Mimoun Azzouz
Sheffield, ENG S102HQ, United Kingdom
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 60 publications
Antisense Dipeptide Repeat Proteins Drive Widescale Purine Metabolism Aberration in C9orf72 Amyotrophic Lateral Sclerosis via ADA.
Journal: International journal of molecular sciences
Published: January 25, 2026
Comparison of AAV9-driven motor neuron transduction following different CNS-directed delivery methods in mice.
Journal: Scientific reports
Published: November 14, 2025
Hypothesis-free evaluation of circulating metabolome provides cell-specific insights regarding the role of energy substrate availability in amyotrophic lateral sclerosis.
Journal: BMC medicine
Published: October 08, 2025
The role of NOTCH3 in CADASIL pathogenesis: insights into novel therapies.
Journal: Brain research
Published: April 17, 2025
Gene editing for collagen disorders: current advances and future perspectives.
Journal: Gene therapy
Published: April 05, 2025
Current regulatory requirements for assessment of immunogenicity for gene therapy medicinal products.
Journal: Cell reports. Medicine
Published: February 17, 2025
Retraction Notice to: Corrigendum to "Development of Nonviral Vectors Targeting the Brain as a Therapeutic Approach For Parkinson's Disease and Other Brain Disorders".
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: April 12, 2024
Retraction Notice to: Development of Nonviral Vectors Targeting the Brain as a Therapeutic Approach For Parkinson's Disease and Other Brain Disorders.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: April 12, 2024
RuvBL1/2 reduce toxic dipeptide repeat protein burden in multiple models of C9orf72-ALS/FTD.
Journal: Life science alliance
Published: April 05, 2024
Pre-clinical development of AP4B1 gene replacement therapy for hereditary spastic paraplegia type 47.
Journal: EMBO molecular medicine
Published: March 15, 2024
A systematic review of immunosuppressive protocols used in AAV gene therapy for monogenic disorders.
A systematic review of immunosuppressive protocols used in AAV gene therapy for monogenic disorders.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: February 06, 2024
A cell-penetrant peptide blocking C9ORF72-repeat RNA nuclear export reduces the neurotoxic effects of dipeptide repeat proteins.
Journal: Science translational medicine
Published: March 01, 2023
Last Updated: 09/26/2026