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The free plasma amyloid Aβ1-42/Aβ1-40 ratio predicts conversion to dementia for subjects with mild cognitive impairment with performance equivalent to that of the total plasma Aβ1-42/Aβ1-40 ratio. The BALTAZAR study.
Schraen-Maschke S, Duhamel A, Vidal JS, Ramdane N, Vaudran L, Dussart C, Buée L, Sablonnière B, Delaby C, Allinquant B, Gabelle A, Bombois S, Lehmann S, Hanon O; BALTAZAR study group. Schraen-Maschke S, et al. Among authors: sablonniere b. Neurobiol Dis. 2024 Apr;193:106459. doi: 10.1016/j.nbd.2024.106459. Epub 2024 Feb 27. Neurobiol Dis. 2024. PMID: 38423192 Free article.
Indication for molecular testing by multiplex ligation-dependent probe amplification in parkinsonism.
Mutez E, Swiderski M, Devos D, Moreau C, Baille G, Degardin A, Ryckewaert G, Carriere N, Kreisler A, Simonin C, Rouaix N, Tir M, Krystkowiak P, Ramdane N, Génin M, Sablonnière B, Defebvre L, Huin V. Mutez E, et al. Among authors: sablonniere b. Eur J Neurol. 2023 Jun;30(6):1667-1675. doi: 10.1111/ene.15788. Epub 2023 Mar 29. Eur J Neurol. 2023. PMID: 36916668
Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex.
Parodi L, Fenu S, Barbier M, Banneau G, Duyckaerts C, Tezenas du Montcel S, Monin ML, Ait Said S, Guegan J, Tallaksen CME, Sablonniere B, Brice A, Stevanin G, Depienne C, Durr A; SPATAX network. Parodi L, et al. Among authors: sablonniere b. Brain. 2018 Dec 1;141(12):3331-3342. doi: 10.1093/brain/awy285. Brain. 2018. PMID: 30476002
Neglected Comorbidity of Chronic Heart Failure: Iron Deficiency.
Manceau H, Ausseil J, Masson D, Feugeas JP, Sablonniere B, Guieu R, Puy H, Peoc'h K. Manceau H, et al. Among authors: sablonniere b. Nutrients. 2022 Aug 5;14(15):3214. doi: 10.3390/nu14153214. Nutrients. 2022. PMID: 35956390 Free PMC article. Review.
[A neglected comorbidity of chronic heart failure: iron deficiency].
Peoc'h K, Ausseil J, Feugeas JP, Guieu R, Masson D, Sablonniere B, Puy H. Peoc'h K, et al. Among authors: sablonniere b. Ann Biol Clin (Paris). 2022 Mar 1;80(2):109-118. doi: 10.1684/abc.2022.1719. Ann Biol Clin (Paris). 2022. PMID: 35766071 French.
Functional Analyses of Two Novel LRRK2 Pathogenic Variants in Familial Parkinson's Disease.
Coku I, Mutez E, Eddarkaoui S, Carrier S, Marchand A, Deldycke C, Goveas L, Baille G, Tir M, Magnez R, Thuru X, Vermeersch G, Vandenberghe W, Buée L, Defebvre L, Sablonnière B, Chartier-Harlin MC, Taymans JM, Huin V. Coku I, et al. Among authors: sablonniere b. Mov Disord. 2022 Aug;37(8):1761-1767. doi: 10.1002/mds.29124. Epub 2022 Jun 16. Mov Disord. 2022. PMID: 35708213 Free PMC article.
Motor neuron pathology in CANVAS due to RFC1 expansions.
Huin V, Coarelli G, Guemy C, Boluda S, Debs R, Mochel F, Stojkovic T, Grabli D, Maisonobe T, Gaymard B, Lenglet T, Tard C, Davion JB, Sablonnière B, Monin ML, Ewenczyk C, Viala K, Charles P, Le Ber I, Reilly MM, Houlden H, Cortese A, Seilhean D, Brice A, Durr A. Huin V, et al. Among authors: sablonniere b. Brain. 2022 Jun 30;145(6):2121-2132. doi: 10.1093/brain/awab449. Brain. 2022. PMID: 34927205 Free article.
Myotonic Dystrophy: an RNA Toxic Gain of Function Tauopathy?
Fernandez-Gomez F, Tran H, Dhaenens CM, Caillet-Boudin ML, Schraen-Maschke S, Blum D, Sablonnière B, Buée-Scherrer V, Buee L, Sergeant N. Fernandez-Gomez F, et al. Among authors: sablonniere b. Adv Exp Med Biol. 2019;1184:207-216. doi: 10.1007/978-981-32-9358-8_17. Adv Exp Med Biol. 2019. PMID: 32096040 Review.
Diagnosis associated with Tau higher than 1200 pg/mL: Insights from the clinical and laboratory practice.
Lehmann S, Paquet C, Malaplate-Armand C, Magnin E, Schraen S, Quillard-Muraine M, Bousiges O, Delaby C, Dumurgier J, Hugon J, Sablonnière B, Blanc F, Wallon D, Gabelle A, Laplanche JL, Bouaziz-Amar E, Peoc'h K; ePLM Group. Lehmann S, et al. Among authors: sablonniere b. Clin Chim Acta. 2019 Aug;495:451-456. doi: 10.1016/j.cca.2019.04.081. Epub 2019 Apr 30. Clin Chim Acta. 2019. PMID: 31051163
103 results