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Results by year

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

Year Number of Results
1975 1
1976 3
1977 5
1978 4
1980 4
1981 1
1982 1
1983 2
1984 6
1985 3
1986 3
1987 3
1988 4
1989 10
1990 7
1991 12
1992 10
1993 5
1994 9
1995 16
1996 11
1997 10
1998 9
1999 5
2000 7
2001 8
2002 11
2003 4
2004 4
2005 9
2006 11
2007 7
2008 12
2009 9
2010 7
2011 9
2012 8
2013 5
2014 8
2015 4
2016 3
2018 1
2023 0

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Search Results

259 results

Results by year

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Page 1
Identification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 gene.
Stheneur C, Collod-Béroud G, Faivre L, Buyck JF, Gouya L, Le Parc JM, Moura B, Muti C, Grandchamp B, Sultan G, Claustres M, Aegerter P, Chevallier B, Jondeau G, Boileau C. Stheneur C, et al. Among authors: grandchamp b. Eur J Hum Genet. 2009 Sep;17(9):1121-8. doi: 10.1038/ejhg.2009.36. Epub 2009 Mar 18. Eur J Hum Genet. 2009. PMID: 19293843 Free PMC article.
Acute intermittent porphyria.
Grandchamp B. Grandchamp B. Semin Liver Dis. 1998;18(1):17-24. doi: 10.1055/s-2007-1007136. Semin Liver Dis. 1998. PMID: 9516674 Review.
Review: molecular pathogenesis of hepatic acute porphyrias.
Grandchamp B, Puy H, Lamoril J, Deybach JC, Nordmann Y. Grandchamp B, et al. J Gastroenterol Hepatol. 1996 Nov;11(11):1046-52. doi: 10.1111/j.1440-1746.1996.tb00035.x. J Gastroenterol Hepatol. 1996. PMID: 8985829 Review.
Molecular genetics of porphyrias.
Nordmann Y, de Verneuil H, Deybach JC, Delfau MH, Grandchamp B. Nordmann Y, et al. Among authors: grandchamp b. Ann Med. 1990 Dec;22(6):387-91. doi: 10.3109/07853899009147275. Ann Med. 1990. PMID: 2076270 Review. No abstract available.
The MUC5B variant is associated with idiopathic pulmonary fibrosis but not with systemic sclerosis interstitial lung disease in the European Caucasian population.
Borie R, Crestani B, Dieude P, Nunes H, Allanore Y, Kannengiesser C, Airo P, Matucci-Cerinic M, Wallaert B, Israel-Biet D, Cadranel J, Cottin V, Gazal S, Peljto AL, Varga J, Schwartz DA, Valeyre D, Grandchamp B. Borie R, et al. Among authors: grandchamp b. PLoS One. 2013 Aug 5;8(8):e70621. doi: 10.1371/journal.pone.0070621. Print 2013. PLoS One. 2013. PMID: 23940607 Free PMC article. Review.
PARKIN Inactivation Links Parkinson's Disease to Melanoma.
Hu HH, Kannengiesser C, Lesage S, André J, Mourah S, Michel L, Descamps V, Basset-Seguin N, Bagot M, Bensussan A, Lebbé C, Deschamps L, Saiag P, Leccia MT, Bressac-de-Paillerets B, Tsalamlal A, Kumar R, Klebe S, Grandchamp B, Andrieu-Abadie N, Thomas L, Brice A, Dumaz N, Soufir N. Hu HH, et al. Among authors: grandchamp b. J Natl Cancer Inst. 2015 Dec 17;108(3). doi: 10.1093/jnci/djv340. Print 2016 Mar. J Natl Cancer Inst. 2015. PMID: 26683220
Coproporphyrinogen III oxidase assay.
Grandchamp B, Nordmann Y. Grandchamp B, et al. Enzyme. 1982;28(2-3):196-205. doi: 10.1159/000459102. Enzyme. 1982. PMID: 7140721
Truncating mutations of TP53AIP1 gene predispose to cutaneous melanoma.
Benfodda M, Gazal S, Descamps V, Basset-Seguin N, Deschamps L, Thomas L, Lebbe C, Saiag P, Zanetti R, Sacchetto L, Chiorino G, Scatolini M, Grandchamp B, Bensussan A, Soufir N. Benfodda M, et al. Among authors: grandchamp b. Genes Chromosomes Cancer. 2018 Jun;57(6):294-303. doi: 10.1002/gcc.22528. Epub 2018 Feb 21. Genes Chromosomes Cancer. 2018. PMID: 29359367
259 results