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G Weber

Showing results (1131-1140 of 1,377) with videos related to

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Epilepsia Open|March 29, 2018
Functional variants in <i>HCN4</i> and <i>CACNA1H</i> may contribute to genetic generalized epilepsyFelicitas Becker, Christopher A Reid, Kerstin Hallmann, et al.
Journal of Virology|April 20, 2018
Subclinical Cytomegalovirus Infection Is Associated with Altered Host Immunity, Gut Microbiota, and Vaccine ResponsesClarissa Santos Rocha, Lauren A Hirao, Mariana G Weber, et al.
Epilepsy & Behavior : E&B|March 28, 2018
Characteristics and healthcare situation of adult patients with tuberous sclerosis complex in German epilepsy centersHajo M Hamer, Margarete Pfäfflin, Hartmut Baier, et al.
The American Journal of Surgical Pathology|December 7, 2007
Angiocentric glioma: report of clinico-pathologic and genetic findings in 8 casesMatthias Preusser, Alexander Hoischen, Klaus Novak, et al.
Chemical Science|January 10, 2025
Unveiling the enzymatic pathway of UMG-SP2 urethanase: insights into polyurethane degradation at the atomic levelP Paiva, L M C Teixeira, R Wei, et al.
Genes|January 21, 2022
Heterozygous <i>DHTKD1</i> Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis PatientsAlma Osmanovic, Isabel Gogol, Helge Martens, et al.
Elife|September 10, 2019
Long-term adult human brain slice cultures as a model system to study human CNS circuitry and diseaseNiklas Schwarz, Betül Uysal, Marc Welzer, et al.
Human Mutation|February 5, 2009
Two novel CLCN2 mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsyCécile Saint-Martin, Grégory Gauvain, Georgeta Teodorescu, et al.
World Journal of Emergency Surgery : WJES|October 27, 2015
WSES position paper on vascular emergency surgeryBruno Monteiro T Pereira, Osvaldo Chiara, Fabio Ramponi, et al.
Neurology|August 12, 2011
Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defectY G Weber, C Kamm, A Suls, et al.
Pageof 138

Showing results (1131-1140 of 1,377) with videos related to

Sort By:
Pageof 138
Epilepsia Open|March 29, 2018
Functional variants in <i>HCN4</i> and <i>CACNA1H</i> may contribute to genetic generalized epilepsyFelicitas Becker, Christopher A Reid, Kerstin Hallmann, et al.
Journal of Virology|April 20, 2018
Subclinical Cytomegalovirus Infection Is Associated with Altered Host Immunity, Gut Microbiota, and Vaccine ResponsesClarissa Santos Rocha, Lauren A Hirao, Mariana G Weber, et al.
Epilepsy & Behavior : E&B|March 28, 2018
Characteristics and healthcare situation of adult patients with tuberous sclerosis complex in German epilepsy centersHajo M Hamer, Margarete Pfäfflin, Hartmut Baier, et al.
The American Journal of Surgical Pathology|December 7, 2007
Angiocentric glioma: report of clinico-pathologic and genetic findings in 8 casesMatthias Preusser, Alexander Hoischen, Klaus Novak, et al.
Chemical Science|January 10, 2025
Unveiling the enzymatic pathway of UMG-SP2 urethanase: insights into polyurethane degradation at the atomic levelP Paiva, L M C Teixeira, R Wei, et al.
Genes|January 21, 2022
Heterozygous <i>DHTKD1</i> Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis PatientsAlma Osmanovic, Isabel Gogol, Helge Martens, et al.
Elife|September 10, 2019
Long-term adult human brain slice cultures as a model system to study human CNS circuitry and diseaseNiklas Schwarz, Betül Uysal, Marc Welzer, et al.
Human Mutation|February 5, 2009
Two novel CLCN2 mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsyCécile Saint-Martin, Grégory Gauvain, Georgeta Teodorescu, et al.
World Journal of Emergency Surgery : WJES|October 27, 2015
WSES position paper on vascular emergency surgeryBruno Monteiro T Pereira, Osvaldo Chiara, Fabio Ramponi, et al.
Neurology|August 12, 2011
Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defectY G Weber, C Kamm, A Suls, et al.
Pageof 138