Frontotemporal dementia: identification of a splicing variant at +1 of Exon 8 in the GRN gene with normal plasma progranulin levels

Autor: Bensalah, M., Nabti, A., Lamari, F., Godefroy, O., Forlani, S., Jornea, L., Le Guern, E., Clot, F.

Publikováno v: In Clinica Chimica Acta 1 May 2024 558 Supplement 1

Comment choisir l’interface au cours du traitement du syndrome d’apnées obstructives du sommeil par pression positive continue

Autor: Borel, J.-C., Chaudot, C., Bresse, C., Clot, F., Deschaux, C.

Publikováno v: In Medecine du Sommeil July-September 2013 10(3):116-123

Atypical clinical presentation and typical FTD atrophy: 17-year clinical follow-up and MRI analysis of a slowly progressive bvFTD associated with C9orf72 expansion

Autor: Géraudie, A. ^*, Guerrier, L., Le Ber, I., Clot, F., Péran, P., Pariente, J.

Publikováno v: In Revue Neurologique September 2020 176(7-8):627-629

Linguistic characteristics of genetic primary progressive aphasias: a retrospective study of 27 cases carrying GRN and c9orf72 mutations

Autor: Saracino, D., Ferrieux, S., Nogues, M., Rinaldi, D., Guignebert, A., Camuzat, A., Clot, F., Coppola, C., Deramecourt, V., Sarazin, Marie, Thauvin, C., Auriacombe, S., Di Iorio, G., Dubois, Bruno, Le Ber, I.

Publikováno v: European Journal of Neurology
the 4th Congress of the European Academy of Neurology
the 4th Congress of the European Academy of Neurology, Jun 2018, Lisbonne, Portugal. pp.451 : EPR2129

IF 4.621; International audience

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a2c864274de877b4c6cbbd0ecfd1349b
https://hal-univ-bourgogne.archives-ouvertes.fr/hal-02049007

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