Resultados da pesquisa - Amouri, Rim

ATP13A2 variability in Parkinson disease Por Vilariño-Güell, Carles, Soto, Alexandra I., Lincoln, Sarah J., Yahmed, Samia Ben, Kefi, Mounir, Heckman, Michael G., Hulihan, Mary M., Chai, Hua, Diehl, Nancy N., Amouri, Rim, Rajput, Alex, Mash, Deborah C., Dickson, Dennis W., Middleton, Lefkos T., Gibson, Rachel A., Hentati, Faycal, Farrer, Matthew J.

Obter o texto integral Obter o texto integral Obter o texto integral

Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity Por Hammer, Monia B., Eleuch-Fayache, Ghada, Schottlaender, Lucia V., Nehdi, Houda, Gibbs, J. Raphael, Arepalli, Sampath K., Chong, Sean B., Hernandez, Dena G., Sailer, Anna, Liu, Guoxiang, Mistry, Pramod K., Cai, Huaibin, Shrader, Ginamarie, Sassi, Celeste, Bouhlal, Yosr, Houlden, Henry, Hentati, Fayçal, Amouri, Rim, Singleton, Andrew B.

Obter o texto integral Obter o texto integral Obter o texto integral

Defects in the CAPN1 gene result in alterations in cerebellar development and in cerebellar ataxia in mice and humans Por Wang, Yubin, Hersheson, Joshua, Lopez, Dulce, Hamad, Monia Ben, Liu, Yan, Lee, Ka-Hung, Pinto, Vanessa, Seinfeld, Jeff, Wiethoff, Sarah, Sun, Jiandong, Amouri, Rim, Hentati, Faycal, Baudry, Neema, Tran, Jennifer, Singleton, Andrew B, Coutelier, Marie, Brice, Alexis, Stevanin, Giovanni, Durr, Alexandra, Bi, Xiaoning, Houlden, Henry, Baudry, Michel

Obter o texto integral Obter o texto integral Obter o texto integral

SLC25A46 mutations associated with Autosomal Recessive Cerebellar Ataxia in North African families Por Hammer, Monia B., Ding, Jinhui, Mochel, Fanny, Eleuch-Fayache, Ghada, Charles, Perrine, Coutelier, Marie, Gibbs, J. Raphael, Arepalli, Sampath K., Chong, Sean B., Hernandez, Dena G., Majounie, Elisa, Clipman, Steven, Bouhlal, Yosr, Nehdi, Houda, Brice, Alexis, Hentati, Faycal, Stevanin, Giovanni, Amouri, Rim, Durr, Alexandra, Singleton, Andrew B.

Obter o texto integral Obter o texto integral Obter o texto integral

Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia Por Wagner, Matias, Osborn, Daniel P. S., Gehweiler, Ina, Nagel, Maike, Ulmer, Ulrike, Bakhtiari, Somayeh, Amouri, Rim, Boostani, Reza, Hentati, Faycal, Hockley, Maryam M., Hölbling, Benedikt, Schwarzmayr, Thomas, Karimiani, Ehsan Ghayoor, Kernstock, Christoph, Maroofian, Reza, Müller-Felber, Wolfgang, Ozkan, Ege, Padilla-Lopez, Sergio, Reich, Selina, Reichbauer, Jennifer, Darvish, Hossein, Shahmohammadibeni, Neda, Tafakhori, Abbas, Vill, Katharina, Zuchner, Stephan, Kruer, Michael C., Winkelmann, Juliane, Jamshidi, Yalda, Schüle, Rebecca

Obter o texto integral Obter o texto integral Obter o texto integral