Rahema Mohammad
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 10 publications
The Genetic Landscape of Hereditary Spastic Paraplegia in Greece.
Journal: Clinical genetics
Published: September 11, 2025
Clinical prognostic indicators in multiple system atrophy.
Journal: Brain : a journal of neurology
Published: September 09, 2025
Clinical and genetic heterogeneity of syndromic hearing loss and its non-syndromic hearing loss mimics.
Journal: Molecular medicine (Cambridge, Mass.)
Published: July 22, 2025
Recurrent and Novel Pathogenic Variants in Genes Involved with Hearing Loss in the Pakistani Population.
Journal: Molecular diagnosis & therapy
Published: April 13, 2025
Elucidating the genomic basis of rare pediatric neurological diseases in Central Asia and Transcaucasia.
Journal: Nature genetics
Published: November 23, 2024
Intronic FGF14 GAA repeat expansions impact progression and survival in multiple system atrophy.
Journal: Brain : a journal of neurology
Published: November 20, 2024
Clinical Practices and Opinions toward Gastrostomy Use in Patients with Atypical Parkinsonian Syndromes: A National Survey in the UK.
Journal: Movement disorders clinical practice
Published: April 07, 2024
Clinical and neuroradiological spectrum of biallelic variants in NOTCH3.
Journal: EBioMedicine
Published: March 03, 2024
Frequency and outcomes of gastrostomy insertion in a longitudinal cohort study of atypical parkinsonism.
Journal: European journal of neurology
Published: October 27, 2023
TRAPPC6B biallelic variants cause a neurodevelopmental disorder with TRAPP II and trafficking disruptions.
Journal: Brain : a journal of neurology
Published: April 18, 2023
Showing 1-10 of 10
Last Updated: 09/26/2026