Biosafety Considerations of Mammalian-Transmissible H5N1 Influenza

by Imperiale, Michael J., Hanna, Michael G.
Published 2012

Update in inclusion body myositis

by Machado, Pedro, Brady, Stefen, Hanna, Michael G.
Published 2013

Progressive neurological disease induced by tacrolimus in a renal transplant recipient: Case presentation

by Chegounchi, Marjan, Hanna, Michael G, Neild, Guy H
Published 2006

Sporadic inclusion body myositis: the genetic contributions to the pathogenesis

by Gang, Qiang, Bettencourt, Conceição, Machado, Pedro, Hanna, Michael G, Houlden, Henry
Published 2014

Reproducibility, and age, body-weight and gender dependency of candidate skeletal muscle MRI outcome measures in healthy volunteers

by Morrow, Jasper M., Sinclair, Christopher D. J., Fischmann, Arne, Reilly, Mary M., Hanna, Michael G., Yousry, Tarek A., Thornton, John S.
Published 2014

Endoplasmic reticulum stress in spinal and bulbar muscular atrophy: a potential target for therapy

by Montague, Karli, Malik, Bilal, Gray, Anna L., La Spada, Albert R., Hanna, Michael G., Szabadkai, Gyorgy, Greensmith, Linda
Published 2014

Sar1 GTPase Activity Is Regulated by Membrane Curvature*♦

by Hanna, Michael G., Mela, Ioanna, Wang, Lei, Henderson, Robert M., Chapman, Edwin R., Edwardson, J. Michael, Audhya, Anjon
Published 2016

Profiling neuronal ion channelopathies with non-invasive brain imaging and dynamic causal models: Case studies of single gene mutations

by Gilbert, Jessica R., Symmonds, Mkael, Hanna, Michael G., Dolan, Raymond J., Friston, Karl J., Moran, Rosalyn J.
Published 2016

Whole-genome sequencing and the clinician: a tale of two cities

by Foley, A Reghan, Pitceathly, Robert D S, He, Jie, Kim, Jihee, Pearson, Nathaniel M, Muntoni, Francesco, Hanna, Michael G
Published 2014

Candidate Screening of the TRPC3 Gene in Cerebellar Ataxia

by Becker, Esther B. E., Fogel, Brent L., Rajakulendran, Sanjeev, Dulneva, Anna, Hanna, Michael G., Perlman, Susan L., Geschwind, Daniel H., Davies, Kay E.
Published 2011

Muscle MRI reveals distinct abnormalities in genetically proven non-dystrophic myotonias☆

by Morrow, Jasper M., Matthews, Emma, Raja Rayan, Dipa L., Fischmann, Arne, Sinclair, Christopher D.J., Reilly, Mary M., Thornton, John S., Hanna, Michael G., Yousry, Tarek A.
Published 2013

Correlation of clinical and molecular features in spinal bulbar muscular atrophy

by Fratta, Pietro, Nirmalananthan, Niranjanan, Masset, Luc, Skorupinska, Iwona, Collins, Toby, Cortese, Andrea, Pemble, Sally, Malaspina, Andrea, Fisher, Elizabeth M.C., Greensmith, Linda, Hanna, Michael G.
Published 2014

Sequencing analysis of the spinal bulbar muscular atrophy CAG expansion reveals absence of repeat interruptions☆

by Fratta, Pietro, Collins, Toby, Pemble, Sally, Nethisinghe, Suran, Devoy, Anny, Giunti, Paola, Sweeney, Mary G., Hanna, Michael G., Fisher, Elizabeth M.C.
Published 2014

SIGMAR1 mutation associated with autosomal recessive Silver-like syndrome

by Horga, Alejandro, Tomaselli, Pedro J., Gonzalez, Michael A., Laurà, Matilde, Muntoni, Francesco, Manzur, Adnan Y., Hanna, Michael G., Blake, Julian C., Houlden, Henry, Züchner, Stephan, Reilly, Mary M.
Published 2016

MRI biomarker assessment of neuromuscular disease progression: a prospective observational cohort study

by Morrow, Jasper M, Sinclair, Christopher D J, Fischmann, Arne, Machado, Pedro M, Reilly, Mary M, Yousry, Tarek A, Thornton, John S, Hanna, Michael G
Published 2016

In vivo impact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2

by Tomlinson, Susan E., Tan, S. Veronica, Burke, David, Labrum, Robyn W., Haworth, Andrea, Gibbons, Vaneesha S., Sweeney, Mary G., Griggs, Robert C., Kullmann, Dimitri M., Bostock, Hugh, Hanna, Michael G.
Published 2016

NDUFA4 Mutations Underlie Dysfunction of a Cytochrome c Oxidase Subunit Linked to Human Neurological Disease

by Pitceathly, Robert D.S., Rahman, Shamima, Wedatilake, Yehani, Polke, James M., Cirak, Sebahattin, Foley, A. Reghan, Sailer, Anna, Hurles, Matthew E., Stalker, Jim, Hargreaves, Iain, Woodward, Cathy E., Sweeney, Mary G., Muntoni, Francesco, Houlden, Henry, Taanman, Jan-Willem, Hanna, Michael G.
Published 2013

Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy☆

by Cortese, Andrea, Plagnol, Vincent, Brady, Stefen, Simone, Roberto, Lashley, Tammaryn, Acevedo-Arozena, Abraham, de Silva, Rohan, Greensmith, Linda, Holton, Janice, Hanna, Michael G., Fisher, Elizabeth M.C., Fratta, Pietro
Published 2014

NDUFA4 Mutations Underlie Dysfunction of a Cytochrome c Oxidase Subunit Linked to Human Neurological Disease

by Pitceathly, Robert D.S., Rahman, Shamima, Wedatilake, Yehani, Polke, James M., Cirak, Sebahattin, Foley, A. Reghan, Sailer, Anna, Hurles, Matthew E., Stalker, Jim, Hargreaves, Iain, Woodward, Cathy E., Sweeney, Mary G., Muntoni, Francesco, Houlden, Henry, Taanman, Jan-Willem, Hanna, Michael G.
Published 2013

Stability and sensitivity of water T 2 obtained with IDEAL‐CPMG in healthy and fat‐infiltrated skeletal muscle

by Sinclair, Christopher D.J., Morrow, Jasper M., Janiczek, Robert L., Evans, Matthew R.B., Rawah, Elham, Shah, Sachit, Hanna, Michael G., Reilly, Mary M., Yousry, Tarek A., Thornton, John S.
Published 2016