Alexander Lossos
The Agnes Ginges Center for Human Neurogenetics
Dept. of Neurology
Hadassah University Hospital
POB 12000
Israel
Name/email consistency: high
- Phenotypic variability among adult siblings with Sjögren-Larsson syndrome. Lossos, A., Khoury, M., Rizzo, W.B., Gomori, J.M., Banin, E., Zlotogorski, A., Jaber, S., Abramsky, O., Argov, Z., Rosenmann, H. Arch. Neurol. (2006)
- Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneity. Lossos, A., Stevanin, G., Meiner, V., Argov, Z., Bouslam, N., Newman, J.P., Gomori, J.M., Klebe, S., Lerer, I., Elleuch, N., Silverstein, S., Durr, A., Abramsky, O., Ben-Nariah, Z., Brice, A. Arch. Neurol. (2006)
- A novel autosomal recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12. Lossos, A., Baala, L., Soffer, D., Averbuch-Heller, L., Dotan, S., Munnich, A., Lyonnet, S., Gomori, J.M., Genem, A., Neufeld, M., Abramsky, O., Zlotogora, J., Argov, Z. Brain (2005)
- Extended phenotype in the transthyretin Tyr77 familial amyloid polyneuropathy. Lossos, A., Soffer, D., Steiner-Birmanns, B., Hassin-Baer, S., Sadeh, M., Sagi, M., Linetski, E., Abramsky, O., Argov, Z., Rosenmann, H. Eur. Neurol. (2005)
- Early clinical heterogeneity in choreoacanthocytosis. Lossos, A., Dobson-Stone, C., Monaco, A.P., Soffer, D., Rahamim, E., Newman, J.P., Mohiddin, S., Fananapazir, L., Lerer, I., Linetsky, E., Reches, A., Argov, Z., Abramsky, O., Gadoth, N., Sadeh, M., Gomori, J.M., Boher, M., Meiner, V. Arch. Neurol. (2005)
- Late-delayed cerebral involvement in systemic non-Hodgkin lymphoma: a second primary tumor or a tardy recurrence?. Lossos, A., Ashhab, Y., Sverdlin, E., Amir, G., Ben-Yehuda, D., Siegal, T. Cancer (2004)
- Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family. Lossos, A., Reches, A., Gal, A., Newman, J.P., Soffer, D., Gomori, J.M., Boher, M., Ekstein, D., Biran, I., Meiner, Z., Abramsky, O., Rosenmann, H. J. Neurol. (2003)