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Molecular Genetics and Metabolism|March 25, 2025
Clinical and biochemical footprints of inherited metabolic diseases: Ia. Movement disorders, updatedDakota J S J Peacock, Carlos R Ferreira, Gabriella Horvath, et al.
Klinische Monatsblatter Fur Augenheilkunde|December 1, 1978
[Osteo-keramo-keratoprosthesis (author's transl)]F Hoffmann, J P Harnisch, V Strunz, et al.
Injury|April 1, 2014
Biomechanical evaluation of fracture fixation constructs using a variable-angle locked periprosthetic femur plate systemMartin F Hoffmann, Travis A Burgers, James J Mason, et al.
Biorxiv : the Preprint Server for Biology|May 7, 2024
Quinoxaline-Based Anti-Schistosomal Compounds Have Potent Anti-Malarial ActivityMukul Rawat, Gilda Padalino, Tomas Yeo, et al.
Orphanet Journal of Rare Diseases|December 5, 2024
Systematic quantitative modeling of the natural history of Aicardi syndrome: A cross sectional study of 245 published casesOliver Y Urban, Jan H Driedger, Sven F Garbade, et al.
Pediatric Pulmonology|November 29, 2022
German newborn screening for Cystic fibrosis: Parental perspectives and suggestions for improvementsSimon Gapp, Sven F Garbade, Patrik Feyh, et al.
Neuropediatrics|March 1, 2002
A new subtype of a congenital disorder of glycosylation (CDG) with mild clinical manifestationsB Assmann, R Hackler, V Peters, et al.
Plos Neglected Tropical Diseases|October 23, 2008
Use of genomic DNA as an indirect reference for identifying gender-associated transcripts in morphologically identical, but chromosomally distinct, Schistosoma mansoni cercariaeJennifer M Fitzpatrick, Anna V Protasio, Andrew J McArdle, et al.
Molecular Genetics and Metabolism|November 17, 2022
Detection of early cardiac disease manifestation in propionic acidemia - Results of a monocentric cross-sectional studyAlexander Kovacevic, Sven F Garbade, Friederike Hörster, et al.
Der Nervenarzt|September 24, 2002
[CDG (congenital disorders of glycosylation). Differential hereditary ataxia in adulthood diagnosis]S Bubel, V Peters, C Klein, et al.
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