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Zugriff
Einrichtung
Medientyp
- Text 5
Karte
Erscheinungsjahr
Autor/in
- Fazeli, Walid
- Isbrandt, Dirk 2
- Altmüller, Janine 1
- Baqi, Younis 1
- Bassot, Emilie 1
- alle zeigen
Sprache
- Englisch 5
5 Einträge gefunden
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A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunction
- Fazeli, Walid
- Herkenrath, Peter
- Stiller, Barbara
- Neugebauer, Antje
- Fricke, Julia
- Lang-Roth, Ruth
- Nürnberg, Gudrun
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Activity of NaV1.2 promotes neurodegeneration in an animal model of multiple sclerosis
- Schattling, Benjamin
- Fazeli, Walid
- Engeland, Birgit
- Liu, Yuanyuan
- Lerche, Holger
- Isbrandt, Dirk
- Friese, Manuel
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A novel mutation within the lactase gene (LCT): the first report of congenital lactase deficiency diagnosed in Central Europe
2015 - Forschungsinformationssystem des UKE - frei zugänglich -
Adenosine receptor antagonists including caffeine alter fetal brain development in mice
- Silva, Carla G
- Métin, Christine
- Fazeli, Walid
- Machado, Nuno J
- Darmopil, Sanja
- Launay, Pierre-Serge
- Ghestem, Antoine