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The European Respiratory Journal|April 28, 2017
Higher serum 25(OH)D concentrations are associated with improved FEV1 and FVC in adolescenceClaudia Flexeder, Elisabeth Thiering, Sibylle Koletzko, et al.
The International Journal of Occupational and Environmental Medicine|July 10, 2017
Residential Air Pollution, Road Traffic, Greenness and Maternal Hypertension: Results from GINIplus and LISAplusMario Jendrossek, Marie Standl, Sibylle Koletzko, et al.
The Journal of Allergy and Clinical Immunology|January 24, 2007
Certain hydrolyzed formulas reduce the incidence of atopic dermatitis but not that of asthma: three-year results of the German Infant Nutritional Intervention StudyAndrea von Berg, Sibylle Koletzko, Birgit Filipiak-Pittroff, et al.
Neurogenetics|February 1, 2012
Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47)Peter Bauer, Esther Leshinsky-Silver, Lubov Blumkin, et al.
International Journal of Paediatric Dentistry|March 6, 2012
Is there a positive relationship between molar incisor hypomineralisations and the presence of dental caries?Daniela Heitmüller, Elisabeth Thiering, Ute Hoffmann, et al.
Cerebellum (London, England)|September 14, 2013
Clinical and neurophysiological profile of four German families with spinocerebellar ataxia type 14Christos Ganos, Simone Zittel, Martina Minnerop, et al.
International Journal of Molecular Sciences|February 25, 2023
Contribution of Glucosylsphingosine (Lyso-Gb1) to Treatment Decisions in Patients with Gaucher DiseaseTama Dinur, Peter Bauer, Christian Beetz, et al.
Pigment Cell & Melanoma Research|June 4, 2026
Copy Number Analysis in Congenital Nevi: Concordance and Diagnostic Limitations of aCGH, sWGS, and Methylation SequencingAnton Karelin, Ines B Brecht, Michaela Pogoda, et al.
Cancers|August 23, 2020
Distinct Mutation Patterns Reveal Melanoma Subtypes and Influence Immunotherapy Response in Advanced Melanoma PatientsFranz J Hilke, Tobias Sinnberg, Axel Gschwind, et al.
European Journal of Human Genetics : EJHG|October 13, 2006
Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approachJürgen Tomiuk, Lutz Bachmann, Claudia Bauer, et al.
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