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Showing results (881-890 of 1,489) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystoniasKathrin Grundmann, Ulrike Laubis-Herrmann, Dirk Dressler, et al.
Human Mutation|April 27, 2004
Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early-onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patientsAna Djarmati, Katja Hedrich, Marina Svetel, et al.
Frontiers in Cardiovascular Medicine|December 6, 2021
Cryoballoon Ablation Strategy in Persistent Atrial FibrillationFlorian Straube, Janis Pongratz, Alexander Kosmalla, et al.
Thrombosis Research|June 11, 2011
Certoparin versus UFH to prevent venous thromboembolic events in the very elderly patient: an analysis of the CERTIFY studyS M Schellong, H-E Gerlach, U Tebbe, et al.
Kidney International|July 1, 1995
Glomerulopathy associated with predominant fibronectin deposits: a newly recognized hereditary diseaseE H Strøm, G Banfi, R Krapf, et al.
Onkologie|June 24, 2009
[Palliative treatment for colorectal cancer]Susanna Hegewisch-Becker, Udo Vanhoefer, Stefan Kubicka, et al.
Molecular and Cellular Neurosciences|June 24, 2008
Blood level of brain-derived neurotrophic factor mRNA is progressively reduced in rodent models of Huntington's disease: restoration by the neuroprotective compound CEP-1347Paola Conforti, Catarina Ramos, Barbara L Apostol, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 10, 1999
Age related axonal neuropathy in spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD)T Klockgether, L Schöls, M Abele, et al.
European Journal of Human Genetics : EJHG|February 11, 2016
Improving the informed consent process in international collaborative rare disease research: effective consent for effective researchSabina Gainotti, Cathy Turner, Simon Woods, et al.
Journal of Clinical and Experimental Hematopathology : JCEH|June 24, 2016
A Rare Case of Acute Myeloid Leukemia with a t(2;3) Chromosomal Translocation Characterized by Thrombophilia and ChemoresistanceCecilia Bozzetti, Seval Türkmen, Ulrich Richter, et al.
Pageof 149

Showing results (881-890 of 1,489) with videos related to

Sort By:
Pageof 149
Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystoniasKathrin Grundmann, Ulrike Laubis-Herrmann, Dirk Dressler, et al.
Human Mutation|April 27, 2004
Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early-onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patientsAna Djarmati, Katja Hedrich, Marina Svetel, et al.
Frontiers in Cardiovascular Medicine|December 6, 2021
Cryoballoon Ablation Strategy in Persistent Atrial FibrillationFlorian Straube, Janis Pongratz, Alexander Kosmalla, et al.
Thrombosis Research|June 11, 2011
Certoparin versus UFH to prevent venous thromboembolic events in the very elderly patient: an analysis of the CERTIFY studyS M Schellong, H-E Gerlach, U Tebbe, et al.
Kidney International|July 1, 1995
Glomerulopathy associated with predominant fibronectin deposits: a newly recognized hereditary diseaseE H Strøm, G Banfi, R Krapf, et al.
Onkologie|June 24, 2009
[Palliative treatment for colorectal cancer]Susanna Hegewisch-Becker, Udo Vanhoefer, Stefan Kubicka, et al.
Molecular and Cellular Neurosciences|June 24, 2008
Blood level of brain-derived neurotrophic factor mRNA is progressively reduced in rodent models of Huntington's disease: restoration by the neuroprotective compound CEP-1347Paola Conforti, Catarina Ramos, Barbara L Apostol, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 10, 1999
Age related axonal neuropathy in spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD)T Klockgether, L Schöls, M Abele, et al.
European Journal of Human Genetics : EJHG|February 11, 2016
Improving the informed consent process in international collaborative rare disease research: effective consent for effective researchSabina Gainotti, Cathy Turner, Simon Woods, et al.
Journal of Clinical and Experimental Hematopathology : JCEH|June 24, 2016
A Rare Case of Acute Myeloid Leukemia with a t(2;3) Chromosomal Translocation Characterized by Thrombophilia and ChemoresistanceCecilia Bozzetti, Seval Türkmen, Ulrich Richter, et al.
Pageof 149