The Role of Interruptions in polyQ in the Pathology of SCA1

Por Menon, Rajesh P., Nethisinghe, Suran, Faggiano, Serena, Vannocci, Tommaso, Rezaei, Human, Pemble, Sally, Sweeney, Mary G., Wood, Nicholas W., Davis, Mary B., Pastore, Annalisa, Giunti, Paola
Publicado em 2013

Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy

Por Rajakulendran, Sanjeev, Graves, Tracey D, Labrum, Robyn W, Kotzadimitriou, Dimitrios, Eunson, Louise, Davis, Mary B, Davies, Rosalyn, Wood, Nicholas W, Kullmann, Dimitri M, Hanna, Michael G, Schorge, Stephanie
Publicado em 2010

Prevalence study of genetically defined skeletal muscle channelopathies in England

Por Horga, Alejandro, Raja Rayan, Dipa L., Matthews, Emma, Sud, Richa, Fialho, Doreen, Durran, Siobhan C.M., Burge, James A., Portaro, Simona, Davis, Mary B., Haworth, Andrea, Hanna, Michael G.
Publicado em 2013

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology

Por Catarino, Claudia B., Liu, Joan Y.W., Liagkouras, Ioannis, Gibbons, Vaneesha S., Labrum, Robyn W., Ellis, Rachael, Woodward, Cathy, Davis, Mary B., Smith, Shelagh J., Cross, J. Helen, Appleton, Richard E., Yendle, Simone C., McMahon, Jacinta M., Bellows, Susannah T., Jacques, Thomas S., Zuberi, Sameer M., Koepp, Matthias J., Martinian, Lillian, Scheffer, Ingrid E., Thom, Maria, Sisodiya, Sanjay M.
Publicado em 2011