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H Kalimo

Showing results (231-240 of 241) with videos related to

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Neurology|August 28, 2002
Narrowing in on the causative defect of an intriguing X-linked myopathy with excessive autophagyB A Minassian, R Aiyar, S Alic, et al.
Muscle & Nerve|March 1, 2005
Enrichment of the R77C alpha-sarcoglycan gene mutation in Finnish LGMD2D patientsP Hackman, V Juvonen, J Sarparanta, et al.
Forensic Science International|December 17, 1998
Alzheimer changes are common in aged drivers killed in single car crashes and at intersectionsM Viitanen, K Johansson, N Bogdanovic, et al.
Current Alzheimer Research|October 26, 2013
Relationships between white matter hyperintensities, cerebral amyloid angiopathy and dementia in a population-based sample of the oldest oldM Tanskanen, R N Kalaria, I-L Notkola, et al.
Nature Medicine|September 30, 1999
Alzheimer disease PS-1 exon 9 deletion definedG Prihar, A Verkkoniem, J Perez-Tur, et al.
Neuromuscular Disorders : NMD|March 17, 2004
New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)R Sallinen, A Vihola, L L Bachinski, et al.
Archives of Pathology|June 1, 1974
Cellular and subcellular alterations of human CNS: studies utilizing in situ perfusion fixation at immediate autopsyH Kalimo, J H Garcia, Y Kamijyo, et al.
Duodecim; Laaketieteellinen Aikakauskirja|November 23, 2001
[CADASIL disease: a hereditary arterial disease leading to brain infarctions and dementia]H Kalimo, T Aho, K Amberla, et al.
Brain : a Journal of Neurology|January 20, 2007
Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASILW C Low, M Junna, A Börjesson-Hanson, et al.
Nature Medicine|April 18, 1998
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1R Crook, A Verkkoniemi, J Perez-Tur, et al.
Pageof 25

Showing results (231-240 of 241) with videos related to

Sort By:
Pageof 25
Neurology|August 28, 2002
Narrowing in on the causative defect of an intriguing X-linked myopathy with excessive autophagyB A Minassian, R Aiyar, S Alic, et al.
Muscle & Nerve|March 1, 2005
Enrichment of the R77C alpha-sarcoglycan gene mutation in Finnish LGMD2D patientsP Hackman, V Juvonen, J Sarparanta, et al.
Forensic Science International|December 17, 1998
Alzheimer changes are common in aged drivers killed in single car crashes and at intersectionsM Viitanen, K Johansson, N Bogdanovic, et al.
Current Alzheimer Research|October 26, 2013
Relationships between white matter hyperintensities, cerebral amyloid angiopathy and dementia in a population-based sample of the oldest oldM Tanskanen, R N Kalaria, I-L Notkola, et al.
Nature Medicine|September 30, 1999
Alzheimer disease PS-1 exon 9 deletion definedG Prihar, A Verkkoniem, J Perez-Tur, et al.
Neuromuscular Disorders : NMD|March 17, 2004
New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)R Sallinen, A Vihola, L L Bachinski, et al.
Archives of Pathology|June 1, 1974
Cellular and subcellular alterations of human CNS: studies utilizing in situ perfusion fixation at immediate autopsyH Kalimo, J H Garcia, Y Kamijyo, et al.
Duodecim; Laaketieteellinen Aikakauskirja|November 23, 2001
[CADASIL disease: a hereditary arterial disease leading to brain infarctions and dementia]H Kalimo, T Aho, K Amberla, et al.
Brain : a Journal of Neurology|January 20, 2007
Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASILW C Low, M Junna, A Börjesson-Hanson, et al.
Nature Medicine|April 18, 1998
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1R Crook, A Verkkoniemi, J Perez-Tur, et al.
Pageof 25