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Matthis Synofzik

Showing results (191-200 of 511) with videos related to

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Acta Neuropathologica|March 14, 2019
The molecular pathogenesis of superoxide dismutase 1-linked ALS is promoted by low oxygen tensionIsil Keskin, Elin Forsgren, Manuela Lehmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 31, 2022
Digital Gait Biomarkers Allow to Capture 1-Year Longitudinal Change in Spinocerebellar Ataxia Type 3Winfried Ilg, Björn Müller, Jennifer Faber, et al.
Clinical Chemistry and Laboratory Medicine|June 29, 2019
Correlations between serum and CSF pNfH levels in ALS, FTD and controls: a comparison of three analytical approachesCarlo Wilke, Fani Pujol-Calderón, Christian Barro, et al.
Annals of Neurology|June 4, 2025
Autosomal Recessive Cerebellar Ataxias: Translating Genes to TherapiesBrent L Fogel, Thomas Klopstock, David R Lynch, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 11, 2026
The Cerebellar Cognitive-Affective Syndrome Scale Reveals Consistent, Early, and Progressive Neuropsychological Deficits in Autosomal-Recessive Spastic Ataxia of Charlevoix-Saguenay: A Large International Cross-Sectional StudyJulie Fortin, Matthis Synofzik, Élyse-Anne Pedneault-Tremblay, et al.
Neurobiology of Aging|November 3, 2015
Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variantsCornelis Blauwendraat, Carlo Wilke, Iris E Jansen, et al.
Frontiers in Cell and Developmental Biology|October 25, 2021
Intracellular Lipid Accumulation and Mitochondrial Dysfunction Accompanies Endoplasmic Reticulum Stress Caused by Loss of the Co-chaperone <i>DNAJC3</i>Matthew J Jennings, Denisa Hathazi, Chi D L Nguyen, et al.
Acta Neuropathologica Communications|April 16, 2016
C9orf72 is differentially expressed in the central nervous system and myeloid cells and consistently reduced in C9orf72, MAPT and GRN mutation carriersPatrizia Rizzu, Cornelis Blauwendraat, Sasja Heetveld, et al.
Journal of Neurology|July 4, 2018
Coordination and timing deficits in speech and swallowing in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)Adam P Vogel, Natalie Rommel, Andreas Oettinger, et al.
Biorxiv : the Preprint Server for Biology|March 13, 2023
Blood neurofilament light chain levels are associated with disease progression in a transgenic SCA3 mouse modelDavid Mengel, Isabel G Wellik, Kristen H Schuster, et al.
Pageof 52

Showing results (191-200 of 511) with videos related to

Sort By:
Pageof 52
Acta Neuropathologica|March 14, 2019
The molecular pathogenesis of superoxide dismutase 1-linked ALS is promoted by low oxygen tensionIsil Keskin, Elin Forsgren, Manuela Lehmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 31, 2022
Digital Gait Biomarkers Allow to Capture 1-Year Longitudinal Change in Spinocerebellar Ataxia Type 3Winfried Ilg, Björn Müller, Jennifer Faber, et al.
Clinical Chemistry and Laboratory Medicine|June 29, 2019
Correlations between serum and CSF pNfH levels in ALS, FTD and controls: a comparison of three analytical approachesCarlo Wilke, Fani Pujol-Calderón, Christian Barro, et al.
Annals of Neurology|June 4, 2025
Autosomal Recessive Cerebellar Ataxias: Translating Genes to TherapiesBrent L Fogel, Thomas Klopstock, David R Lynch, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 11, 2026
The Cerebellar Cognitive-Affective Syndrome Scale Reveals Consistent, Early, and Progressive Neuropsychological Deficits in Autosomal-Recessive Spastic Ataxia of Charlevoix-Saguenay: A Large International Cross-Sectional StudyJulie Fortin, Matthis Synofzik, Élyse-Anne Pedneault-Tremblay, et al.
Neurobiology of Aging|November 3, 2015
Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variantsCornelis Blauwendraat, Carlo Wilke, Iris E Jansen, et al.
Frontiers in Cell and Developmental Biology|October 25, 2021
Intracellular Lipid Accumulation and Mitochondrial Dysfunction Accompanies Endoplasmic Reticulum Stress Caused by Loss of the Co-chaperone <i>DNAJC3</i>Matthew J Jennings, Denisa Hathazi, Chi D L Nguyen, et al.
Acta Neuropathologica Communications|April 16, 2016
C9orf72 is differentially expressed in the central nervous system and myeloid cells and consistently reduced in C9orf72, MAPT and GRN mutation carriersPatrizia Rizzu, Cornelis Blauwendraat, Sasja Heetveld, et al.
Journal of Neurology|July 4, 2018
Coordination and timing deficits in speech and swallowing in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)Adam P Vogel, Natalie Rommel, Andreas Oettinger, et al.
Biorxiv : the Preprint Server for Biology|March 13, 2023
Blood neurofilament light chain levels are associated with disease progression in a transgenic SCA3 mouse modelDavid Mengel, Isabel G Wellik, Kristen H Schuster, et al.
Pageof 52