Michael Hanna

234 th ENMC International Workshop: Chaperone dysfunction in muscle disease December 8-10th 2017, Naarden, Netherlands

C. Weihl, B. Udd, Michael Hanna, 2019 .

Bi-allelic LETM1 variants perturb mitochondrial ion homeostasis leading to a clinical spectrum with predominant nervous system involvement

E. Bertini, R. Carrozzo, H. Prokisch, 2022, American journal of human genetics.

PRRT2 gene mutations

D. Kullmann, S. Schneider, M. Stamelou, 2012, Neurology.

Downregulation of myostatin pathway in neuromuscular diseases may explain challenges of anti-myostatin therapeutic approaches

F. Muntoni, L. Servais, T. Maisonobe, 2017, Nature Communications.

Expanding SPTAN1 monoallelic variant associated disorders: From epileptic encephalopathy to pure spastic paraplegia and ataxia

A. Need, C. Tregidgo, J. Clayton-Smith, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

The mutational profile in a South African cohort with inherited neuropathies and spastic paraplegia

M. Benatar, M. Reilly, J. Wilmshurst, 2023, Frontiers in neurology.

Amplifying the Heat Shock Response Ameliorates ALS and FTD Pathology in Mouse and Human Models

L. Greensmith, R. Patani, Mhoriam Ahmed, 2023, Molecular Neurobiology.