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Showing results (341-350 of 511) with videos related to

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European Journal of Human Genetics : EJHG|August 13, 2021
Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseasesBirte Zurek, Kornelia Ellwanger, Lisenka E L M Vissers, et al.
Orphanet Journal of Rare Diseases|August 14, 2020
A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a TreatabolomeAntonio Atalaia, Rachel Thompson, Alberto Corvo, et al.
Orphanet Journal of Rare Diseases|March 23, 2021
Correction to: A guide to writing systematic reviews of rare disease treatments to generate FAIRcompliant datasets: building a TreatabolomeAntonio Atalaia, Rachel Thompson, Alberto Corvo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 8, 2020
Abnormal pain perception is associated with thalamo-cortico-striatal atrophy in <i>C9orf72</i> expansion carriers in the GENFI cohortRhian S Convery, Martina Bocchetta, Caroline V Greaves, et al.
Human Genomics|April 3, 2024
The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous populationNejat Mahdieh, Morteza Heidari, Zahra Rezaei, et al.
European Journal of Human Genetics : EJHG|June 2, 2021
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseasesBirte Zurek, Kornelia Ellwanger, Lisenka E L M Vissers, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2021
Practice effects in genetic frontotemporal dementia and at-risk individuals: a GENFI studyLinn Öijerstedt, Christin Andersson, Vesna Jelic, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 16, 2021
MRI data-driven algorithm for the diagnosis of behavioural variant frontotemporal dementiaAna L Manera, Mahsa Dadar, John Cornelis Van Swieten, et al.
Neuroimage. Clinical|January 8, 2021
Disease-related cortical thinning in presymptomatic granulin mutation carriersSergi Borrego-Écija, Roser Sala-Llonch, John van Swieten, et al.
Brain Communications|July 28, 2022
Hierarchical spectral clustering reveals brain size and shape changes in asymptomatic carriers of <i>C9orf72</i>Rose Bruffaerts, Dorothy Gors, Alicia Bárcenas Gallardo, et al.
Pageof 52

Showing results (341-350 of 511) with videos related to

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Pageof 52
European Journal of Human Genetics : EJHG|August 13, 2021
Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseasesBirte Zurek, Kornelia Ellwanger, Lisenka E L M Vissers, et al.
Orphanet Journal of Rare Diseases|August 14, 2020
A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a TreatabolomeAntonio Atalaia, Rachel Thompson, Alberto Corvo, et al.
Orphanet Journal of Rare Diseases|March 23, 2021
Correction to: A guide to writing systematic reviews of rare disease treatments to generate FAIRcompliant datasets: building a TreatabolomeAntonio Atalaia, Rachel Thompson, Alberto Corvo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 8, 2020
Abnormal pain perception is associated with thalamo-cortico-striatal atrophy in <i>C9orf72</i> expansion carriers in the GENFI cohortRhian S Convery, Martina Bocchetta, Caroline V Greaves, et al.
Human Genomics|April 3, 2024
The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous populationNejat Mahdieh, Morteza Heidari, Zahra Rezaei, et al.
European Journal of Human Genetics : EJHG|June 2, 2021
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseasesBirte Zurek, Kornelia Ellwanger, Lisenka E L M Vissers, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2021
Practice effects in genetic frontotemporal dementia and at-risk individuals: a GENFI studyLinn Öijerstedt, Christin Andersson, Vesna Jelic, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 16, 2021
MRI data-driven algorithm for the diagnosis of behavioural variant frontotemporal dementiaAna L Manera, Mahsa Dadar, John Cornelis Van Swieten, et al.
Neuroimage. Clinical|January 8, 2021
Disease-related cortical thinning in presymptomatic granulin mutation carriersSergi Borrego-Écija, Roser Sala-Llonch, John van Swieten, et al.
Brain Communications|July 28, 2022
Hierarchical spectral clustering reveals brain size and shape changes in asymptomatic carriers of <i>C9orf72</i>Rose Bruffaerts, Dorothy Gors, Alicia Bárcenas Gallardo, et al.
Pageof 52