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

Year Number of Results
1986 1
1989 4
1990 1
1991 3
1992 3
1993 3
1994 3
1995 4
1996 4
1997 3
1998 3
1999 3
2000 5
2001 1
2002 2
2003 1
2004 1
2005 2
2007 2
2009 1
2010 2
2011 2
2012 2
2013 1
2015 3
2016 1
2018 2
2019 2
2024 0

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62 results

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Page 1
Molecular genetics of cystic fibrosis.
Tsui LC, Rommens J, Kerem B, Rozmahel R, Zielenski J, Kennedy D, Markiewicz D, Plavsic N, Chou JL, Bozon D, et al. Tsui LC, et al. Among authors: bozon d. Adv Exp Med Biol. 1991;290:9-17; discussion 17-8. doi: 10.1007/978-1-4684-5934-0_2. Adv Exp Med Biol. 1991. PMID: 1719772 Review. No abstract available.
Combined liver-kidney transplantation in primary hyperoxaluria type 1.
Cochat P, Gaulier JM, Koch Nogueira PC, Feber J, Jamieson NV, Rolland MO, Divry P, Bozon D, Dubourg L. Cochat P, et al. Among authors: bozon d. Eur J Pediatr. 1999 Dec;158 Suppl 2:S75-80. doi: 10.1007/pl00014327. Eur J Pediatr. 1999. PMID: 10603104 Review.
Mucopolysaccharidosis type II--genotype/phenotype aspects.
Froissart R, Moreira da Silva I, Guffon N, Bozon D, Maire I. Froissart R, et al. Among authors: bozon d. Acta Paediatr Suppl. 2002;91(439):82-7. doi: 10.1111/j.1651-2227.2002.tb03116.x. Acta Paediatr Suppl. 2002. PMID: 12572848
SURF1 deficiency causes demyelinating Charcot-Marie-Tooth disease.
Echaniz-Laguna A, Ghezzi D, Chassagne M, Mayençon M, Padet S, Melchionda L, Rouvet I, Lannes B, Bozon D, Latour P, Zeviani M, Mousson de Camaret B. Echaniz-Laguna A, et al. Among authors: bozon d. Neurology. 2013 Oct 22;81(17):1523-30. doi: 10.1212/WNL.0b013e3182a4a518. Epub 2013 Sep 11. Neurology. 2013. PMID: 24027061 Free PMC article.
Genetics of congenital heart defects.
el Zein L, Schön P, Chhin B, Guichard C, Sauer U, Bozon D, Baptista MJ, Bouvagnet P. el Zein L, et al. Among authors: bozon d. Rev Port Cardiol. 2004 Jan;23(1):137-42. Rev Port Cardiol. 2004. PMID: 15058152 Review. No abstract available.
Hunter syndrome: gene deletions and rearrangements.
Froissart R, Blond JL, Maire I, Guibaud P, Hopwood JJ, Mathieu M, Bozon D. Froissart R, et al. Among authors: bozon d. Hum Mutat. 1993;2(2):138-40. doi: 10.1002/humu.1380020214. Hum Mutat. 1993. PMID: 8318991 No abstract available.
Processing of iduronate 2-sulphatase in human fibroblasts.
Froissart R, Millat G, Mathieu M, Bozon D, Maire I. Froissart R, et al. Among authors: bozon d. Biochem J. 1995 Jul 15;309 ( Pt 2)(Pt 2):425-30. doi: 10.1042/bj3090425. Biochem J. 1995. PMID: 7626005 Free PMC article.
U1 snRNA mis-binding: a new cause of CMT1B.
Crehalet H, Latour P, Bonnet V, Attarian S, Labauge P, Bonello N, Bernard R, Millat G, Rousson R, Bozon D. Crehalet H, et al. Among authors: bozon d. Neurogenetics. 2010 Feb;11(1):13-9. doi: 10.1007/s10048-009-0199-8. Epub 2009 May 28. Neurogenetics. 2010. PMID: 19475438
62 results