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Erscheinungsjahr
72765 Treffer
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Publikationen
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< 2021
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Johannes Gutenberg-Universität Mainz
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Universität Koblenz
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Hochschule Mainz
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Hochschule für Wirtschaft und Gesellschaft Ludwigshafen
- Imrie, Jackie; Mengel, Karl Eugen; Cassiman, David et al.
- Cause of death in patients with attenuated acid sphingomyelinase deficiency: Comprehensive literature review and report of new cases
- MOLECULAR GENETICS AND METABOLISM. Bd. 117. H. 2. 2016 S. S60-S60
- van Capelle, C. I.; van der Meijden, J. C.; van den Hout, J. M. P. et al.
- Childhood Pompe disease: clinical spectrum and genotype in 31 patients
- ORPHANET JOURNAL OF RARE DISEASES. Bd. 11. 2016
- Fischer, J*; Paret, C*; El Malki, K et al.
- CD19 isoforms lacking the CART-19 epitope are expressed before any therapy
- Journal of Immunotherapy. 2016 S. ff
- Knoll, RL; Forslund, K; Kultima, JR et al.
- Gut microbiota differs between children with Inflammatory Bowel Disease and healthy siblings in taxonomic and functional composition – a metagenomic analysis
- Am J Physiol Gastrointest Liver Physiol. 2016 S. ff
- Kampmann, Christoph; Abu-Tair, Tariq; Goekce, Seyfullah et al.
- Heart and Cardiovascular Involvement in Patients with Mucopolysaccharidosis Type IVA (Morquio-A Syndrome)
- PLOS ONE. Bd. 11. H. 9. 2016
- Bettendorf, M.; Binder, G.; Hauffa, B. P. et al.
- Growth in thyroid disorders in childhood and adolescence. Thyroid dysfunction and growth
- MONATSSCHRIFT KINDERHEILKUNDE. Bd. 164. H. 8. 2016 S. 689-696
- Wirth, S.; Zepp, F.
- Hepatic Diseases during Infancy, Childhood and Adolescence
- MONATSSCHRIFT KINDERHEILKUNDE. Bd. 164. H. 6. 2016 S. 434-435
- Pena, Loren; Baron, Richard; Byrne, Barry et al.
- Phase 1 exploratory efficacy of the novel enzyme replacement therapy neoGAA in treatment-naive and alglucosidase alfa-treated late-onset Pompe disease patients
- MOLECULAR GENETICS AND METABOLISM. Bd. 117. H. 2. 2016 S. S92-S92
- Ladha, Shafeeq; Laforet, Pascal; Mengel, Eugen et al.
- Phase 1 safety and pharmacokinetics of the novel enzyme replacement therapy neoGAA in treatment-naive and alglucosidase alfa-treated late-onset Pompe disease patients
- MOLECULAR GENETICS AND METABOLISM. Bd. 117. H. 2. 2016 S. S117-S118
- Eggermann, Thomas; Brioude, Frederic; Russo, Silvia et al.
- Prenatal molecular testing for Beckwith-Wiedemann and Silver-Russell syndromes: a challenge for molecular analysis and genetic counseling
- EUROPEAN JOURNAL OF HUMAN GENETICS. Bd. 24. H. 6. 2016 S. 784-793