Associated Papers
Novel and rare variants in amyotrophic lateral sclerosis genes identified in Malaysian patients.
Zulhairy-Liong NA et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2025
ANXA11 Mutations in the FTD Spectrum: A Novel Finding in a Patient With Semantic Variant Primary Progressive Aphasia.
Meng Y et al.
European Journal of Neurology, 2025
40345169 (PubMed )
Supplement: ENE-32-e70187-s001.docx
Episodic Memory Loss: When Alzheimer's Disease Is Not the Answer.
García-Roldán E et al.
Journal of Alzheimer's Disease Reports, 2024
Expanding the Genetic Landscape of Usher-Like Phenotypes.
Fuster-García C et al.
Investigative Ophthalmology & Visual Science, 2019
Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families.
Cruchaga C et al.
Plos One, 2012
A variant in GRN of Spanish origin presenting with heterogeneous phenotypes.
Menéndez-González M et al.
Neurologia, 0
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