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

Year Number of Results
1975 2
1976 1
1980 1
1981 1
1982 5
1983 5
1984 7
1985 13
1986 12
1987 9
1988 4
1989 10
1990 2
1991 5
1992 17
1993 5
1994 7
1995 8
1996 11
1997 8
1998 5
1999 9
2000 9
2001 8
2002 9
2003 7
2004 11
2005 10
2006 11
2007 13
2008 11
2009 17
2010 11
2011 13
2012 8
2013 15
2014 16
2015 23
2016 11
2017 9
2018 9
2019 7
2020 4
2021 1
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Search Results

354 results
Results by year
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Page 1
Safety, tolerability, pharmacokinetics, pharmacodynamics, and exploratory efficacy of the novel enzyme replacement therapy avalglucosidase alfa (neoGAA) in treatment-naïve and alglucosidase alfa-treated patients with late-onset Pompe disease: A phase 1, open-label, multicenter, multinational, ascending dose study.
Pena LDM, Barohn RJ, Byrne BJ, Desnuelle C, Goker-Alpan O, Ladha S, Laforêt P, Mengel KE, Pestronk A, Pouget J, Schoser B, Straub V, Trivedi J, Van Damme P, Vissing J, Young P, Kacena K, Shafi R, Thurberg BL, Culm-Merdek K, van der Ploeg AT; NEO1 Investigator Group. Pena LDM, et al. Among authors: pouget j. Neuromuscul Disord. 2019 Mar;29(3):167-186. doi: 10.1016/j.nmd.2018.12.004. Epub 2018 Dec 17. Neuromuscul Disord. 2019. PMID: 30770310 Free article. Clinical Trial.
Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia Genes.
Coutelier M, Hammer MB, Stevanin G, Monin ML, Davoine CS, Mochel F, Labauge P, Ewenczyk C, Ding J, Gibbs JR, Hannequin D, Melki J, Toutain A, Laugel V, Forlani S, Charles P, Broussolle E, Thobois S, Afenjar A, Anheim M, Calvas P, Castelnovo G, de Broucker T, Vidailhet M, Moulignier A, Ghnassia RT, Tallaksen C, Mignot C, Goizet C, Le Ber I, Ollagnon-Roman E, Pouget J, Brice A, Singleton A, Durr A; Spastic Paraplegia and Ataxia Network. Coutelier M, et al. Among authors: pouget j. JAMA Neurol. 2018 May 1;75(5):591-599. doi: 10.1001/jamaneurol.2017.5121. JAMA Neurol. 2018. PMID: 29482223 Free PMC article.
Hommage à Georges Serratrice (1927-2019).
Pouget J. Pouget J. Med Sci (Paris). 2020 Dec;36 Hors série n° 2:7-9. doi: 10.1051/medsci/2020267. Epub 2021 Jan 11. Med Sci (Paris). 2020. PMID: 33427628 French.
[A dream becoming reality].
Pouget J. Pouget J. Med Sci (Paris). 2019 Mar;35 Hors série n° 1:7. doi: 10.1051/medsci/2019050. Epub 2019 Apr 3. Med Sci (Paris). 2019. PMID: 30943152 Free article. French. No abstract available.
[Georges Serratrice].
Pouget J. Pouget J. Rev Neurol (Paris). 2021 Jan-Feb;177(1-2):3-6. doi: 10.1016/j.neurol.2021.01.001. Rev Neurol (Paris). 2021. PMID: 33583557 French. No abstract available.
Novel CAPN3 variant associated with an autosomal dominant calpainopathy.
Cerino M, Campana-Salort E, Salvi A, Cintas P, Renard D, Juntas Morales R, Tard C, Leturcq F, Stojkovic T, Bonello-Palot N, Gorokhova S, Mortreux J, Maues De Paula A, Lévy N, Pouget J, Cossée M, Bartoli M, Krahn M, Attarian S. Cerino M, et al. Among authors: pouget j. Neuropathol Appl Neurobiol. 2020 Oct;46(6):564-578. doi: 10.1111/nan.12624. Epub 2020 Jun 10. Neuropathol Appl Neurobiol. 2020. PMID: 32342993
Myofibrillar myopathies: State of the art, present and future challenges.
Béhin A, Salort-Campana E, Wahbi K, Richard P, Carlier RY, Carlier P, Laforêt P, Stojkovic T, Maisonobe T, Verschueren A, Franques J, Attarian S, Maues de Paula A, Figarella-Branger D, Bécane HM, Nelson I, Duboc D, Bonne G, Vicart P, Udd B, Romero N, Pouget J, Eymard B. Béhin A, et al. Among authors: pouget j. Rev Neurol (Paris). 2015 Oct;171(10):715-29. doi: 10.1016/j.neurol.2015.06.002. Epub 2015 Sep 3. Rev Neurol (Paris). 2015. PMID: 26342832 Review.
Single-fiber studies for assigning pathogenicity of eight mitochondrial DNA variants associated with mitochondrial diseases.
Zereg E, Chaussenot A, Morel G, Bannwarth S, Sacconi S, Soriani MH, Attarian S, Cano A, Pouget J, Bellance R, Tranchant C, Lannes B, de Paula AM, Saadi Ait-El-Mkadem S, Chafino B, Berthet M, Fragaki K, Paquis-Flucklinger V, Rouzier C. Zereg E, et al. Among authors: pouget j. Hum Mutat. 2020 Aug;41(8):1394-1406. doi: 10.1002/humu.24037. Epub 2020 Jun 12. Hum Mutat. 2020. PMID: 32419253
[Necrotizing myopathies: From genetic to acquired forms].
Salort-Campana E, De Paula AM, Figarella-Branger D, Pouget J. Salort-Campana E, et al. Among authors: pouget j. Rev Med Interne. 2014 Jul;35(7):430-6. doi: 10.1016/j.revmed.2013.11.012. Epub 2013 Dec 19. Rev Med Interne. 2014. PMID: 24359726 Review. French.
354 results
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