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

Year Number of Results
1951 50
1952 64
1953 113
1954 104
1955 119
1956 110
1957 127
1958 183
1959 104
1960 132
1961 170
1962 97
1963 135
1964 159
1965 154
1966 137
1967 175
1968 323
1969 157
1970 332
1971 170
1972 171
1973 185
1974 191
1975 215
1976 251
1977 235
1978 261
1979 341
1980 294
1981 385
1982 324
1983 386
1984 432
1985 476
1986 419
1987 484
1988 515
1989 486
1990 543
1991 563
1992 653
1993 744
1994 717
1995 688
1996 933
1997 913
1998 1039
1999 1099
2000 1270
2001 1185
2002 1278
2003 1394
2004 1644
2005 1554
2006 1730
2007 1550
2008 1516
2009 1514
2010 1568
2011 1671
2012 1798
2013 2031
2014 2059
2015 2214
2016 2316
2017 2190
2018 2232
2019 2386
2020 2587
2021 1058
Text availability
Article attribute
Article type
Publication date

Search Results

54,471 results
Results by year
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Antisense oligonucleotides: A primer.
Scoles DR, Minikel EV, Pulst SM. Scoles DR, et al. Neurol Genet. 2019 Apr 1;5(2):e323. doi: 10.1212/NXG.0000000000000323. eCollection 2019 Apr. Neurol Genet. 2019. PMID: 31119194 Free PMC article. Review.
Diabetic neuropathy--a review.
Said G. Said G. Nat Clin Pract Neurol. 2007 Jun;3(6):331-40. doi: 10.1038/ncpneuro0504. Nat Clin Pract Neurol. 2007. PMID: 17549059 Review.
Epilepsy in children.
Arnold ST, Dodson WE. Arnold ST, et al. Baillieres Clin Neurol. 1996 Dec;5(4):783-802. Baillieres Clin Neurol. 1996. PMID: 9068881 Review.
Next-generation sequencing approach to hyperCKemia: A 2-year cohort study.
Rubegni A, Malandrini A, Dosi C, Astrea G, Baldacci J, Battisti C, Bertocci G, Donati MA, Dotti MT, Federico A, Giannini F, Grosso S, Guerrini R, Lenzi S, Maioli MA, Melani F, Mercuri E, Sacchini M, Salvatore S, Siciliano G, Tolomeo D, Tonin P, Volpi N, Santorelli FM, Cassandrini D. Rubegni A, et al. Neurol Genet. 2019 Aug 16;5(5):e352. doi: 10.1212/NXG.0000000000000352. eCollection 2019 Oct. Neurol Genet. 2019. PMID: 31517061 Free PMC article.
CONCLUSIONS: This study of patients with undiagnosed hyperCKemia, highlighting the advantages of NGS used as a first-tier diagnostic approach in genetically heterogeneous conditions, illustrates the ongoing evolution of molecular diagnosis in the field of clinical neurology
CONCLUSIONS: This study of patients with undiagnosed hyperCKemia, highlighting the advantages of NGS used as a first-tier diagnostic approac …
Epilepsy with migrating focal seizures: KCNT1 mutation hotspots and phenotype variability.
Barcia G, Chemaly N, Kuchenbuch M, Eisermann M, Gobin-Limballe S, Ciorna V, Macaya A, Lambert L, Dubois F, Doummar D, Billette de Villemeur T, Villeneuve N, Barthez MA, Nava C, Boddaert N, Kaminska A, Bahi-Buisson N, Milh M, Auvin S, Bonnefont JP, Nabbout R. Barcia G, et al. Neurol Genet. 2019 Oct 25;5(6):e363. doi: 10.1212/NXG.0000000000000363. eCollection 2019 Dec. Neurol Genet. 2019. PMID: 31872048 Free PMC article.
Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts.
Iwaki H, Blauwendraat C, Leonard HL, Liu G, Maple-Grødem J, Corvol JC, Pihlstrøm L, van Nimwegen M, Hutten SJ, Nguyen KH, Rick J, Eberly S, Faghri F, Auinger P, Scott KM, Wijeyekoon R, Van Deerlin VM, Hernandez DG, Day-Williams AG, Brice A, Alves G, Noyce AJ, Tysnes OB, Evans JR, Breen DP, Estrada K, Wegel CE, Danjou F, Simon DK, Ravina B, Toft M, Heutink P, Bloem BR, Weintraub D, Barker RA, Williams-Gray CH, van de Warrenburg BP, Van Hilten JJ, Scherzer CR, Singleton AB, Nalls MA. Iwaki H, et al. Neurol Genet. 2019 Jul 9;5(4):e348. doi: 10.1212/NXG.0000000000000348. eCollection 2019 Aug. Neurol Genet. 2019. PMID: 31404238 Free PMC article.
Headaches and polygenic scores.
Vilhjálmsson BJ, Privé F. Vilhjálmsson BJ, et al. Neurol Genet. 2019 Oct 24;5(6):e368. doi: 10.1212/NXG.0000000000000368. eCollection 2019 Dec. Neurol Genet. 2019. PMID: 31872052 Free PMC article. No abstract available.
Ethics.
Young GB. Young GB. Baillieres Clin Neurol. 1996 Oct;5(3):673-84. Baillieres Clin Neurol. 1996. PMID: 9117081 Review.
Infections.
Bolton CF. Bolton CF. Baillieres Clin Neurol. 1996 Oct;5(3):599-626. Baillieres Clin Neurol. 1996. PMID: 9117078 Review. No abstract available.
Splitting vs lumping: Does the phenotype matter anymore?
Pavlakis S. Pavlakis S. Neurol Genet. 2020 Jan 13;6(1):e395. doi: 10.1212/NXG.0000000000000395. eCollection 2020 Feb. Neurol Genet. 2020. PMID: 32043493 Free PMC article. No abstract available.
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