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Hannu Kalimo

Showing results (41-50 of 83) with videos related to

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Brain : a Journal of Neurology|May 26, 2007
Distal myopathy caused by homozygous missense mutations in the nebulin geneCarina Wallgren-Pettersson, Vilma-Lotta Lehtokari, Hannu Kalimo, et al.
Ophthalmology|August 1, 2006
Ophthalmologic findings in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a cross-sectional studySusanna Roine, Mika Harju, Tero T Kivelä, et al.
BMC Cancer|February 19, 2009
Absence of polysialylated NCAM is an unfavorable prognostic phenotype for advanced stage neuroblastomaMiikka Korja, Anne Jokilammi, Toivo T Salmi, et al.
Neuromuscular Disorders : NMD|April 8, 2015
No cardiomyopathy in X-linked myopathy with excessive autophagyAntti Saraste, Juha W Koskenvuo, Juhani Airaksinen, et al.
Journal of Neuro-Oncology|August 7, 2008
Decreased expression of antioxidant enzymes is associated with aggressive features in ependymomasSally Järvelä, Kristiina Nordfors, Miia Jansson, et al.
Neuromuscular Disorders : NMD|March 8, 2011
Four new Finnish families with LGMD1D; refinement of the clinical phenotype and the linked 7q36 locusPeter Hackman, Satu Sandell, Jaakko Sarparanta, et al.
Annals of Neurology|July 12, 2002
Electrophysiological findings in X-linked myopathy with excessive autophagySatu K Jääskeläinen, Vern C Juel, Bjarne Udd, et al.
Journal of Alzheimer'S Disease : JAD|July 24, 2009
Neuropathologic findings of dementia with lewy bodies (DLB) in a population-based Vantaa 85+ studyMinna Oinas, Tuomo Polvikoski, Raimo Sulkava, et al.
Stroke|March 16, 2004
Positron emission tomography examination of cerebral blood flow and glucose metabolism in young CADASIL patientsSusanna Tuominen, Qing Miao, Timo Kurki, et al.
Molecular Medicine (Cambridge, Mass.)|July 12, 2007
Proteome analysis of cultivated vascular smooth muscle cells from a CADASIL patientSaara Ihalainen, Rabah Soliymani, Erika Iivanainen, et al.
Pageof 9

Showing results (41-50 of 83) with videos related to

Sort By:
Pageof 9
Brain : a Journal of Neurology|May 26, 2007
Distal myopathy caused by homozygous missense mutations in the nebulin geneCarina Wallgren-Pettersson, Vilma-Lotta Lehtokari, Hannu Kalimo, et al.
Ophthalmology|August 1, 2006
Ophthalmologic findings in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a cross-sectional studySusanna Roine, Mika Harju, Tero T Kivelä, et al.
BMC Cancer|February 19, 2009
Absence of polysialylated NCAM is an unfavorable prognostic phenotype for advanced stage neuroblastomaMiikka Korja, Anne Jokilammi, Toivo T Salmi, et al.
Neuromuscular Disorders : NMD|April 8, 2015
No cardiomyopathy in X-linked myopathy with excessive autophagyAntti Saraste, Juha W Koskenvuo, Juhani Airaksinen, et al.
Journal of Neuro-Oncology|August 7, 2008
Decreased expression of antioxidant enzymes is associated with aggressive features in ependymomasSally Järvelä, Kristiina Nordfors, Miia Jansson, et al.
Neuromuscular Disorders : NMD|March 8, 2011
Four new Finnish families with LGMD1D; refinement of the clinical phenotype and the linked 7q36 locusPeter Hackman, Satu Sandell, Jaakko Sarparanta, et al.
Annals of Neurology|July 12, 2002
Electrophysiological findings in X-linked myopathy with excessive autophagySatu K Jääskeläinen, Vern C Juel, Bjarne Udd, et al.
Journal of Alzheimer'S Disease : JAD|July 24, 2009
Neuropathologic findings of dementia with lewy bodies (DLB) in a population-based Vantaa 85+ studyMinna Oinas, Tuomo Polvikoski, Raimo Sulkava, et al.
Stroke|March 16, 2004
Positron emission tomography examination of cerebral blood flow and glucose metabolism in young CADASIL patientsSusanna Tuominen, Qing Miao, Timo Kurki, et al.
Molecular Medicine (Cambridge, Mass.)|July 12, 2007
Proteome analysis of cultivated vascular smooth muscle cells from a CADASIL patientSaara Ihalainen, Rabah Soliymani, Erika Iivanainen, et al.
Pageof 9