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Efthymia Kafantari

Showing results (1-10 of 7) with videos related to

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Genes|December 30, 2025
WES-Based Screening of a Swedish Patient Series with Parkinson's DiseaseEfthymia Kafantari, Kajsa Atterling Brolin, Joel Wallenius, et al.
Parkinsonism & Related Disorders|April 11, 2020
New generation genetic testing entering the clinicSorina Gorcenco, Andreea Ilinca, Wejdan Almasoudi, et al.
Stroke|November 5, 2024
Diagnosing Monogenic Stroke at Younger AgeAndreea Ilinca, Efthymia Kafantari, Joel Wallenius, et al.
Neurology. Genetics|March 17, 2021
<i>MAP3K6</i> Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and TremorAndreea Ilinca, Elisabet Englund, Sofie Samuelsson, et al.
Parkinsonism & Related Disorders|March 15, 2025
TOR1AIP2 as a candidate gene for dystonia-hemichorea/hemiballismEfthymia Kafantari, Victoria J Hernandez, Ján Necpál, et al.
Journal of Neurology|October 3, 2023
Clinical and genetic analyses of a Swedish patient series diagnosed with ataxiaSorina Gorcenco, Efthymia Kafantari, Joel Wallenius, et al.
American Journal of Human Genetics|November 30, 2023
Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine diseaseJoel Wallenius, Efthymia Kafantari, Emma Jhaveri, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Genes|December 30, 2025
WES-Based Screening of a Swedish Patient Series with Parkinson's DiseaseEfthymia Kafantari, Kajsa Atterling Brolin, Joel Wallenius, et al.
Parkinsonism & Related Disorders|April 11, 2020
New generation genetic testing entering the clinicSorina Gorcenco, Andreea Ilinca, Wejdan Almasoudi, et al.
Stroke|November 5, 2024
Diagnosing Monogenic Stroke at Younger AgeAndreea Ilinca, Efthymia Kafantari, Joel Wallenius, et al.
Neurology. Genetics|March 17, 2021
<i>MAP3K6</i> Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and TremorAndreea Ilinca, Elisabet Englund, Sofie Samuelsson, et al.
Parkinsonism & Related Disorders|March 15, 2025
TOR1AIP2 as a candidate gene for dystonia-hemichorea/hemiballismEfthymia Kafantari, Victoria J Hernandez, Ján Necpál, et al.
Journal of Neurology|October 3, 2023
Clinical and genetic analyses of a Swedish patient series diagnosed with ataxiaSorina Gorcenco, Efthymia Kafantari, Joel Wallenius, et al.
American Journal of Human Genetics|November 30, 2023
Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine diseaseJoel Wallenius, Efthymia Kafantari, Emma Jhaveri, et al.
Pageof 1