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

Year Number of Results
1984 1
1985 4
1986 4
1987 1
1988 2
1989 2
1990 2
1991 3
1992 1
1993 2
1994 1
1996 1
1998 1
1999 4
2000 3
2001 1
2003 1
2008 1
2012 1
2014 1
2015 1
2016 1
2017 1
2024 0

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38 results

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Page 1
Homozygous SLC4A11 mutation in a large Irish CHED2 pedigree.
Hand CK, McGuire M, Parfrey NA, Murphy CC. Hand CK, et al. Among authors: parfrey na. Ophthalmic Genet. 2017 Mar-Apr;38(2):148-151. doi: 10.3109/13816810.2016.1151901. Epub 2016 Apr 8. Ophthalmic Genet. 2017. PMID: 27057589
Phenotypic Variation in a Caucasian Kindred with Chorea-Acanthocytosis.
Merwick Á, Mok T, McNamara B, Parfrey NA, Moore H, Sweeney BJ, Hand CK, Ryan AM. Merwick Á, et al. Among authors: parfrey na. Mov Disord Clin Pract. 2014 Dec 6;2(1):86-89. doi: 10.1002/mdc3.12117. eCollection 2015 Mar. Mov Disord Clin Pract. 2014. PMID: 30713887 Free PMC article. No abstract available.
Role of T helper lymphocytes in autoimmune diseases.
Prud'homme GJ, Parfrey NA. Prud'homme GJ, et al. Among authors: parfrey na. Lab Invest. 1988 Aug;59(2):158-72. Lab Invest. 1988. PMID: 2969996 Review. No abstract available.
Association of NOD2 with Crohn's disease in a homogenous Irish population.
Bairead E, Harmon DL, Curtis AM, Kelly Y, O'Leary C, Gardner M, Leahy DT, Vaughan P, Keegan D, O'Morain C, O'Donoghue D, Shanahan F, Parfrey NA, Quane KA. Bairead E, et al. Among authors: parfrey na. Eur J Hum Genet. 2003 Mar;11(3):237-44. doi: 10.1038/sj.ejhg.5200954. Eur J Hum Genet. 2003. PMID: 12673278
38 results