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Martin Berghoff

Showing results (21-30 of 41) with videos related to

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Scientific Reports|August 17, 2025
Characterization of growth differentiation factor 15 (GDF15) as a neurotropic adipokine permeable to the brainAndreas Schmid, Emily Wilfurth, Alexandra Höpfinger, et al.
Molecular and Cellular Neurosciences|December 21, 2004
Neuroprotective effect of the immune system in a mouse model of severe dysmyelinating hereditary neuropathy: enhanced axonal degeneration following disruption of the RAG-1 geneMartin Berghoff, Mohtashem Samsam, Marcus Müller, et al.
International Journal of Molecular Sciences|October 27, 2022
Interferon Beta-1a versus Combined Interferon Beta-1a and Oligodendrocyte-Specific FGFR1 Deletion in Experimental Autoimmune EncephalomyelitisRanjithkumar Rajendran, Vinothkumar Rajendran, Liza Gupta, et al.
Cells|June 2, 2021
Effects of FGFR Tyrosine Kinase Inhibition in OLN-93 OligodendrocytesRanjithkumar Rajendran, Gregor Böttiger, Niklas Dentzien, et al.
Revista De Biologia Tropical|February 28, 2015
A Costa Rican family affected with Charcot-Marie-Tooth disease due to the myelin protein zero (MPZ) p.Thr124Met mutation shares the Belgian haplotypeAlejandro Leal, Corinna Berghoff, Martin Berghoff, et al.
International Journal of Molecular Sciences|September 10, 2021
Oligodendrocyte-Specific Deletion of <i>FGFR1</i> Reduces Cerebellar Inflammation and Neurodegeneration in MOG<sub>35-55</sub>-Induced EAERanjithkumar Rajendran, Vinothkumar Rajendran, Mario Giraldo-Velasquez, et al.
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|September 3, 2011
Sonographic assessment of the optic nerve sheath and transorbital monitoring of treatment effects in a patient with spontaneous intracranial hypotension: case reportJochen Bäuerle, Elke R Gizewski, Kerstin von Stockhausen, et al.
Neurological Research|October 2, 2008
Late onset autosomal dominant Charcot-Marie-Tooth 2 neuropathy in a Costa Rican familyCorinna Berghoff, Martin Berghoff, Alejandro Leal, et al.
Leukemia & Lymphoma|October 27, 2012
Development of progressive multifocal leukoencephalopathy in a patient with non-Hodgkin lymphoma 13 years after treatment with cladribineMartin Berghoff, Anne Schänzer, Gerhard C Hildebrandt, et al.
Neuromuscular Disorders : NMD|April 22, 2004
Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3Corinna Berghoff, Martin Berghoff, Alejandro Leal, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Scientific Reports|August 17, 2025
Characterization of growth differentiation factor 15 (GDF15) as a neurotropic adipokine permeable to the brainAndreas Schmid, Emily Wilfurth, Alexandra Höpfinger, et al.
Molecular and Cellular Neurosciences|December 21, 2004
Neuroprotective effect of the immune system in a mouse model of severe dysmyelinating hereditary neuropathy: enhanced axonal degeneration following disruption of the RAG-1 geneMartin Berghoff, Mohtashem Samsam, Marcus Müller, et al.
International Journal of Molecular Sciences|October 27, 2022
Interferon Beta-1a versus Combined Interferon Beta-1a and Oligodendrocyte-Specific FGFR1 Deletion in Experimental Autoimmune EncephalomyelitisRanjithkumar Rajendran, Vinothkumar Rajendran, Liza Gupta, et al.
Cells|June 2, 2021
Effects of FGFR Tyrosine Kinase Inhibition in OLN-93 OligodendrocytesRanjithkumar Rajendran, Gregor Böttiger, Niklas Dentzien, et al.
Revista De Biologia Tropical|February 28, 2015
A Costa Rican family affected with Charcot-Marie-Tooth disease due to the myelin protein zero (MPZ) p.Thr124Met mutation shares the Belgian haplotypeAlejandro Leal, Corinna Berghoff, Martin Berghoff, et al.
International Journal of Molecular Sciences|September 10, 2021
Oligodendrocyte-Specific Deletion of <i>FGFR1</i> Reduces Cerebellar Inflammation and Neurodegeneration in MOG<sub>35-55</sub>-Induced EAERanjithkumar Rajendran, Vinothkumar Rajendran, Mario Giraldo-Velasquez, et al.
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|September 3, 2011
Sonographic assessment of the optic nerve sheath and transorbital monitoring of treatment effects in a patient with spontaneous intracranial hypotension: case reportJochen Bäuerle, Elke R Gizewski, Kerstin von Stockhausen, et al.
Neurological Research|October 2, 2008
Late onset autosomal dominant Charcot-Marie-Tooth 2 neuropathy in a Costa Rican familyCorinna Berghoff, Martin Berghoff, Alejandro Leal, et al.
Leukemia & Lymphoma|October 27, 2012
Development of progressive multifocal leukoencephalopathy in a patient with non-Hodgkin lymphoma 13 years after treatment with cladribineMartin Berghoff, Anne Schänzer, Gerhard C Hildebrandt, et al.
Neuromuscular Disorders : NMD|April 22, 2004
Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3Corinna Berghoff, Martin Berghoff, Alejandro Leal, et al.
Pageof 5