Simon M - Search Results

1

A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA association.

Simon M, Le Mignon L, Fauchet R, Yaouanq J, David V, Edan G, Bourel M. Simon M, et al. Am J Hum Genet. 1987 Aug;41(2):89-105. Am J Hum Genet. 1987. PMID: 3475981 Free PMC article.

2

DNA polymorphism related to the idiopathic hemochromatosis gene: evidence in a recombinant family.

David V, Paul P, Simon M, Le Gall JY, Fauchet R, Gicquel I, Dugast I, Le Mignon L, Yaouanq J, Cohen D, et al. David V, et al. Among authors: simon m. Hum Genet. 1986 Oct;74(2):113-20. doi: 10.1007/BF00282073. Hum Genet. 1986. PMID: 2876944

3

An HLA-All association with the hemochromatosis allele?

Le Mignon L, Simon M, Fauchet R, Edan G, Le Reun M, Brissot P, Genetet B, Bourel M. Le Mignon L, et al. Among authors: simon m. Clin Genet. 1983 Sep;24(3):171-6. doi: 10.1111/j.1399-0004.1983.tb02234.x. Clin Genet. 1983. PMID: 6578890

4

Genetic analysis of idiopathic hemochromatosis using both qualitative (disease status) and quantitative (serum iron) information.

Lalouel JM, Le Mignon L, Simon M, Fauchet R, Bourel M, Rao DC, Morton NE. Lalouel JM, et al. Among authors: simon m. Am J Hum Genet. 1985 Jul;37(4):700-18. Am J Hum Genet. 1985. PMID: 9556659 Free PMC article.

5

Ferritin H gene polymorphism in idiopathic hemochromatosis.

David V, Papadopoulos P, Yaouanq J, Blayau M, Abel L, Zappone E, Perichon M, Drysdale J, Le Gall JY, Simon M. David V, et al. Among authors: simon m. Hum Genet. 1989 Jan;81(2):123-6. doi: 10.1007/BF00293887. Hum Genet. 1989. PMID: 2563249

6

HLA determinants in idiopathic hemochromatosis.

Fauchet R, Genetet N, Genetet B, Simon M, Bourel M. Fauchet R, et al. Among authors: simon m. Tissue Antigens. 1979 Jul;14(1):10-4. doi: 10.1111/j.1399-0039.1979.tb00815.x. Tissue Antigens. 1979. PMID: 91216

7

Idiopathic hemochromatosis and iron overload in alcoholic liver disease: differentiation by HLA phenotype.

Simon M, Bourel M, Genetet B, Fauchet R, Edan G, Brissot P. Simon M, et al. Gastroenterology. 1977 Oct;73(4 Pt 1):655-8. Gastroenterology. 1977. PMID: 892369

8

Idiopathic hemochromatosis. Demonstration of recessive transmission and early detection by family HLA typing.

Simon M, Bourel M, Genetet B, Fauchet R. Simon M, et al. N Engl J Med. 1977 Nov 10;297(19):1017-21. doi: 10.1056/NEJM197711102971901. N Engl J Med. 1977. PMID: 909547

9

Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis.

Simon M, Bourel M, Fauchet R, Genetet B. Simon M, et al. Gut. 1976 May;17(5):332-4. doi: 10.1136/gut.17.5.332. Gut. 1976. PMID: 1278715 Free PMC article.

10

HLA alleles, hemochromatosis allele, and serum ferritin in hemodialysis patients.

Yaouanq J, Simon M. Yaouanq J, et al. Among authors: simon m. Nephron. 1988;50(3):259-60. doi: 10.1159/000185174. Nephron. 1988. PMID: 3226462 Free article. No abstract available.

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