José Luís Muñoz-Blanco

King's College London — United Kingdom

Medicine · Health Sciences

22h-index3.2kcitations60works1.02yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Amyotrophic Lateral Sclerosis Research(20), Neurological diseases and metabolism(11), Genetic Neurodegenerative Diseases(10), Neurogenetic and Muscular Disorders Research(8), Mitochondrial Function and Pathology(7)

Publications57 total

Dynamic modelling of the ALSFRS-R: leveraging population-based scores using neural networks
EBioMedicine·2025· 1 citedOpen Access
Entering the era of precision medicine to treat amyotrophic lateral sclerosis
Molecular Neurodegeneration·2025· 2 citedOpen Access
Immune-mediated necrotizing myopathy: an emerging disorder
Neurología (English Edition)·2025· 1 citedOpen Access
Miopatía necrosante inmunomediada: experiencia en una unidad neuromuscular
Neurología·2024Open Access
Patients with transthyretin amyloidosis enrolled in THAOS between 2018 and 2021 continue to experience substantial diagnostic delay
Amyloid·2023· 13 citedOpen Access
Should Advanced Friedreich’s Ataxia Be a Contraindication for Heart Transplantation? A Case Report of a Successful Procedure in a 58-Year-Old Patient
Journal of Cardiovascular Development and Disease·2022· 1 citedOpen Access
Tract-specific damage at spinal cord level in pure hereditary spastic paraplegia type 4: a diffusion tensor imaging study
Journal of Neurology·2022· 6 cited
Corticospinal tract and motor cortex degeneration in pure hereditary spastic paraparesis type 4 (SPG4)
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration·2021· 11 cited
Thalamic atrophy in patients with pure hereditary spastic paraplegia type 4
Journal of Neurology·2021· 11 cited
Neurological complications of COVID‐19 in hospitalized patients: The registry of a neurology department in the first wave of the pandemic
European Journal of Neurology·2021· 41 citedOpen Access
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis
Neuron·2020· 80 citedOpen Access
Altered Secretome and ROS Production in Olfactory Mucosa Stem Cells Derived from Friedreich’s Ataxia Patients
International Journal of Molecular Sciences·2020· 8 citedOpen Access
Upper trunk brachial plexopathy as a consequence of prone positioning due to <scp>SARS‐CoV</scp>‐2 acute respiratory distress syndrome
Muscle & Nerve·2020· 21 cited
Immunoserologic Detection and Diagnostic Relevance of Cross-Reactive Autoantibodies in Coronavirus Disease 2019 Patients
The Journal of Infectious Diseases·2020· 22 citedOpen Access
Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease
Neurología (English Edition)·2020· 26 citedOpen Access
Ocular Involvement in Friedreich Ataxia Patients and Its Relationship with Neurological Disability, a Follow-Up Study
Diagnostics·2020· 17 citedOpen Access
Spanish Pompe registry: Baseline characteristics of first 49 patients with adult onset of Pompe disease
Medicina Clínica (English Edition)·2020· 9 cited
Reply to: “Mitochondrial Parkinsonism due to <i>SPG7/Paraplegin</i> variants with secondary mtDNA depletion”
Movement Disorders·2019
Changes in Retinal OCT and Their Correlations with Neurological Disability in Early ALS Patients, a Follow-Up Study
Brain Sciences·2019· 38 citedOpen Access
P.395Spanish Pompe registry: baseline characteristics of first 49 patients with adult onset of Pompe disease
Neuromuscular Disorders·2019
page 1 of 3Next →

Frequent Co-authors

Alberto García‐Redondo(11), Jesús Esteban‐Pérez(10), Roberto Fernández‐Torrón(10), Jordi Díaz‐Manera(8), Pamela J. Shaw(7), Ricard Rojas‐García(7), Irene Catalina(7), Ivonne Jericó(7), Francisco Grandas(7), Kevin P. Kenna(6), Orla Hardiman(6), Adolfo López de Munaín(6), Míriam Almendrote(6), Alba Ramos‐Fransí(6), Nicola Ticozzi(5), Simon Topp(5), Jack W. Miller(5), Caroline Vance(5), Meraida Polak(5), Isabel Illa(5)