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Brain : a Journal of Neurology|August 16, 2021
Neurofilament light chain and glial fibrillary acidic protein levels in metachromatic leukodystrophyShanice Beerepoot, Hans Heijst, Birthe Roos, et al.
Journal of Huntington'S Disease|September 4, 2015
FDG μPET Fails to Detect a Disease-Specific Phenotype in Rats Transgenic for Huntington's Disease – A 15 Months Follow-up StudyRalf Reilmann, Veronika Lippross, Eva Hölzner, et al.
Molecular Therapy. Methods & Clinical Development|May 29, 2020
Lentiviral Hematopoietic Stem Cell Gene Therapy Corrects Murine Pompe DiseaseMerel Stok, Helen de Boer, Marshall W Huston, et al.
BMC Geriatrics|April 16, 2024
Which Comprehensive Geriatric Assessment (CGA) instruments are currently used in Germany: a surveyJennifer Kudelka, Malte Ollenschläger, Richard Dodel, et al.
Orphanet Journal of Rare Diseases|May 15, 2021
Presymptomatic treatment of classic late-infantile neuronal ceroid lipofuscinosis with cerliponase alfaJ Schaefers, L J van der Giessen, C Klees, et al.
Blood|February 8, 2011
Murine prolylcarboxypeptidase depletion induces vascular dysfunction with hypertension and faster arterial thrombosisGregory N Adams, Gretchen A LaRusch, Evi Stavrou, et al.
Technology in Cancer Research & Treatment|March 8, 2003
Molecular and functional imaging technology for the development of efficient treatment strategies for gliomasA H Jacobs, A Winkler, C Dittmar, et al.
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