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Michel Koenig

Showing results (101-110 of 126) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|June 24, 2015
Developed turbulence and nonlinear amplification of magnetic fields in laboratory and astrophysical plasmasJena Meinecke, Petros Tzeferacos, Anthony Bell, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 22, 2015
Delayed-onset Friedreich's ataxia revisitedClaire Lecocq, Perrine Charles, Jean-Philippe Azulay, et al.
Journal of Neurology|January 8, 2021
Expanding the clinical spectrum of STIP1 homology and U-box containing protein 1-associated ataxiaJean-Marie Ravel, Mehdi Benkirane, Nadège Calmels, et al.
Genes|August 27, 2021
An Integrated Clinical-Biological Approach to Identify Interindividual Variability and Atypical Phenotype-Genotype Correlations in Myopathies: Experience on A Cohort of 156 FamiliesRaul Juntas Morales, Aurélien Perrin, Guilhem Solé, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 21, 2019
Correction: The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literatureJuliette Piard, Lara Hawkes, Mathieu Milh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 26, 2018
The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literatureJuliette Piard, Lara Hawkes, Mathieu Milh, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 2021
Time-resolved turbulent dynamo in a laser plasmaArchie F A Bott, Petros Tzeferacos, Laura Chen, et al.
American Journal of Human Genetics|November 25, 2010
Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxiaSascha Vermeer, Alexander Hoischen, Rowdy P P Meijer, et al.
Acta Neuropathologica Communications|July 3, 2026
Phenotype-specific muscle proteomic profiling in titinopathiesAurélien Perrin, Marie-Rocio Casenave-Camgaston, Baptiste Rabillard, et al.
The Journal of Allergy and Clinical Immunology|June 14, 2011
Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotypeRomain Micol, Lilia Ben Slama, Felipe Suarez, et al.
Pageof 13

Showing results (101-110 of 126) with videos related to

Sort By:
Pageof 13
Proceedings of the National Academy of Sciences of the United States of America|June 24, 2015
Developed turbulence and nonlinear amplification of magnetic fields in laboratory and astrophysical plasmasJena Meinecke, Petros Tzeferacos, Anthony Bell, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 22, 2015
Delayed-onset Friedreich's ataxia revisitedClaire Lecocq, Perrine Charles, Jean-Philippe Azulay, et al.
Journal of Neurology|January 8, 2021
Expanding the clinical spectrum of STIP1 homology and U-box containing protein 1-associated ataxiaJean-Marie Ravel, Mehdi Benkirane, Nadège Calmels, et al.
Genes|August 27, 2021
An Integrated Clinical-Biological Approach to Identify Interindividual Variability and Atypical Phenotype-Genotype Correlations in Myopathies: Experience on A Cohort of 156 FamiliesRaul Juntas Morales, Aurélien Perrin, Guilhem Solé, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 21, 2019
Correction: The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literatureJuliette Piard, Lara Hawkes, Mathieu Milh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 26, 2018
The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literatureJuliette Piard, Lara Hawkes, Mathieu Milh, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 2021
Time-resolved turbulent dynamo in a laser plasmaArchie F A Bott, Petros Tzeferacos, Laura Chen, et al.
American Journal of Human Genetics|November 25, 2010
Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxiaSascha Vermeer, Alexander Hoischen, Rowdy P P Meijer, et al.
Acta Neuropathologica Communications|July 3, 2026
Phenotype-specific muscle proteomic profiling in titinopathiesAurélien Perrin, Marie-Rocio Casenave-Camgaston, Baptiste Rabillard, et al.
The Journal of Allergy and Clinical Immunology|June 14, 2011
Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotypeRomain Micol, Lilia Ben Slama, Felipe Suarez, et al.
Pageof 13