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Results by year

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

Year Number of Results
1971 2
1975 7
1976 6
1977 6
1978 4
1979 13
1980 2
1981 5
1982 4
1983 5
1984 11
1985 13
1986 9
1987 4
1988 7
1989 11
1990 16
1991 20
1992 18
1993 30
1994 15
1995 25
1996 24
1997 30
1998 26
1999 26
2000 32
2001 28
2002 40
2003 26
2004 31
2005 30
2006 48
2007 47
2008 52
2009 55
2010 47
2011 42
2012 70
2013 75
2014 66
2015 77
2016 69
2017 78
2018 73
2019 73
2020 80
2021 84
2022 96
2023 93
2024 43

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Article type

Publication date

PubMed for id: 347171

1,596 results

Results by year

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Page 1
Identification of a Novel Indel Variant in the DARS2 Gene in Russian Patients with Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation.
Bostanova FM, Tsygankova PG, Larshina EA, Nagornov IO, Evseeva YV, Krutikhina IL, Dzhentemirova ME, Kashlakova MN, Petukhova MS, Sharkova IV, Zakharova EY. Bostanova FM, et al. Genes (Basel). 2024 May 11;15(5):615. doi: 10.3390/genes15050615. Genes (Basel). 2024. PMID: 38790244 Free PMC article.
Traditional versus progressive robot-assisted gait training in people with multiple sclerosis and severe gait disability: study protocol for the PROGR-EX randomised controlled trial.
Baroni A, Lamberti N, Gandolfi M, Rimondini M, Bertagnolo V, Grassilli S, Zerbinati L, Manfredini F, Straudi S. Baroni A, et al. BMJ Open Sport Exerc Med. 2024 May 21;10(2):e002039. doi: 10.1136/bmjsem-2024-002039. eCollection 2024. BMJ Open Sport Exerc Med. 2024. PMID: 38779575 Free PMC article.
AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia.
Diarra S, Ghosh S, Cissé L, Coulibaly T, Yalcouyé A, Harmison G, Diallo S, Diallo SH, Coulibaly O, Schindler A, Cissé CAK, Maiga AB, Bamba S, Samassekou O, Khokha MK, Mis EK, Lakhani SA, Donovan FX, Jacobson S, Blackstone C, Guinto CO, Landouré G, Bonifacino JS, Fischbeck KH, Grunseich C. Diarra S, et al. Neurobiol Dis. 2024 Aug;198:106537. doi: 10.1016/j.nbd.2024.106537. Epub 2024 May 19. Neurobiol Dis. 2024. PMID: 38772452 Free article.
Spectrum of ERCC6-Related Cockayne Syndrome (Type B): From Mild to Severe Forms.
Sartorelli J, Travaglini L, Macchiaiolo M, Garone G, Gonfiantini MV, Vecchio D, Sinibaldi L, Frascarelli F, Ceccatelli V, Petrillo S, Piemonte F, Piccolo G, Novelli A, Longo D, Pro S, D'Amico A, Bertini ES, Nicita F. Sartorelli J, et al. Genes (Basel). 2024 Apr 18;15(4):508. doi: 10.3390/genes15040508. Genes (Basel). 2024. PMID: 38674442 Free PMC article.
1,596 results