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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A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease von Nishioka, Kenya, Kefi, Mounir, Jasinska-Myga, Barbara, Wider, Christian, Vilariño-Güell, Carles, Ross, Owen A, Heckman, Michael G, Middleton, Lefkos T, Ishihara-Paul, Lianna, Gibson, Rachel A, Amouri, Rim, Ben Yahmed, Samia, Ben Sassi, Samia, Zouari, Mourad, El Euch, Ghada, Farrer, Matthew J, Hentati, Faycal

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A recessive ataxia diagnosis algorithm for the next generation sequencing era von Renaud, Mathilde, Tranchant, Christine, Martin, Juan Vicente Torres, Mochel, Fanny, Synofzik, Matthis, van de Warrenburg, Bart, Pandolfo, Massimo, Koenig, Michel, Kolb, Stefan A., Anheim, Mathieu, Alonso, Isabel, Azzedine, Hamid, Barbot, Clara, Bereau, Matthieu, Berkovic, Sam, Bernard, Geneviéve, Bindoff, Laurence A., Bompaire, Flavie, Bonneau, Dominique, Bonneau, Patrizia, Boycott, Kym M., Bras, Jose, Brais, Bernard, Brigatti, Karlla W., Cameron, Jillian, Chamova, Teodora, Choquet, Karine, Delague, Valérie, Denizeau, Philippe, Dotti, Maria Teresa, El‐Euch, Ghada, Elmalik, Salah A., Federico, Antonio, Fiskerstrand, Torunn, Gagnon, Cynthia, Guerreiro, Rita, Guissart, Claire, Hassin‐Baer, Sharon, Heimdal, Ketil Riddervold, Héron, Bénédicte, Isohanni, Pirjo, Kalaydijeva, Luba, Kawarai, Toshitaka, Koht, Jeanette Aimee, Lai, Szu‐Chia, Piana, Roberta La, Lecocq, Claire, Linnankivi, Tarja, Lönnqvist, Tuula, Lu, Chin‐Song, Maas, Roderick, Mahlaoui, Nizar, Mallaret, Martial, Marelli, Cecilia, Mariotti, Caterina, Mathieu, Jean, Méneret, Aurélie, Mignarri, Andrea, Monin, Marie Lorraine, Montaut, Solveig, Nanetti, Lorenzo, Nadjar, Yann, Poujois, Aurélia, Salih, Mustafa A., Sousa, Sergio, Stanier, Philip, Stoppa‐Lyonnet, Dominique, Strauss, Kevin, Tallaksen, Chantal, Tarnopolsky, Mark, Tinant, Nadége, Tournev, Ivailo, Topaloglu, Haluk, Varhaug, Kristin Nielsen, Woimant, France, Wolf, Nicole I., Yahalom, Gilad, Yoon, Grace, Young, Millie

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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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Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families von Ishihara, Lianna, Gibson, Rachel A., Warren, Liling, Amouri, Rim, Lyons, Kelly, Wielinski, Catherine, Hunter, Christine, Swartz, Jina E., Elango, Ramu, Akkari, P. Anthony, Leppert, David, Surh, Linda, Reeves, Kevin H., Thomas, Siwan, Ragone, Leigh, Hattori, Nobutaka, Pahwa, Rajesh, Jankovic, Joseph, Nance, Martha, Freeman, Alan, Gouider-Khouja, Neziha, Kefi, Mounir, Zouari, Mourad, Ben Sassi, Samia, Ben Yahmed, Samia, El Euch-Fayeche, Ghada, Middleton, Lefkos, Burn, David J., Watts, Ray L., Hentati, Faycal

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Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa von Jasinska-Myga, Barbara, Kachergus, Jennifer, Vilariño-Güell, Carles, Wider, Christian, Soto-Ortolaza, Alexandra I., Kefi, Mounir, Middleton, Lefkos T., Ishihara-Paul, Lianna, Gibson, Rachel A., Amouri, Rim, Yahmed, Samia Ben, Sassi, Samia Ben, Zouari, Mourad, Euch, Ghada El, Ross, Owen A., Hentati, Faycal, Farrer, Matthew J.

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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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Clinical features and molecular genetics of two Tunisian families with abetalipoproteinemia von Hammer, Monia Benhamed, El Euch-Fayache, Ghada, Nehdi, Houda, Feki, Moncef, Maamouri-Hicheri, Wieme, Hentati, Fayçal, Amouri, Rim

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A Novel SACS Gene Mutation in a Tunisian Family von Bouhlal, Yosr, El Euch-Fayeche, Ghada, Hentati, Fayçal, Amouri, Rim

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Clinical and Molecular Findings of Ataxia With Oculomotor Apraxia Type 2 (AOA2) in 5 Tunisian Families von Hammer, Monia Benhamed, El Euch-Fayache, Ghada, Nehdi, Houda, Saidi, Dalel, Nasri, Amira, Nabli, Fatma, Bouhlal, Yosr, Maamouri-Hicheri, Wieme, Hentati, Fayçal, Amouri, Rim

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