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Results: 1-25 | 26-49
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GENERATION OF A TRANSCRIPTION MAP OF A 1 MBASE REGION CONTAINING THE HFE GENE (6P22)
Authors: TOTARO A ROETTO A ROMMENS JM GRIFA A CARELLA M DAGRUMA L VALENTINO MA DAMBROSIO L CICILANO M CAMASCHELLA C FRANCO B GASPARINI P
Citation: A. Totaro et al., GENERATION OF A TRANSCRIPTION MAP OF A 1 MBASE REGION CONTAINING THE HFE GENE (6P22), European journal of human genetics, 6(2), 1998, pp. 105-113
SEARCH FOR CANDIDATE GENES OF JUVENILE HEMOCHROMATOSIS, A DISORDER DISTINCT FROM ADULT HEMOCHROMATOSIS
Authors: ROETTO A CICILANO M BOSIO S TOTARO A CARELLA M GRIFA A CAMASCHELLA C GASPARINI P
Citation: A. Roetto et al., SEARCH FOR CANDIDATE GENES OF JUVENILE HEMOCHROMATOSIS, A DISORDER DISTINCT FROM ADULT HEMOCHROMATOSIS, European journal of human genetics, 6, 1998, pp. 4149-4149
JUVENILE HEMOCHROMATOSIS
Authors: CAMASCHELLA C
Citation: C. Camaschella, JUVENILE HEMOCHROMATOSIS, Bailliere's clinical gastroenterology, 12(2), 1998, pp. 227-235
MOLECULAR-GENETICS AND CONTROL OF IRON-METABOLISM IN HEMOCHROMATOSIS
Authors: PIETRANGELO A CAMASCHELLA C
Citation: A. Pietrangelo et C. Camaschella, MOLECULAR-GENETICS AND CONTROL OF IRON-METABOLISM IN HEMOCHROMATOSIS, Haematologica, 83(5), 1998, pp. 456-461
HETEROGENEITY OF HEMOCHROMATOSIS IN ITALY
Authors: PIPERNO A SAMPIETRO M PIETRANGELO A AROSIO C LUPICA L MONTOSI G VERGANI A FRAQUELLI M GIRELLI D PASQUERO P ROETTO A GASPARINI P FARGION S CONTE D CAMASCHELLA C
Citation: A. Piperno et al., HETEROGENEITY OF HEMOCHROMATOSIS IN ITALY, Gastroenterology, 114(5), 1998, pp. 996-1002
JUVENILE AND ADULT HEMOCHROMATOSIS ARE DISTINCT GENETIC-DISORDERS
Authors: CAMASCHELLA C ROETTO A CICILANO M PASQUERO P BOSIO S GUBETTA L DIVITO F GIRELLI D TOTARO A CARELLA M GRIFA A GASPARINI P
Citation: C. Camaschella et al., JUVENILE AND ADULT HEMOCHROMATOSIS ARE DISTINCT GENETIC-DISORDERS, European journal of human genetics, 5(6), 1997, pp. 371-375
A FREQUENT POLYMORPHISM IN THE 5'-REGION OF THE BCMA GENE
Authors: ROETTO A CICILANO M GOTTARDI E TOTARO A CARELLA M GASPARINI P CAMASCHELLA C
Citation: A. Roetto et al., A FREQUENT POLYMORPHISM IN THE 5'-REGION OF THE BCMA GENE, Molecular and cellular probes, 11(4), 1997, pp. 311-312
HEREDITARY HEMOCHROMATOSIS - A HPAL POLYMORPHISM WITHIN THE HLA-H GENE
Authors: TOTARO A GRIFA A CARELLA M DAMBROSIO L VALENTINO M ROTH MP BOROT N COPPIN H ROETTO A CAMASCHELLA C GASPARINI P
Citation: A. Totaro et al., HEREDITARY HEMOCHROMATOSIS - A HPAL POLYMORPHISM WITHIN THE HLA-H GENE, Molecular and cellular probes, 11(3), 1997, pp. 229-230
FEASIBILITY OF MOLECULAR DIAGNOSIS OF ALPHA-THALASSEMIA IN THE EVALUATION OF MICROCYTOSIS
Authors: SIVERA P ROETTO A MAZZA U CAMASCHELLA C
Citation: P. Sivera et al., FEASIBILITY OF MOLECULAR DIAGNOSIS OF ALPHA-THALASSEMIA IN THE EVALUATION OF MICROCYTOSIS, Haematologica, 82(5), 1997, pp. 592-593
HEREDITARY HEMOCHROMATOSIS - RECENT ADVANCES IN MOLECULAR-GENETICS AND CLINICAL MANAGEMENT
Authors: CAMASCHELLA C PIPERNO A
Citation: C. Camaschella et A. Piperno, HEREDITARY HEMOCHROMATOSIS - RECENT ADVANCES IN MOLECULAR-GENETICS AND CLINICAL MANAGEMENT, Haematologica, 82(1), 1997, pp. 77-84
DIFFERENT HEMATOLOGICAL PHENOTYPES CAUSED BY THE INTERACTION OF TRIPLICATED ALPHA-GLOBIN GENES AND HETEROZYGOUS BETA-THALASSEMIA
Authors: CAMASCHELLA C KATTAMIS AC PETRONI D ROETTO A SIVERA P SBAIZ L COHEN A OHENEFREMPONG K TRIFILLIS P SURREY S FORTINA P
Citation: C. Camaschella et al., DIFFERENT HEMATOLOGICAL PHENOTYPES CAUSED BY THE INTERACTION OF TRIPLICATED ALPHA-GLOBIN GENES AND HETEROZYGOUS BETA-THALASSEMIA, American journal of hematology, 55(2), 1997, pp. 83-88
AN ARG403GLN BETA-MYOSIN HEAVY-CHAIN GENE MUTATION IDENTIFIED IN AN ITALIAN FAMILY WITH HYPERTROPHIC CARDIOMYOPATHY - DESCRIPTION OF CLINICAL-FEATURES OF THE FAMILY MEMBERS
Authors: CONTE MR MORELLO M MANGIARDI L ORZAN L CHECCO L BONFIGLIO G ALFARANO A CAMASCHELLA C BRUSCA A
Citation: Mr. Conte et al., AN ARG403GLN BETA-MYOSIN HEAVY-CHAIN GENE MUTATION IDENTIFIED IN AN ITALIAN FAMILY WITH HYPERTROPHIC CARDIOMYOPATHY - DESCRIPTION OF CLINICAL-FEATURES OF THE FAMILY MEMBERS, European heart journal, 18(6), 1997, pp. 1033-1034
JUVENILE HEMOCHROMATOSIS IS A DISEASE UNRELATED TO HEMOCHROMATOSIS AND UNLINKED TO 6P
Authors: CAMASCHELLA C ROETTO A CICILANO M BOSIO S GUBETTA L GIRELLI D TOTARO A CARELLA M GRIFA A GASPARINI P
Citation: C. Camaschella et al., JUVENILE HEMOCHROMATOSIS IS A DISEASE UNRELATED TO HEMOCHROMATOSIS AND UNLINKED TO 6P, Blood, 90(10), 1997, pp. 2681-2681
A RECOMBINATION EVENT CLOSE TO HFE GENE IN HEREDITARY HEMOCHROMATOSIS
Authors: ROETTO A SBAIZ L BOSIO S PIPERNO A FARGION S CARELLA M TOTARO A GRIFA A GASPARINI P CAMASCHELLA C
Citation: A. Roetto et al., A RECOMBINATION EVENT CLOSE TO HFE GENE IN HEREDITARY HEMOCHROMATOSIS, Annales de genetique, 40(3), 1997, pp. 150-153
MUTATION ANALYSIS OF THE HLA-H GENE IN ITALIAN HEMOCHROMATOSIS PATIENTS
Authors: CARELLA M DAMBROSIO L TOTARO A GRIFA A VALENTINO MA PIPERNO A GIRELLI D ROETTO A FRANCO B GASPARINI P CAMASCHELLA C
Citation: M. Carella et al., MUTATION ANALYSIS OF THE HLA-H GENE IN ITALIAN HEMOCHROMATOSIS PATIENTS, American journal of human genetics, 60(4), 1997, pp. 828-832
ANALYSIS OF MICROSATELLITE INSTABILITY IN CHRONIC LYMPHOPROLIFERATIVEDISORDERS
Authors: VOLPE G GAMBERI B PASTORE C ROETTO A PAUTASSO M PARVIS G CAMASCHELLA C MAZZA U SAGLIO G GAIDANO G
Citation: G. Volpe et al., ANALYSIS OF MICROSATELLITE INSTABILITY IN CHRONIC LYMPHOPROLIFERATIVEDISORDERS, Annals of hematology, 72(2), 1996, pp. 67-71
2 POLYMORPHIC REPEATS IN THE CANDIDATE REGION FOR THE HEMOCHROMATOSISGENE
Authors: GRIFA A TOTARO A CARELLA M DAMBROSIO L SBAIZ L ROETTO A CAMASCHELLA C GASPARINI P
Citation: A. Grifa et al., 2 POLYMORPHIC REPEATS IN THE CANDIDATE REGION FOR THE HEMOCHROMATOSISGENE, Molecular and cellular probes, 10(6), 1996, pp. 469-470
CONSTRUCTION OF A YAC CONTIG COVERING HUMAN-CHROMOSOME 6P22
Authors: MALASPINA P ROETTO A TRETTEL F JODICE C BLASI P FRONTALI M CARELLA M FRANCO B CAMASCHELLA C NOVELLETO A
Citation: P. Malaspina et al., CONSTRUCTION OF A YAC CONTIG COVERING HUMAN-CHROMOSOME 6P22, Genomics, 36(3), 1996, pp. 399-407
HEREDITARY HEMOCHROMATOSIS - GENERATION OF A TRANSCRIPTION MAP WITHINA REFINED AND EXTENDED MAP OF THE HLA CLASS-I REGION
Authors: TOTARO A ROMMENS JM GRIFA A LUNARDI C CARELLA M HUIZENGA JJ ROETTO A CAMASCHELLA C DESANDRE G GASPARINI P
Citation: A. Totaro et al., HEREDITARY HEMOCHROMATOSIS - GENERATION OF A TRANSCRIPTION MAP WITHINA REFINED AND EXTENDED MAP OF THE HLA CLASS-I REGION, Genomics, 31(3), 1996, pp. 319-326
SERUM ERYTHROPOIETIN AND CIRCULATING TRANSFERRIN RECEPTOR IN THALASSEMIA-INTERMEDIA PATIENTS WITH HETEROGENEOUS GENOTYPES
Authors: CAMASCHELLA C GONELLA S CALABRESE R VISCHIA F ROETTO A GRAZIADEI G MAZZA U CAPPELLINI MD
Citation: C. Camaschella et al., SERUM ERYTHROPOIETIN AND CIRCULATING TRANSFERRIN RECEPTOR IN THALASSEMIA-INTERMEDIA PATIENTS WITH HETEROGENEOUS GENOTYPES, Haematologica, 81(5), 1996, pp. 397-403
HUMAN ALPHA-THALASSEMIA SYNDROMES - DETECTION OF MOLECULAR DEFECTS
Authors: KATTAMIS AC CAMASCHELLA C SIVERA P SURREY S FORTINA P
Citation: Ac. Kattamis et al., HUMAN ALPHA-THALASSEMIA SYNDROMES - DETECTION OF MOLECULAR DEFECTS, American journal of hematology, 53(2), 1996, pp. 81-91
ALLELIC ASSOCIATION OF MICROSATELLITES OF 6P IN ITALIAN HEMOCHROMATOSIS PATIENTS
Authors: CAMASCHELLA C ROETTO A GASPARINI P PIPERNO A FORTINA P SURREY S RAPPAPORT E
Citation: C. Camaschella et al., ALLELIC ASSOCIATION OF MICROSATELLITES OF 6P IN ITALIAN HEMOCHROMATOSIS PATIENTS, Human genetics, 97(4), 1996, pp. 476-481
THE ANCESTRAL HEMOCHROMATOSIS HAPLOTYPE IS ASSOCIATED WITH A SEVERE PHENOTYPE EXPRESSION IN ITALIAN PATIENTS
Authors: PIPERNO A AROSIO C FARGION S ROETTO A NICOLI C GIRELLI D SBAIZ L GASPARINI P BOARI G SAMPIETRO M CAMASCHELLA C
Citation: A. Piperno et al., THE ANCESTRAL HEMOCHROMATOSIS HAPLOTYPE IS ASSOCIATED WITH A SEVERE PHENOTYPE EXPRESSION IN ITALIAN PATIENTS, Hepatology, 24(1), 1996, pp. 43-46
NOVEL MISSENSE MUTATION IN THE PHENYLALANINE-HYDROXYLASE GENE LEADINGTO COMPLETE LOSS OF ENZYMATIC-ACTIVITY
Authors: DIANZANI I KNAPPSKOG PM DESANCTIS L GIANNATTASIO S RIVA E PONZONE A APOLD J CAMASCHELLA C
Citation: I. Dianzani et al., NOVEL MISSENSE MUTATION IN THE PHENYLALANINE-HYDROXYLASE GENE LEADINGTO COMPLETE LOSS OF ENZYMATIC-ACTIVITY, Human mutation, 6(3), 1995, pp. 247-249
AN EFFICIENT METHOD FOR PCR ANALYSIS OF MITOCHONDRIAL-DNA FROM PARAFFIN-EMBEDDED ARCHIVAL HEART-TISSUE
Authors: BOBBA A LIPPOLIS R GIANNATTASIO S CAMASCHELLA C MARRA E
Citation: A. Bobba et al., AN EFFICIENT METHOD FOR PCR ANALYSIS OF MITOCHONDRIAL-DNA FROM PARAFFIN-EMBEDDED ARCHIVAL HEART-TISSUE, PCR methods and applications, 4(5), 1995, pp. 309-310
Risultati: 1-25 | 26-49