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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1971 1
1973 3
1974 1
1979 7
1980 1
1981 8
1982 2
1983 2
1984 1
1989 1
1997 1
2001 1
2009 1
2013 1
2018 1
2022 2
2023 4
2024 0

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36 results

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Page 1
Pourquoi et comment améliorer l’information des patients et de leurs aidants au bon usage de leurs dispositifs médicaux tout au long du parcours de soin ?
Thiveaud D, Orlikowski D, Ollé F, Camus D, Josseran A, Degon PF, Ferracci C, Fraysse JL, Germe AF, Grumblat A, Guido-Morin P, Jarraya B, Joly AS, Lanier C, Pelayo S, Racle G, Teyssie M. Thiveaud D, et al. Among authors: ferracci c. Therapie. 2023 Jan-Feb;78(1):39-52. doi: 10.1016/j.therap.2022.10.070. Epub 2022 Nov 1. Therapie. 2023. PMID: 36424211 French. No abstract available.
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. Brain. 2023 Apr 19;146(4):1496-1510. doi: 10.1093/brain/awac326. Brain. 2023. PMID: 36073231 Free PMC article.
Why and how can we improve patient and caregiver information for the proper use of their medical devices throughout the care pathway?
Thiveaud D, Orlikowski D, Ollé F, Camus D, Josseran A, Degon PF, Ferracci C, Fraysse JL, Germe AF, Grumblat A, Guido-Morin P, Jarraya B, Joly AS, Lanier C, Pelayo S, Racle G, Teyssie M. Thiveaud D, et al. Among authors: ferracci c. Therapie. 2023 Jan-Feb;78(1):53-65. doi: 10.1016/j.therap.2022.11.002. Epub 2022 Nov 12. Therapie. 2023. PMID: 36435676
Outbreak of Locally Acquired Mosquito-Transmitted (Autochthonous) Malaria - Florida and Texas, May-July 2023.
Blackburn D, Drennon M, Broussard K, Morrison AM, Stanek D, Sarney E, Ferracci C, Huard S, Brennan W, Eaton J, Nealeigh S, Barber N, Zimler RA, Adams JN, Blackmore C, Gordillo M, Mercado R, Vore H, Scanlan K, Motie I, Stanfield L, Farooq A, Widel K, Tomson K, Kerr N, Nasir J, Cone M, Rice C, Larkin T, Hernandez E, Bencie J, Lesser CR, Dersch M, Ramirez-Lachmann S, Clark M, Rollo S, Bashadi A, Tyler R, Bolling B, Moore B, Sullivan B, Fonken E, Castillo R, Gonzalez Y, Olivares G, Mace KE, Sayre D, Lenhart A, Sutcliffe A, Dotson E, Corredor C, Rogers E, Raphael BH, Sapp SGH, Qvarnstrom Y, Ridpath AD, McElroy PD. Blackburn D, et al. Among authors: ferracci c. MMWR Morb Mortal Wkly Rep. 2023 Sep 8;72(36):973-978. doi: 10.15585/mmwr.mm7236a1. MMWR Morb Mortal Wkly Rep. 2023. PMID: 37676839 Free PMC article.
GIGYF2 mutations are not a frequent cause of familial Parkinson's disease.
Di Fonzo A, Fabrizio E, Thomas A, Fincati E, Marconi R, Tinazzi M, Breedveld GJ, Simons EJ, Chien HF, Ferreira JJ, Horstink MW, Abbruzzese G, Borroni B, Cossu G, Dalla Libera A, Fabbrini G, Guidi M, De Mari M, Lopiano L, Martignoni E, Marini P, Onofrj M, Padovani A, Stocchi F, Toni V, Sampaio C, Barbosa ER, Meco G; Italian Parkinson Genetics Network; Oostra BA, Bonifati V. Di Fonzo A, et al. Parkinsonism Relat Disord. 2009 Nov;15(9):703-5. doi: 10.1016/j.parkreldis.2009.05.001. Epub 2009 May 31. Parkinsonism Relat Disord. 2009. PMID: 19482505
Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism.
Quadri M, Fang M, Picillo M, Olgiati S, Breedveld GJ, Graafland J, Wu B, Xu F, Erro R, Amboni M, Pappatà S, Quarantelli M, Annesi G, Quattrone A, Chien HF, Barbosa ER; International Parkinsonism Genetics Network; Oostra BA, Barone P, Wang J, Bonifati V. Quadri M, et al. Hum Mutat. 2013 Sep;34(9):1208-15. doi: 10.1002/humu.22373. Epub 2013 Aug 6. Hum Mutat. 2013. PMID: 23804577
LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study.
Quadri M, Mandemakers W, Grochowska MM, Masius R, Geut H, Fabrizio E, Breedveld GJ, Kuipers D, Minneboo M, Vergouw LJM, Carreras Mascaro A, Yonova-Doing E, Simons E, Zhao T, Di Fonzo AB, Chang HC, Parchi P, Melis M, Correia Guedes L, Criscuolo C, Thomas A, Brouwer RWW, Heijsman D, Ingrassia AMT, Calandra Buonaura G, Rood JP, Capellari S, Rozemuller AJ, Sarchioto M, Fen Chien H, Vanacore N, Olgiati S, Wu-Chou YH, Yeh TH, Boon AJW, Hoogers SE, Ghazvini M, IJpma AS, van IJcken WFJ, Onofrj M, Barone P, Nicholl DJ, Puschmann A, De Mari M, Kievit AJ, Barbosa E, De Michele G, Majoor-Krakauer D, van Swieten JC, de Jong FJ, Ferreira JJ, Cossu G, Lu CS, Meco G, Cortelli P, van de Berg WDJ, Bonifati V; International Parkinsonism Genetics Network. Quadri M, et al. Lancet Neurol. 2018 Jul;17(7):597-608. doi: 10.1016/S1474-4422(18)30179-0. Epub 2018 Jun 7. Lancet Neurol. 2018. PMID: 29887161
Dapsone-resistant leprosy in a population of Bamako (Mali).
Baquillon G, Ferracci C, Saint Andre P, Pattyn SR. Baquillon G, et al. Among authors: ferracci c. Lepr Rev. 1980 Dec;51(4):315-9. doi: 10.5935/0305-7518.19800032. Lepr Rev. 1980. PMID: 7012500 No abstract available.
36 results