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Sorina Gorcenco

Showing results (1-10 of 13) with videos related to

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Cerebellum (London, England)|December 16, 2022
Patients' Perspective in Hereditary AtaxiaSorina Gorcenco, Christin Karremo, Andreas Puschmann
Frontiers in Systems Neuroscience|September 4, 2024
Corrigendum: Neurocognitive and cerebellar function in ADHD, autism and spinocerebellar ataxiaMaurizio Cundari, Susanna Vestberg, Peik Gustafsson, et al.
Frontiers in Systems Neuroscience|July 7, 2023
Neurocognitive and cerebellar function in ADHD, autism and spinocerebellar ataxiaMaurizio Cundari, Susanna Vestberg, Peik Gustafsson, et al.
Parkinsonism & Related Disorders|April 11, 2020
New generation genetic testing entering the clinicSorina Gorcenco, Andreea Ilinca, Wejdan Almasoudi, et al.
Frontiers in Computational Neuroscience|December 25, 2025
Neurocognition, cerebellar functions and psychiatric features in spinocerebellar ataxia type 34: a case seriesMaurizio Cundari, Lena Kirchhoff, Susanna Vestberg, 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.
Parkinsonism & Related Disorders|October 23, 2018
Oral therapy for riboflavin transporter deficiency - What is the regimen of choice?Sorina Gorcenco, Frédéric M Vaz, Anna Tracewska-Siemiatkowska, 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.
Neurology. Genetics|August 31, 2017
Ataxia-pancytopenia syndrome with <i>SAMD9L</i> mutationsSorina Gorcenco, Jonna Komulainen-Ebrahim, Karin Nordborg, et al.
Blood|February 17, 2017
Gain-of-function <i>SAMD9L</i> mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptomsBianca Tesi, Josef Davidsson, Matthias Voss, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Cerebellum (London, England)|December 16, 2022
Patients' Perspective in Hereditary AtaxiaSorina Gorcenco, Christin Karremo, Andreas Puschmann
Frontiers in Systems Neuroscience|September 4, 2024
Corrigendum: Neurocognitive and cerebellar function in ADHD, autism and spinocerebellar ataxiaMaurizio Cundari, Susanna Vestberg, Peik Gustafsson, et al.
Frontiers in Systems Neuroscience|July 7, 2023
Neurocognitive and cerebellar function in ADHD, autism and spinocerebellar ataxiaMaurizio Cundari, Susanna Vestberg, Peik Gustafsson, et al.
Parkinsonism & Related Disorders|April 11, 2020
New generation genetic testing entering the clinicSorina Gorcenco, Andreea Ilinca, Wejdan Almasoudi, et al.
Frontiers in Computational Neuroscience|December 25, 2025
Neurocognition, cerebellar functions and psychiatric features in spinocerebellar ataxia type 34: a case seriesMaurizio Cundari, Lena Kirchhoff, Susanna Vestberg, 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.
Parkinsonism & Related Disorders|October 23, 2018
Oral therapy for riboflavin transporter deficiency - What is the regimen of choice?Sorina Gorcenco, Frédéric M Vaz, Anna Tracewska-Siemiatkowska, 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.
Neurology. Genetics|August 31, 2017
Ataxia-pancytopenia syndrome with <i>SAMD9L</i> mutationsSorina Gorcenco, Jonna Komulainen-Ebrahim, Karin Nordborg, et al.
Blood|February 17, 2017
Gain-of-function <i>SAMD9L</i> mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptomsBianca Tesi, Josef Davidsson, Matthias Voss, et al.
Pageof 2