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Showing results (341-350 of 712) with videos related to

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Biomicrofluidics|November 8, 2014
Modulating patterns of two-phase flow with electric fieldsDingsheng Liu, Bejan Hakimi, Michael Volny, et al.
Plos One|February 12, 2011
CAG repeats determine brain atrophy in spinocerebellar ataxia 17: a VBM studyKathrin Reetz, Alexandra Kleiman, Christine Klein, et al.
BMC Cardiovascular Disorders|February 2, 2011
Persistent increase in cardiac troponin I in Fabry disease: a case reportChristian Tanislav, Andreas Feustel, Wolfgang Franzen, et al.
Clinical Genetics|February 17, 2016
A homozygous nonsense variant in IFT52 is associated with a human skeletal ciliopathyK M Girisha, A Shukla, D Trujillano, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 22, 2008
The microstructure of cornea verticillata in Fabry disease and amiodarone-induced keratopathy: a confocal laser-scanning microscopy studyKaren Falke, Armin Büttner, Michael Schittkowski, et al.
Neurology. Genetics|September 27, 2016
Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disabilitySofia Steinrücke, Katja Lohmann, Aloysius Domingo, et al.
Immunopharmacology|May 24, 2000
K(+) channel-blocking alkoxypsoralens inhibit the immune response of encephalitogenic T line cells and lymphocytes from Lewis rats challenged for experimental autoimmune encephalomyelitisU Strauss, K Wissel, S Jung, et al.
International Journal of Molecular Sciences|April 17, 2025
Sidransky Syndrome-<i>GBA1</i>-Related Parkinson's Disease and Its Targeted TherapiesMajdolen Istaiti, Gilad Yahalom, Mikhal Cohen, et al.
International Journal of Molecular Sciences|January 8, 2023
Organ Weights in <i>NPC1</i> Mutant Mice Partly Normalized by Various Pharmacological Treatment ApproachesVeronica Antipova, Lisa-Marie Steinhoff, Carsten Holzmann, et al.
Plos One|March 15, 2014
Continuous cardiac troponin I release in Fabry diseaseAndreas Feustel, Andreas Hahn, Christian Schneider, et al.
Pageof 72

Showing results (341-350 of 712) with videos related to

Sort By:
Pageof 72
Biomicrofluidics|November 8, 2014
Modulating patterns of two-phase flow with electric fieldsDingsheng Liu, Bejan Hakimi, Michael Volny, et al.
Plos One|February 12, 2011
CAG repeats determine brain atrophy in spinocerebellar ataxia 17: a VBM studyKathrin Reetz, Alexandra Kleiman, Christine Klein, et al.
BMC Cardiovascular Disorders|February 2, 2011
Persistent increase in cardiac troponin I in Fabry disease: a case reportChristian Tanislav, Andreas Feustel, Wolfgang Franzen, et al.
Clinical Genetics|February 17, 2016
A homozygous nonsense variant in IFT52 is associated with a human skeletal ciliopathyK M Girisha, A Shukla, D Trujillano, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 22, 2008
The microstructure of cornea verticillata in Fabry disease and amiodarone-induced keratopathy: a confocal laser-scanning microscopy studyKaren Falke, Armin Büttner, Michael Schittkowski, et al.
Neurology. Genetics|September 27, 2016
Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disabilitySofia Steinrücke, Katja Lohmann, Aloysius Domingo, et al.
Immunopharmacology|May 24, 2000
K(+) channel-blocking alkoxypsoralens inhibit the immune response of encephalitogenic T line cells and lymphocytes from Lewis rats challenged for experimental autoimmune encephalomyelitisU Strauss, K Wissel, S Jung, et al.
International Journal of Molecular Sciences|April 17, 2025
Sidransky Syndrome-<i>GBA1</i>-Related Parkinson's Disease and Its Targeted TherapiesMajdolen Istaiti, Gilad Yahalom, Mikhal Cohen, et al.
International Journal of Molecular Sciences|January 8, 2023
Organ Weights in <i>NPC1</i> Mutant Mice Partly Normalized by Various Pharmacological Treatment ApproachesVeronica Antipova, Lisa-Marie Steinhoff, Carsten Holzmann, et al.
Plos One|March 15, 2014
Continuous cardiac troponin I release in Fabry diseaseAndreas Feustel, Andreas Hahn, Christian Schneider, et al.
Pageof 72