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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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A D Sperfeld

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Neurology|October 13, 2006

High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegiaC Beetz, A O H Nygren, J Schickel, et al.

Journal of Neural Transmission (Vienna, Austria : 1996)|February 24, 2007

Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutationY Baba, M C Baker, I Le Ber, et al.

European Journal of Human Genetics : EJHG|July 4, 2001

Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the worldA Lund, B Udd, V Juvonen, et al.

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Search research articles

Showing results (21-30 of 23) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 23 results.

Neurology|October 13, 2006

High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegiaC Beetz, A O H Nygren, J Schickel, et al.

Journal of Neural Transmission (Vienna, Austria : 1996)|February 24, 2007

Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutationY Baba, M C Baker, I Le Ber, et al.

European Journal of Human Genetics : EJHG|July 4, 2001

Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the worldA Lund, B Udd, V Juvonen, et al.

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