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Florentine Radelfahr

Showing results (1-10 of 8) with videos related to

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Fortschritte Der Neurologie-Psychiatrie|September 25, 2018
[Diagnostic and Therapeutic Approaches for Mitochondrial Diseases]Florentine Radelfahr, Thomas Klopstock
Der Nervenarzt|January 16, 2019
[Mitochondrial diseases]Florentine Radelfahr, Thomas Klopstock
Neurology. Genetics|November 2, 2020
Biotinidase deficiency: A treatable cause of hereditary spastic paraparesisFlorentine Radelfahr, Korbinian M Riedhammer, Leonie F Keidel, et al.
Annals of Clinical and Translational Neurology|October 31, 2014
Intrathecal anti-CD20 efficiently depletes meningeal B cells in CNS autoimmunityKlaus Lehmann-Horn, Silke Kinzel, Linda Feldmann, et al.
Journal of Lipid Research|April 23, 2021
Metabolic profiling in serum, cerebrospinal fluid, and brain of patients with cerebrotendinous xanthomatosisPhilip Höflinger, Stefan Hauser, Eylan Yutuc, et al.
Journal of Neurology|June 25, 2023
Economic evaluation of Motor Neuron Diseases: a nationwide cross-sectional analysis in GermanyFelix Heinrich, Isabell Cordts, René Günther, et al.
American Journal of Human Genetics|July 25, 2020
Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic ParaplegiaRalf A Husain, Mona Grimmel, Matias Wagner, et al.
Nature Communications|February 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxiaBenita Menden, Rana D Incebacak Eltemur, German Demidov, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Fortschritte Der Neurologie-Psychiatrie|September 25, 2018
[Diagnostic and Therapeutic Approaches for Mitochondrial Diseases]Florentine Radelfahr, Thomas Klopstock
Der Nervenarzt|January 16, 2019
[Mitochondrial diseases]Florentine Radelfahr, Thomas Klopstock
Neurology. Genetics|November 2, 2020
Biotinidase deficiency: A treatable cause of hereditary spastic paraparesisFlorentine Radelfahr, Korbinian M Riedhammer, Leonie F Keidel, et al.
Annals of Clinical and Translational Neurology|October 31, 2014
Intrathecal anti-CD20 efficiently depletes meningeal B cells in CNS autoimmunityKlaus Lehmann-Horn, Silke Kinzel, Linda Feldmann, et al.
Journal of Lipid Research|April 23, 2021
Metabolic profiling in serum, cerebrospinal fluid, and brain of patients with cerebrotendinous xanthomatosisPhilip Höflinger, Stefan Hauser, Eylan Yutuc, et al.
Journal of Neurology|June 25, 2023
Economic evaluation of Motor Neuron Diseases: a nationwide cross-sectional analysis in GermanyFelix Heinrich, Isabell Cordts, René Günther, et al.
American Journal of Human Genetics|July 25, 2020
Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic ParaplegiaRalf A Husain, Mona Grimmel, Matias Wagner, et al.
Nature Communications|February 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxiaBenita Menden, Rana D Incebacak Eltemur, German Demidov, et al.
Pageof 1