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S-M Pulst

Showing results (51-60 of 106) with videos related to

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Fortschritte Der Neurologie-Psychiatrie|July 24, 1998
[Neurofibromatosis versus schwannomatosis]V F Mautner, S Schröder, S M Pulst, et al.
Human Molecular Genetics|December 1, 1993
CA-repeat polymorphism at the D22S430 locus adjacent to NF2J Sainz, A Nechiporuk, U J Kim, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 27, 2001
Identification and expression of a mouse ortholog of A2BP1T R Kiehl, H Shibata, T Vo, et al.
Brain Research. Developmental Brain Research|October 25, 2001
Differential expression and tissue distribution of parkin isoforms during mouse developmentD P Huynh, M Dy, D Nguyen, et al.
Neurology|October 1, 1993
Familial meningioma is not allelic to neurofibromatosis 2S M Pulst, G A Rouleau, C Marineau, et al.
Journal of Neuropathology and Experimental Neurology|April 1, 1997
Immunohistochemical detection of schwannomin and neurofibromin in vestibular schwannomas, ependymomas and meningiomasD P Huynh, V Mautner, M E Baser, et al.
Muscle & Nerve|May 16, 2001
Rippling muscle disease: evidence for phenotypic and genetic heterogeneityY T So, L Zu, C Barraza, et al.
Human Molecular Genetics|January 1, 1995
High frequency of nonsense mutations in the NF2 gene caused by C to T transitions in five CGA codonsJ Sainz, K Figueroa, M E Baser, et al.
Annals of Neurology|February 16, 1999
Expression of ataxin-2 in brains from normal individuals and patients with Alzheimer's disease and spinocerebellar ataxia 2D P Huynh, M R Del Bigio, D H Ho, et al.
American Journal of Human Genetics|April 1, 1997
The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxiaD H Geschwind, S Perlman, C P Figueroa, et al.
Pageof 11

Showing results (51-60 of 106) with videos related to

Sort By:
Pageof 11
Fortschritte Der Neurologie-Psychiatrie|July 24, 1998
[Neurofibromatosis versus schwannomatosis]V F Mautner, S Schröder, S M Pulst, et al.
Human Molecular Genetics|December 1, 1993
CA-repeat polymorphism at the D22S430 locus adjacent to NF2J Sainz, A Nechiporuk, U J Kim, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 27, 2001
Identification and expression of a mouse ortholog of A2BP1T R Kiehl, H Shibata, T Vo, et al.
Brain Research. Developmental Brain Research|October 25, 2001
Differential expression and tissue distribution of parkin isoforms during mouse developmentD P Huynh, M Dy, D Nguyen, et al.
Neurology|October 1, 1993
Familial meningioma is not allelic to neurofibromatosis 2S M Pulst, G A Rouleau, C Marineau, et al.
Journal of Neuropathology and Experimental Neurology|April 1, 1997
Immunohistochemical detection of schwannomin and neurofibromin in vestibular schwannomas, ependymomas and meningiomasD P Huynh, V Mautner, M E Baser, et al.
Muscle & Nerve|May 16, 2001
Rippling muscle disease: evidence for phenotypic and genetic heterogeneityY T So, L Zu, C Barraza, et al.
Human Molecular Genetics|January 1, 1995
High frequency of nonsense mutations in the NF2 gene caused by C to T transitions in five CGA codonsJ Sainz, K Figueroa, M E Baser, et al.
Annals of Neurology|February 16, 1999
Expression of ataxin-2 in brains from normal individuals and patients with Alzheimer's disease and spinocerebellar ataxia 2D P Huynh, M R Del Bigio, D H Ho, et al.
American Journal of Human Genetics|April 1, 1997
The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxiaD H Geschwind, S Perlman, C P Figueroa, et al.
Pageof 11