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

Year Number of Results
1984 1
1985 1
1986 1
1987 1
1988 4
1989 5
1990 1
1991 4
1992 4
1994 3
1995 2
1996 2
1997 2
1999 1
2000 1
2001 1
2003 1
2004 2
2005 1
2006 1
2007 1
2008 1
2009 3
2011 2
2015 1
2016 1
2017 2
2024 0

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48 results

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Page 1
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.
Crow YJ, Chase DS, Lowenstein Schmidt J, Szynkiewicz M, Forte GM, Gornall HL, Oojageer A, Anderson B, Pizzino A, Helman G, Abdel-Hamid MS, Abdel-Salam GM, Ackroyd S, Aeby A, Agosta G, Albin C, Allon-Shalev S, Arellano M, Ariaudo G, Aswani V, Babul-Hirji R, Baildam EM, Bahi-Buisson N, Bailey KM, Barnerias C, Barth M, Battini R, Beresford MW, Bernard G, Bianchi M, Billette de Villemeur T, Blair EM, Bloom M, Burlina AB, Carpanelli ML, Carvalho DR, Castro-Gago M, Cavallini A, Cereda C, Chandler KE, Chitayat DA, Collins AE, Sierra Corcoles C, Cordeiro NJ, Crichiutti G, Dabydeen L, Dale RC, D'Arrigo S, De Goede CG, De Laet C, De Waele LM, Denzler I, Desguerre I, Devriendt K, Di Rocco M, Fahey MC, Fazzi E, Ferrie CD, Figueiredo A, Gener B, Goizet C, Gowrinathan NR, Gowrishankar K, Hanrahan D, Isidor B, Kara B, Khan N, King MD, Kirk EP, Kumar R, Lagae L, Landrieu P, Lauffer H, Laugel V, La Piana R, Lim MJ, Lin JP, Linnankivi T, Mackay MT, Marom DR, Marques Lourenço C, McKee SA, Moroni I, Morton JE, Moutard ML, Murray K, Nabbout R, Nampoothiri S, Nunez-Enamorado N, Oades PJ, Olivieri I, Ostergaard JR, Pérez-Dueñas B, Prendiville JS, Ramesh V, Rasmussen M, Régal L, Ricci F, Rio M, Ro… See abstract for full author list ➔ Crow YJ, et al. Among authors: prendiville js. Am J Med Genet A. 2015 Feb;167A(2):296-312. doi: 10.1002/ajmg.a.36887. Epub 2015 Jan 16. Am J Med Genet A. 2015. PMID: 25604658 Free PMC article.
Childhood dermatitis herpetiformis.
Prendiville JS, Esterly NB. Prendiville JS, et al. Clin Dermatol. 1991 Jul-Sep;9(3):375-81. doi: 10.1016/0738-081x(91)90029-k. Clin Dermatol. 1991. PMID: 1806225 Review. No abstract available.
Skin signs of nutritional disorders.
Prendiville JS, Manfredi LN. Prendiville JS, et al. Semin Dermatol. 1992 Mar;11(1):88-97. Semin Dermatol. 1992. PMID: 1550720 Review.
Hereditary benign telangiectasia.
Gold MH, Eramo L, Prendiville JS. Gold MH, et al. Among authors: prendiville js. Pediatr Dermatol. 1989 Sep;6(3):194-7. doi: 10.1111/j.1525-1470.1989.tb00816.x. Pediatr Dermatol. 1989. PMID: 2798257
Transient erythroporphyria of infancy.
Crawford RI, Lawlor ER, Wadsworth LD, Prendiville JS. Crawford RI, et al. Among authors: prendiville js. J Am Acad Dermatol. 1996 Nov;35(5 Pt 2):833-4. doi: 10.1016/s0190-9622(96)90096-1. J Am Acad Dermatol. 1996. PMID: 8912598
Kindler syndrome and epidermolysis bullosa simplex.
Prendiville JS, Fine JD, Esterly NB. Prendiville JS, et al. J Am Acad Dermatol. 1990 Aug;23(2 Pt 1):327-8. doi: 10.1016/s0190-9622(08)81248-0. J Am Acad Dermatol. 1990. PMID: 2212134 No abstract available.
Kindler syndrome: report of two cases and review of the literature.
Forman AB, Prendiville JS, Esterly NB, Hebert AA, Duvic M, Horiguchi Y, Fine JD. Forman AB, et al. Among authors: prendiville js. Pediatr Dermatol. 1989 Jun;6(2):91-101. doi: 10.1111/j.1525-1470.1989.tb01004.x. Pediatr Dermatol. 1989. PMID: 2664740 Review.
48 results