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Fritz Zimprich

Showing results (81-90 of 103) with videos related to

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Journal of Clinical Medicine|March 14, 2026
Hereditary Transthyretin Amyloidosis in Austria: Clinical, Genetic, and Demographic Insights from a Nationwide CohortNikita Ermolaev, Wolfgang N Löscher, Nicolas Verheyen, 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.
Epilepsia|March 7, 2020
Testing association of rare genetic variants with resistance to three common antiseizure medicationsStefan Wolking, Claudia Moreau, Anne T Nies, et al.
Annals of Neurology|March 3, 2015
Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromesEva M Reinthaler, Borislav Dejanovic, Dennis Lal, et al.
Brain : a Journal of Neurology|April 21, 2021
Antibodies to the Caspr1/contactin-1 complex in chronic inflammatory demyelinating polyradiculoneuropathyElba Pascual-Goñi, Janev Fehmi, Cinta Lleixà, et al.
Pharmacogenomics|April 21, 2020
Pharmacoresponse in genetic generalized epilepsy: a genome-wide association studyStefan Wolking, Herbert Schulz, Anne T Nies, et al.
American Journal of Human Genetics|July 19, 2011
A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson diseaseAlexander Zimprich, Anna Benet-Pagès, Walter Struhal, et al.
Eclinicalmedicine|November 3, 2025
Efficacy and safety of risdiplam in adults with 5q-associated spinal muscular atrophy: a nationwide observational cohort study in AustriaOmar Keritam, Marcus Erdler, Bernhard Fasching, et al.
Human Molecular Genetics|June 19, 2014
16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsyEva M Reinthaler, Dennis Lal, Sebastien Lebon, et al.
European Journal of Human Genetics : EJHG|December 20, 2012
Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversityTõnu Esko, Massimo Mezzavilla, Mari Nelis, et al.
Pageof 11

Showing results (81-90 of 103) with videos related to

Sort By:
Pageof 11
Journal of Clinical Medicine|March 14, 2026
Hereditary Transthyretin Amyloidosis in Austria: Clinical, Genetic, and Demographic Insights from a Nationwide CohortNikita Ermolaev, Wolfgang N Löscher, Nicolas Verheyen, 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.
Epilepsia|March 7, 2020
Testing association of rare genetic variants with resistance to three common antiseizure medicationsStefan Wolking, Claudia Moreau, Anne T Nies, et al.
Annals of Neurology|March 3, 2015
Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromesEva M Reinthaler, Borislav Dejanovic, Dennis Lal, et al.
Brain : a Journal of Neurology|April 21, 2021
Antibodies to the Caspr1/contactin-1 complex in chronic inflammatory demyelinating polyradiculoneuropathyElba Pascual-Goñi, Janev Fehmi, Cinta Lleixà, et al.
Pharmacogenomics|April 21, 2020
Pharmacoresponse in genetic generalized epilepsy: a genome-wide association studyStefan Wolking, Herbert Schulz, Anne T Nies, et al.
American Journal of Human Genetics|July 19, 2011
A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson diseaseAlexander Zimprich, Anna Benet-Pagès, Walter Struhal, et al.
Eclinicalmedicine|November 3, 2025
Efficacy and safety of risdiplam in adults with 5q-associated spinal muscular atrophy: a nationwide observational cohort study in AustriaOmar Keritam, Marcus Erdler, Bernhard Fasching, et al.
Human Molecular Genetics|June 19, 2014
16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsyEva M Reinthaler, Dennis Lal, Sebastien Lebon, et al.
European Journal of Human Genetics : EJHG|December 20, 2012
Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversityTõnu Esko, Massimo Mezzavilla, Mari Nelis, et al.
Pageof 11