The inherited ataxias and the new genetics.

Por Hammans, S R
Publicado em 1996

Superior sagittal sinus thrombosis in Wegener's granulomatosis.

Por Hammans, S R, Ginsberg, L
Publicado em 1989

Chronic relapsing inflammatory polyneuropathy complicating sicca syndrome.

Por Barnes, D, Hammans, S R, Legg, N J
Publicado em 1988

Influence of obtaining a neurological opinion on the diagnosis and management of hospital inpatients.

Por Steiger, M J, Enevoldson, T P, Hammans, S R, Ginsberg, L
Publicado em 1996

Oculopharyngeal muscular dystrophy: a point mutation which mimics the effect of the PABPN1 gene triplet repeat expansion mutation

Por Robinson, D O, Wills, A J, Hammans, S R, Read, S P, Sillibourne, J
Publicado em 2006

Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA.

Por McShane, M A, Hammans, S R, Sweeney, M, Holt, I J, Beattie, T J, Brett, E M, Harding, A E
Publicado em 1991

ADCY5-related dyskinesia presenting as familial myoclonus-dystonia

Por Douglas, Andrew G. L., Andreoletti, Gaia, Talbot, Kevin, Hammans, Simon R., Singh, Jaspal, Whitney, Andrea, Ennis, Sarah, Foulds, Nicola C.
Publicado no Neurogenetics (2017)

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia Caused by a Novel R782G Mutation in CSF1R

Por Foulds, Nicola, Pengelly, Reuben J., Hammans, Simon R., Nicoll, James A. R., Ellison, David W., Ditchfield, Adam, Beck, Sarah, Ennis, Sarah
Publicado no Sci Rep (2015)

Pathogenic Mitochondrial tRNA Point Mutations: Nine Novel Mutations Affirm Their Importance as a Cause of Mitochondrial Disease

Por Blakely, Emma L, Yarham, John W, Alston, Charlotte L, Craig, Kate, Poulton, Joanna, Brierley, Charlotte, Park, Soo-Mi, Dean, Andrew, Xuereb, John H, Anderson, Kirstie N, Compston, Alistair, Allen, Chris, Sharif, Saba, Enevoldson, Peter, Wilson, Martin, Hammans, Simon R, Turnbull, Douglass M, McFarland, Robert, Taylor, Robert W
Publicado em 2013

New NBIA subtype: Genetic, clinical, pathologic, and radiographic features of MPAN

Por Hogarth, Penelope, Gregory, Allison, Kruer, Michael C., Sanford, Lynn, Wagoner, Wendy, Natowicz, Marvin R., Egel, Robert T., Subramony, S.H., Goldman, Jennifer G., Berry-Kravis, Elizabeth, Foulds, Nicola C., Hammans, Simon R., Desguerre, Isabelle, Rodriguez, Diana, Wilson, Callum, Diedrich, Andrea, Green, Sarah, Tran, Huong, Reese, Lindsay, Woltjer, Randall L., Hayflick, Susan J.
Publicado em 2013

Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy

Por Halter, Joerg P., Michael, W., Schüpbach, M., Mandel, Hanna, Casali, Carlo, Orchard, Kim, Collin, Matthew, Valcarcel, David, Rovelli, Attilio, Filosto, Massimiliano, Dotti, Maria T., Marotta, Giuseppe, Pintos, Guillem, Barba, Pere, Accarino, Anna, Ferra, Christelle, Illa, Isabel, Beguin, Yves, Bakker, Jaap A., Boelens, Jaap J., de Coo, Irenaeus F. M., Fay, Keith, Sue, Carolyn M., Nachbaur, David, Zoller, Heinz, Sobreira, Claudia, Pinto Simoes, Belinda, Hammans, Simon R., Savage, David, Martí, Ramon, Chinnery, Patrick F., Elhasid, Ronit, Gratwohl, Alois, Hirano, Michio
Publicado no Brain (2015)