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Dagmar Timmann

Showing results (201-210 of 269) with videos related to

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Brain : a Journal of Neurology|February 21, 2013
Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6Kathrin Reetz, Ana S Costa, Shahram Mirzazade, et al.
Brain : a Journal of Neurology|February 1, 2017
Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78)Alejandro Estrada-Cuzcano, Shaun Martin, Teodora Chamova, et al.
Brain : a Journal of Neurology|April 23, 2021
Biallelic loss-of-function variations in PRDX3 cause cerebellar ataxiaAdriana P Rebelo, Ilse Eidhof, Vivian P Cintra, et al.
Cerebellum (London, England)|December 14, 2011
Consensus paper: roles of the cerebellum in motor control--the diversity of ideas on cerebellar involvement in movementMario Manto, James M Bower, Adriana Bastos Conforto, et al.
Cerebellum (London, England)|December 10, 2013
Consensus paper: Language and the cerebellum: an ongoing enigmaPeter Mariën, Herman Ackermann, Michael Adamaszek, et al.
Journal of Visualized Experiments : Jove|December 2, 2024
Neuronavigated Focalized Transcranial Direct Current Stimulation Administered During Functional Magnetic Resonance ImagingFilip Niemann, Alireza Shahbabaie, Sven Paßmann, et al.
Cerebellum (London, England)|March 6, 2024
Correction: Cerebellar Volumetry in Ataxias: Relation to Ataxia Severity and DurationMónica Ferreira, Tamara Schaprian, David Kügler, et al.
Neurology|April 1, 2016
Diffuse hypomyelination is not obligate for POLR3-related disordersRoberta La Piana, Ferdy K Cayami, Luan T Tran, et al.
Research Square|November 28, 2023
Cerebellar volumetry in ataxias: Relation to ataxia severity and durationMónica Ferreira, Tamara Schaprian, David Kügler, et al.
Cerebellum (London, England)|February 16, 2024
Cerebellar Volumetry in Ataxias: Relation to Ataxia Severity and DurationMónica Ferreira, Tamara Schaprian, David Kügler, et al.
Pageof 27

Showing results (201-210 of 269) with videos related to

Sort By:
Pageof 27
Brain : a Journal of Neurology|February 21, 2013
Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6Kathrin Reetz, Ana S Costa, Shahram Mirzazade, et al.
Brain : a Journal of Neurology|February 1, 2017
Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78)Alejandro Estrada-Cuzcano, Shaun Martin, Teodora Chamova, et al.
Brain : a Journal of Neurology|April 23, 2021
Biallelic loss-of-function variations in PRDX3 cause cerebellar ataxiaAdriana P Rebelo, Ilse Eidhof, Vivian P Cintra, et al.
Cerebellum (London, England)|December 14, 2011
Consensus paper: roles of the cerebellum in motor control--the diversity of ideas on cerebellar involvement in movementMario Manto, James M Bower, Adriana Bastos Conforto, et al.
Cerebellum (London, England)|December 10, 2013
Consensus paper: Language and the cerebellum: an ongoing enigmaPeter Mariën, Herman Ackermann, Michael Adamaszek, et al.
Journal of Visualized Experiments : Jove|December 2, 2024
Neuronavigated Focalized Transcranial Direct Current Stimulation Administered During Functional Magnetic Resonance ImagingFilip Niemann, Alireza Shahbabaie, Sven Paßmann, et al.
Cerebellum (London, England)|March 6, 2024
Correction: Cerebellar Volumetry in Ataxias: Relation to Ataxia Severity and DurationMónica Ferreira, Tamara Schaprian, David Kügler, et al.
Neurology|April 1, 2016
Diffuse hypomyelination is not obligate for POLR3-related disordersRoberta La Piana, Ferdy K Cayami, Luan T Tran, et al.
Research Square|November 28, 2023
Cerebellar volumetry in ataxias: Relation to ataxia severity and durationMónica Ferreira, Tamara Schaprian, David Kügler, et al.
Cerebellum (London, England)|February 16, 2024
Cerebellar Volumetry in Ataxias: Relation to Ataxia Severity and DurationMónica Ferreira, Tamara Schaprian, David Kügler, et al.
Pageof 27