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

Year Number of Results
1974 1
1975 2
1976 3
1977 1
1978 1
1979 9
1980 3
1981 2
1982 4
1983 6
1984 4
1985 4
1986 3
1987 1
1988 4
1989 5
1990 5
1991 6
1992 8
1993 5
1994 5
1995 5
1996 3
1997 4
1998 6
1999 4
2000 8
2001 3
2002 1
2003 5
2004 2
2005 1
2006 3
2007 3
2008 7
2009 4
2010 2
2011 2
2012 6
2013 3
2014 3
2015 2
2016 6
2017 7
2018 4
2021 1
2022 2
2024 1

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176 results

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Page 1
IRDiRC-recommended.
Aymé S. Aymé S. Eur J Hum Genet. 2016 Jul;24(7):955. doi: 10.1038/ejhg.2015.236. Eur J Hum Genet. 2016. PMID: 27307111 Free PMC article. No abstract available.
Editorial: Prevention, diagnosis and treatment of rare disorders.
Cox TM, Tylki-Szymańska A, Aymé S, Dooms M. Cox TM, et al. Among authors: ayme s. Front Pharmacol. 2022 Sep 28;13:1026064. doi: 10.3389/fphar.2022.1026064. eCollection 2022. Front Pharmacol. 2022. PMID: 36249823 Free PMC article. No abstract available.
Introduction.
Matthijs G, Aymé S. Matthijs G, et al. Among authors: ayme s. Eur J Hum Genet. 2008 May;16 Suppl 1:S1-2. doi: 10.1038/ejhg.2008.35. Eur J Hum Genet. 2008. PMID: 18432280 No abstract available.
The Human Phenotype Ontology in 2017.
Köhler S, Vasilevsky NA, Engelstad M, Foster E, McMurry J, Aymé S, Baynam G, Bello SM, Boerkoel CF, Boycott KM, Brudno M, Buske OJ, Chinnery PF, Cipriani V, Connell LE, Dawkins HJ, DeMare LE, Devereau AD, de Vries BB, Firth HV, Freson K, Greene D, Hamosh A, Helbig I, Hum C, Jähn JA, James R, Krause R, F Laulederkind SJ, Lochmüller H, Lyon GJ, Ogishima S, Olry A, Ouwehand WH, Pontikos N, Rath A, Schaefer F, Scott RH, Segal M, Sergouniotis PI, Sever R, Smith CL, Straub V, Thompson R, Turner C, Turro E, Veltman MW, Vulliamy T, Yu J, von Ziegenweidt J, Zankl A, Züchner S, Zemojtel T, Jacobsen JO, Groza T, Smedley D, Mungall CJ, Haendel M, Robinson PN. Köhler S, et al. Among authors: ayme s. Nucleic Acids Res. 2017 Jan 4;45(D1):D865-D876. doi: 10.1093/nar/gkw1039. Epub 2016 Nov 28. Nucleic Acids Res. 2017. PMID: 27899602 Free PMC article. Review.
Constitutional chromosomal breakage.
Giraud F, Ayme S, Mattei JF, Mattei MG. Giraud F, et al. Among authors: ayme s. Hum Genet. 1976 Oct 28;34(2):125-36. doi: 10.1007/BF00278880. Hum Genet. 1976. PMID: 1033912
The OrphanAnaesthesia project.
Becke K, Aymé S, Strau J, Veyckemans F, Emmig U. Becke K, et al. Among authors: ayme s. Eur J Anaesthesiol. 2011 Oct;28(10):678-9. doi: 10.1097/EJA.0b013e32834a28ee. Eur J Anaesthesiol. 2011. PMID: 21912238 No abstract available.
Prenatal diagnosis of Fryns' syndrome.
Pellissier MC, Philip N, Potier A, Scheiner C, Aymé S, Mattei JF, Giraud F. Pellissier MC, et al. Among authors: ayme s. Prenat Diagn. 1992 Apr;12(4):299-303. doi: 10.1002/pd.1970120410. Prenat Diagn. 1992. PMID: 1614987 Review.
Networking for rare diseases: a necessity for Europe.
Aymé S, Schmidtke J. Aymé S, et al. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2007 Dec;50(12):1477-83. doi: 10.1007/s00103-007-0381-9. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2007. PMID: 18026888 Review.
176 results