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Results: 1-25 | 26-50 | 51-75 | 76-90
Results: 1-25/90
UGT1A PROMOTER POLYMORPHISM DIFFERENTLY CONTRIBUTES TO JAUNDICE IN INHERITED HEMOLYTIC-ANEMIAS OF NEWBORN
Authors: IOLASCON A FAIENZA MF GIORDANI L PERROTTA S MELONI MF GUGGIU G DELGIUDICE EM
Citation: A. Iolascon et al., UGT1A PROMOTER POLYMORPHISM DIFFERENTLY CONTRIBUTES TO JAUNDICE IN INHERITED HEMOLYTIC-ANEMIAS OF NEWBORN, European journal of human genetics, 6, 1998, pp. 4085-4085
REFINEMENT OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II LOCUS ON CHROMOSOME-20
Authors: TOTARO A CARELLA M GRIFA A VALENTINO MA GASPARINI P ZELANTE L DELGIUDICE EM DELAUNAY J PERROTTA S IOLASCON A
Citation: A. Totaro et al., REFINEMENT OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II LOCUS ON CHROMOSOME-20, European journal of human genetics, 6, 1998, pp. 4128-4128
MOLECULAR-GENETICS OF OSTEOPOROSIS IN ITALY
Authors: DAGRUMA L BISCEGLIA L GASPARINI P ZELANTE L IOLASCON A IOLASCON G COLAPIETRO F FURLAN F BERTOLDO F
Citation: L. Dagruma et al., MOLECULAR-GENETICS OF OSTEOPOROSIS IN ITALY, European journal of human genetics, 6, 1998, pp. 4129-4129
THE THROMBOPOIETIN RECEPTOR (C-MPL) IS NOT INVOLVED IN CONGENITAL THROMBOCYTOPENIA AND ABSENT RADII (TAR)
Authors: SAVOIA A TONELLI R GIORDANO P SAVINO M STRIPPOLI PL DEMATTIA D ZELANTE L BAGNARA GP IOLASCON A
Citation: A. Savoia et al., THE THROMBOPOIETIN RECEPTOR (C-MPL) IS NOT INVOLVED IN CONGENITAL THROMBOCYTOPENIA AND ABSENT RADII (TAR), European journal of human genetics, 6, 1998, pp. 4144-4144
RESISTANCE TO ACTIVATED PROTEIN-C IN THALASSEMIC PATIENTS - AN UNDERLYING CAUSE OF THROMBOSIS
Authors: GIORDANO P DELVECCHIO GC ALTOMARE M COPPOLA B SCHETTINI F IOLASCON A DEMATTIA D
Citation: P. Giordano et al., RESISTANCE TO ACTIVATED PROTEIN-C IN THALASSEMIC PATIENTS - AN UNDERLYING CAUSE OF THROMBOSIS, European journal of haematology, 61(2), 1998, pp. 123-127
EXPRESSION OF CELL-CYCLE REGULATORY GENES IN CHRONIC MYELOGENOUS LEUKEMIA
Authors: IOLASCON A DELLARAGIONE F GIORDANI L SERRA A SAGLIO G FAIENZA MF
Citation: A. Iolascon et al., EXPRESSION OF CELL-CYCLE REGULATORY GENES IN CHRONIC MYELOGENOUS LEUKEMIA, Haematologica, 83(9), 1998, pp. 771-777
DECISION-MAKING AT THE BEDSIDE - DIAGNOSIS OF HEREDITARY SPHEROCYTOSIS IN A TRANSFUSED INFANT
Authors: DELGIUDICE EM PERROTTA S LOMBARDI C IOLASCON A
Citation: Em. Delgiudice et al., DECISION-MAKING AT THE BEDSIDE - DIAGNOSIS OF HEREDITARY SPHEROCYTOSIS IN A TRANSFUSED INFANT, Haematologica, 83(4), 1998, pp. 347-349
HEREDITARY SPHEROCYTOSIS - FROM CLINICAL TO MOLECULAR DEFECTS
Authors: IOLASCON A DELGIUDICE EM PERROTTA S ALLOISIO N MORLE L DELAUNAY J
Citation: A. Iolascon et al., HEREDITARY SPHEROCYTOSIS - FROM CLINICAL TO MOLECULAR DEFECTS, Haematologica, 83(3), 1998, pp. 240-257
INTERSTITIAL AND LARGE CHROMOSOME 1P DELETION OCCURS IN LOCALIZED ANDDISSEMINATED NEUROBLASTOMAS AND PREDICTS AN UNFAVORABLE OUTCOME
Authors: IOLASCON A LOCUNSOLO C GIORDANI L CUSANO R MAZZOCCO K BOUMGARTNER M GHISELLINI P FAIENZA MF BONI L DEBERNARDI B CONTE M ROMEO G TONINI GP
Citation: A. Iolascon et al., INTERSTITIAL AND LARGE CHROMOSOME 1P DELETION OCCURS IN LOCALIZED ANDDISSEMINATED NEUROBLASTOMAS AND PREDICTS AN UNFAVORABLE OUTCOME, Cancer letters, 130(1-2), 1998, pp. 83-92
DECREASED BAND-3 ANION TRANSPORT ACTIVITY AND BAND-3 CLUSTERIZATION IN CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II
Authors: DEFRANCESCHI L TURRINI F DELGIUDICE EM PERROTTA S OLIVIERI O CORROCHER R MANNU F IOLASCON A
Citation: L. Defranceschi et al., DECREASED BAND-3 ANION TRANSPORT ACTIVITY AND BAND-3 CLUSTERIZATION IN CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II, Experimental hematology, 26(9), 1998, pp. 869-873
ANALYSIS OF CDKN2A, CDKN2B, CDKN2C, AND CYCLIN DS GENE STATUS IN HEPATOBLASTOMA
Authors: IOLASCON A GIORDANI L MORETTI A BASSO G BORRIELLO A DELLARAGIONE F
Citation: A. Iolascon et al., ANALYSIS OF CDKN2A, CDKN2B, CDKN2C, AND CYCLIN DS GENE STATUS IN HEPATOBLASTOMA, Hepatology, 27(4), 1998, pp. 989-995
CYTOGENETIC ANALYSIS OF HEPATOBLASTOMA - HYPOTHESIS OF CYTOGENETIC EVOLUTION IN SUCH TUMORS AND RESULTS OF A MULTICENTRIC STUDY
Authors: SAINATI L LESZL A STELLA M MONTALDI A PERILONGO G RUGGE M BOLCATO S IOLASCON A BASSO G
Citation: L. Sainati et al., CYTOGENETIC ANALYSIS OF HEPATOBLASTOMA - HYPOTHESIS OF CYTOGENETIC EVOLUTION IN SUCH TUMORS AND RESULTS OF A MULTICENTRIC STUDY, Cancer genetics and cytogenetics, 104(1), 1998, pp. 39-44
INTERACTION OF 3 GENETIC POLYMORPHISMS AS THROMBOSIS RISK-FACTORS
Authors: GIORDANO P MICELLI M COPPOLA B GILIBERTI MG CIAVARELLA N DELUCIA D IOLASCON A
Citation: P. Giordano et al., INTERACTION OF 3 GENETIC POLYMORPHISMS AS THROMBOSIS RISK-FACTORS, Thrombosis research, 91(3), 1998, pp. 68-68
STRUCTURAL AND FUNCTIONAL-ANALYSIS OF CYCLIN-DEPENDENT KINASE INHIBITOR GENES (CDKN2A, CDKN2B, AND CDKN2C) IN NEUROBLASTOMA
Authors: IOLASCON A GIORDANI L MORETTI A TONINI GP LOCUNSOLO C MASTROPIETRO S BORRIELLO A DELLARAGIONE F
Citation: A. Iolascon et al., STRUCTURAL AND FUNCTIONAL-ANALYSIS OF CYCLIN-DEPENDENT KINASE INHIBITOR GENES (CDKN2A, CDKN2B, AND CDKN2C) IN NEUROBLASTOMA, Pediatric research, 43(1), 1998, pp. 139-144
MUTATIONAL SCREENING OF THROMBOPOIETIN RECEPTOR GENE (C-MPL) IN PATIENTS WITH CONGENITAL THROMBOCYTOPENIA AND ABSENT RADII (TAR)
Authors: STRIPPOLI P SAVOIA A IOLASCON A TONELLI R SAVINO M GIORDANO P DAVANZO M MASSOLO F LOCATELLI F BORGNA C DEMATTIA D ZELANTE L PAOLUCCI G BAGNARA GP
Citation: P. Strippoli et al., MUTATIONAL SCREENING OF THROMBOPOIETIN RECEPTOR GENE (C-MPL) IN PATIENTS WITH CONGENITAL THROMBOCYTOPENIA AND ABSENT RADII (TAR), British Journal of Haematology, 103(2), 1998, pp. 311-314
CHROMOSOMAL LOCALIZATION OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II (CDA-II)
Authors: IOLASCON A DELGIUDICE EM PERROTTA S NOBILI B ZELANTE L GRANATIERO M MELCHIONDA S DELAUNAY J GASPARINI P
Citation: A. Iolascon et al., CHROMOSOMAL LOCALIZATION OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II (CDA-II), British Journal of Haematology, 102(1), 1998, pp. 3-3
ANALYSIS OF 3 GENETIC POLYMORPHISMS AS THROMBOSIS RISK-FACTORS
Authors: GIORDANO P COPPOLA B MICELLI M GILIBERTI MG CIAVARELLA N DELUCIA D IOLASCON A
Citation: P. Giordano et al., ANALYSIS OF 3 GENETIC POLYMORPHISMS AS THROMBOSIS RISK-FACTORS, British Journal of Haematology, 102(1), 1998, pp. 253-253
CLINICAL AND MOLECULAR EVALUATION OF NONDOMINANT HEREDITARY SPHEROCYTOSIS (HS)
Authors: DELGIUDICE EM NOBILI B DURZO G ILARDO R FRANCESE M CONTE ML EBER SW IOLASCON A PERROTTA S
Citation: Em. Delgiudice et al., CLINICAL AND MOLECULAR EVALUATION OF NONDOMINANT HEREDITARY SPHEROCYTOSIS (HS), British Journal of Haematology, 102(1), 1998, pp. 302-302
FREQUENT DE-NOVO MONOALLELIC EXPRESSION OF BETA-SPECTRIN GENE (SPTB) IN CHILDREN WITH HEREDITARY SPHEROCYTOSIS AND ISOLATED SPECTRIN DEFICIENCY
Authors: DELGIUDICE EM LOMBARDI C FRANCESE M NOBILI B CONTE ML AMENDOLA G CUTILLO S IOLASCON A PERROTTA S
Citation: Em. Delgiudice et al., FREQUENT DE-NOVO MONOALLELIC EXPRESSION OF BETA-SPECTRIN GENE (SPTB) IN CHILDREN WITH HEREDITARY SPHEROCYTOSIS AND ISOLATED SPECTRIN DEFICIENCY, British Journal of Haematology, 101(2), 1998, pp. 251-254
GENETIC-HETEROGENEITY OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II
Authors: IOLASCON A DEMATTIA D PERROTTA S CARELLA M GASPARINI P DELILIERS GL
Citation: A. Iolascon et al., GENETIC-HETEROGENEITY OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II, Blood, 92(7), 1998, pp. 2593-2594
UGT1 PROMOTER POLYMORPHISM ACCOUNTS FOR INCREASED NEONATAL APPEARANCEOF HEREDITARY SPHEROCYTOSIS
Authors: IOLASCON A FAIENZA MF MORETTI A PERROTTA S DELGIUDICE EM
Citation: A. Iolascon et al., UGT1 PROMOTER POLYMORPHISM ACCOUNTS FOR INCREASED NEONATAL APPEARANCEOF HEREDITARY SPHEROCYTOSIS, Blood, 91(3), 1998, pp. 1093-1093
MATERNAL AND NEONATAL LEAD-EXPOSURE IN SOUTHERN ITALY
Authors: CARBONE R LAFORGIA N CROLLO E MAUTONE A IOLASCON A
Citation: R. Carbone et al., MATERNAL AND NEONATAL LEAD-EXPOSURE IN SOUTHERN ITALY, Biology of the neonate, 73(6), 1998, pp. 362-366
GENOMEWIDE SEARCH FOR DEHYDRATED HEREDITARY STOMATOCYTOSIS (HEREDITARY XEROCYTOSIS) - MAPPING OF LOCUS TO CHROMOSOME-16 (16Q23-QTER)
Authors: CARELLA M STEWART G AJETUNMOBI JF PERROTTA S GROOTENBOER S TCHERNIA G DELAUNAY J TOTARO A ZELANTE L GASPARINI P IOLASCON A
Citation: M. Carella et al., GENOMEWIDE SEARCH FOR DEHYDRATED HEREDITARY STOMATOCYTOSIS (HEREDITARY XEROCYTOSIS) - MAPPING OF LOCUS TO CHROMOSOME-16 (16Q23-QTER), American journal of human genetics, 63(3), 1998, pp. 810-816
INACTIVATION OF CYCLIN-DEPENDENT KINASE INHIBITOR GENES AND DEVELOPMENT OF HUMAN ACUTE LEUKEMIAS
Authors: DELLARAGIONE F IOLASCON A
Citation: F. Dellaragione et A. Iolascon, INACTIVATION OF CYCLIN-DEPENDENT KINASE INHIBITOR GENES AND DEVELOPMENT OF HUMAN ACUTE LEUKEMIAS, Leukemia & lymphoma, 25(1-2), 1997, pp. 23-35
RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM ANALYSIS REVEALS DIFFERENT ALLELE FREQUENCY AND A LINKAGE DISEQUILIBRIUM AT LOCUS D1S94 IN NEUROBLASTOMA PATIENTS
Authors: PERRI P PESSION A MAZZOCCO K SCARUFFI P STRIGINI P IOLASCON A ALBERGONI MP BASSO G TONINI GP
Citation: P. Perri et al., RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM ANALYSIS REVEALS DIFFERENT ALLELE FREQUENCY AND A LINKAGE DISEQUILIBRIUM AT LOCUS D1S94 IN NEUROBLASTOMA PATIENTS, European journal of cancer, 33(12), 1997, pp. 1949-1952
Risultati: 1-25 | 26-50 | 51-75 | 76-90