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Results: 1-22 |
Results: 22
HIGH-FREQUENCY OF DE-NOVO MUTATIONS IN ANKYRIN GENE (ANK1) IN CHILDREN WITH HEREDITARY SPHEROCYTOSIS
Authors: DELGIUDICE EM FRANCESE M NOBILI B MORLE L CUTILLO S DELAUNAY J PERROTTA S
Citation: Em. Delgiudice et al., HIGH-FREQUENCY OF DE-NOVO MUTATIONS IN ANKYRIN GENE (ANK1) IN CHILDREN WITH HEREDITARY SPHEROCYTOSIS, The Journal of pediatrics, 132(1), 1998, pp. 117-120
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
DYSKERATOSIS-CONGENITA - A CASE WITH EARLY-ONSET
Authors: NOBILI B MATARESE SMR DELGIUDICE EM PERROTTA S DURZO G
Citation: B. Nobili et al., DYSKERATOSIS-CONGENITA - A CASE WITH EARLY-ONSET, British Journal of Haematology, 102(1), 1998, pp. 44-45
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
APPARENTLY NORMAL ANKYRIN CONTENT IN UNSPLENECTOMIZED HEREDITARY SPHEROCYTOSIS PATIENTS WITH THE INACTIVATION OF ONE ANKYRIN (ANK1) ALLELE
Authors: DELGIUDICE EM FRANCESE M POLITO R NOBILI B IOLASCON A PERROTTA S
Citation: Em. Delgiudice et al., APPARENTLY NORMAL ANKYRIN CONTENT IN UNSPLENECTOMIZED HEREDITARY SPHEROCYTOSIS PATIENTS WITH THE INACTIVATION OF ONE ANKYRIN (ANK1) ALLELE, Haematologica, 82(3), 1997, pp. 332-333
DIAMOND-BLACKFAN ANEMIA - EXPANSION OF ERYTHROID PROGENITORS IN-VITROBY IL-9, BUT EXCLUSION OF A SIGNIFICANT PATHOGENETIC ROLE FOR THE IL-9 GENE AND THE HEMATOPOIETIC GENE-CLUSTER ON CHROMOSOME-5Q
Authors: DIANZANI I GARELLI E CRESCENZIO N TIMEUS F MORI PG VAROTTO S NOBILI B BRANDALISE S OLIVIERI NF GABUTTI V RAMENGHI U
Citation: I. Dianzani et al., DIAMOND-BLACKFAN ANEMIA - EXPANSION OF ERYTHROID PROGENITORS IN-VITROBY IL-9, BUT EXCLUSION OF A SIGNIFICANT PATHOGENETIC ROLE FOR THE IL-9 GENE AND THE HEMATOPOIETIC GENE-CLUSTER ON CHROMOSOME-5Q, Experimental hematology, 25(12), 1997, pp. 1270-1277
A TRIAL OF HIGH-DOSE DEXAMETHASONE THERAPY FOR CHRONIC IDIOPATHIC THROMBOCYTOPENIC PURPURA IN CHILDHOOD
Authors: BORGNAPIGNATTI C RUGOLOTTO S NOBILI B AMENDOLA G DESTEFANO P MACCARIO R LOCATELLI F
Citation: C. Borgnapignatti et al., A TRIAL OF HIGH-DOSE DEXAMETHASONE THERAPY FOR CHRONIC IDIOPATHIC THROMBOCYTOPENIC PURPURA IN CHILDHOOD, The Journal of pediatrics, 130(1), 1997, pp. 13-16
PHLEBOTOMY TO REDUCE IRON OVERLOAD IN PATIENTS CURED OF THALASSEMIA BY BONE-MARROW TRANSPLANTATION
Authors: ANGELUCCI E MURETTO P LUCARELLI G RIPALTI M BARONCIANI D ERER B GALIMBERTI M GIARDINI C GAZIEV D POLCHI P ROVELLI A MONGUZZI W MASERA G PIGA A GAROFALO F GABUTTI V DIGREGORIO F ROMEO MA CAMMELLA A RUSSO G GALLISAI D BURRAI C COSTI C MARINARO AM ERBEIA M MAZZANI D NOBILI B PERROTTA S",FERRARA,"CUTILLO S MULAS G CAREDDU F MANCINI E ARGIOLU F ADDARI C RUGGIERO L DENUNZIO A TERZOLI S DASCOLA G BRUCIATELLI M SATTA AM BORGNAPIGNATTI C MARRADI P PUGGIONI G MURGIA T PORTA E POGGI V PINTABOCCALATTE MF POLIZZI B MARONI P CHELAZZI G ROCCO S ROTOLI B MANGIAGLI G BELLOMO G MINELLI P LAMANTIA A COLAROSSI M MARTINELLI L FERNANDO V TOMMASI G DEROSA C BUFARDI S MELCHIORRI G CARUSO V
Citation: E. Angelucci et al., PHLEBOTOMY TO REDUCE IRON OVERLOAD IN PATIENTS CURED OF THALASSEMIA BY BONE-MARROW TRANSPLANTATION, Blood, 90(3), 1997, pp. 994-998
HEREDITARY SPHEROCYTOSIS PATIENT WITH PROTEIN-4.2 NIPPON - THE FIRST CASE IN A NON-JAPANESE POPULATION
Authors: PERROTTA S POLITO R DEVIVO M NOBILI B CONTE ML IOLASCON A CUTILLO S DELGIUDICE EM
Citation: S. Perrotta et al., HEREDITARY SPHEROCYTOSIS PATIENT WITH PROTEIN-4.2 NIPPON - THE FIRST CASE IN A NON-JAPANESE POPULATION, Blood, 90(10), 1997, pp. 2714-2714
SHORT-TERM CYCLOSPORINE-A THERAPY FOR CHRONIC THROMBOCYTOPENIC PURPURA (ITP) IN CHILDHOOD
Authors: AMENDOLA G POGGI V PERROTTA S SPIEZA M DELVECCHIO L MATARESE SMR MIRAGLIA E DELGIUDICE EM NOBILI B
Citation: G. Amendola et al., SHORT-TERM CYCLOSPORINE-A THERAPY FOR CHRONIC THROMBOCYTOPENIC PURPURA (ITP) IN CHILDHOOD, Blood, 90(10), 1997, pp. 3069-3069
FACTORS PREDICTIVE OF RESPONSE TO SPLENECTOMY IN CHILDREN AFFECTED BYCHRONIC ITP
Authors: NOBILI B AMENDOLA G LOCATELLI F ZECCA M MARTIRE B DURZO G MATARESE SMR DESTEFANO P DEMATTIA D
Citation: B. Nobili et al., FACTORS PREDICTIVE OF RESPONSE TO SPLENECTOMY IN CHILDREN AFFECTED BYCHRONIC ITP, Blood, 90(10), 1997, pp. 3098-3098
HEREDITARY SPHEROCYTOSIS DUE TO AN ELONGATED BAND-3 - BAND-3 VESUVIO
Authors: PERROTTA S NIGRO V POLITO R NOBILI B AMENDOLA G DEVIVO M CONTE ML CUTILLO S DELGIUDICE EM
Citation: S. Perrotta et al., HEREDITARY SPHEROCYTOSIS DUE TO AN ELONGATED BAND-3 - BAND-3 VESUVIO, Blood, 90(10), 1997, pp. 1186-1186
HETEROGENEITY OF THE MOLECULAR MECHANISMS UNDERLYING NONDOMINANT HEREDITARY SPHEROCYTOSIS
Authors: DELGIUDICE EM LOMBARDI C NOBILI B FRANCESE M DEVIVO M CONTE ML IOLASCON A CUTILLO S PERROTTA S
Citation: Em. Delgiudice et al., HETEROGENEITY OF THE MOLECULAR MECHANISMS UNDERLYING NONDOMINANT HEREDITARY SPHEROCYTOSIS, Blood, 90(10), 1997, pp. 1190-1190
LOSS OF EXPRESSION OF ONE BETA-SPECTRIN ALLELE IN NOT DOMINANT HEREDITARY SPHEROCYTOSIS WITH ISOLATED SPECTRIN DEFICIENCY
Authors: DELGIUDICE EM LOMBARDI C NOBILI B FRANCESE M AMENDOLA G DEVIVO M CUTILLO S PERROTTA S
Citation: Em. Delgiudice et al., LOSS OF EXPRESSION OF ONE BETA-SPECTRIN ALLELE IN NOT DOMINANT HEREDITARY SPHEROCYTOSIS WITH ISOLATED SPECTRIN DEFICIENCY, Blood, 88(10), 1996, pp. 6-6
THE ITALIAN PEDIATRIC SURVEY ON HEREDITARY SPHEROCYTOSIS
Authors: PINTO L IOLASCON A DELGIUDICE EM MATARESE SMR NOBILI B PERROTTA S
Citation: L. Pinto et al., THE ITALIAN PEDIATRIC SURVEY ON HEREDITARY SPHEROCYTOSIS, International journal of pediatric hematology/oncology, 2(1), 1995, pp. 43-47
TREATMENT OF CHILDHOOD CHRONIC IDIOPATHIC THROMBOCYTOPENIC PURPURA WITH HIGH-DOSE DEXAMETHASONE
Authors: PINATTI CB RUGOLOTTO S NOBILI B AMENDOLA G DESTEFANO P MACCARIO R LOCATELLI F
Citation: Cb. Pinatti et al., TREATMENT OF CHILDHOOD CHRONIC IDIOPATHIC THROMBOCYTOPENIC PURPURA WITH HIGH-DOSE DEXAMETHASONE, Blood, 86(10), 1995, pp. 3376-3376
MOLECULAR HETEROGENEITY OF HEREDITARY ELLIPTOCYTOSIS IN ITALY
Authors: DELGIUDICE EM PERROTTA S SANNINO E DEANGELIS F NOBILI B IOLASCON A
Citation: Em. Delgiudice et al., MOLECULAR HETEROGENEITY OF HEREDITARY ELLIPTOCYTOSIS IN ITALY, Haematologica, 79(5), 1994, pp. 400-405
MOLECULAR HETEROGENEITY OF HEREDITARY ELLIPTOCYTOSIS IN ITALY
Authors: DELGIUDICE EM PERROTTA S SANNINO E DEANGELIS F NOBILI B IOLASCON A
Citation: Em. Delgiudice et al., MOLECULAR HETEROGENEITY OF HEREDITARY ELLIPTOCYTOSIS IN ITALY, Haematologica, 79(5), 1994, pp. 400-405
ERYTHROCYTE-MEMBRANE PROTEIN ALTERATIONS UNDERLYING CLINICAL HETEROGENEITY IN HEREDITARY SPHEROCYTOSIS
Authors: DELGIUDICE EM IOLASCON A PINTO L NOBILI B PERROTTA S
Citation: Em. Delgiudice et al., ERYTHROCYTE-MEMBRANE PROTEIN ALTERATIONS UNDERLYING CLINICAL HETEROGENEITY IN HEREDITARY SPHEROCYTOSIS, British Journal of Haematology, 88(1), 1994, pp. 52-55
COEXISTENCE OF HEREDITARY SPHEROCYTOSIS (HS) DUE TO BAND-3 DEFICIENCYAND BETA-THALASSEMIA TRAIT - PARTIAL CORRECTION OF HS PHENOTYPE
Authors: DELGIUDICE EM PERROTTA S NOBILI B PINTO L CUTILLO L IOLASCON A
Citation: Em. Delgiudice et al., COEXISTENCE OF HEREDITARY SPHEROCYTOSIS (HS) DUE TO BAND-3 DEFICIENCYAND BETA-THALASSEMIA TRAIT - PARTIAL CORRECTION OF HS PHENOTYPE, British Journal of Haematology, 85(3), 1993, pp. 553-557
BIOCHEMICAL BASIS OF NEONATAL HEREDITARY SPHEROCYTOSIS
Authors: PERROTTA S DELGIUDICE EM PINTO L SANNINO E NOBILI B CUTILLO S IOLASCON A
Citation: S. Perrotta et al., BIOCHEMICAL BASIS OF NEONATAL HEREDITARY SPHEROCYTOSIS, Blood, 82(10), 1993, pp. 10000459-10000459
Risultati: 1-22 |