Search Results - Gallenmüller, Constanze

Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients by Schüle-Freyer, Rebecca (Author) , Wiethoff, Sarah (Author) , Martus, Peter (Author) , Karle, Kathrin Nora (Author) , Otto, Susanne (Author) , Klebe, Stephan (Author) , Klimpe, Sven (Author) , Gallenmüller, Constanze (Author) , Kurzwelly, Delia (Author) , Henkel, Dorothea (Author) , Rimmele, Florian D. (Author) , Stolze, Henning Wolfgang (Author) , Kohl, Zacharias (Author) , Kassubek, Jan Rainer (Author) , Klockgether, Thomas (Author) , Vielhaber, Stefan (Author) , Kamm, Christoph (Author) , Klopstock, Thomas (Author) , Bauer, Peter (Author) , Züchner, Stephan (Author) , Liepelt-Scarfone, Inga (Author) , Schöls, Ludger (Author) ,

Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients by Schüle-Freyer, Rebecca (Author) , Wiethoff, Sarah (Author) , Martus, Peter (Author) , Karle, Kathrin Nora (Author) , Otto, Susanne (Author) , Klebe, Stephan (Author) , Klimpe, Sven (Author) , Gallenmüller, Constanze (Author) , Kurzwelly, Delia (Author) , Henkel, Dorothea (Author) , Rimmele, Florian D. (Author) , Stolze, Henning Wolfgang (Author) , Kohl, Zacharias (Author) , Kassubek, Jan Rainer (Author) , Klockgether, Thomas (Author) , Vielhaber, Stefan (Author) , Kamm, Christoph (Author) , Klopstock, Thomas (Author) , Bauer, Peter (Author) , Züchner, Stephan (Author) , Liepelt-Scarfone, Inga (Author) , Schöls, Ludger (Author) ,

• Resolving-System, Volltext

Paranoid delusion as lead symptom in two siblings with late-onset Tay-Sachs disease and a novel mutation in the HEXA gene by Stendel, Claudia (Author) , Gallenmüller, Constanze (Author) , Peters, Katrin (Author) , Bürger, Friederike (Author) , Gramer, Gwendolyn (Author) , Biskup, Saskia (Author) , Klopstock, Thomas (Author) ,

• Verlag, lizenzpflichtig, Volltext