Glial fibrillary acidic protein in cerebrospinal fluid of patients with spinal muscular atrophy-Reference-Cited by-同舟云学术

Glial fibrillary acidic protein in cerebrospinal fluid of patients with spinal muscular atrophy

Published:2022-08-11 Issue:9 Volume:9 Page:1437-1448
ISSN:2328-9503
Container-title:Annals of Clinical and Translational Neurology
language:en
Short-container-title:Ann Clin Transl Neurol

Author:

Freigang Maren¹^ORCID,Steinacker Petra²³,Wurster Claudia D.³,Schreiber‐Katz Olivia⁴,Osmanovic Alma⁴⁵,Petri Susanne⁴,Koch Jan C.⁶,Rostásy Kevin⁷,Huss André³⁸,Tumani Hayrettin³,Winter Benedikt⁹,Falkenburger Björn¹¹⁰,Ludolph Albert C.³⁸,Otto Markus²^ORCID,Hermann Andreas¹¹¹²^ORCID,Günther René¹¹⁰

Affiliation:

1. Department of Neurology University Hospital Carl Gustav Carus, Technische Universität Dresden Dresden Germany

2. Department of Neurology Universitätsklinikum Halle (Saale) Halle (Saale) Germany

3. Department of Neurology Ulm University Ulm Germany

4. Department of Neurology Hannover Medical School Hannover Germany

5. Essener Zentrum für Seltene Erkrankungen (EZSE) University Hospital Essen Essen Germany

6. Department of Neurology University Medicine Göttingen Göttingen Germany

7. Department of Pediatric Neurology Children's Hospital Datteln, University Witten/Herdecke Datteln Germany

8. Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE) Ulm Ulm Germany

9. Department of Pediatric Neurology University Hospital Mannheim Mannheim Germany

10. Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE) Dresden Dresden Germany

11. Translational Neurodegeneration Section “Albrecht‐Kossel”, Department of Neurology, and Center for Transdisciplinary Neurosciences Rostock (CTNR) University Medical Center Rostock, University of Rostock Rostock Germany

12. Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE) Rostock/Greifswald Rostock Germany

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.51645

Reference40 articles.

1. Identification and characterization of a spinal muscular atrophy-determining gene

2. Reduced Survival of Motor Neuron (SMN) Protein in Motor Neuronal Progenitors Functions Cell Autonomously to Cause Spinal Muscular Atrophy in Model Mice Expressing the Human Centromeric (SMN2) Gene

3. Astrocytes influence the severity of spinal muscular atrophy

4. Role and therapeutic potential of astrocytes in amyotrophic lateral sclerosis;Pehar M;Curr Pharm Des,2017

5. Glial cells in amyotrophic lateral sclerosis

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