Blayau M - Search Results

1

Short-term prednisolone followed by recombinant human alpha-interferon alone or combined with adenine-arabinoside in chronic hepatitis B. A prospective and randomized trial.

Brissot P, Jacquelinet C, Jouanolle H, David V, Guyader D, Guéguen M, Blayau M, Lescoat G, Messner M, Deugnier Y. Brissot P, et al. Among authors: blayau m. J Hepatol. 1991 Mar;12(2):181-9. doi: 10.1016/0168-8278(91)90936-6. J Hepatol. 1991. PMID: 2050997 Clinical Trial.

2

A new mutation of E-cadherin gene in familial gastric linitis plastica cancer with extra-digestive dissemination.

Dussaulx-Garin L, Blayau M, Pagenault M, Le Berre-Heresbach N, Raoul JL, Campion JP, David V, Bretagne JF. Dussaulx-Garin L, et al. Among authors: blayau m. Eur J Gastroenterol Hepatol. 2001 Jun;13(6):711-5. doi: 10.1097/00042737-200106000-00016. Eur J Gastroenterol Hepatol. 2001. PMID: 11434599

3

[Biological markers in hepatocellular carcinoma].

Deugnier Y, David V, Leray G, Blayau M, Le Gall JY. Deugnier Y, et al. Among authors: blayau m. Ann Biol Clin (Paris). 1988;46(1):85-8. Ann Biol Clin (Paris). 1988. PMID: 2455460 Review. French.

4

Dinucleotide repeat polymorphism at the FTHPI locus of chromosome 6.

Mauvieux V, Jouanolle AM, el Kahloun A, Blayau M, Le Gall JY, David V. Mauvieux V, et al. Among authors: blayau m. Nucleic Acids Res. 1991 Dec 25;19(24):6969. doi: 10.1093/nar/19.24.6969. Nucleic Acids Res. 1991. PMID: 1762936 Free PMC article.

5

Two polymorphisms at the locus D698 defined by a YAC.

David V, Boretto J, Jouanolle AM, Mauvieux V, el Khaloun A, Périchon M, Blayau M, Pontarotti P. David V, et al. Among authors: blayau m. Nucleic Acids Res. 1990 Sep 25;18(18):5582. doi: 10.1093/nar/18.18.5582-a. Nucleic Acids Res. 1990. PMID: 1977128 Free PMC article.

6

Identification of three novel mutations in the dystrophin gene detected by the heteroduplex/SSCA screening procedure. Mutations in brief no. 222. Online.

Dubourg C, Odent S, Fergelot P, Le Gall JY, David V, Blayau M. Dubourg C, et al. Among authors: blayau m. Hum Mutat. 1999;13(2):173. doi: 10.1002/(SICI)1098-1004(1999)13:2<173::AID-HUMU20>3.0.CO;2-3. Hum Mutat. 1999. PMID: 10094565

7

HLA class I gene polymorphism in genetic hemochromatosis.

Jouanolle AM, Yaouanq J, Blayau M, Périchon M, Fauchet R, Font MP, Le Gall JY, David V. Jouanolle AM, et al. Among authors: blayau m. Hum Genet. 1990 Aug;85(3):279-82. doi: 10.1007/BF00206746. Hum Genet. 1990. PMID: 1975556

8

A new mutation in the six-domain of SIX3 gene causes holoprosencephaly.

Pasquier L, Dubourg C, Blayau M, Lazaro L, Le Marec B, David V, Odent S. Pasquier L, et al. Among authors: blayau m. Eur J Hum Genet. 2000 Oct;8(10):797-800. doi: 10.1038/sj.ejhg.5200540. Eur J Hum Genet. 2000. PMID: 11039582

9

Molecular screening of the CFTR gene in men with anomalies of the vas deferens: identification of three novel mutations.

Jézéquel P, Dubourg C, Le Lannou D, Odent S, Le Gall JY, Blayau M, Le Treut A, David V. Jézéquel P, et al. Among authors: blayau m. Mol Hum Reprod. 2000 Dec;6(12):1063-7. doi: 10.1093/molehr/6.12.1063. Mol Hum Reprod. 2000. PMID: 11101688

10

[Genetic study of holoprosencephaly].

Dubourg C, Lazaro L, Blayau M, Pasquier L, Durou MR, Odent S, David V. Dubourg C, et al. Among authors: blayau m. Ann Biol Clin (Paris). 2003 Nov-Dec;61(6):679-87. Ann Biol Clin (Paris). 2003. PMID: 14711609 Free article. French.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

61 results

Search Page

Filters