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

Year Number of Results
1952 1
1953 2
1956 1
1959 2
1960 1
1963 3
1964 1
1965 1
1966 2
1967 3
1968 4
1969 1
1970 2
1971 2
1973 6
1975 3
1976 8
1977 3
1978 5
1979 5
1980 4
1981 5
1982 7
1983 5
1984 5
1985 3
1986 3
1987 3
1988 1
1989 1
1991 3
1992 3
1993 2
1995 4
1996 1
1997 3
1998 5
1999 6
2000 7
2001 9
2002 5
2003 5
2004 3
2005 7
2006 8
2007 9
2008 10
2009 9
2010 8
2011 9
2012 4
2013 6
2014 4
2015 1
2016 4
2017 4
2018 3
2019 2
2020 9
2021 2
2022 3
2024 2
2025 5

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249 results

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Page 1
Pompe disease diagnosis and management guideline.
Kishnani PS, Steiner RD, Bali D, Berger K, Byrne BJ, Case LE, Crowley JF, Downs S, Howell RR, Kravitz RM, Mackey J, Marsden D, Martins AM, Millington DS, Nicolino M, O'Grady G, Patterson MC, Rapoport DM, Slonim A, Spencer CT, Tifft CJ, Watson MS. Kishnani PS, et al. Among authors: slonim a. Genet Med. 2006 May;8(5):267-88. doi: 10.1097/01.gim.0000218152.87434.f3. Genet Med. 2006. PMID: 16702877 Free PMC article. No abstract available.
Population genetic screening efficiently identifies carriers of autosomal dominant diseases.
Grzymski JJ, Elhanan G, Morales Rosado JA, Smith E, Schlauch KA, Read R, Rowan C, Slotnick N, Dabe S, Metcalf WJ, Lipp B, Reed H, Sharma L, Levin E, Kao J, Rashkin M, Bowes J, Dunaway K, Slonim A, Washington N, Ferber M, Bolze A, Lu JT. Grzymski JJ, et al. Among authors: slonim a. Nat Med. 2020 Aug;26(8):1235-1239. doi: 10.1038/s41591-020-0982-5. Epub 2020 Jul 27. Nat Med. 2020. PMID: 32719484
Diencephalic syndrome revisited.
Burr IM, Slonim AE, Danish RK, Gadoth N, Butler IJ. Burr IM, et al. Among authors: slonim ae. J Pediatr. 1976 Mar;88(3):439-44. doi: 10.1016/s0022-3476(76)80260-0. J Pediatr. 1976. PMID: 1245953
Developing a framework and priorities to promote mobility among older adults.
Anderson LA, Slonim A, Yen IH, Jones DL, Allen P, Hunter RH, Goins RT, Leith KH, Rosenberg D, Satariano WA, McPhillips-Tangum C. Anderson LA, et al. Among authors: slonim a. Health Educ Behav. 2014 Oct;41(1 Suppl):10S-8S. doi: 10.1177/1090198114537492. Health Educ Behav. 2014. PMID: 25274706 Free PMC article.
Epimerase-deficiency galactosemia is not a binary condition.
Openo KK, Schulz JM, Vargas CA, Orton CS, Epstein MP, Schnur RE, Scaglia F, Berry GT, Gottesman GS, Ficicioglu C, Slonim AE, Schroer RJ, Yu C, Rangel VE, Keenan J, Lamance K, Fridovich-Keil JL. Openo KK, et al. Among authors: slonim ae. Am J Hum Genet. 2006 Jan;78(1):89-102. doi: 10.1086/498985. Epub 2005 Nov 14. Am J Hum Genet. 2006. PMID: 16385452 Free PMC article.
249 results