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

Year Number of Results
1932 2
1950 1
1959 1
1963 1
1970 1
1973 2
1974 1
1976 3
1977 6
1978 3
1979 7
1980 9
1981 10
1982 9
1983 4
1984 2
1985 3
1987 4
1988 11
1989 8
1990 6
1991 9
1992 5
1993 6
1994 6
1995 6
1996 5
1997 5
1998 2
1999 4
2000 7
2001 2
2002 1
2003 2
2004 2
2005 2
2006 3
2009 4
2010 3
2011 2
2012 1
2013 2
2014 4
2015 6
2016 5
2017 7
2018 7
2019 6
2020 7
2021 10
2022 6
Text availability
Article attribute
Article type
Publication date

Search Results

221 results
Results by year
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Page 1
Opsoclonus-myoclonus-ataxia syndrome in children.
Bhatia P, Heim J, Cornejo P, Kane L, Santiago J, Kruer MC. Bhatia P, et al. Among authors: heim j. J Neurol. 2022 Feb;269(2):750-757. doi: 10.1007/s00415-021-10536-3. Epub 2021 Mar 29. J Neurol. 2022. PMID: 33779841 Review.
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Jin SC, Lewis SA, Bakhtiari S, Zeng X, Sierant MC, Shetty S, Nordlie SM, Elie A, Corbett MA, Norton BY, van Eyk CL, Haider S, Guida BS, Magee H, Liu J, Pastore S, Vincent JB, Brunstrom-Hernandez J, Papavasileiou A, Fahey MC, Berry JG, Harper K, Zhou C, Zhang J, Li B, Zhao H, Heim J, Webber DL, Frank MSB, Xia L, Xu Y, Zhu D, Zhang B, Sheth AH, Knight JR, Castaldi C, Tikhonova IR, López-Giráldez F, Keren B, Whalen S, Buratti J, Doummar D, Cho M, Retterer K, Millan F, Wang Y, Waugh JL, Rodan L, Cohen JS, Fatemi A, Lin AE, Phillips JP, Feyma T, MacLennan SC, Vaughan S, Crompton KE, Reid SM, Reddihough DS, Shang Q, Gao C, Novak I, Badawi N, Wilson YA, McIntyre SJ, Mane SM, Wang X, Amor DJ, Zarnescu DC, Lu Q, Xing Q, Zhu C, Bilguvar K, Padilla-Lopez S, Lifton RP, Gecz J, MacLennan AH, Kruer MC. Jin SC, et al. Among authors: heim j. Nat Genet. 2020 Oct;52(10):1046-1056. doi: 10.1038/s41588-020-0695-1. Epub 2020 Sep 28. Nat Genet. 2020. PMID: 32989326
Cataplexy in Patients Harboring the KCNMA1 p.N999S Mutation.
Heim J, Vemuri A, Lewis S, Guida B, Troester M, Keros S, Meredith A, Kruer MC. Heim J, et al. Mov Disord Clin Pract. 2020 Aug 21;7(7):861-862. doi: 10.1002/mdc3.13024. eCollection 2020 Oct. Mov Disord Clin Pract. 2020. PMID: 33043086 Free PMC article. No abstract available.
Prospects for the next anti-Pseudomonas drug.
Page MG, Heim J. Page MG, et al. Among authors: heim j. Curr Opin Pharmacol. 2009 Oct;9(5):558-65. doi: 10.1016/j.coph.2009.08.006. Epub 2009 Sep 12. Curr Opin Pharmacol. 2009. PMID: 19748829 Review.
Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Jin SC, Lewis SA, Bakhtiari S, Zeng X, Sierant MC, Shetty S, Nordlie SM, Elie A, Corbett MA, Norton BY, van Eyk CL, Haider S, Guida BS, Magee H, Liu J, Pastore S, Vincent JB, Brunstrom-Hernandez J, Papavasileiou A, Fahey MC, Berry JG, Harper K, Zhou C, Zhang J, Li B, Zhao H, Heim J, Webber DL, Frank MSB, Xia L, Xu Y, Zhu D, Zhang B, Sheth AH, Knight JR, Castaldi C, Tikhonova IR, López-Giráldez F, Keren B, Whalen S, Buratti J, Doummar D, Cho M, Retterer K, Millan F, Wang Y, Waugh JL, Rodan L, Cohen JS, Fatemi A, Lin AE, Phillips JP, Feyma T, MacLennan SC, Vaughan S, Crompton KE, Reid SM, Reddihough DS, Shang Q, Gao C, Novak I, Badawi N, Wilson YA, McIntyre SJ, Mane SM, Wang X, Amor DJ, Zarnescu DC, Lu Q, Xing Q, Zhu C, Bilguvar K, Padilla-Lopez S, Lifton RP, Gecz J, MacLennan AH, Kruer MC. Jin SC, et al. Among authors: heim j. Nat Genet. 2021 Mar;53(3):412. doi: 10.1038/s41588-021-00780-8. Nat Genet. 2021. PMID: 33432185 No abstract available.
Second-site NMR screening and linker design.
Jahnke W, Flörsheimer A, Blommers MJ, Paris CG, Heim J, Nalin CM, Perez LB. Jahnke W, et al. Among authors: heim j. Curr Top Med Chem. 2003;3(1):69-80. doi: 10.2174/1568026033392778. Curr Top Med Chem. 2003. PMID: 12570778 Review.
The biosynthesis of sulfur-containing beta-lactam antibiotics.
Nüesch J, Heim J, Treichler HJ. Nüesch J, et al. Among authors: heim j. Annu Rev Microbiol. 1987;41:51-75. doi: 10.1146/annurev.mi.41.100187.000411. Annu Rev Microbiol. 1987. PMID: 3120640 Review. No abstract available.
Soluble guanylyl cyclase and platelet function.
Buechler WA, Ivanova K, Wolfram G, Drummer C, Heim JM, Gerzer R. Buechler WA, et al. Among authors: heim jm. Ann N Y Acad Sci. 1994 Apr 18;714:151-7. doi: 10.1111/j.1749-6632.1994.tb12039.x. Ann N Y Acad Sci. 1994. PMID: 7912486 Review. No abstract available.
Biallelic mutations of TBC1D24 in exercise-induced paroxysmal dystonia.
Steel D, Heim J, Kruer MC, Sanchis-Juan A, Raymond LF, Eunson P, Kurian MA. Steel D, et al. Among authors: heim j. Mov Disord. 2020 Feb;35(2):372-373. doi: 10.1002/mds.27981. Epub 2020 Jan 10. Mov Disord. 2020. PMID: 31922275 No abstract available.
221 results