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Items: 30

1.

Pure-tone threshold description of an elderly French screened population.

Blanchet C, Pommie C, Mondain M, Berr C, Hillaire D, Puel JL.

Otol Neurotol. 2008 Jun;29(4):432-40. doi: 10.1097/MAO.0b013e3181719746.

PMID:
18520580
2.

Genome search for additional human loci controlling infection levels by Schistosoma mansoni.

Zinn-Justin A, Marquet S, Hillaire D, Dessein A, Abel L.

Am J Trop Med Hyg. 2001 Dec;65(6):754-8.

PMID:
11791970
3.

Genetics of parasitic infections.

Dessein AJ, Chevillard C, Marquet S, Henri S, Hillaire D, Dessein H.

Drug Metab Dispos. 2001 Apr;29(4 Pt 2):484-8.

PMID:
11259337
4.

[Genetic predisposition to bilharziasis in humans: research methods and application to the study of Schistosoma mansoni infection].

Abel L, Marquet S, Chevillard C, elWali NE, Hillaire D, Dessein A.

J Soc Biol. 2000;194(1):15-8. Review. French.

PMID:
11107544
5.

Infection and disease in human schistosomiasis mansoni are under distinct major gene control.

Dessein AJ, Marquet S, Henri S, El Wali NE, Hillaire D, Rodrigues V, Prata A, Ali QM, Gharib B, de Reggi M, Magzoub MM, Saeed OK, Abdelhameed AA, Abel L.

Microbes Infect. 1999 Jun;1(7):561-7. Review. No abstract available.

PMID:
10603573
6.

Severe hepatic fibrosis in Schistosoma mansoni infection is controlled by a major locus that is closely linked to the interferon-gamma receptor gene.

Dessein AJ, Hillaire D, Elwali NE, Marquet S, Mohamed-Ali Q, Mirghani A, Henri S, Abdelhameed AA, Saeed OK, Magzoub MM, Abel L.

Am J Hum Genet. 1999 Sep;65(3):709-21.

7.
8.

Linkage analysis of blood Plasmodium falciparum levels: interest of the 5q31-q33 chromosome region.

Garcia A, Marquet S, Bucheton B, Hillaire D, Cot M, Fievet N, Dessein AJ, Abel L.

Am J Trop Med Hyg. 1998 Jun;58(6):705-9.

PMID:
9660449
9.

Genetic localization of a locus controlling the intensity of infection by Schistosoma mansoni on chromosome 5q31-q33.

Marquet S, Abel L, Hillaire D, Dessein H, Kalil J, Feingold J, Weissenbach J, Dessein AJ.

Nat Genet. 1996 Oct;14(2):181-4.

PMID:
8841190
10.

Juvenile limb-girdle muscular dystrophy. Clinical, histopathological and genetic data from a small community living in the Reunion Island.

Fardeau M, Hillaire D, Mignard C, Feingold N, Feingold J, Mignard D, de Ubeda B, Collin H, Tome FM, Richard I, Beckmann J.

Brain. 1996 Feb;119 ( Pt 1):295-308.

PMID:
8624690
11.

[Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis].

Fardeau M, Tomé FM, Helbling-Leclerc A, Evangelista T, Ottolini A, Chevallay M, Barois A, Estournet B, Harpey JP, Fauré S, Guicheney P, Hillaire D.

Rev Neurol (Paris). 1996 Jan;152(1):11-9. French.

PMID:
8729391
12.

Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping.

Hillaire D, Leclerc A, Fauré S, Topaloglu H, Chiannilkulchaï N, Guicheney P, Grinas L, Legos P, Philpot J, Evangelista T, et al.

Hum Mol Genet. 1994 Sep;3(9):1657-61.

PMID:
7833925
13.

Malignant hyperthermia and central core disease: analysis of two families with heterogeneous clinical expression.

Romero NB, Nivoche Y, Lunardi J, Bruneau B, Cheval MA, Hillaire D, Fardeau M.

Neuromuscul Disord. 1993 Sep-Nov;3(5-6):547-51.

PMID:
8186709
14.

Failure to replicate linkage between chromosome 5q11-q13 markers and schizophrenia in 28 families.

Campion D, d'Amato T, Laklou H, Sabate O, Jay M, Leboyer M, Malafosse A, Gorwood P, Babron MC, Hillaire D, et al.

Psychiatry Res. 1992 Dec;44(3):171-9.

PMID:
1363250
15.

Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophy.

Richard I, Broux O, Hillaire D, Cherif D, Fougerousse F, Cohen D, Beckmann JS.

Hum Mol Genet. 1992 Nov;1(8):621-4.

PMID:
1363783
16.

A nonsense mutation in exon 4 of the cystic fibrosis gene frequent among the population of the Reunion Island.

Chevalier-Porst F, Chomel JC, Hillaire D, Kitzis A, Kaplan JC, Goutaland R, Mathieu M, Bozon D.

Hum Mol Genet. 1992 Nov;1(8):647-8. No abstract available.

PMID:
1284471
17.

Evidence for a pseudoautosomal locus for schizophrenia. II: Replication of a non-random segregation of alleles at the DXYS14 locus.

d'Amato T, Campion D, Gorwood P, Jay M, Sabate O, Petit C, Abbar M, Malafosse A, Leboyer M, Hillaire D, et al.

Br J Psychiatry. 1992 Jul;161:59-62.

PMID:
1638330
18.

Evidence for a pseudoautosomal locus for schizophrenia. I: A replication study using phenotype analysis.

Gorwood P, Leboyer M, d'Amato T, Jay M, Campion D, Hillaire D, Mallet J, Feingold J.

Br J Psychiatry. 1992 Jul;161:55-8.

PMID:
1638329
19.

Relationship of HLA to schizophrenia not supported in multiplex families.

Campion D, Leboyer M, Hillaire D, Halle L, Gorwood P, Cavelier B, Soufflet MF, d'Amato T, Muller B, Kaplan C, et al.

Psychiatry Res. 1992 Feb;41(2):99-105.

PMID:
1574545
20.

Clinical subtypes and age at onset in schizophrenic siblings.

Leboyer M, Filteau MJ, Jay M, Campion D, d'Amato T, Guilloud-Bataille M, Hillaire D, Feingold J, des Lauriers A, Widlöcher D.

Psychiatry Res. 1992 Feb;41(2):107-14.

PMID:
1574538
21.

[Familial forms of schizophrenia. Cytogenetic study].

Gorwood P, Leboyer M, Jay M, Hillaire D, Carteault F, Dugain AM, Berg S, Des Lauriers A, Feingold J.

Encephale. 1991 Nov-Dec;17(6):525-9. Review. French.

PMID:
1806361
22.

Linkage analysis in spinal muscular atrophy, by six closely flanking markers on chromosome 5.

Sheth P, Abdelhak S, Bachelot MF, Burlet P, Masset M, Hillaire D, Clerget-Darpoux F, Frézal J, Lathrop GM, Munnich A, et al.

Am J Hum Genet. 1991 Apr;48(4):764-8.

23.

Cytogenetic studies of familial schizophrenics.

Gorwood P, Leboyer M, Hillaire D, Jay M, Carteault F, Dugain AM, Berg S, Bois E, Feingold J.

Biol Psychiatry. 1991 Mar 15;29(6):624-5. No abstract available.

PMID:
2054433
24.

A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage.

Beckmann JS, Richard I, Hillaire D, Broux O, Antignac C, Bois E, Cann H, Cottingham RW Jr, Feingold N, Feingold J, et al.

C R Acad Sci III. 1991;312(4):141-8.

PMID:
1901754
25.

Cystic fibrosis in the population of Reunion Island.

Hillaire D, Chomel JC, Lesure F, Renouil M, Musenger C, Pierson F, Berthelon M, Lenoir G, Gérard G, Bois E, et al.

Ann Genet. 1991;34(1):5-7.

PMID:
1952795
26.

Subtyping familial schizophrenia: reliability, concordance, and stability.

Leboyer M, Jay M, D'Amato T, Campion D, Guilloud-Bataille M, Hillaire D, Drouet A, Lépine JP, Bois E, Feingold J.

Psychiatry Res. 1990 Oct;34(1):77-88.

PMID:
2267264
27.

Use of a simple method for the Epstein-Barr virus transformation of lymphocytes from members of large families of Réunion Island.

Ventura M, Gibaud A, Le Pendu J, Hillaire D, Gérard G, Vitrac D, Oriol R.

Hum Hered. 1988;38(1):36-43.

PMID:
2832305
28.

Cryoenzymic studies on myosin subfragment 1: perturbation of an enzyme reaction by temperature and solvent.

Biosca JA, Travers F, Hillaire D, Barman TE.

Biochemistry. 1984 Apr 24;23(9):1947-55.

PMID:
6232952
29.
30.

Cryoenzymological studies on myosin subfragment 1. Solvent, temperature and pH effects on the overall reaction.

Travers F, Hillaire D.

Eur J Biochem. 1979 Jul;98(1):293-9. No abstract available.

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