N
N. Gouider-Khouja
Researcher at French Institute of Health and Medical Research
Publications - 23
Citations - 1208
N. Gouider-Khouja is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Striatonigral Degeneration & Antisaccade task. The author has an hindex of 15, co-authored 22 publications receiving 1137 citations.
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Journal ArticleDOI
Eye movements in parkinsonian syndromes.
Marie Vidailhet,S. Rivaud,N. Gouider-Khouja,Bernard Pillon,Anne-Marie Bonnet,Bertrand Gaymard,Yves Agid,Charles Pierrot-Deseilligny +7 more
TL;DR: It is concluded that saccade abnormalities are clearly different in SND, CBD, and PSP, and might help in early differential diagnosis in individual patients, but that SND cannot be differentiated from PD on the simple basis of eye movement abnormalities.
Journal ArticleDOI
Neuropsychological pattern of striatonigral degeneration: comparison with Parkinson's disease and progressive supranuclear palsy.
Bernard Pillon,N. Gouider-Khouja,Bernard Deweer,M. Vidailhet,Chara Malapani,Bruno Dubois,Yves Agid +6 more
TL;DR: The results showed that the dysexecutive syndrome of SND is similar to that of Parkinson's disease and less severe than in PSP.
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Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries
Hiroyuki Tomiyama,Yuanzhe Li,Manabu Funayama,Kazuko Hasegawa,Hiroyo Yoshino,Shin-ichiro Kubo,Kenichi Sato,Tatsuya Hattori,Chin-Song Lu,Rivka Inzelberg,Ruth Djaldetti,Eldad Melamed,Rim Amouri,N. Gouider-Khouja,Fayçal Hentati,Yasuko Hatano,Mei Wang,Yoko Imamichi,Koichi Mizoguchi,Hiroaki Miyajima,Fumiya Obata,Tatsushi Toda,Matthew J. Farrer,Yoshikuni Mizuno,Nobutaka Hattori +24 more
TL;DR: Clinical phenotypes including psychosis, dementia, and MIBG ratios are also heterogeneous, similar to neuropathology, in PD associated with LRRK2 mutations, and I2020T mutation has a single‐founder effect in Japanese patients.
Journal ArticleDOI
Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency
S. Gabsi,N. Gouider-Khouja,Samir Belal,M. Fki,M. Kefi,Ilhem Turki,M. Ben Hamida,Herbert J. Kayden,R. Mebazaa,Fayçel Hentati +9 more
TL;DR: Vit E supplementation in AVED patients stabilizes the neurological signs and can lead to mild improvement of cerebellar ataxia, especially in early stages of the disease.
Journal ArticleDOI
Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study
N. Gouider-Khouja,A. Larnaout,Rim Amouri,Sana Sfar,Samir Belal,Christiane Ben Hamida,Mongi Ben Hamida,Nobutaka Hattori,Yoshikuni Mizuno,Fayçal Hentati +9 more
TL;DR: This Tunisian kindred with AR-JP linked to a micro-deletion of the parkin gene shows clinical similarities with the previously reported Japanese and European families.