Biosafety Considerations of Mammalian-Transmissible H5N1 Influenza

por Imperiale, Michael J., Hanna, Michael G.
Publicado 2012

Update in inclusion body myositis

por Machado, Pedro, Brady, Stefen, Hanna, Michael G.
Publicado 2013

COVID‐19 infection and vaccination in patients with skeletal muscle channelopathies

por Vivekanandam, Vinojini, Jayaseelan, Dipa, Hanna, Michael G.
Publicado 2022

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

por Chegounchi, Marjan, Hanna, Michael G, Neild, Guy H
Publicado 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 2010

Sporadic inclusion body myositis: the genetic contributions to the pathogenesis

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

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 2017

Cardiolipin, Mitochondria, and Neurological Disease

por Falabella, Micol, Vernon, Hilary J., Hanna, Michael G., Claypool, Steven M., Pitceathly, Robert D.S.
Publicado 2021

SHIP164 is a chorein motif lipid transfer protein that controls endosome–Golgi membrane traffic

por Hanna, Michael G., Suen, Patreece H., Wu, Yumei, Reinisch, Karin M., De Camilli, Pietro
Publicado 2022

Gene expression analysis reveals early dysregulation of disease pathways and links Chmp7 to pathogenesis of spinal and bulbar muscular atrophy

por Malik, Bilal, Devine, Helen, Patani, Rickie, La Spada, Albert R., Hanna, Michael G., Greensmith, Linda
Publicado 2019

Sodium channel myotonia may be associated with high-risk brief resolved unexplained events

por Cea, Gabriel, Andreu, Daniel, Fletcher, Elaine, Ramdas, Sithara, Sud, Richa, Hanna, Michael G., Matthews, Emma
Publicado 2020

VPS13D bridges the ER to mitochondria and peroxisomes via Miro

por Guillén-Samander, Andrés, Leonzino, Marianna, Hanna, Michael G., Tang, Ni, Shen, Hongying, De Camilli, Pietro
Publicado 2021

Correction: VPS13D bridges the ER to mitochondria and peroxisomes via Miro

por Guillén-Samander, Andrés, Leonzino, Marianna, Hanna, Michael G., Tang, Ni, Shen, Hongying, De Camilli, Pietro
Publicado 2021

Mitochondrial Strokes: Diagnostic Challenges and Chameleons

por Pizzamiglio, Chiara, Bugiardini, Enrico, Macken, William L., Woodward, Cathy E., Hanna, Michael G., Pitceathly, Robert D. S.
Publicado 2021

The Sar1 GTPase is dispensable for COPII-dependent cargo export from the ER

por Kasberg, William, Luong, Peter, Hanna, Michael G., Minushkin, Kayla, Tsao, Annabelle, Shankar, Raakhee, Block, Samuel, Audhya, Anjon
Publicado 2023

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 2016

Correction to: Episodic Ataxia Type 1: Natural History and Effect on Quality of Life

por Graves, Tracey D., Griggs, Robert C., Bundy, Brian N., Jen, Joanna C., Baloh, Robert W., Hanna, Michael G.
Publicado 2022

Episodic Ataxia Type 1: Natural History and Effect on Quality of Life

por Graves, Tracey D., Griggs, Robert C., Bundy, Brian N., Jen, Joanna C., Baloh, Robert W., Hanna, Michael G.
Publicado 2022

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 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 2014