Kireshnee Naidu
Cape Town, WC, South Africa
Last Updated: 09/26/2026
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Found 8 publications
Phenotypic characterization of dominantly inherited distal nebulin myopathy.
Journal: Neuromuscular disorders : NMD
Published: December 23, 2025
Structural variation in nebulin and its implications on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletions.
Journal: medRxiv : the preprint server for health sciences
Published: January 13, 2025
Structural variation in nebulin and its impact on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletions.
Journal: European journal of human genetics : EJHG
Published: January 07, 2025
Mitochondrial DNA disorders in neuromuscular diseases in diverse populations.
Journal: Annals of clinical and translational neurology
Published: May 22, 2024
Extended Phenotype of PEX11B Pathogenic Variants: Ataxia, Tremor, and Dystonia Due to a Novel C.2T > G Variant.
Journal: Movement disorders clinical practice
Published: October 18, 2023
Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study.
Journal: Orphanet journal of rare diseases
Published: July 07, 2023
The mutational profile in a South African cohort with inherited neuropathies and spastic paraplegia.
The mutational profile in a South African cohort with inherited neuropathies and spastic paraplegia.
Journal: Frontiers in neurology
Published: June 13, 2023
Neuromuscular disease genetics in under-represented populations: increasing data diversity.
Journal: Brain : a journal of neurology
Published: May 22, 2023
Showing 1-8 of 8
Last Updated: 09/26/2026