Motor phenotype of LRRK2-associated Parkinson's disease: A tunisian longitudinal study von Nabli, Fatma, Ben Sassi, Samia, Amouri, Rim, Duda, John E., Farrer, Matthew J., Hentati, Fayçal

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Cerebral Venous Thrombosis: A Tunisian Monocenter Study on 160 Patients von Sassi, Samia Ben, Touati, Nahla, Baccouche, Hela, Drissi, Cyrine, Romdhane, Neila Ben, Hentati, Fayçal

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DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study von Trinh, Joanne, BSc, Gustavsson, Emil K, MSc, Vilariño-Güell, Carles, PhD, Bortnick, Stephanie, BSc, Latourelle, Jeanne, PhD, McKenzie, Marna B, BSc, Tu, Chelsea Szu, MSc, Nosova, Ekaterina, PhD, Khinda, Jaskaran, BSc, Milnerwood, Austen, PhD, Lesage, Suzanne, PhD, Brice, Alexis, MD, Tazir, Meriem, MD, Aasly, Jan O, MD, Parkkinen, Laura, PhD, Haytural, Hazal, MSc, Foroud, Tatiana, PhD, Myers, Richard H, PhD, Sassi, Samia Ben, MD, Hentati, Emna, MD, Nabli, Fatma, MD, Farhat, Emna, MD, Amouri, Rim, PhD, Hentati, Fayçal, MD, Farrer, Matthew J, Dr

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Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiency von EL EUCH-FAYACHE, Ghada, BOUHLAL, Yosr, AMOURI, Rim, FEKI, Moncef, HENTATI, Fayçal

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LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic study von Hulihan, Mary M, MPH, Ishihara-Paul, Lianna, PhD, Kachergus, Jennifer, BSc, Warren, Liling, PhD, Amouri, Rim, PhD, Elango, Ramu, PhD, Prinjha, Rab K, PhD, Upmanyu, Ruchi, MSc, Kefi, Mounir, MD, Zouari, Mourad, MD, Sassi, Samia Ben, MD, Yahmed, Samia Ben, MD, El Euch-Fayeche, Ghada, MD, Matthews, Paul M, PhD, Middleton, Lefkos T, MD, Gibson, Rachel A, PhD, Hentati, Fayçal, MD, Farrer, Matthew J, PhD

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Inhibition of LRRK2 kinase activity leads to dephosphorylation of Ser910/Ser935, disruption of 14-3-3 binding and altered cytoplasmic localization von Dzamko, Nicolas, Deak, Maria, Hentati, Faycal, Reith, Alastair D., Prescott, Alan R., Alessi, Dario R., Nichols, R. Jeremy

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Stroke revealing Neuro-Behçet's disease with parenchymal and extensive vascular involvement von Hamza, Nouha, Ben Sassi, Samia, Nabli, Fatma, Nagi, Sonia, Mahmoud, Maha, Ben Abdelaziz, Ines, Hentati, Fayçal

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Autosomal recessive spastic ataxia of Charlevoix–Saguenay: An overview von Bouhlal, Yosr, Amouri, Rim, El Euch-Fayeche, Ghada, Hentati, Fayçal

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Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity von 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.

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Disability progression in multiple sclerosis: a Tunisian prospective cohort study von Hentati, Emna, Ben Sassi, Samia, Nabli, Fatma, Mabrouk, Tarek, Zouari, Mourad, Hentati, Fayçal

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

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A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia von 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

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Cerebral venous thrombosis in inflammatory bowel disease: a case series von Samia, Ben Sassi, Lamia, Kallel, Fatma, Nabli, Sawssen, Ben Romdhane, Rim, Ellouze, Mourad, Zouari, Neila, Ben Romdhane, Azza, Filali, Fayçal, Hentati

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Defects in the CAPN1 Gene Result in Alterations in Cerebellar Development and Cerebellar Ataxia in Mice and Humans von Wang, Yubin, Hersheson, Joshua, Lopez, Dulce, Hammer, Monia, 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

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Cerebral Venous Thrombosis Presenting With Cerebellar Ataxia and Cortical Blindness von Ben Sassi, Samia, MD, Mizouni, Habiba, MD, Nabli, Fatma, MD, Kallel, Lamia, MD, Kefi, Mounir, MD, Hentati, Fayçal, MD

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The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis von Yang, Yi, Hentati, Afif, Deng, Han-Xiang, Dabbagh, Omar, Sasaki, Toru, Hirano, Makito, Hung, Wu-Yen, Ouahchi, Karim, Yan, Jianhua, Azim, Anser C., Cole, Natalie, Gascon, Generoso, Yagmour, Ayesha, Ben-Hamida, Mongi, Pericak-Vance, Margaret, Hentati, Fayçal, Siddique, Teepu

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Primary Spinal Hydatidosis Revealed by Spinal Cord Compression von Bouattour, Nadia, Nabli, Fatma, Nagi, Sonia, Saied, Zakaria, Ben Abdelaziz, Ines, Hentati, Fayçal, Belal, Samir, Ben Sassi, Samia

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The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy von Bomont, Pascale, Cavalier, Laurent, Blondeau, François, Hamida, Christiane Ben, Belal, Samir, Tazir, Meriem, Demir, Ercan, Topaloglu, Haluk, Korinthenberg, Rudolf, Tüysüz, Beyhan, Landrieu, Pierre, Hentati, Fayçal, Koenig, Michel

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Cognitive dysfunction in Tunisian LRRK2 associated Parkinson’s disease von Ben Sassi, Samia, Nabli, Fatma, Hentati, Emna, Nahdi, Houda, Trabelsi, Meriam, Ben Ayed, Hela, Amouri, Rim, Duda, John Eric, Farrer, Matthew John, Hentati, Fayçal

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

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