AAAAAA

   
Results: 1-25 | 26-43
Results: 1-25/43

Authors: ROBERTS AG PUY H DAILEY TA MORGAN RR WHATLEY SD DAILEY HA MARTASEK P NORDMANN Y DEYBACH JC ELDER GH
Citation: Ag. Roberts et al., MOLECULAR CHARACTERIZATION OF HOMOZYGOUS VARIEGATE PORPHYRIA, Human molecular genetics (Print), 7(12), 1998, pp. 1921-1925

Authors: LAMORIL J ANDANT C BOGARD C PUY H GOUYA L PAWLOTSKY JM DASILVA V SOULE JC DEYBACH JC NORDMANN Y
Citation: J. Lamoril et al., EPIDEMIOLOGY OF HEPATITIS-C AND HEPATITIS-G IN SPORADIC AND FAMILIAL PORPHYRIA-CUTANEA-TARDA, Hepatology, 27(3), 1998, pp. 848-852

Authors: LAGARDE C HAMELTEILLAC D DEFROST Y BLANCHE S THOMAS C FISCHER A NORDMANN Y GED C DEVERNEUIL H
Citation: C. Lagarde et al., ALLOGENEIC BONE-MARROW TRANSPLANTATION IN CONGENITAL ERYTHROPOIETIC PORPHYRIA (GUNTHERS-DISEASE), Annales de dermatologie et de venereologie, 125(2), 1998, pp. 114-117

Authors: LYOUMI S PUY H TAMION F SCOTTE M DAVEAU M NORDMANN Y LEBRETON JP DEYBACH JC
Citation: S. Lyoumi et al., NITRIC-OXIDE SYNTHASE INHIBITION AND THE INDUCTION OF CYTOCHROME-P-450 AFFECT HEME OXYGENASE-1 MESSENGER-RNA EXPRESSION AFTER PARTIAL-HEPATECTOMY AND ACUTE-INFLAMMATION IN RATS, Critical care medicine, 26(10), 1998, pp. 1683-1689

Authors: GROSS U SASSA S JACOB K DEYBACH JC NORDMANN Y FRANK M DOSS MO
Citation: U. Gross et al., 5-AMINOLEVULINIC ACID DEHYDRATASE DEFICIENCY PORPHYRIA - A 20-YEAR CLINICAL AND BIOCHEMICAL FOLLOW-UP, Clinical chemistry, 44(9), 1998, pp. 1892-1896

Authors: LAMORIL J PUY H GOUYA L ROSIPAL R DASILVA V GRANDCHAMP B FOINT T BADERMEUNIER B DOMMERGUES JP DEYBACH JC NORDMANN Y
Citation: J. Lamoril et al., NEONATAL HEMOLYTIC-ANEMIA DUE TO INHERITED HARDEROPORPHYRIA - CLINICAL CHARACTERISTICS AND MOLECULAR-BASIS, Blood, 91(4), 1998, pp. 1453-1457

Authors: RUFENACHT UB GOUYA L SCHNEIDERYIN X PUY H SCHAFER BW AQUARON R NORDMANN Y MINDER EI DEYBACH JC
Citation: Ub. Rufenacht et al., SYSTEMATIC ANALYSIS OF MOLECULAR DEFECTS IN THE FERROCHELATASE GENE FROM PATIENTS WITH ERYTHROPOIETIC PROTOPORPHYRIA, American journal of human genetics, 62(6), 1998, pp. 1341-1352

Authors: LAMORIL J DEYBACH JC PUY H GRANDCHAMP B NORDMANN Y
Citation: J. Lamoril et al., 3 NOVEL MUTATIONS IN THE COPROPORPHYRINOGEN OXIDASE GENE, Human mutation, 9(1), 1997, pp. 78-80

Authors: NORDMANN Y PUY H DASILVA V SIMONIN S ROBREAU AM BONAITI C PHUNG LN DEYBACH JC
Citation: Y. Nordmann et al., ACUTE INTERMITTENT PORPHYRIA - PREVALENCE OF MUTATIONS IN THE PORPHOBILINOGEN DEAMINASE GENE IN BLOOD-DONORS IN FRANCE, Journal of internal medicine, 242(3), 1997, pp. 213-217

Authors: ANDANT C LAMORIL J BOGARD C PUY H DEVARS JC SOULE JC NORDMANN Y DEYBACH JC
Citation: C. Andant et al., PREVALENCE OF HEPATITIS-C VIRUS-INFECTION IN SPORADIC AND FAMILIAL PORPHYRIA-CUTANEA-TARDA IN FRANCE, Hepatology, 26(4), 1997, pp. 334-334

Authors: PUY H AQUARON R LAMORIL J ROBREAU AM NORDMANN Y DEYBACH JC
Citation: H. Puy et al., ACUTE INTERMITTENT PORPHYRIA - RAPID MOLECULAR DIAGNOSIS, Cellular and molecular biology, 43(1), 1997, pp. 37-45

Authors: ROSIPAL R PUY H LAMORIL J MARTASEK P NORDMANN Y DEYBACH JC
Citation: R. Rosipal et al., MOLECULAR ANALYSIS OF PORPHOBILINOGEN (PEG) DEAMINASE GENE-MUTATIONS IN ACUTE INTERMITTENT PORPHYRIA - FIRST STUDY IN PATIENTS OF SLAVIC ORIGIN, Scandinavian journal of clinical & laboratory investigation, 57(3), 1997, pp. 217-224

Authors: POUX JM DEMONTIS R CADRANEL JF GHAZALI A FIEVET P NORDMANN Y
Citation: Jm. Poux et al., PORPHYRIA-CUTANEA-TARDA IN DIALYZED PATIENT WITH HEPATITIS-C VIRUS-INFECTION - DRAMATIC EFFICACY OF SMALL REPEATED PHLEBOTOMIES, The American journal of medicine, 103(2), 1997, pp. 163-164

Authors: PUY H DEYBACH JC LAMORIL J ROBREAU AM DASILVA V GOUYA L GRANDCHAMP B NORDMANN Y
Citation: H. Puy et al., MOLECULAR EPIDEMIOLOGY AND DIAGNOSIS OF PBG DEAMINASE GENE DEFECTS INACUTE INTERMITTENT PORPHYRIA, American journal of human genetics, 60(6), 1997, pp. 1373-1383

Authors: ANDANT C PUY H DEYBACH JC SOULE JC NORDMANN Y
Citation: C. Andant et al., OCCURRENCE OF HEPATOCELLULAR-CARCINOMA IN A CASE OF HEREDITARY COPROPORPHYRIA, The American journal of gastroenterology, 92(8), 1997, pp. 1389-1390

Authors: DEYBACH JC PUY H ROBREAU AM LAMORIL J DASILVA V GRANDCHAMP B NORDMANN Y
Citation: Jc. Deybach et al., MUTATIONS IN THE PROTOPORPHYRINOGEN OXIDASE GENE IN PATIENTS WITH VARIEGATE PORPHYRIA, Human molecular genetics, 5(3), 1996, pp. 407-410

Authors: GRANDCHAMP B PUY H LAMORIL J DEYBACH JC NORDMANN Y
Citation: B. Grandchamp et al., REVIEW - MOLECULAR PATHOGENESIS OF HEPATIC ACUTE PORPHYRIAS, Journal of gastroenterology and hepatology, 11(11), 1996, pp. 1046-1052

Authors: MOULY F JANIER M NORDMANN Y FLAGEUL B
Citation: F. Mouly et al., URINARY PORPHYRIN EXCRETION IN HUMAN-IMMU NODEFICIENCY-VIRUS INFECTION, La Presse medicale, 25(32), 1996, pp. 1541-1545

Authors: ANDANT C PUY H DEYBACH JC ZEITOUN E DUMAYNE JFD SOULE JC NORDMANN Y
Citation: C. Andant et al., ACUTE HEPATIC PORPHYRIAS - A NEW ETIOLOGIC FACTOR OF HEPATOCELLULAR-CARCINOMA, Hepatology, 24(4), 1996, pp. 294-294

Authors: NORDMANN Y
Citation: Y. Nordmann, HOW DO YOU TREAT PORPHYRIA-CUTANEA-TARDA - RESPONSE, Annales de dermatologie et de venereologie, 123(4), 1996, pp. 294-294

Authors: THOMAS C GED C NORDMANN Y DEVERNEUIL H PELLIER I FISCHER A BLANCHE S
Citation: C. Thomas et al., CORRECTION OF CONGENITAL ERYTHROPOIETIC PORPHYRIA BY BONE-MARROW TRANSPLANTATION, The Journal of pediatrics, 129(3), 1996, pp. 453-456

Authors: PUY H DEYBACH JC BOGDAN A CALLEBERT J BAUMGARTNER M VOISIN P NORDMANN Y TOUITOU Y
Citation: H. Puy et al., INCREASED DELTA-AMINOLEVULINIC-ACID AND DECREASED PINEAL MELATONIN PRODUCTION - A COMMON EVENT IN ACUTE PORPHYRIA STUDIES IN THE RAT, The Journal of clinical investigation, 97(1), 1996, pp. 104-110

Authors: PUY H ROBREAU AM ROSIPAL R NORDMANN Y DEYBACH JC
Citation: H. Puy et al., PROTOPORPHYRINOGEN OXIDASE - COMPLETE GENOMIC SEQUENCE AND POLYMORPHISMS IN THE HUMAN GENE, Biochemical and biophysical research communications, 226(1), 1996, pp. 226-230

Authors: GOUYA L DEYBACH JC LAMORIL J DASILVA V BEAUMONT C GRANDCHAMP B NORDMANN Y
Citation: L. Gouya et al., MODULATION OF THE PHENOTYPE IN DOMINANT ERYTHROPOIETIC PROTOPORPHYRIABY A LOW EXPRESSION OF THE NORMAL FERROCHELATASE ALLELE, American journal of human genetics, 58(2), 1996, pp. 292-299

Authors: PUY H DEYBACH JC LAMORIL J ROBREAU AM NORDMANN Y
Citation: H. Puy et al., DETECTION OF 4 NOVEL MUTATIONS IN THE PORPHOBILINOGEN DEAMINASE GENE IN FRENCH CAUCASIAN PATIENTS WITH ACUTE INTERMITTENT PORPHYRIA, Human heredity, 46(3), 1996, pp. 177-180
Risultati: 1-25 | 26-43