Biblio

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Filters: Author is Trempe, Jean-Francois  [Clear All Filters]
2020
Estiar MA, Leveille E, Spiegelman D, Dupré N, Trempe J-F, Rouleau GA, Gan-Or, iv Z. Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype. Mol Genet Genomic Med. 2020;:e1052.
2019
Alcalay RN, Mallett V, Vanderperre B, Tavassoly O, Dauvilliers Y, Wu RYJ, Ruskey JA, Leblond CS, Ambalavanan A, Laurent SB, Spiegelman D, Dionne-Laporte A, Liong C, Levy OA, Fahn S, Waters C, Kuo S-H, Chung WK, Ford B, Marder KS, Kang UJung, Hassin-Baer S, Greenbaum L, Trempe J-F, Wolf P, Oliva P, Zhang XKate, Clark LN, Langlois M, Dion PA, Fon EA, Dupré N, Rouleau GA, Gan-Or, iv Z. SMPD1 mutations, activity, and α-synuclein accumulation in Parkinson's disease. Mov Disord. 2019;34(4):526-535.