Search Results - "Barbier, Mathieu"

Lipschitz Pruning: Hierarchical Simplification of Primitive‐Based SDFs.

Authors: Barbier, Wilhem Sanchez, Mathieu Paris, Axel et al.

Source: Computer Graphics Forum; May2025, Vol. 44 Issue 2, p1-12, 12p

SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration.

Authors: Barbier, Mathieu Camuzat, Agnès Hachimi, Khalid El et al.

Source: Brain: A Journal of Neurology; Sep2021, Vol. 144 Issue 9, p2798-2811, 14p

Robust trajectory forecasting in autonomous systems using mixtures of Student's T-distributions with T-DistNet.

Authors: Lafage, Adrien Franchi, Gianni Barbier, Mathieu et al.

Source: Pattern Recognition; Sep2025, Vol. 165, pN.PAG-N.PAG, 1p

Homozygous GRN mutations: new phenotypes and new insights into pathological and molecular mechanisms.

Authors: Huin, Vincent Barbier, Mathieu Bottani, Armand et al.

Source: Brain: A Journal of Neurology; Jan2020, Vol. 143 Issue 1, p303-319, 17p

Homozygous GRN mutations: new phenotypes and new insights into pathological and molecular mechanisms.

Authors: Huin, Vincent Barbier, Mathieu Bottani, Armand et al.

Source: Brain: A Journal of Neurology; Jan2019, Vol. 142 Issue 1, p303-319, 17p

CD1 Gene Polymorphisms and Phenotypic Variability in X-Linked Adrenoleukodystrophy.

Authors: Barbier, Mathieu Sabbagh, Audrey Kasper, Edwige et al.

Source: PLoS ONE. Jan2012, Vol. 7 Issue 1, p1-7. 7p.

Platelets Alter Gene Expression Profile in Human Brain Endothelial Cells in an In Vitro Model of Cerebral Malaria.

Authors: Barbier, Mathieu Faille, Dorotheé atrice^Loriod, Bé et al.

Source: PLoS ONE. 2011, Vol. 6 Issue 5, p1-14. 14p.

Reply: Two heterozygous progranulin mutations in progressive supranuclear palsy.

Authors: Huin, Vincent Barbier, Mathieu Durr, Alexandra et al.

Source: Brain: A Journal of Neurology; Mar2021, Vol. 144 Issue 3, pe28-e28, 1p

Reply: Early-onset phenotype of bi-allelic GRN mutations.

Authors: Huin, Vincent Barbier, Mathieu Durr, Alexandra et al.

Source: Brain: A Journal of Neurology; Feb2021, Vol. 144 Issue 2, pe23-e23, 1p

Front Matter.

Source: Computer Graphics Forum; May2025, Vol. 44 Issue 2, pi-xxvii, 1p

Interrupted CAG expansions in ATXN2 gene expand the genetic spectrum of frontotemporal dementias.

Authors: Fournier, Clémence Anquetil, Vincent Camuzat, Agnès et al.

Source: Acta Neuropathologica Communications. 5/30/2018, Vol. 6 Issue 1, pN.PAG-N.PAG. 1p.

Baseline individual factors associated with clinical outcomes in adults with non-specific low back pain following manual therapy: a systematic review.

Authors: Barbier G Picchiottino M Delafontaine A et al.

Source: BMC complementary medicine and therapies [BMC Complement Med Ther] 2025 Sep 18; Vol. 25 (1), pp. 330. Date of Electronic Publication: 2025 Sep 18.

Publication Type: Journal Article; Systematic Review

Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101761232 Publication Model: Electronic Cited Medium: Internet ISSN: 2662-7671 (Electronic) Linking ISSN: 26627671 NLM ISO Abbreviation: BMC Complement Med Ther Subsets: MEDLINE