Related Experiment Videos
[Molecular pediatrics: "childhood illnesses" as pioneers in medicine]
1Abteilung für Stoffwechselkrankheiten und Molekulare Pädiatrie, Universitäts-Kinderklinik, Zürich. binges@kispi.unizh.ch
Schweizerische Medizinische Wochenschrift
|March 5, 1999
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Zurich Fabry study - prevalence of Fabry disease in young patients with first cryptogenic ischaemic stroke or TIA.
European journal of neurology·2012
[Benefit of clinical and laboratory parameters for the diagnosis of endometritis in dairy cows].
Schweizer Archiv fur Tierheilkunde·2010
[Swiss warmblood horse with symptoms of hereditary equine regional dermal asthenia without mutation in the cyclophylin B gene (PPIB)].
Schweizer Archiv fur Tierheilkunde·2010
Elevated serum biotinidase activity in hepatic glycogen storage disorders--a convenient biomarker.
Journal of inherited metabolic disease·2007
Pyridoxal 5'-phosphate may be curative in early-onset epileptic encephalopathy.
Journal of inherited metabolic disease·2007
Marfan syndrome--a diagnostic challenge caused by phenotypic and genetic heterogeneity.
Methods of information in medicine·2005
Altered m 6 A methylation across eight reward- and motor-related brain regions in alcohol use disorder.
medRxiv : the preprint server for health sciences·2026
P5 promoter-mediated incorporation explains REP/CAP manufacturing contaminants in patient liver after rAAV gene therapy.
medRxiv : the preprint server for health sciences·2026
Spatiotemporal control of STING activation and saRNA delivery decouples humoral and cellular immunity.
bioRxiv : the preprint server for biology·2026