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Computational Analysis of a Novel SACS Gene Mutation with BioExtract Server.
Published in:
Journal of Molecular Neuroscience, 2011, v. 44, n. 1, p. 53, doi. 10.1007/s12031-011-9512-8
By:
- Bouhlal, Yosr;
- Jennewein, Douglas;
- Anderson, Brent;
- Reynoldson, Joe;
- Maamouri, Wiem;
- Hentati, Fayçal;
- Amouri, Rim;
- Lushbough, Carol
Publication type:
Article
A Novel SACS Gene Mutation in a Tunisian Family.
Published in:
Journal of Molecular Neuroscience, 2009, v. 39, n. 3, p. 333, doi. 10.1007/s12031-009-9212-9
By:
- Bouhlal, Yosr;
- Euch-Fayeche, Ghada;
- Hentati, Fayçal;
- Amouri, Rim
Publication type:
Article
Allelic ROBO3 Heterogeneity in Tunisian Patients with Horizontal Gaze Palsy with Progressive Scoliosis.
Published in:
Journal of Molecular Neuroscience, 2009, v. 39, n. 3, p. 337, doi. 10.1007/s12031-009-9217-4
By:
- Amouri, Rim;
- Nehdi, Houda;
- Bouhlal, Yosr;
- Kefi, Mounir;
- Larnaout, Abdelmajid;
- Hentati, Fayçal
Publication type:
Article
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families.
Published in:
Neurodegenerative Diseases, 2017, v. 17, n. 4/5, p. 208, doi. 10.1159/000464445
By:
- 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.
Publication type:
Article
Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia.
Published in:
Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12620-9
By:
- 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
Publication type:
Article
Giant axonal neuropathy locus refinement to a < 590 kb critical interval.
Published in:
European Journal of Human Genetics, 2000, v. 8, n. 7, p. 527, doi. 10.1038/sj.ejhg.5200476
By:
- Cavalier, Laurent;
- BenHamida, Christiane;
- Amouri, Rim;
- Belal, Samir;
- Bomont, Pascale;
- Lagarde, Nadège;
- Gressin, Laëtitia;
- Callen, David;
- Demir, Ercan;
- Topaloglu, Haluk;
- Landrieu, Pierre;
- Ioos, Catherine;
- Hamida, Mongi Ben;
- Kœnig, Michel;
- Hentati, Fayçal
Publication type:
Article
Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiency.
Published in:
Brain: A Journal of Neurology, 2014, v. 137, n. 2, p. 402, doi. 10.1093/brain/awt339
By:
- Euch-Fayache, Ghada El;
- Bouhlal, Yosr;
- Amouri, Rim;
- Feki, Moncef;
- Hentati, Fayçal
Publication type:
Article
A phase I trial of adeno-associated virus serotype 1-γ-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2C.
Published in:
Brain: A Journal of Neurology, 2012, v. 135, n. 2, p. 483, doi. 10.1093/brain/awr342
By:
- Herson, Serge;
- Hentati, Faycal;
- Rigolet, Aude;
- Behin, Anthony;
- Romero, Norma B.;
- Leturcq, France;
- Laforêt, Pascal;
- Maisonobe, Thierry;
- Amouri, Rim;
- Haddad, Hafedh;
- Audit, Muriel;
- Montus, Marie;
- Masurier, Carole;
- Gjata, Bernard;
- Georger, Christophe;
- Cheraï, Mustapha;
- Carlier, Pierre;
- Hogrel, Jean-Yves;
- Herson, Ariane;
- Allenbach, Yves
Publication type:
Article
A Tunisian patient with CLCN2‐related leukoencephalopathy.
Published in:
2022
By:
- Ben Mohamed, Dina;
- Saied, Zacharia;
- Ben Sassi, Samia;
- Ben Said, Mariem;
- Nabli, Fatma;
- Achouri, Afef;
- Jeridi, Cyrine;
- Masmoudi, Saber;
- Amouri, Rim
Publication type:
Case Study
Genetic Modifiers of LRRK2 Parkinson’s Disease: A Replication Study in Arab-Berbers.
Published in:
Movement Disorders, 2024, v. 39, n. 4, p. 751, doi. 10.1002/mds.29735
By:
- Follett, Jordan;
- Guenther, Dylan;
- Xoi, Leyna;
- Amouri, Rim;
- Sassi, Samia Ben;
- Hentati, Faycel;
- Farrer, Matthew J.
Publication type:
Article
Interaction of Mitochondrial Polygenic Score and Lifestyle Factors in LRRK2 p.Gly2019Ser Parkinsonism.
Published in:
Movement Disorders, 2023, v. 38, n. 10, p. 1837, doi. 10.1002/mds.29563
By:
- 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
Publication type:
Article
ATP13A2 variability in Parkinson disease.
Published in:
Human Mutation, 2009, v. 30, n. 3, p. 406, doi. 10.1002/humu.20877
By:
- 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.
Publication type:
Article
The Evolution of Genetic Variability at the LRRK2 Locus.
Published in:
Genes, 2024, v. 15, n. 7, p. 878, doi. 10.3390/genes15070878
By:
- Guenther, Dylan T.;
- Follett, Jordan;
- Amouri, Rim;
- Sassi, Samia Ben;
- Hentati, Faycel;
- Farrer, Matthew J.
Publication type:
Article
Motor phenotype of LRRK2-associated Parkinson's disease: A tunisian longitudinal study.
Published in:
Movement Disorders, 2015, v. 30, n. 2, p. 253, doi. 10.1002/mds.26097
By:
- Nabli, Fatma;
- Ben Sassi, Samia;
- Amouri, Rim;
- Duda, John E.;
- Farrer, Matthew J.;
- Hentati, Fayçal
Publication type:
Article
Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa.
Published in:
Movement Disorders, 2010, v. 25, n. 13, p. 2052, doi. 10.1002/mds.23283
By:
- 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.
Publication type:
Article
Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families.
Published in:
2007
By:
- 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
Publication type:
journal article
Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries.
Published in:
Movement Disorders, 2006, v. 21, n. 8, p. 1102, doi. 10.1002/mds.20886
By:
- Tomiyama, Hiroyuki;
- Li, Yuanzhe;
- Funayama, Manabu;
- Hasegawa, Kazuko;
- Yoshino, Hiroyo;
- Kubo, Shin-Ichiro;
- Sato, Kenichi;
- Hattori, Tatsuya;
- Lu, Chin-Song;
- Inzelberg, Rivka;
- Djaldetti, Ruth;
- Melamed, Eldad;
- Amouri, Rim;
- Gouider-Khouja, Neziha;
- Hentati, Faycal;
- Hatano, Yasuko;
- Wang, Mei;
- Imamichi, Yoko;
- Mizoguchi, Koichi;
- Miyajima, Hiroaki
Publication type:
Article

Found: 17