGFβ1, interleukin-8, and tumor necrosis factor alpha in induced sputum and blood in cystic fibrosis.

Transforming growth factor β1 genotypes in relation to TGFβ1, interleukin-8, and tumor necrosis factor alpha in induced sputum and blood in cystic fibrosis.

Journal: Mediators of inflammation

Published: April 21, 2013

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Last Updated: 09/26/2026