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M Andersen

Showing results (531-540 of 1,540) with videos related to

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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|January 4, 2013
Progressive aphasia as the presenting symptom in a patient with amyotrophic lateral sclerosis with a novel mutation in the OPTN geneDavid Czell, Peter M Andersen, Christoph Neuwirth, et al.
Annals of Internal Medicine|June 1, 1989
National Study of Internal Medicine Manpower: XV. A decade of change in residency training in internal medicineR M Andersen, C Lyttle, C Kohrman, et al.
Behaviour Research and Therapy|December 6, 2016
Induced optimism as mental rehearsal to decrease depressive predictive certaintyRegina Miranda, Mariann Weierich, Valerie Khait, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|February 18, 2024
Functional characterization of <i>SORL1</i> variants in cell-based assays to investigate variant pathogenicityElnaz Fazeli, Elham Fazeli, Petr Fojtík, et al.
Human Molecular Genetics|June 2, 2009
Variation in aggregation propensities among ALS-associated variants of SOD1: correlation to human diseaseMercedes Prudencio, P John Hart, David R Borchelt, et al.
Physical Review Letters|May 7, 2016
Magnetic Fluctuations in Pair-Density-Wave SuperconductorsMorten H Christensen, Henrik Jacobsen, Thomas A Maier, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 10, 2016
Comment on "Cutting Edge: Inhibiting TBK1 by Compound II Ameliorates Autoimmune Disease in Mice"David Brenner, Peter M Andersen, Albert C Ludolph, et al.
Phytochemistry|October 16, 2003
Anthocyanins acylated with gallic acid from chenille plant, Acalypha hispidaBergitte Reiersen, Bernard T Kiremire, Robert Byamukama, et al.
Social Science & Medicine (1982)|April 1, 1992
Child developmental delay and socio-economic disadvantage in Australia: a longitudinal studyJ M Najman, W Bor, J Morrison, et al.
Journal of the Neurological Sciences|December 14, 1999
Motor system abnormalities in heterozygous relatives of a D90A homozygous CuZn-SOD ALS patient of finnish extractionM Mezei, P M Andersen, H Stewart, et al.
Pageof 154

Showing results (531-540 of 1,540) with videos related to

Sort By:
Pageof 154
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|January 4, 2013
Progressive aphasia as the presenting symptom in a patient with amyotrophic lateral sclerosis with a novel mutation in the OPTN geneDavid Czell, Peter M Andersen, Christoph Neuwirth, et al.
Annals of Internal Medicine|June 1, 1989
National Study of Internal Medicine Manpower: XV. A decade of change in residency training in internal medicineR M Andersen, C Lyttle, C Kohrman, et al.
Behaviour Research and Therapy|December 6, 2016
Induced optimism as mental rehearsal to decrease depressive predictive certaintyRegina Miranda, Mariann Weierich, Valerie Khait, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|February 18, 2024
Functional characterization of <i>SORL1</i> variants in cell-based assays to investigate variant pathogenicityElnaz Fazeli, Elham Fazeli, Petr Fojtík, et al.
Human Molecular Genetics|June 2, 2009
Variation in aggregation propensities among ALS-associated variants of SOD1: correlation to human diseaseMercedes Prudencio, P John Hart, David R Borchelt, et al.
Physical Review Letters|May 7, 2016
Magnetic Fluctuations in Pair-Density-Wave SuperconductorsMorten H Christensen, Henrik Jacobsen, Thomas A Maier, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 10, 2016
Comment on "Cutting Edge: Inhibiting TBK1 by Compound II Ameliorates Autoimmune Disease in Mice"David Brenner, Peter M Andersen, Albert C Ludolph, et al.
Phytochemistry|October 16, 2003
Anthocyanins acylated with gallic acid from chenille plant, Acalypha hispidaBergitte Reiersen, Bernard T Kiremire, Robert Byamukama, et al.
Social Science & Medicine (1982)|April 1, 1992
Child developmental delay and socio-economic disadvantage in Australia: a longitudinal studyJ M Najman, W Bor, J Morrison, et al.
Journal of the Neurological Sciences|December 14, 1999
Motor system abnormalities in heterozygous relatives of a D90A homozygous CuZn-SOD ALS patient of finnish extractionM Mezei, P M Andersen, H Stewart, et al.
Pageof 154