An update on advances in magnetic resonance imaging of multiple system atrophy

por Chelban, Viorica, Bocchetta, Martina, Hassanein, Sara, Haridy, Nourelhoda A., Houlden, Henry, Rohrer, Jonathan D.
Publicado 2018

Severe axonal neuropathy is a late manifestation of SPG11

por Manole, Andreea, Chelban, Viorica, Haridy, Nourelhoda A., Hamed, Sherifa A., Berardo, Andrés, Reilly, Mary M., Houlden, Henry
Publicado 2016

Myasthenia gravis with achalasia secondary to thymoma: a case report and literature review

por Haridy, Nourelhoda A., Khedr, Eman M., Hasan, Asmaa M., Maghraby, Ahmed A., Abdelmohsen, Essam, Aly, AbdelHamid M.
Publicado 2023

Sequencing analysis of the SCA6 CAG expansion excludes an influence of repeat interruptions on disease onset

por Wiethoff, Sarah, O’Connor, Emer, Haridy, Nourelhoda A, Nethisinghe, Suran, Wood, Nicholas, Giunti, Paola, Bettencourt, Conceição, Houlden, Henry
Publicado 2018

Genotype‐phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14

por Chelban, Viorica, Wiethoff, Sarah, Fabian‐Jessing, Bjørn K., Haridy, Nourelhoda A., Khan, Alaa, Efthymiou, Stephanie, Becker, Esther B. E., O'Connor, Emer, Hersheson, Joshua, Newland, Katrina, Hojland, Allan Thomas, Gregersen, Pernille A., Lindquist, Suzanne G., Petersen, Michael B., Nielsen, Jørgen E., Nielsen, Michael, Wood, Nicholas W., Giunti, Paola, Houlden, Henry
Publicado 2018

Genetic and phenotypic characterization of complex hereditary spastic paraplegia

por Kara, Eleanna, Tucci, Arianna, Manzoni, Claudia, Lynch, David S., Elpidorou, Marilena, Bettencourt, Conceicao, Chelban, Viorica, Manole, Andreea, Hamed, Sherifa A., Haridy, Nourelhoda A., Federoff, Monica, Preza, Elisavet, Hughes, Deborah, Pittman, Alan, Jaunmuktane, Zane, Brandner, Sebastian, Xiromerisiou, Georgia, Wiethoff, Sarah, Schottlaender, Lucia, Proukakis, Christos, Morris, Huw, Warner, Tom, Bhatia, Kailash P., Korlipara, L.V. Prasad, Singleton, Andrew B., Hardy, John, Wood, Nicholas W., Lewis, Patrick A., Houlden, Henry
Publicado 2016

PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation

por Chelban, Viorica, Wilson, Matthew P., Warman Chardon, Jodi, Vandrovcova, Jana, Zanetti, M. Natalia, Zamba‐Papanicolaou, Eleni, Efthymiou, Stephanie, Pope, Simon, Conte, Maria R., Abis, Giancarlo, Liu, Yo‐Tsen, Tribollet, Eloise, Haridy, Nourelhoda A., Botía, Juan A., Ryten, Mina, Nicolaou, Paschalis, Minaidou, Anna, Christodoulou, Kyproula, Kernohan, Kristin D., Eaton, Alison, Osmond, Matthew, Ito, Yoko, Bourque, Pierre, Jepson, James E. C., Bello, Oscar, Bremner, Fion, Cordivari, Carla, Reilly, Mary M., Foiani, Martha, Heslegrave, Amanda, Zetterberg, Henrik, Heales, Simon J. R., Wood, Nicholas W., Rothman, James E., Boycott, Kym M., Mills, Philippa B., Clayton, Peter T., Houlden, Henry
Publicado 2019