The Role of Calcium Channels in Epilepsy

Por Rajakulendran, Sanjeev, Hanna, Michael G.
Publicado no Cold Spring Harb Perspect Med (2016)

Channeling into the Epilepsies

Por Graves, Tracey D, Hanna, Michael G
Publicado em 2008

Biosafety Considerations of Mammalian-Transmissible H5N1 Influenza

Por Imperiale, Michael J., Hanna, Michael G.
Publicado em 2012

Acute neurology

Por Tomlinson, Susan E, Hanna, Michael G
Publicado no Clin Med (Lond) (2007)

Update in inclusion body myositis

Por Machado, Pedro, Brady, Stefen, Hanna, Michael G.
Publicado em 2013

Active specific immunotherapy: Using tumor heterogeneity to successfully fight cancer

Por Hanna, Michael G, Howard, Jason, Vermorken, Jan
Publicado no Hum Vaccin Immunother (2014)

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

Por Chegounchi, Marjan, Hanna, Michael G, Neild, Guy H
Publicado em 2006

Dysfunction of the Ca(V)2.1 calcium channel in cerebellar ataxias

Por Rajakulendran, Sanjeev, Schorge, Stephanie, Kullmann, Dimitri M, Hanna, Michael G
Publicado em 2010

Sporadic inclusion body myositis: the genetic contributions to the pathogenesis

Por Gang, Qiang, Bettencourt, Conceição, Machado, Pedro, Hanna, Michael G, Houlden, Henry
Publicado em 2014

Variable K(+) channel subunit dysfunction in inherited mutations of KCNA1

Por Rea, Ruth, Spauschus, Alexander, Eunson, Louise H, Hanna, Michael G, Kullmann, Dimitri M
Publicado em 2002

Predominantly myalgic phenotype caused by the c.3466G>A p.A1156T mutation in SCN4A gene

Por Palmio, Johanna, Sandell, Satu, Hanna, Michael G., Männikkö, Roope, Penttilä, Sini, Udd, Bjarne
Publicado no Neurology (2017)

Episodic ataxia type 1 mutations differentially affect neuronal excitability and transmitter release

Por Heeroma, Joost H., Henneberger, Christian, Rajakulendran, Sanjeev, Hanna, Michael G., Schorge, Stephanie, Kullmann, Dimitri M.
Publicado em 2009

IN VIVO ASSESSMENT OF MUSCLE MEMBRANE PROPERTIES IN MYOTONIC DYSTROPHY

Por Tan, S Veronica, Z’Graggen, Werner J, Boërio, Delphine, Turner, Christopher, Hanna, Michael G, Bostock, Hugh
Publicado no Muscle Nerve (2016)

Co-induction of the heat shock response ameliorates disease progression in a mouse model of human spinal and bulbar muscular atrophy: implications for therapy

Por Malik, Bilal, Nirmalananthan, Niranjanan, Gray, Anna L., La Spada, Albert R., Hanna, Michael G., Greensmith, Linda
Publicado em 2013

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

Por Gilbert, Jessica R., Symmonds, Mkael, Hanna, Michael G., Dolan, Raymond J., Friston, Karl J., Moran, Rosalyn J.
Publicado no Neuroimage (2016)

Nerve excitability studies characterize K(V)1.1 fast potassium channel dysfunction in patients with episodic ataxia type 1

Por Tomlinson, Susan E., Tan, S. Veronica, Kullmann, Dimitri M., Griggs, Robert C., Burke, David, Hanna, Michael G., Bostock, Hugh
Publicado em 2010

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

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

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

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

Sar1 GTPase Activity Is Regulated by Membrane Curvature

Por Hanna, Michael G., Mela, Ioanna, Wang, Lei, Henderson, Robert M., Chapman, Edwin R., Edwardson, J. Michael, Audhya, Anjon
Publicado no J Biol Chem (2016)

Familial childhood-onset progressive cerebellar syndrome associated with the ATP1A3 mutation

Por Jaffer, Fatima, Fawcett, Katherine, Sims, David, Heger, Andreas, Houlden, Henry, Hanna, Michael G., Kingston, Helen, Sisodiya, Sanjay M.
Publicado no Neurol Genet (2017)