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Maija Siitonen

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Journal of Alzheimer'S Disease : JAD|October 22, 2016
A Novel Loss-of-Function GRN Mutation p.(Tyr229*): Clinical and Neuropathological FeaturesLiina Kuuluvainen, Minna Pöyhönen, Petra Pasanen, et al.
Neurobiology of Aging|April 22, 2014
Novel α-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinson's disease-type pathologyPetra Pasanen, Liisa Myllykangas, Maija Siitonen, et al.
Brain Pathology (Zurich, Switzerland)|October 18, 2014
CADASIL and CARASILSaara Tikka, Marc Baumann, Maija Siitonen, et al.
European Journal of Human Genetics : EJHG|February 25, 2018
Genetics of dementia in a Finnish cohortPetra Pasanen, Liisa Myllykangas, Minna Pöyhönen, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|September 6, 2012
CADASIL mutations and shRNA silencing of NOTCH3 affect actin organization in cultured vascular smooth muscle cellsSaara Tikka, Yan Peng Ng, Giuseppe Di Maio, et al.
Brain : a Journal of Neurology|April 4, 2017
Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1Maija Siitonen, Anne Börjesson-Hanson, Minna Pöyhönen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2025
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
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Showing results (1-10 of 7) with videos related to

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Pageof 1
Journal of Alzheimer'S Disease : JAD|October 22, 2016
A Novel Loss-of-Function GRN Mutation p.(Tyr229*): Clinical and Neuropathological FeaturesLiina Kuuluvainen, Minna Pöyhönen, Petra Pasanen, et al.
Neurobiology of Aging|April 22, 2014
Novel α-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinson's disease-type pathologyPetra Pasanen, Liisa Myllykangas, Maija Siitonen, et al.
Brain Pathology (Zurich, Switzerland)|October 18, 2014
CADASIL and CARASILSaara Tikka, Marc Baumann, Maija Siitonen, et al.
European Journal of Human Genetics : EJHG|February 25, 2018
Genetics of dementia in a Finnish cohortPetra Pasanen, Liisa Myllykangas, Minna Pöyhönen, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|September 6, 2012
CADASIL mutations and shRNA silencing of NOTCH3 affect actin organization in cultured vascular smooth muscle cellsSaara Tikka, Yan Peng Ng, Giuseppe Di Maio, et al.
Brain : a Journal of Neurology|April 4, 2017
Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1Maija Siitonen, Anne Börjesson-Hanson, Minna Pöyhönen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2025
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
Pageof 1