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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
1954 3
1956 2
1957 5
1958 3
1959 8
1960 4
1961 4
1962 4
1963 5
1964 9
1965 3
1966 4
1967 4
1968 6
1969 6
1970 5
1971 8
1972 3
1973 3
1974 1
1975 6
1976 5
1977 2
1978 6
1979 7
1980 5
1981 10
1982 6
1983 3
1984 3
1985 1
1986 2
1987 3
1988 6
1989 9
1990 10
1991 13
1992 12
1993 11
1994 12
1995 15
1996 9
1997 5
1998 6
1999 2
2000 2
2001 1
2002 1
2003 1
2004 1
2007 4
2008 1
2009 6
2010 13
2011 12
2012 11
2013 13
2014 14
2015 15
2016 11
2017 17
2018 15
2019 26
2020 30
2021 23
2022 14
Text availability
Article attribute
Article type
Publication date

Search Results

456 results
Results by year
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Page 1
The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant.
Koolen DA, Pfundt R, Linda K, Beunders G, Veenstra-Knol HE, Conta JH, Fortuna AM, Gillessen-Kaesbach G, Dugan S, Halbach S, Abdul-Rahman OA, Winesett HM, Chung WK, Dalton M, Dimova PS, Mattina T, Prescott K, Zhang HZ, Saal HM, Hehir-Kwa JY, Willemsen MH, Ockeloen CW, Jongmans MC, Van der Aa N, Failla P, Barone C, Avola E, Brooks AS, Kant SG, Gerkes EH, Firth HV, Õunap K, Bird LM, Masser-Frye D, Friedman JR, Sokunbi MA, Dixit A, Splitt M; DDD Study, Kukolich MK, McGaughran J, Coe BP, Flórez J, Nadif Kasri N, Brunner HG, Thompson EM, Gecz J, Romano C, Eichler EE, de Vries BB. Koolen DA, et al. Among authors: fortuna am. Eur J Hum Genet. 2016 May;24(5):652-9. doi: 10.1038/ejhg.2015.178. Epub 2015 Aug 26. Eur J Hum Genet. 2016. PMID: 26306646 Free PMC article.
Congenital Disorders of Glycosylation in Portugal-Two Decades of Experience.
Quelhas D, Martins E, Azevedo L, Bandeira A, Diogo L, Garcia P, Sequeira S, Ferreira AC, Teles EL, Rodrigues E, Fortuna AM, Mendonça C, Fernandes HC, Medeira A, Gaspar A, Janeiro P, Oliveira A, Laranjeira F, Ribeiro I, Souche E, Race V, Keldermans L, Matthijs G, Jaeken J. Quelhas D, et al. Among authors: fortuna am. J Pediatr. 2021 Apr;231:148-156. doi: 10.1016/j.jpeds.2020.12.026. Epub 2020 Dec 17. J Pediatr. 2021. PMID: 33340551
Paediatric intracranial meningiomas.
Ferrante L, Acqui M, Artico M, Mastronardi L, Fortuna A. Ferrante L, et al. Among authors: fortuna a. Br J Neurosurg. 1989;3(2):189-96. doi: 10.3109/02688698909002794. Br J Neurosurg. 1989. PMID: 2679687 Review.
Genomic Landscape of Malignant Peripheral Nerve Sheath Tumor‒Like Melanoma.
Muniz TP, Sorotsky H, Kanjanapan Y, Rose AAN, Araujo DV, Fortuna A, Ghazarian D, Kamil ZS, Pugh T, Mah M, Thiagarajah M, Torti D, Spreafico A, Hogg D. Muniz TP, et al. Among authors: fortuna a. J Invest Dermatol. 2021 Oct;141(10):2470-2479. doi: 10.1016/j.jid.2021.03.016. Epub 2021 Apr 6. J Invest Dermatol. 2021. PMID: 33831431
456 results