The Evolution of Genetic Variability at the LRRK2 Locus
Guenther, Dylan T, Follett, Jordan, Amouri, Rim, Sassi, Samia Ben, Hentati, Faycel, Farrer, Matthew J
Published in Genes (01.07.2024)
Published in Genes (01.07.2024)
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Age at Onset of LRRK2 p.Gly2019Ser Is Related to Environmental and Lifestyle Factors
Lüth, Theresa, König, Inke R., Grünewald, Anne, Kasten, Meike, Klein, Christine, Hentati, Faycel, Farrer, Matthew, Trinh, Joanne
Published in Movement disorders (01.10.2020)
Published in Movement disorders (01.10.2020)
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Genetic Modifiers of LRRK2 Parkinson's Disease: A Replication Study in Arab‐Berbers
Follett, Jordan, Guenther, Dylan, Xoi, Leyna, Amouri, Rim, Ben Sassi, Samia, Hentati, Faycel, Farrer, Matthew J.
Published in Movement disorders (01.04.2024)
Published in Movement disorders (01.04.2024)
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Impacts of Iron Metabolism Dysregulation on Alzheimer's Disease
Jouini, Najla, Saied, Zakaria, Ben Sassi, Samia, Nebli, Fatma, Messaoud, Taieb, Hentati, Faycel, Belal, Samir
Published in Journal of Alzheimer's disease (01.01.2021)
Published in Journal of Alzheimer's disease (01.01.2021)
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Interaction of Mitochondrial Polygenic Score and Lifestyle Factors in LRRK2 p. Gly2019Ser Parkinsonism
Lüth, Theresa, Gabbert, Carolin, Koch, Sebastian, König, Inke R., Caliebe, Amke, Laabs, Björn‐Hergen, Hentati, Faycel, Sassi, Samia Ben, Amouri, Rim, Spielmann, Malte, Klein, Christine, Grünewald, Anne, Farrer, Matthew J., Trinh, Joanne
Published in Movement disorders (01.10.2023)
Published in Movement disorders (01.10.2023)
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Journal Article
Age at Onset of LRRK2 p. Gly2019Ser Is Related to Environmental and Lifestyle Factors
Lüth, Theresa, König, Inke R., Grünewald, Anne, Kasten, Meike, Klein, Christine, Hentati, Faycel, Farrer, Matthew, Trinh, Joanne
Published in Movement disorders (01.10.2020)
Published in Movement disorders (01.10.2020)
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LRRK2 parkinsonism in Tunisia and Norway: a comparative analysis of disease penetrance
Hentati, Faycel, Trinh, Joanne, Thompson, Christina, Nosova, Ekaterina, Farrer, Matthew J, Aasly, Jan O
Published in Neurology (05.08.2014)
Published in Neurology (05.08.2014)
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Interaction of Mitochondrial Polygenic Score and Lifestyle Factors in LRRK2 p.Gly2019Ser Parkinsonism
Lüth, Theresa, Gabbert, Carolin, Koch, Sebastian, König, Inke R, Caliebe, Amke, Laabs, Björn-Hergen, Hentati, Faycel, Sassi, Samia Ben, Amouri, Rim, Spielmann, Malte, Klein, Christine, Grünewald, Anne, Farrer, Matthew J, Trinh, Joanne
Published in Movement disorders (01.10.2023)
Published in Movement disorders (01.10.2023)
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Discriminative expression of CD39 and CD73 in Cerebrospinal fluid of patients with Multiple Sclerosis and Neuro-Behçet’s disease
Bahrini, Khadija, Belghith, Meriam, Maghrebi, Olfa, Bekir, Jihène, Kchaou, Mariem, Jeridi, Cyrine, Amouri, Rim, Hentati, Faycel, Belal, Samir, Ben Sassi, Samia, Barbouche, Mohamed-Ridha
Published in Cytokine (Philadelphia, Pa.) (01.06.2020)
Published in Cytokine (Philadelphia, Pa.) (01.06.2020)
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Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1/PRKN-linked Parkinson’s disease
Trinh, Joanne, Hicks, Andrew A, König, Inke R, Delcambre, Sylvie, Lüth, Theresa, Schaake, Susen, Wasner, Kobi, Ghelfi, Jenny, Borsche, Max, Vilariño-Güell, Carles, Hentati, Faycel, Germer, Elisabeth L, Bauer, Peter, Takanashi, Masashi, Kostić, Vladimir, Lang, Anthony E, Brüggemann, Norbert, Pramstaller, Peter P, Pichler, Irene, Rajput, Alex, Hattori, Nobutaka, Farrer, Matthew J, Lohmann, Katja, Weissensteiner, Hansi, May, Patrick, Klein, Christine, Grünewald, Anne
Published in Brain (London, England : 1878) (03.07.2023)
Published in Brain (London, England : 1878) (03.07.2023)
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RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses
Gustavsson, Emil K, Follett, Jordan, Trinh, Joanne, Barodia, Sandeep K, Real, Raquel, Liu, Zhiyong, Grant-Peters, Melissa, Fox, Jesse D, Appel-Cresswell, Silke, Stoessl, A Jon, Rajput, Alex, Rajput, Ali H, Auer, Roland, Tilney, Russel, Sturm, Marc, Haack, Tobias B, Lesage, Suzanne, Tesson, Christelle, Brice, Alexis, Vilariño-Güell, Carles, Ryten, Mina, Goldberg, Matthew S, West, Andrew B, Hu, Michele T, Morris, Huw R, Sharma, Manu, Gan-Or, Ziv, Samanci, Bedia, Lis, Pawel, Periñan, Maria Teresa, Amouri, Rim, Ben Sassi, Samia, Hentati, Faycel, Tonelli, Francesca, Alessi, Dario R, Farrer, Matthew J
Published in Lancet neurology (01.06.2024)
Published in Lancet neurology (01.06.2024)
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A comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism
Trinh, Joanne, Amouri, Rim, Duda, John E, Morley, James F, Read, Matthew, Donald, Alan, Vilariño-Güell, Carles, Thompson, Christina, Szu Tu, Chelsea, Gustavsson, Emil K, Ben Sassi, Samia, Hentati, Emna, Zouari, Mourad, Farhat, Emna, Nabli, Fatma, Hentati, Faycel, Farrer, Matthew J
Published in Neurobiology of aging (01.05.2014)
Published in Neurobiology of aging (01.05.2014)
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Accident vasculaire cérébral ischémique du sujet jeune : principales étiologies
Melliti, Maroua, Bradai, Nesrine, Ines, Benabdelaziz, Zakaria, Said, Samir, Blel, Samia, Ben Sassi, Faycel, Hentati
Published in Revue neurologique (01.04.2019)
Published in Revue neurologique (01.04.2019)
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Uvéite et sclérose en plaque
Benabdelaziz, Ines, Moalla, Khadija, Farhat, Emna, Brahem, Zaineb, Ben Sassi, Samia, Hentati, Faycel, Zouari, Mourad
Published in Revue neurologique (01.04.2015)
Published in Revue neurologique (01.04.2015)
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Hypotension intracrânienne spontanée associée à une syringomyélie
Moalla, Khadija Senda, Nabli, Fatma, Brahim, Zeineb, Saied, Zakaria, Sassi, Samia Ben, Zouari, Mourad, Hentati, Faycel
Published in Revue neurologique (01.04.2015)
Published in Revue neurologique (01.04.2015)
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Ureteral stenosis in Wegener's granulomatosis. Case report
Ben Ghorbel, Imed, Chebbi, Waffa, Zouari, Mourad, Hentati, Faycel, Miled, Mohamed, Houman, Mohamed Habib
Published in La Presse médicale (1983) (01.11.2006)
Published in La Presse médicale (1983) (01.11.2006)
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Journal Article
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinase
Gustavsson, Emil K, Follett, Jordan, Trinh, Joanne, Barodia, Sandeep K, Real, Raquel, Liu, Zhiyong, Grant-Peters, Melissa, Fox, Jesse D, Appel-Cresswell, Silke, Stoessl, A Jon, Rajput, Alex, Rajput, Ali H, Auer, Roland, Tilney, Russel, Sturm, Marc, Haack, Tobias B, Lesage, Suzanne, Tesson, Christelle, Brice, Alexis, Vilariño-Güell, Carles, Ryten, Mina, Goldberg, Matthew S, West, Andrew B, Hu, Michele T, Morris, Huw R, Sharma, Manu, Gan-Or, Ziv, Samanci, Bedia, Lis, Pawel, Tocino, Teresa, Amouri, Rim, Sassi, Samia Ben, Hentati, Faycel, Tonelli, Francesca, Alessi, Dario R, Farrer, Matthew J
Published in medRxiv : the preprint server for health sciences (18.01.2024)
Published in medRxiv : the preprint server for health sciences (18.01.2024)
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Molecular analysis of the SMN1 and NAIP genes in 60 Tunisian spinal muscular atrophy patients
Mrad, Ridha, Dorboz, Imen, Ben Jemaa, Lamia, Maazoul, Faouzi, Trabelsi, Madiha, Chaabouni, Meriem, Mlaiki, Brahim, Miladi, Nakjoua, Hentati, Faycel, Chaabouni, Habiba
Published in Tunisie Medicale (01.08.2006)
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Published in Tunisie Medicale (01.08.2006)
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