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Results by year

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

Year Number of Results
1972 1
1974 1
1978 1
1980 2
1981 1
1982 1
1983 1
1984 6
1985 3
1986 1
1987 4
1988 2
1989 7
1990 1
1991 3
1992 4
1994 3
1995 4
1996 4
1997 2
1998 3
1999 3
2000 3
2001 2
2002 2
2003 3
2004 6
2005 5
2006 2
2007 4
2008 1
2009 5
2010 3
2011 2
2012 7
2013 4
2014 4
2015 3
2016 1
2017 1
2018 2
2019 1
2020 3
2022 1
2023 3
2024 1

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Search Results

120 results

Results by year

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Page 1
[Argentine consensus on late-onset Pompe's disease].
Dubrovsky A, Fulgenzi E, De Vito EL, Barroso F, Berardo A, Bettini M, Binaghi D, Calabrese E, Carlés D, Chaves M, Chloca F, Conti E, Corderi J, Di Gennaro F, Ferradás N, Jáuregui A, Lubieniecki F, Mazia C, Medina M, Pirra L, Politei J, Reisin R, Rosa AL, Rugiero M, Salutto V, Schenone A, Sussini M, Taratuto AL. Dubrovsky A, et al. Among authors: carles d. Medicina (B Aires). 2018;78 Suppl 1:1-23. Medicina (B Aires). 2018. PMID: 30179846 Free article. Spanish.
[Smith-Lemli-Opitz syndrome].
Pelluard-Nehmé F, Carles D, Alberti EM, Saura R, Wong C, Wolf C. Pelluard-Nehmé F, et al. Among authors: carles d. Ann Pathol. 2005 Sep;25(4):318-21. doi: 10.1016/s0242-6498(05)80136-1. Ann Pathol. 2005. PMID: 16327658 French.
Ellis-Van Creveld Syndrome: Clinical and Molecular Analysis of 50 Individuals.
Aubert-Mucca M, Huber C, Baujat G, Michot C, Zarhrate M, Bras M, Boutaud L, Malan V, Attie-Bitach T; Clinical Contributors; Cormier-Daire V. Aubert-Mucca M, et al. J Med Genet. 2023 Apr;60(4):337-345. doi: 10.1136/jmg-2022-108435. Epub 2022 Aug 4. J Med Genet. 2023. PMID: 35927022
Donnai-Barrow syndrome: four additional patients.
Chassaing N, Lacombe D, Carles D, Calvas P, Saura R, Bieth E. Chassaing N, et al. Among authors: carles d. Am J Med Genet A. 2003 Sep 1;121A(3):258-62. doi: 10.1002/ajmg.a.20266. Am J Med Genet A. 2003. PMID: 12923867 Review.
Fryns syndrome: report on 8 new cases.
Aymé S, Julian C, Gambarelli D, Mariotti B, Luciani A, Sudan N, Maurin N, Philip N, Serville F, Carles D, et al. Aymé S, et al. Among authors: carles d. Clin Genet. 1989 Mar;35(3):191-201. doi: 10.1111/j.1399-0004.1989.tb02927.x. Clin Genet. 1989. PMID: 2650934 Review.
[Placental pathology of uteroplacental vascular deficiency].
Carles D, Pelluard F, André G, Naudion S, Poingt M, Castain C, Sauvestre F. Carles D, et al. Ann Pathol. 2013 Aug;33(4):230-6. doi: 10.1016/j.annpat.2013.04.018. Epub 2013 Jul 31. Ann Pathol. 2013. PMID: 23954115 Review. French.
Pathological Findings in Feto-maternal Hemorrhage.
Carles D, André G, Pelluard F, Martin O, Sauvestre F. Carles D, et al. Pediatr Dev Pathol. 2014 Mar-Apr;17(2):102-6. doi: 10.2350/13-12-1419-OA.1. Epub 2014 Feb 27. Pediatr Dev Pathol. 2014. PMID: 24575782
In utero seizures revealing dentato-olivary dysplasia caused by SCN2A mutation.
Sauvestre F, Moutton S, Badens C, Broussin B, Carles D, Houcinat N, Lacoste C, Marguet F, Pecheux C, Villard L, Pelluard F, Laquerrière A, André G. Sauvestre F, et al. Among authors: carles d. Neuropathol Appl Neurobiol. 2017 Dec;43(7):631-635. doi: 10.1111/nan.12409. Epub 2017 Jun 9. Neuropathol Appl Neurobiol. 2017. PMID: 28489313 No abstract available.
120 results