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Results: 1-14 |
Results: 14

Authors: MENDLER MH CORBINAIS S SAPEY T LUCASCLERC C TIISMA V GUYADER D DEUGNIER Y LETREUT A BRISSOT P
Citation: Mh. Mendler et al., IN PATIENTS WITH CIRRHOSIS, SHOULD SERUM-ALBUMIN DETERMINATION BE CARRIED OUT BY IMMUNONEPHELEMETRY OR BY PROTEIN ELECTROPHORESIS, Gastroenterology, 114(4), 1998, pp. 116-116

Authors: FROUGE C CAZENAVE A PHAM E JURAS J LETREUT A DILHUYDY MH BLERY M
Citation: C. Frouge et al., MAMMOGRAPHIC PATTERN DUE TO RESIDUAL LIPIODOL AFTER GALACTOGRAPHY, European radiology, 7(2), 1997, pp. 204-207

Authors: THOMAS L CHACON B KIND M LASBAREILLES O MUYLDERMANS P CHEMIN A LETREUT A PIGNEUX J KANTOR G
Citation: L. Thomas et al., MAGNETIC-RESONANCE-IMAGING IN THE TREATMENT PLANNING OF RADIATION-THERAPY IN CARCINOMA OF THE CERVIX TREATED WITH THE 4-FIELD PELVIC TECHNIQUE, International journal of radiation oncology, biology, physics, 37(4), 1997, pp. 827-832

Authors: JEZEQUEL P GUILHEM I HESPEL JP LETREUT A LEGALL JY ALLANNIC H BLAYAU M
Citation: P. Jezequel et al., IDENTIFICATION OF A NOVEL MUTATION (A268G) IN EXON-8 OF THE HTR-BETA GENE IN A LARGE FAMILY WITH THYROID-HORMONE RESISTANCE, Human mutation, 8(4), 1996, pp. 396-396

Authors: JEZEQUEL P CHAUVEL B LETREUT A LEGALL JY DAVID V LELANNOU D BLAYAU M
Citation: P. Jezequel et al., IDENTIFICATION OF A NOVEL MUTATION IN CFTR GENE EXON-8 (L375F) IN A CUAVD PHENOTYPE, Human genetics, 97(4), 1996, pp. 548-549

Authors: GANDON G JOUANOLLE AM CHAUVEL B MAUVIEUX V LETREUT A FEINGOLD J LEGALL JY DAVID V YAOUANQ J
Citation: G. Gandon et al., LINKAGE DISEQUILIBRIUM AND EXTENDED HAPLOTYPES IN THE HLA-A TO D6S105REGION - IMPLICATIONS FOR MAPPING THE HEMOCHROMATOSIS GENE (HFE), Human genetics, 97(1), 1996, pp. 103-113

Authors: THOMAS L CHACON B KIND M LASBAREILLES O MUYLDERMANS P PIGNEUX J LETREUT A KANTOR G
Citation: L. Thomas et al., MRI IN THE TREATMENT PLANNING OF RADIATION-THERAPY IN CERVICAL CARCINOMAS, European journal of cancer, 31A, 1995, pp. 191-191

Authors: JEZEQUEL P DORVAL I FERGELOT P CHAUVEL B LETREUT A LEGALL JY LELANNOU D BLAYAU M
Citation: P. Jezequel et al., STRUCTURAL-ANALYSIS OF CFTR GENE IN CONGENITAL BILATERAL ABSENCE OF VAS-DEFERENS, Clinical chemistry, 41(6), 1995, pp. 833-835

Authors: STINES J BOUHNIK H MARELLE P LETREUT A MASSELOT J BOUHNIK H NOEL A PAGE M ANDRE J ASTIE T BARON PL BARREAU B BENMUSSA M BERTRAND AF BOISSERIELACROIX M BOULET P CAMBIER L CASELLES O CASILE MC CHEMIN A CHERIFCHEIKH J DILHUYDY MH GRUMBACH Y GUERRIN B HAGAY C ISNARD A KAEMMERLEN P KLEITZ C LEGAL M MALET C MARIE B MARTY MH MEUNIER M RICAUD M SALICRU B SERADOUR B VAILLANT D
Citation: J. Stines et al., GROUPE-INTERDISCIPLINAIRE-DE-MAMMOGRAPHIE (GIM) - QUALITY-CONTROL OF MAMMOGRAPHY, Journal de radiologie, 75(5), 1994, pp. 295-301

Authors: LEGALL JY DAVID V YAOUANQ J PERICHON M BLAYAU M JOUANOLLE AM MAUVIEUX V ELKAHLOUN A CHAUVEL B DORVAL I LETREUT A
Citation: Jy. Legall et al., MOLECULAR-GENETICS OF HEMOCHROMATOSIS, La Semaine des hopitaux de Paris, 70(21-22), 1994, pp. 644-650

Authors: DORVAL I FERGELOT P DUBOURG C JEZEQUEL P CHAUVEL B LEGALL JY LETREUT A
Citation: I. Dorval et al., RAPID DETECTION OF 1078-DELT MUTATION BY PCR-MEDIATED SITE-DIRECTED MUTAGENESIS - DETECTION OF CYSTIC-FIBROSIS CARRIERS IN A CELTIC POPULATION, Clinical chemistry, 40(12), 1994, pp. 2318-2319

Authors: YAOUANQ J PERICHON M CHORNEY M PONTAROTTI P LETREUT A ELKAHLOUN A MAUVIEUX V BLAYAU M JOUANOLLE AM CHAUVEL B MOIRAND R NOUEL O LEGALL JY FEINGOLD J DAVID V
Citation: J. Yaouanq et al., ANONYMOUS MARKER LOCI WITHIN 400 KB OF HLA-A GENERATE HAPLOTYPES IN LINKAGE DISEQUILIBRIUM WITH THE HEMOCHROMATOSIS GENE (HFE), American journal of human genetics, 54(2), 1994, pp. 252-263

Authors: LEGALL JY DAVID V YAOUANQ J PERICHON M BLAYAU M JOUANOLLE AM MAUVIEUX V ELKAHLOUN A CHAUVEL B DORVAL I LETREUT A
Citation: Jy. Legall et al., MOLECULAR-GENETICS OF HEMOCHROMATOSIS, Annales de Gastroenterologie et d'Hepatologie, 29(6), 1993, pp. 292-299

Authors: LEGALL JY DAVID V YAOUANQ J PERICHON M BLAYAU M JOUANOLLE AM MAUVIEUX V ELKAHLOUN A CHAUVEL B DORVAL I LETREUT A
Citation: Jy. Legall et al., MOLECULAR-GENETICS OF HEMOCHROMATOSIS, Bulletin de l'Academie nationale de medecine, 177(2), 1993, pp. 187-201
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