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Hannu Kalimo

Showing results (31-40 of 83) with videos related to

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Neuromuscular Disorders : NMD|November 26, 2009
Adult course in dynamin 2 dominant centronuclear myopathy with neonatal onsetAtle Melberg, Christine Kretz, Hannu Kalimo, et al.
Acta Neuropathologica|October 13, 2006
Genetically distinct astrocytic and oligodendroglial components in oligoastrocytomasMingqi Qu, Tommie Olofsson, Sunna Sigurdardottir, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 4, 2008
Duchenne muscular dystrophy and idiopathic hyperCKemia in the same familyOrvar Eeg-Olofsson, Hannu Kalimo, Karin Edebol Eeg-Olofsson, et al.
Molecular and Cellular Biology|July 2, 2003
Cdk5 regulates the organization of Nestin and its association with p35Cecilia M Sahlgren, Andrey Mikhailov, Samuli Vaittinen, et al.
Neuro-Oncology|November 16, 2007
Gene expression analyses of grade II gliomas and identification of rPTPbeta/zeta as a candidate oligodendroglioma markerDaniel Hägerstrand, Anja Smits, Anna Eriksson, et al.
Best Practice & Research. Clinical Rheumatology|May 22, 2007
Muscle injuries: optimising recoveryTero A H Järvinen, Teppo L N Järvinen, Minna Kääriäinen, et al.
Journal of the Neurological Sciences|February 5, 2004
Neuropsychological functions in variant Alzheimer's disease with spastic paraparesisAuli Verkkoniemi, Raija Ylikoski, Juha O Rinne, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|May 21, 2016
Gelsolin amyloid angiopathy causes severe disruption of the arterial wallSusanna Koskelainen, Tiia Pihlamaa, Sinikka Suominen, et al.
Circulation Research|May 17, 2008
Notch signaling regulates platelet-derived growth factor receptor-beta expression in vascular smooth muscle cellsShaobo Jin, Emil M Hansson, Saara Tikka, et al.
Neurogenetics|June 30, 2006
Mitochondrial DNA sequence variation and mutation rate in patients with CADASILJohanna Annunen-Rasila, Saara Finnilä, Kati Mykkänen, et al.
Pageof 9

Showing results (31-40 of 83) with videos related to

Sort By:
Pageof 9
Neuromuscular Disorders : NMD|November 26, 2009
Adult course in dynamin 2 dominant centronuclear myopathy with neonatal onsetAtle Melberg, Christine Kretz, Hannu Kalimo, et al.
Acta Neuropathologica|October 13, 2006
Genetically distinct astrocytic and oligodendroglial components in oligoastrocytomasMingqi Qu, Tommie Olofsson, Sunna Sigurdardottir, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 4, 2008
Duchenne muscular dystrophy and idiopathic hyperCKemia in the same familyOrvar Eeg-Olofsson, Hannu Kalimo, Karin Edebol Eeg-Olofsson, et al.
Molecular and Cellular Biology|July 2, 2003
Cdk5 regulates the organization of Nestin and its association with p35Cecilia M Sahlgren, Andrey Mikhailov, Samuli Vaittinen, et al.
Neuro-Oncology|November 16, 2007
Gene expression analyses of grade II gliomas and identification of rPTPbeta/zeta as a candidate oligodendroglioma markerDaniel Hägerstrand, Anja Smits, Anna Eriksson, et al.
Best Practice & Research. Clinical Rheumatology|May 22, 2007
Muscle injuries: optimising recoveryTero A H Järvinen, Teppo L N Järvinen, Minna Kääriäinen, et al.
Journal of the Neurological Sciences|February 5, 2004
Neuropsychological functions in variant Alzheimer's disease with spastic paraparesisAuli Verkkoniemi, Raija Ylikoski, Juha O Rinne, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|May 21, 2016
Gelsolin amyloid angiopathy causes severe disruption of the arterial wallSusanna Koskelainen, Tiia Pihlamaa, Sinikka Suominen, et al.
Circulation Research|May 17, 2008
Notch signaling regulates platelet-derived growth factor receptor-beta expression in vascular smooth muscle cellsShaobo Jin, Emil M Hansson, Saara Tikka, et al.
Neurogenetics|June 30, 2006
Mitochondrial DNA sequence variation and mutation rate in patients with CADASILJohanna Annunen-Rasila, Saara Finnilä, Kati Mykkänen, et al.
Pageof 9