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Ingo Kurth

Showing results (31-40 of 145) with videos related to

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Neurogenetics|August 28, 2025
Familial cerebral cavernous malformations caused by a novel germline structural variant in the KRIT1 geneRobin A Pilz, Matthias Begemann, Surema Pfister, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 3, 2017
Posterior column ataxia with retinitis pigmentosa coexisting with sensory-autonomic neuropathy and leukemia due to the homozygous p.Pro221Ser FLVCR1 mutationMarco Castori, Silvia Morlino, Martin Ungelenk, et al.
BMC Bioinformatics|December 17, 2024
CNVizard-a lightweight streamlit application for an interactive analysis of copy number variantsJeremias Krause, Carlos Classen, Daniela Dey, et al.
Neuromuscular Disorders : NMD|November 4, 2018
Microangiopathy and mild mixed neuromyopathic alterations in a patient with homozygous PIEZO-2 mutationAnnegret Quade, Joachim Weis, Ingo Kurth, et al.
Journal of Neurology|June 18, 2009
Missense exchanges in the TTBK2 gene mutated in SCA11Ulf Edener, Ingo Kurth, Annechristin Meiner, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 8, 2019
Paroxysmal tonic upgaze: A heterogeneous clinical condition responsive to carbonic anhydrase inhibitionAnnegret Quade, Anne Thiel, Ingo Kurth, et al.
Gene|June 5, 2016
Identification of the first multi-exonic WDR72 deletion in isolated amelogenesis imperfecta, and generation of a WDR72-specific copy number screening toolJulia Hentschel, Dana Tatun, Dmitri Parkhomchuk, et al.
Frontiers in Molecular Neuroscience|January 9, 2023
Isolation and transfection of myenteric neurons from mice for patch-clamp applicationsSamuel Kuehs, Laura Teege, Ann-Katrin Hellberg, et al.
Neurology India|March 10, 2022
Hereditary Sensory and Autonomic Neuropathy: A Case Series of Six ChildrenRenu Suthar, Indar K Sharawat, Katja Eggermann, et al.
Vascular Medicine (London, England)|October 29, 2011
Severe case and literature review of primary erythromelalgia: novel SCN9A gene mutationNedaa Skeik, Thom W Rooke, Mark Denis P Davis, et al.
Pageof 15

Showing results (31-40 of 145) with videos related to

Sort By:
Pageof 15
Neurogenetics|August 28, 2025
Familial cerebral cavernous malformations caused by a novel germline structural variant in the KRIT1 geneRobin A Pilz, Matthias Begemann, Surema Pfister, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 3, 2017
Posterior column ataxia with retinitis pigmentosa coexisting with sensory-autonomic neuropathy and leukemia due to the homozygous p.Pro221Ser FLVCR1 mutationMarco Castori, Silvia Morlino, Martin Ungelenk, et al.
BMC Bioinformatics|December 17, 2024
CNVizard-a lightweight streamlit application for an interactive analysis of copy number variantsJeremias Krause, Carlos Classen, Daniela Dey, et al.
Neuromuscular Disorders : NMD|November 4, 2018
Microangiopathy and mild mixed neuromyopathic alterations in a patient with homozygous PIEZO-2 mutationAnnegret Quade, Joachim Weis, Ingo Kurth, et al.
Journal of Neurology|June 18, 2009
Missense exchanges in the TTBK2 gene mutated in SCA11Ulf Edener, Ingo Kurth, Annechristin Meiner, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 8, 2019
Paroxysmal tonic upgaze: A heterogeneous clinical condition responsive to carbonic anhydrase inhibitionAnnegret Quade, Anne Thiel, Ingo Kurth, et al.
Gene|June 5, 2016
Identification of the first multi-exonic WDR72 deletion in isolated amelogenesis imperfecta, and generation of a WDR72-specific copy number screening toolJulia Hentschel, Dana Tatun, Dmitri Parkhomchuk, et al.
Frontiers in Molecular Neuroscience|January 9, 2023
Isolation and transfection of myenteric neurons from mice for patch-clamp applicationsSamuel Kuehs, Laura Teege, Ann-Katrin Hellberg, et al.
Neurology India|March 10, 2022
Hereditary Sensory and Autonomic Neuropathy: A Case Series of Six ChildrenRenu Suthar, Indar K Sharawat, Katja Eggermann, et al.
Vascular Medicine (London, England)|October 29, 2011
Severe case and literature review of primary erythromelalgia: novel SCN9A gene mutationNedaa Skeik, Thom W Rooke, Mark Denis P Davis, et al.
Pageof 15