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

Year Number of Results
1968 1
1972 1
1973 2
1976 1
1978 2
1979 1
1980 5
1981 2
1982 2
1983 7
1984 6
1985 5
1986 6
1987 5
1988 3
1989 2
1990 5
1991 3
1992 3
1993 4
1994 3
1995 5
1996 2
1997 9
1998 1
1999 9
2000 2
2001 3
2002 3
2003 4
2004 4
2005 2
2006 3
2007 2
2008 4
2009 4
2010 3
2011 1
2012 2
2013 3
2014 3
2015 3
2016 2
2018 4
2019 3
2020 4
2021 9
2022 1
2023 3
2024 0

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160 results

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Page 1
Achondroplasia: a comprehensive clinical review.
Pauli RM. Pauli RM. Orphanet J Rare Dis. 2019 Jan 3;14(1):1. doi: 10.1186/s13023-018-0972-6. Orphanet J Rare Dis. 2019. PMID: 30606190 Free PMC article. Review.
Warfarin embryopathy.
Pauli RM, Hall JG. Pauli RM, et al. Lancet. 1979 Jul 21;2(8134):144. doi: 10.1016/s0140-6736(79)90017-5. Lancet. 1979. PMID: 88569 No abstract available.
Acanthosis nigricans in achondroplasia.
Smid CJ, Modaff P, Alade A, Legare JM, Pauli RM. Smid CJ, et al. Among authors: pauli rm. Am J Med Genet A. 2018 Dec;176(12):2630-2636. doi: 10.1002/ajmg.a.40506. Epub 2018 Oct 31. Am J Med Genet A. 2018. PMID: 30380187
Stillbirth: fetal disorders.
Pauli RM. Pauli RM. Clin Obstet Gynecol. 2010 Sep;53(3):646-55. doi: 10.1097/GRF.0b013e3181eb6755. Clin Obstet Gynecol. 2010. PMID: 20661049 Review.
Achondroplasia natural history study (CLARITY): 60-year experience in orthopedic surgery from four skeletal dysplasia centers.
Nahm NJ, Mackenzie WGS, Mackenzie WG, Gough E, Hashmi SS, Hecht JT, Legare JM, Little ME, Modaff P, Pauli RM, Rodriguez-Buritica DF, Serna ME, Smid CJ, Hoover-Fong J, Bober MB. Nahm NJ, et al. Among authors: pauli rm. Orphanet J Rare Dis. 2023 Jun 6;18(1):139. doi: 10.1186/s13023-023-02738-x. Orphanet J Rare Dis. 2023. PMID: 37280669 Free PMC article.
Familial agnathia-holoprosencephaly.
Pauli RM, Pettersen JC, Arya S, Gilbert EF. Pauli RM, et al. Am J Med Genet. 1983 Apr;14(4):677-98. doi: 10.1002/ajmg.1320140411. Am J Med Genet. 1983. PMID: 6846401
Multicenter study of mortality in achondroplasia.
Hashmi SS, Gamble C, Hoover-Fong J, Alade AY, Pauli RM, Modaff P, Carney M, Brown C, Bober MB, Hecht JT. Hashmi SS, et al. Among authors: pauli rm. Am J Med Genet A. 2018 Nov;176(11):2359-2364. doi: 10.1002/ajmg.a.40528. Epub 2018 Oct 1. Am J Med Genet A. 2018. PMID: 30276962
Syringomyelia in hereditary multiple exostosis.
Legare JM, Modaff P, Iskandar BJ, Pauli RM. Legare JM, et al. Among authors: pauli rm. Am J Med Genet A. 2016 Nov;170(11):2956-2959. doi: 10.1002/ajmg.a.37854. Epub 2016 Aug 2. Am J Med Genet A. 2016. PMID: 27480811
160 results