Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
5 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Genotype-phenotype correlation in PRKN-associated Parkinson's disease.
NPJ Parkinsons Dis. 2024 Mar 29;10(1):72. doi: 10.1038/s41531-024-00677-3.
NPJ Parkinsons Dis. 2024.
PMID: 38553467
Free PMC article.
Identification of a DAGLB Mutation in a Non-Chinese Patient with Parkinson's Disease.
Tesson C, Bouchetara MS, Ferrien M, Lesage S, Brice A.
Tesson C, et al. Among authors: ferrien m.
Mov Disord. 2023 Sep;38(9):1756-1757. doi: 10.1002/mds.29533. Epub 2023 Jul 11.
Mov Disord. 2023.
PMID: 37431851
No abstract available.
Item in Clipboard
Detection of ATXN2 Expansions in an Exome Dataset: An Underdiagnosed Cause of Parkinsonism.
Casse F, Courtin T, Tesson C, Ferrien M, Noël S, Fauret-Amsellem AL, Gareau T, Guegan J, Anheim M, Mariani LL, Le Forestier N, Tranchant C, Corvol JC, Lesage S, Brice A; French Parkinson's disease genetics study group (PDG).
Casse F, et al. Among authors: ferrien m.
Mov Disord Clin Pract. 2023 Mar 7;10(4):664-669. doi: 10.1002/mdc3.13699. eCollection 2023 Apr.
Mov Disord Clin Pract. 2023.
PMID: 37070044
Free PMC article.
Item in Clipboard
PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disability.
Fevga C, Tesson C, Carreras Mascaro A, Courtin T, van Coller R, Sakka S, Ferraro F, Farhat N, Bardien S, Damak M, Carr J, Ferrien M, Boumeester V, Hundscheid J, Grillenzoni N, Kessissoglou IA, Kuipers DJS, Quadri M; French and Mediterranean Parkinson disease Genetics Study Group; International Parkinsonism Genetics Network; Corvol JC, Mhiri C, Hassan BA, Breedveld GJ, Lesage S, Mandemakers W, Brice A, Bonifati V.
Fevga C, et al. Among authors: ferrien m.
Brain. 2023 Apr 19;146(4):1496-1510. doi: 10.1093/brain/awac326.
Brain. 2023.
PMID: 36073231
Free PMC article.
Item in Clipboard
Genetic screening of ANXA11 revealed novel mutations linked to amyotrophic lateral sclerosis.
Teyssou E, Muratet F, Amador MD, Ferrien M, Lautrette G, Machat S, Boillée S, Larmonier T, Saker S, Leguern E, Cazeneuve C, Marie Y, Guegan J, Gyorgy B, Cintas P, Meininger V, Le Forestier N, Salachas F, Couratier P, Camu W, Seilhean D, Millecamps S.
Teyssou E, et al. Among authors: ferrien m.
Neurobiol Aging. 2021 Mar;99:102.e11-102.e20. doi: 10.1016/j.neurobiolaging.2020.10.015. Epub 2020 Oct 23.
Neurobiol Aging. 2021.
PMID: 33218681
Item in Clipboard
Cite
Cite