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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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120 results

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Page 1
Genotype-phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease.
Denamur E, Delezoide AL, Alberti C, Bourillon A, Gubler MC, Bouvier R, Pascaud O, Elion J, Grandchamp B, Michel-Calemard L, Missy P, Zaccaria I, Le Nagard H, Gerard B, Loirat C; Société Française de Foetopathologie; Barbet J, Beaufrère AM, Berchel C, Bessières B, Boudjemaa S, Buenerd A, Carles D, Clemenson A, Dechelotte P, Devisme L, Dijoud F, Espérandieu O, Fallet C, Gonzalès M, Hillion Y, Jacob B, Joubert M, Kermanach P, Lallemand A, Laquerrière A, Laurent N, Liprandi A, Loeuillet L, Loget P, Martinovic J, Ménez F, Narcy F, Roux JJ, Rouleau-Dubois C, Sinico M, Tantau J, Wann AR. Denamur E, et al. Among authors: carles d. Kidney Int. 2010 Feb;77(4):350-8. doi: 10.1038/ki.2009.440. Epub 2009 Nov 25. Kidney Int. 2010. PMID: 19940839 Free article.
[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
Clinical and bronchial parameters associated with the exacerbation frequency of severe preschool wheezers.
Beaufils F, Esteves P, Enaud R, Prevel R, Henrot P, Campagnac M, Maurat E, Michelet M, Lavrand F, Begueret H, Trian T, Fayon M, Berger P; P’tit Asthme Study Group. Beaufils F, et al. J Allergy Clin Immunol Pract. 2024 Apr;12(4):1067-1070. doi: 10.1016/j.jaip.2023.12.017. Epub 2023 Dec 19. J Allergy Clin Immunol Pract. 2024. PMID: 38128699 Free article. No abstract available.
120 results