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G Weber

Showing results (1201-1210 of 1,377) with videos related to

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The Journal of Clinical Investigation|May 3, 2008
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leakYvonne G Weber, Alexander Storch, Thomas V Wuttke, et al.
Annals of Neurology|December 18, 2015
Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutationElena Gardella, Felicitas Becker, Rikke S Møller, et al.
Epilepsia|May 30, 2020
Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizuresShan Tang, Laura Addis, Anna Smith, et al.
Plos One|March 19, 2016
Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy SyndromesDennis Lal, Eva M Reinthaler, Borislav Dejanovic, et al.
Physical Review Letters|May 21, 2005
Evidence for strange-quark contributions to the nucleon's form factors at Q2=0.108 (GeV/c)2F E Maas, K Aulenbacher, S Baunack, et al.
Nature Genetics|June 27, 2018
De novo variants in neurodevelopmental disorders with epilepsyHenrike O Heyne, Tarjinder Singh, Hannah Stamberger, et al.
Acta Neuropathologica|March 19, 2015
Molecular classification of diffuse cerebral WHO grade II/III gliomas using genome- and transcriptome-wide profiling improves stratification of prognostically distinct patient groupsMichael Weller, Ruthild G Weber, Edith Willscher, et al.
Physical Review Letters|June 11, 2013
Electron- and proton-impact excitation of hydrogenlike uranium in relativistic collisionsA Gumberidze, D B Thorn, C J Fontes, et al.
Pharmacogenomics|April 21, 2020
Pharmacoresponse in genetic generalized epilepsy: a genome-wide association studyStefan Wolking, Herbert Schulz, Anne T Nies, et al.
World Journal of Emergency Surgery : WJES|January 11, 2020
Perforated and bleeding peptic ulcer: WSES guidelinesAntonio Tarasconi, Federico Coccolini, Walter L Biffl, et al.
Pageof 138

Showing results (1201-1210 of 1,377) with videos related to

Sort By:
Pageof 138
The Journal of Clinical Investigation|May 3, 2008
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leakYvonne G Weber, Alexander Storch, Thomas V Wuttke, et al.
Annals of Neurology|December 18, 2015
Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutationElena Gardella, Felicitas Becker, Rikke S Møller, et al.
Epilepsia|May 30, 2020
Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizuresShan Tang, Laura Addis, Anna Smith, et al.
Plos One|March 19, 2016
Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy SyndromesDennis Lal, Eva M Reinthaler, Borislav Dejanovic, et al.
Physical Review Letters|May 21, 2005
Evidence for strange-quark contributions to the nucleon's form factors at Q2=0.108 (GeV/c)2F E Maas, K Aulenbacher, S Baunack, et al.
Nature Genetics|June 27, 2018
De novo variants in neurodevelopmental disorders with epilepsyHenrike O Heyne, Tarjinder Singh, Hannah Stamberger, et al.
Acta Neuropathologica|March 19, 2015
Molecular classification of diffuse cerebral WHO grade II/III gliomas using genome- and transcriptome-wide profiling improves stratification of prognostically distinct patient groupsMichael Weller, Ruthild G Weber, Edith Willscher, et al.
Physical Review Letters|June 11, 2013
Electron- and proton-impact excitation of hydrogenlike uranium in relativistic collisionsA Gumberidze, D B Thorn, C J Fontes, et al.
Pharmacogenomics|April 21, 2020
Pharmacoresponse in genetic generalized epilepsy: a genome-wide association studyStefan Wolking, Herbert Schulz, Anne T Nies, et al.
World Journal of Emergency Surgery : WJES|January 11, 2020
Perforated and bleeding peptic ulcer: WSES guidelinesAntonio Tarasconi, Federico Coccolini, Walter L Biffl, et al.
Pageof 138