Progressive cerebellar degeneration revealing Primary Sjögren Syndrome: a case report

द्वारा Farhat, Emna, Zouari, Mourad, Abdelaziz, Ines Ben, Drissi, Cyrine, Beyrouti, Rahma, Hammouda, Mohamed Ben, Hentati, Fayçal
में प्रकाशित Cerebellum Ataxias (2016)

Inhibition of LRRK2 kinase activity leads to dephosphorylation of Ser(910)/Ser(935), disruption of 14-3-3 binding and altered cytoplasmic localization

द्वारा Dzamko, Nicolas, Deak, Maria, Hentati, Faycal, Reith, Alastair D., Prescott, Alan R., Alessi, Dario R., Nichols, R. Jeremy
प्रकाशित 2010

Primary Spinal Hydatidosis Revealed by Spinal Cord Compression

द्वारा Bouattour, Nadia, Nabli, Fatma, Nagi, Sonia, Saied, Zakaria, Ben Abdelaziz, Ines, Hentati, Fayçal, Belal, Samir, Ben Sassi, Samia
में प्रकाशित Neurol Clin Pract (2021)

Genetic variation of the mitochondrial Complex I subunit NDUFV2 and Parkinson disease

द्वारा Nishioka, Kenya, Vilariño-Güell, Carles, Cobb, Stephanie A., Kachergus, Jennifer M., Ross, Owen A., Hentati, Emna, Hentati, Faycal, Farrer, Matthew J.
में प्रकाशित Parkinsonism Relat Disord (2010)

Glucocerebrosidase mutations are not a common risk factor for Parkinson disease in North Africa

द्वारा Nishioka, Kenya, Vilariño-Güell, Carles, Cobb, Stephanie A., Kachergus, Jennifer M., Ross, Owen A., Wider, Christian, Gibson, Rachel A., Hentati, Faycal, Farrer, Matthew J.
प्रकाशित 2009

Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus

द्वारा Belal, Samir, Panayides, Kyproula, Sirugo, Giorgio, Hamida, Christiane Ben, Ioannou, Panos, Hentati, Fayçal, Beckmann, Jacques, Koenig, Michel, Mandel, Jean-Louis, Hamida, Mongi Ben, Middleton, Lefkos T.
प्रकाशित 1992

Exome sequencing: an efficient diagnostic tool for complex neurodegenerative disorders

द्वारा Hammer, Monia B, Eleuch-Fayache, Ghada, Gibbs, J Raphael, Arepalli, Sampath K, Chong, Sean B, Sassi, Celeste, Bouhlal, Yosr, Hentati, Fayçal, Amouri, Rim, Singleton, Andrew B
में प्रकाशित Eur J Neurol (2012)

Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron Degeneration

द्वारा Tsaousidou, Maria K., Ouahchi, Karim, Warner, Tom T., Yang, Yi, Simpson, Michael A., Laing, Nigel G., Wilkinson, Philip A., Madrid, Ricardo E., Patel, Heema, Hentati, Faycal, Patton, Michael A., Hentati, Afif, Lamont, Philippa J., Siddique, Teepu, Crosby, Andrew H.
प्रकाशित 2008

Recombinations in Individuals Homozygous by Descent Localize the Friedreich Ataxia Locus in a Cloned 450-kb Interval

द्वारा Rodius, François, Duclos, Franck, Wrogemann, Klaus, Le Paslier, Denis, Ougen, Pierre, Billault, Alain, Belal, Samir, Musenger, Christine, Brice, Alexis, Dürr, Alexandra, Mignard, Claude, Sirugo, Giorgio, Weissenbach, Jean, Cohen, Daniel, Hentati, Fayçal, Hamida, Mongi Ben, Mandel, Jean-Louis, Koenig, Michel
प्रकाशित 1994

Heterodimerization of Lrrk1-Lrrk2: Implications for LRRK2-associated Parkinson disease

द्वारा Dachsel, Justus C., Nishioka, Kenya, Vilariño-Güell, Carles, Lincoln, Sarah J., Soto-Ortolaza, Alexandra I., Kachergus, Jennifer, Hinkle, Kelly M., Heckman, Michael G., Jasinska-Myga, Barbara, Taylor, Julie P., Dickson, Dennis W., Gibson, Rachel A., Hentati, Faycal, Ross, Owen A., Farrer, Matthew J.
प्रकाशित 2010

ATP13A2 variability in Parkinson disease

द्वारा 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.
प्रकाशित 2009

A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia

द्वारा Ben Ammar, Asma, Soltanzadeh, Payam, Bauché, Stéphanie, Richard, Pascale, Goillot, Evelyne, Herbst, Ruth, Gaudon, Karen, Huzé, Caroline, Schaeffer, Laurent, Yamanashi, Yuji, Higuchi, Osamu, Taly, Antoine, Koenig, Jeanine, Leroy, Jean-Paul, Hentati, Fayçal, Najmabadi, Hossein, Kahrizi, Kimia, Ilkhani, Manouchehr, Fardeau, Michel, Eymard, Bruno, Hantaï, Daniel
प्रकाशित 2013

Correction: A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia

द्वारा Ben Ammar, Asma, Soltanzadeh, Payam, Bauché, Stéphanie, Richard, Pascale, Goillot, Evelyne, Herbst, Ruth, Gaudon, Karen, Huzé, Caroline, Schaeffer, Laurent, Yamanashi, Yuji, Higuchi, Osamu, Taly, Antoine, Koenig, Jeanine, Leroy, Jean-Paul, Hentati, Fayçal, Najmabadi, Hossein, Kahrizi, Kimia, Ilkhani, Manouchehr, Fardeau, Michel, Eymard, Bruno, Hantaï, Daniel
प्रकाशित 2013

Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity

द्वारा 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.
प्रकाशित 2013

Defects in the CAPN1 gene result in alterations in cerebellar development and in cerebellar ataxia in mice and humans

द्वारा 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
में प्रकाशित Cell Rep (2016)

SLC25A46 mutations associated with Autosomal Recessive Cerebellar Ataxia in North African families

द्वारा 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.
में प्रकाशित Neurodegener Dis (2017)

Ataxia with Vitamin E Deficiency: Refinement of Genetic Localization and Analysis of Linkage Disequilibrium by Using New Markers in 14 Families

द्वारा Doerflinger, Nathalie, Linder, Catherine, Ouahchi, Karim, Gyapay, Gabor, Weissenbach, Jean, Le Paslier, Denis, Rigault, Philippe, Belal, Samir, Hamida, Christiane Ben, Hentati, Faycal, Hamida, Mongi Ben, Pandolfo, Massimo, DiDonato, Stephano, Sokol, Ronald, Kayden, Herbert, Landrieu, Pierre, Durr, Alexandra, Brice, Alexis, Goutières, Françoise, Kohlschütter, Alfried, Sabouraud, Pascal, Benomar, Ali, Yahyaoui, Mohamed, Mandel, Jean-Louis, Koenig, Michel
प्रकाशित 1995

Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia

द्वारा 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
में प्रकाशित Nat Commun (2019)

Michael J. Fox Foundation Consortium: Geographical Differences in Returning Genetic Research Data to Study Participants

द्वारा Alcalay, Roy N., Aasly, Jan, Berg, Daniela, Bressman, Susan, Brice, Alexis, Brockmann, Kathrin, Chan, Piu, Clark, Lorraine, Corvol, Jean-Christophe, Durr, Alexandra, Farrer, Matthew, Foroud, Tatiana M., Gasser, Thomas, Giladi, Nir, Halter, Cheryl, Hentati, Fayçal, Lang, Anthony, Langston, J. William, Marder, Karen, Marras, Connie, Marti-Masso, Jose-Felix, Martinez, Javier Ruiz, Mejia-Santana, Helen, Mirelman, Anat, Pont, Claustre, Orr-Urtreger, Avi, Raymond, Deborah, Saunders-Pullman, Rachel, Schüle, Birgitt, Tanner, Caroline, Tolosa, Eduardo, Vilas, Dolores, Wise, Adina, Facheris, Maurizio
में प्रकाशित Genet Med (2014)

VPS35 Mutations in Parkinson Disease

द्वारा Vilariño-Güell, Carles, Wider, Christian, Ross, Owen A., Dachsel, Justus C., Kachergus, Jennifer M., Lincoln, Sarah J., Soto-Ortolaza, Alexandra I., Cobb, Stephanie A., Wilhoite, Greggory J., Bacon, Justin A., Behrouz, Bahareh, Melrose, Heather L., Hentati, Emna, Puschmann, Andreas, Evans, Daniel M., Conibear, Elizabeth, Wasserman, Wyeth W., Aasly, Jan O., Burkhard, Pierre R., Djaldetti, Ruth, Ghika, Joseph, Hentati, Faycal, Krygowska-Wajs, Anna, Lynch, Tim, Melamed, Eldad, Rajput, Alex, Rajput, Ali H., Solida, Alessandra, Wu, Ruey-Meei, Uitti, Ryan J., Wszolek, Zbigniew K., Vingerhoets, François, Farrer, Matthew J.
प्रकाशित 2011