Miren Zulaica
Madrid, MD 28029, Spain
Last Updated: 09/26/2026
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Found 33 publications
Mitochondria and Lipid Defects in Hereditary Progranulin-Related Frontotemporal Dementia.
Journal: Cells
Published: December 31, 2025
Clinical and imaging spectrum of non-congenital dominant ACTN2 myopathy.
Journal: Journal of neurology
Published: September 17, 2024
Dysregulated FOXO1 activity drives skeletal muscle intrinsic dysfunction in amyotrophic lateral sclerosis.
Journal: Acta neuropathologica
Published: June 27, 2024
Altered tubulin detyrosination due to SVBP malfunction induces cytokinesis failure and senescence, underlying a complex hereditary spastic paraplegia.
Journal: Aging cell
Published: May 10, 2024
Author Correction: Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.
Journal: Nature communications
Published: February 09, 2023
Expanding the phenotypic spectrum of TRAPPC11-related muscular dystrophy: 25 Roma individuals carrying a founder variant.
Journal: Journal of medical genetics
Published: December 30, 2022
Shedding light on motor premanifest myotonic dystrophy type 1: A molecular, muscular and central nervous system follow-up study.
Journal: European journal of neurology
Published: February 21, 2022
Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers.
Journal: Acta neuropathologica
Published: February 16, 2022
Senescence plays a role in myotonic dystrophy type 1.
Journal: JCI insight
Published: February 14, 2022
Description of Two Families with New Mutations in Familial Cerebral Cavernous Malformations Genes.
Journal: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association
Published: July 08, 2021
New insights into the genetic etiology of Alzheimer's disease and related dementias.
Journal: Nature genetics
Published: June 16, 2021
Last Updated: 09/26/2026