30 May 2026Open access
COXFA4L2 upregulation preserves residual cytochrome c oxidase activity in COXFA4-related Leigh-like encephalopathyPublisher siteNature Communications, Mitochondrial Function and Pathology
UniversitiesMichael G. Hanna
Active, last published 2026
In genetic neurodegenerative diseases
Michael G.
Hanna
Scholar“Research focused on Genetic Neurodegenerative Diseases and adjacent fields.”
National Hospital for Neurology and Neurosurgery
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01 · About the work
What I study
ichael G. Hanna is a researcher working on Genetic Neurodegenerative Diseases. A fuller summary will appear once they update their profile.
02 · Reach
Publication output and reach
Michael's work has been cited 41,546 times across 2 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
03 · Research focus
Topics
Genetic Neurodegenerative Diseases×223Ion channel regulation and function×180Mitochondrial Function and Pathology×176Metabolism and Genetic Disorders×111Muscle Physiology and Disorders×100
04 · Where I am
Affiliations
Affiliation on published researchNational Hospital for Neurology and NeurosurgeryDrawn from the institution listed on this researcher’s published work.
05 · Selected work
Recent publications
5 works1 Oct 2024
Comparative Study between Ultrasound Guided Quadratus Lumborum Block vs Intraperitoneal and Perioportal Bupivacaine Infiltration as Post Operative Analgesia after Laparoscopic CholecystectomyPublisher siteQJM, Anesthesia and Pain Management
2 Aug 2024Open access1cites
Extended Phenotype of <i>PEX11B</i> Pathogenic Variants: Ataxia, Tremor, and Dystonia Due to a Novel C.2T > G VariantPublisher siteMovement Disorders Clinical Practice, Genetics and Neurodevelopmental Disorders
2 Aug 2024Open access2cites
Mitochondrial DNA disorders in neuromuscular diseases in diverse populationsPublisher siteAnnals of Clinical and Translational Neurology, Mitochondrial Function and Pathology
14 May 2024Open access1cites
Biallelic variants in <i>ARHGAP19</i> cause a motor-predominant neuropathy with asymmetry and conduction slowingPublisher siteExpert Academic Profiles go further
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