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Publications by Verena Schneider

Genotype/Phenotype Association in Cystic Fibrosis: Analyses of the ΔF508, R553X, and 3905insT Mutations

Pediatric Research

English

Related publications

Chloride Conductance and Genetic Background Modulate the Cystic Fibrosis Phenotype of ΔF508 Homozygous Twins and Siblings

Journal of Clinical Investigation

English

Prevalence of deltaF508, G551D, G542X, and R553X Mutations Among Cystic Fibrosis Patients in the North of Brazil

Brazilian Journal of Medical and Biological Research

English

Genotype-Phenotype Relationship in 12 Patients Carrying Cystic Fibrosis Mutation R334W.

Journal of Medical Genetics

English

A Cystic Fibrosis Patient Homozygous for the Nonsense Mutation R553X.

Journal of Medical Genetics

English

Association Between Haplotypes and Specific Mutations in Swiss Cystic Fibrosis Families

Pediatric Research

English

Functional Stability of Rescued ΔF508 Cystic Fibrosis Transmembrane Conductance Regulator in Airway Epithelial Cells

American Journal of Respiratory Cell and Molecular Biology

Respiratory Medicine

Clinical Biochemistry

Molecular Biology

English

Distribution and Genotype-Phenotype Correlation of GDAP1 Mutations in Spain

Scientific Reports

Multidisciplinary

English

Energy Expenditure and Genotype of Children With Cystic Fibrosis

Pediatric Research

English

Point Mutations in Ferroportin Disease: Genotype/Phenotype Correlation

English