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H Kalimo

Showing results (221-230 of 241) with videos related to

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Journal of Cell Science|August 27, 1999
Mechanical loading regulates tenascin-C expression in the osteotendinous junctionT A Järvinen, L Jozsa, P Kannus, et al.
Neuropathology and Applied Neurobiology|April 24, 1999
Clinicopathological correlation of cell proliferation, apoptosis and p53 in cerebellar pilocytic astrocytomasH Haapasalo, S Sallinen, P Sallinen, et al.
Neuropathology and Applied Neurobiology|December 21, 2000
High topoisomerase IIalpha expression associates with high proliferation rate and and poor prognosis in oligodendrogliomasH E Miettinen, T A Järvinen, U Kellner, et al.
Neuropathology and Applied Neurobiology|September 4, 1999
CADASIL: hereditary disease of arteries causing brain infarcts and dementiaH Kalimo, M Viitanen, K Amberla, et al.
American Journal of Human Genetics|April 1, 1989
Gene deletions in X-linked muscular dystrophyM Lindlöf, A Kiuru, H Kääriäinen, et al.
Neuropathology and Applied Neurobiology|August 10, 2000
Grading of diffusely infiltrating astrocytomas by quantitative histopathology, cell proliferation and image cytometric DNA analysis. Comparison of 133 tumours in the context of the WHO 1979 and WHO 1993 grading schemesP K Sallinen, S L Sallinen, P T Helén, et al.
Neuropathology and Applied Neurobiology|August 8, 2001
Cases of Alzheimer's disease due to deletion of exon 9 of the presenilin-1 gene show an unusual but characteristic beta-amyloid pathology known as 'cotton wool' plaquesD M Mann, A Takeuchi, S Sato, et al.
Neuromuscular Disorders : NMD|March 11, 2000
Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain diseaseM Auranen, J Rapola, H Pihko, et al.
Brain : a Journal of Neurology|June 28, 2008
PET amyloid ligand [11C]PIB uptake shows predominantly striatal increase in variant Alzheimer's diseaseJ Koivunen, A Verkkoniemi, S Aalto, et al.
Stroke|August 4, 2001
Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutationS Tuominen, V Juvonen, K Amberla, et al.
Pageof 25

Showing results (221-230 of 241) with videos related to

Sort By:
Pageof 25
Journal of Cell Science|August 27, 1999
Mechanical loading regulates tenascin-C expression in the osteotendinous junctionT A Järvinen, L Jozsa, P Kannus, et al.
Neuropathology and Applied Neurobiology|April 24, 1999
Clinicopathological correlation of cell proliferation, apoptosis and p53 in cerebellar pilocytic astrocytomasH Haapasalo, S Sallinen, P Sallinen, et al.
Neuropathology and Applied Neurobiology|December 21, 2000
High topoisomerase IIalpha expression associates with high proliferation rate and and poor prognosis in oligodendrogliomasH E Miettinen, T A Järvinen, U Kellner, et al.
Neuropathology and Applied Neurobiology|September 4, 1999
CADASIL: hereditary disease of arteries causing brain infarcts and dementiaH Kalimo, M Viitanen, K Amberla, et al.
American Journal of Human Genetics|April 1, 1989
Gene deletions in X-linked muscular dystrophyM Lindlöf, A Kiuru, H Kääriäinen, et al.
Neuropathology and Applied Neurobiology|August 10, 2000
Grading of diffusely infiltrating astrocytomas by quantitative histopathology, cell proliferation and image cytometric DNA analysis. Comparison of 133 tumours in the context of the WHO 1979 and WHO 1993 grading schemesP K Sallinen, S L Sallinen, P T Helén, et al.
Neuropathology and Applied Neurobiology|August 8, 2001
Cases of Alzheimer's disease due to deletion of exon 9 of the presenilin-1 gene show an unusual but characteristic beta-amyloid pathology known as 'cotton wool' plaquesD M Mann, A Takeuchi, S Sato, et al.
Neuromuscular Disorders : NMD|March 11, 2000
Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain diseaseM Auranen, J Rapola, H Pihko, et al.
Brain : a Journal of Neurology|June 28, 2008
PET amyloid ligand [11C]PIB uptake shows predominantly striatal increase in variant Alzheimer's diseaseJ Koivunen, A Verkkoniemi, S Aalto, et al.
Stroke|August 4, 2001
Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutationS Tuominen, V Juvonen, K Amberla, et al.
Pageof 25