Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Franclo Henning

Showing results (11-20 of 24) with videos related to

Pageof 3
Sort By:
Journal of the Neurological Sciences|April 23, 2019
C9orf72 repeat expansions in South Africans with amyotrophic lateral sclerosisMelissa Nel, Gloudi M Agenbag, Franclo Henning, et al.
Journal of Medical Case Reports|October 16, 2023
Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) and Human Immunodeficiency virus infection: dilemmas in diagnosis and management: a case seriesYohane Gadama, Marié Du Preez, Jonathan Carr, et al.
Muscle & Nerve|November 19, 2016
Muscle fiber type proportion and size is not altered in mcardle diseaseFranclo Henning, Carol Anne Cunninghame, Miguel Angel Martín, et al.
The British Journal of Nutrition|May 21, 2009
Immune cell membrane fatty acids and inflammatory marker, C-reactive protein, in patients with multiple sclerosisGloudina Hon, Mogamat Hassan, Susan Janse van Rensburg, et al.
Biochemical and Biophysical Research Communications|April 12, 2014
Mitochondrial impairment observed in fibroblasts from South African Parkinson's disease patients with parkin mutationsCelia van der Merwe, Ben Loos, Chrisna Swart, et al.
Neuromuscular Disorders : NMD|March 26, 2026
Phenotypic characterization of dominantly inherited distal nebulin myopathyFranclo Henning, Kireshnee Naidu, Pearl Thomas, et al.
Movement Disorders Clinical Practice|August 2, 2024
Extended Phenotype of PEX11B Pathogenic Variants: Ataxia, Tremor, and Dystonia Due to a Novel C.2T > G VariantFranclo Henning, Kireshnee Naidu, Christopher J Record, et al.
Orphanet Journal of Rare Diseases|January 14, 2024
Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD studyMichelle Bisschoff, Izelle Smuts, Marli Dercksen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 23, 2018
Clinical features and prognosis of amyotrophic lateral sclerosis in Africa: the TROPALS studyJaime Luna, Mouhamadou Diagana, Leila Ait Aissa, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|August 30, 2021
Clinical management and disease-modifying treatment for amyotrophic lateral sclerosis in African hospital centers: the TROPALS studyJaime Luna, Jeremy Jost, Mouhamadou Diagana, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Journal of the Neurological Sciences|April 23, 2019
C9orf72 repeat expansions in South Africans with amyotrophic lateral sclerosisMelissa Nel, Gloudi M Agenbag, Franclo Henning, et al.
Journal of Medical Case Reports|October 16, 2023
Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) and Human Immunodeficiency virus infection: dilemmas in diagnosis and management: a case seriesYohane Gadama, Marié Du Preez, Jonathan Carr, et al.
Muscle & Nerve|November 19, 2016
Muscle fiber type proportion and size is not altered in mcardle diseaseFranclo Henning, Carol Anne Cunninghame, Miguel Angel Martín, et al.
The British Journal of Nutrition|May 21, 2009
Immune cell membrane fatty acids and inflammatory marker, C-reactive protein, in patients with multiple sclerosisGloudina Hon, Mogamat Hassan, Susan Janse van Rensburg, et al.
Biochemical and Biophysical Research Communications|April 12, 2014
Mitochondrial impairment observed in fibroblasts from South African Parkinson's disease patients with parkin mutationsCelia van der Merwe, Ben Loos, Chrisna Swart, et al.
Neuromuscular Disorders : NMD|March 26, 2026
Phenotypic characterization of dominantly inherited distal nebulin myopathyFranclo Henning, Kireshnee Naidu, Pearl Thomas, et al.
Movement Disorders Clinical Practice|August 2, 2024
Extended Phenotype of PEX11B Pathogenic Variants: Ataxia, Tremor, and Dystonia Due to a Novel C.2T > G VariantFranclo Henning, Kireshnee Naidu, Christopher J Record, et al.
Orphanet Journal of Rare Diseases|January 14, 2024
Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD studyMichelle Bisschoff, Izelle Smuts, Marli Dercksen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 23, 2018
Clinical features and prognosis of amyotrophic lateral sclerosis in Africa: the TROPALS studyJaime Luna, Mouhamadou Diagana, Leila Ait Aissa, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|August 30, 2021
Clinical management and disease-modifying treatment for amyotrophic lateral sclerosis in African hospital centers: the TROPALS studyJaime Luna, Jeremy Jost, Mouhamadou Diagana, et al.
Pageof 3