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Results: 1-25 | 26-50 | 51-75 | 76-86
Results: 51-75/86
ATOPIC-DERMATITIS IN CHILDREN - EXPRESSION OF CD30 IN CUTANEOUS BIOPSIES AND EVALUATION OF SERUM LEVELS OF SOLUBLE CD30
Authors: CAVAGNI G BRUGNONI D FACCHETTI F LODIRIZZINI F GARDENGHI M SALVIONI F PORTERI V ALTOBELLI R CATTANEO R DUSE M NOTARANGELO LD TOSONI C UGAZIO UG
Citation: G. Cavagni et al., ATOPIC-DERMATITIS IN CHILDREN - EXPRESSION OF CD30 IN CUTANEOUS BIOPSIES AND EVALUATION OF SERUM LEVELS OF SOLUBLE CD30, Journal of investigative dermatology, 107(4), 1996, pp. 53-53
IN-VITRO CORRECTION OF JAK3-DEFICIENT SEVERE COMBINED IMMUNODEFICIENCY BY RETROVIRAL-MEDIATED GENE TRANSDUCTION
Authors: CANDOTTI F OAKES SA JOHNSTON JA NOTARANGELO LD OSHEA JJ BLAESE RM
Citation: F. Candotti et al., IN-VITRO CORRECTION OF JAK3-DEFICIENT SEVERE COMBINED IMMUNODEFICIENCY BY RETROVIRAL-MEDIATED GENE TRANSDUCTION, The Journal of experimental medicine, 183(6), 1996, pp. 2687-2692
CD30 CELL EXPRESSION AND ABNORMAL SOLUBLE CD30 SERUM ACCUMULATION IN OMENNS SYNDROME - EVIDENCE FOR A T-HELPER 2-MEDIATED CONDITION
Authors: CHILOSI M FACCHETTI F NOTARANGELO LD ROMAGNANI S DELPRETE G ALMERIGOGNA F DECARLI M PIZZOLO G
Citation: M. Chilosi et al., CD30 CELL EXPRESSION AND ABNORMAL SOLUBLE CD30 SERUM ACCUMULATION IN OMENNS SYNDROME - EVIDENCE FOR A T-HELPER 2-MEDIATED CONDITION, European Journal of Immunology, 26(2), 1996, pp. 329-334
INTRAVENOUS IMMUNE GLOBULIN IN THE TREATMENT OF INTRACTABLE CHILDHOODEPILEPSY
Authors: DUSE M NOTARANGELO LD TIBERTI S MENEGATI E PLEBANI A UGAZIO AG
Citation: M. Duse et al., INTRAVENOUS IMMUNE GLOBULIN IN THE TREATMENT OF INTRACTABLE CHILDHOODEPILEPSY, Clinical and experimental immunology, 104, 1996, pp. 71-76
MONOCYTE FUNCTION IN A SEVERE COMBINED IMMUNODEFICIENT PATIENT WITH ADONOR SPLICE-SITE MUTATION IN THE JAK3 GENE
Authors: VILLA A SIRONI M MACCHI P MATTEUCCI C NOTARANGELO LD VEZZONI P MANTOVANI A
Citation: A. Villa et al., MONOCYTE FUNCTION IN A SEVERE COMBINED IMMUNODEFICIENT PATIENT WITH ADONOR SPLICE-SITE MUTATION IN THE JAK3 GENE, Blood, 88(3), 1996, pp. 817-823
MULTIPLE MONOCLONAL-ANTIBODIES FLOW CYTOMETRIC ANALYSIS OF CD95 IN CHILDREN CARRYING 2 DISTINCT MUTATIONS OF THE GENE RESULTING IN AUTOIMMUNE-LYMPHOPROLIFERATIVE SYNDROME
Authors: BRUGNONI D BETTINARDI A AIRO P CATTANEO R NOTARANGELO LD
Citation: D. Brugnoni et al., MULTIPLE MONOCLONAL-ANTIBODIES FLOW CYTOMETRIC ANALYSIS OF CD95 IN CHILDREN CARRYING 2 DISTINCT MUTATIONS OF THE GENE RESULTING IN AUTOIMMUNE-LYMPHOPROLIFERATIVE SYNDROME, Tissue antigens, 48(4-II), 1996, pp. 614-614
FLOW-CYTOMETRY ANALYSIS OF OX40 AND 4-1BB ON HUMAN PURIFIED T-CELL SUBSETS
Authors: BRUGNONI D NESTA F NOTARANGELO LD CATTANEO R AIRO P
Citation: D. Brugnoni et al., FLOW-CYTOMETRY ANALYSIS OF OX40 AND 4-1BB ON HUMAN PURIFIED T-CELL SUBSETS, Tissue antigens, 48(4-II), 1996, pp. 616-616
EFFECT OF INTERFERON-ALPHA THERAPY IN A PATIENT WITH COMMON VARIABLE IMMUNODEFICIENCY AND CHRONIC EPSTEIN-BARR-VIRUS INFECTION
Authors: TORALDO R DAVANZO M TOLONE C CANINO G IAFUSCO F NOTARANGELO LD UGAZIO A CIRILLO C
Citation: R. Toraldo et al., EFFECT OF INTERFERON-ALPHA THERAPY IN A PATIENT WITH COMMON VARIABLE IMMUNODEFICIENCY AND CHRONIC EPSTEIN-BARR-VIRUS INFECTION, Pediatric hematology and oncology, 12(5), 1995, pp. 489-493
CONGENITAL AGAMMAGLOBULINEMIA IN A FEMALE CHILD
Authors: CALABRI G SALVI G NIERI RM ROSSI ME PAROLINI O NOTARANGELO LD GIOVANNUCCI ML COCCHI P
Citation: G. Calabri et al., CONGENITAL AGAMMAGLOBULINEMIA IN A FEMALE CHILD, Rivista italiana di pediatria, 21(6), 1995, pp. 880-884
MEMBRANES IN INTERCELLULAR COMMUNICATION
Authors: NOTARANGELO LD
Citation: Ld. Notarangelo, MEMBRANES IN INTERCELLULAR COMMUNICATION, Rivista italiana di pediatria, 21(4), 1995, pp. 411-415
EXPANSION OF LARGE GRANULAR LYMPHOCYTE SUBSETS IN WISKOTT-ALDRICH SYNDROME
Authors: PLEBANI A AIRO P BRUGNONI D LEBOWITZ M CATTANEO R MONAFO V MEINI A NOTARANGELO LD DUSE M UGAZIO AG
Citation: A. Plebani et al., EXPANSION OF LARGE GRANULAR LYMPHOCYTE SUBSETS IN WISKOTT-ALDRICH SYNDROME, Haematologica, 80(6), 1995, pp. 521-525
PSEUDOHYPOALDOSTERONISM - REPORT OF A CASE PRESENTING AS FAILURE-TO-THRIVE
Authors: BUZI F BEZANTE T BRUNORI A NOTARANGELO LD UGAZIO AG
Citation: F. Buzi et al., PSEUDOHYPOALDOSTERONISM - REPORT OF A CASE PRESENTING AS FAILURE-TO-THRIVE, Journal of pediatric endocrinology & metabolism, 8(1), 1995, pp. 61-65
BTKBASE - A DATABASE OF XLA-CAUSING MUTATIONS
Authors: VIHINEN M COOPER MD DESAINTBASILE G FISCHER A GOOD RA HENDRIKS RW KINNON C KWAN SP LITMAN GW NOTARANGELO LD OCHS HD ROSEN FS VETRIE D WEBSTER ADB ZEGERS BJM SMITH CIE
Citation: M. Vihinen et al., BTKBASE - A DATABASE OF XLA-CAUSING MUTATIONS, Immunology today, 16(10), 1995, pp. 460-465
MUTATION ANALYSIS IN WISKOTT-ALDRICH SYNDROME ON CHORIONIC VILLUS DNA
Authors: WENGLER GS NOTARANGELO LD GILIANI S PIRASTRU MG UGAZIO AG PAROLINI O
Citation: Gs. Wengler et al., MUTATION ANALYSIS IN WISKOTT-ALDRICH SYNDROME ON CHORIONIC VILLUS DNA, Lancet, 346(8975), 1995, pp. 641-642
GENE-THERAPY IN PERIPHERAL-BLOOD LYMPHOCYTES AND BONE-MARROW FOR ADA(-) IMMUNODEFICIENT PATIENTS
Authors: BORDIGNON C NOTARANGELO LD NOBILI N FERRARI G CASORATI G PANINA P MAZZOLARI E MAGGIONI D ROSSI C SERVIDA P UGAZIO AG MAVILIO F
Citation: C. Bordignon et al., GENE-THERAPY IN PERIPHERAL-BLOOD LYMPHOCYTES AND BONE-MARROW FOR ADA(-) IMMUNODEFICIENT PATIENTS, Science, 270(5235), 1995, pp. 470-475
MUTATIONS OF JAK-3 GENE IN PATIENTS WITH AUTOSOMAL SEVERE COMBINED IMMUNE-DEFICIENCY (SCID)
Authors: MACCHI P VILLA A GILIANI S SACCO MG FRATTINI A PORTA F UGAZIO AG JOHNSTON JA CANDOTTI F OSHEA JJ VEZZONI P NOTARANGELO LD
Citation: P. Macchi et al., MUTATIONS OF JAK-3 GENE IN PATIENTS WITH AUTOSOMAL SEVERE COMBINED IMMUNE-DEFICIENCY (SCID), Nature, 377(6544), 1995, pp. 65-68
MOLECULAR-GENETIC ANALYSIS OF X-LINKED HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH-HORMONE DEFICIENCY
Authors: STEWART DM NOTARANGELO LD KURMAN CC STAUDT LM NELSON DL
Citation: Dm. Stewart et al., MOLECULAR-GENETIC ANALYSIS OF X-LINKED HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH-HORMONE DEFICIENCY, The Journal of immunology, 155(5), 1995, pp. 2770-2774
IMMUNOHISTOLOGIC ANALYSIS OF INEFFECTIVE CD40-CD40 LIGAND INTERACTIONIN LYMPHOID-TISSUES FROM PATIENTS WITH X-LINKED IMMUNODEFICIENCY WITHHYPER-IGM - ABORTIVE GERMINAL CENTER CELL REACTION AND SEVERE DEPLETION OF FOLLICULAR DENDRITIC CELLS
Authors: FACCHETTI F APPIANI C SALVI L LEVY J NOTARANGELO LD
Citation: F. Facchetti et al., IMMUNOHISTOLOGIC ANALYSIS OF INEFFECTIVE CD40-CD40 LIGAND INTERACTIONIN LYMPHOID-TISSUES FROM PATIENTS WITH X-LINKED IMMUNODEFICIENCY WITHHYPER-IGM - ABORTIVE GERMINAL CENTER CELL REACTION AND SEVERE DEPLETION OF FOLLICULAR DENDRITIC CELLS, The Journal of immunology, 154(12), 1995, pp. 6624-6633
EFFECT OF HIV VERTICAL TRANSMISSION ON THE ONTOGENY OF T-CELL ANTIGENS INVOLVED IN THE REGULATION OF HUMORAL IMMUNE-RESPONSE
Authors: BRUGNONI D SORESINA A AIRO P UGAZIO AG NOTARANGELO LD CATTANEO R DUSE M
Citation: D. Brugnoni et al., EFFECT OF HIV VERTICAL TRANSMISSION ON THE ONTOGENY OF T-CELL ANTIGENS INVOLVED IN THE REGULATION OF HUMORAL IMMUNE-RESPONSE, Clinical and experimental immunology, 102(2), 1995, pp. 238-242
HIGH PREVALENCE OF NONSENSE, FRAME-SHIFT, AND SPLICE-SITE MUTATIONS IN 16 PATIENTS WITH FULL-BLOWN WISKOTT-ALDRICH SYNDROME
Authors: WENGLER GS NOTARANGELO LD BERARDELLI S POLLONNI G MELLA P FASTH A UGAZIO AG PAROLINI O
Citation: Gs. Wengler et al., HIGH PREVALENCE OF NONSENSE, FRAME-SHIFT, AND SPLICE-SITE MUTATIONS IN 16 PATIENTS WITH FULL-BLOWN WISKOTT-ALDRICH SYNDROME, Blood, 86(10), 1995, pp. 3648-3654
ENGRAFTED MATERNAL T-CELLS IN A SEVERE COMBINED IMMUNODEFICIENCY PATIENT EXPRESS T-CELL RECEPTOR VARIABLE BETA-SEGMENTS CHARACTERIZED BY A RESTRICTED V-D-J JUNCTIONAL DIVERSITY
Authors: SOTTINI A QUIROSROLDAN E NOTARANGELO LD MALAGOLI A PRIMI D IMBERTI L
Citation: A. Sottini et al., ENGRAFTED MATERNAL T-CELLS IN A SEVERE COMBINED IMMUNODEFICIENCY PATIENT EXPRESS T-CELL RECEPTOR VARIABLE BETA-SEGMENTS CHARACTERIZED BY A RESTRICTED V-D-J JUNCTIONAL DIVERSITY, Blood, 85(8), 1995, pp. 2105-2113
CHARACTERIZATION OF 9 NOVEL MUTATIONS IN THE CD40 LIGAND GENE IN PATIENTS WITH X-LINKED HYPER IGM SYNDROME OF VARIOUS ANCESTRY
Authors: MACCHI P VILLA A STRINA D SACCO MG MORALI F BRUGNONI D GILIANI S MANTUANO E FASTH A ANDERSSON B ZEGERS BJM CAVAGNI G REZNICK I LEVY J ZANBAR I PORAT Y AIRO P PLEBANI A VEZZONI P NOTARANGELO LD
Citation: P. Macchi et al., CHARACTERIZATION OF 9 NOVEL MUTATIONS IN THE CD40 LIGAND GENE IN PATIENTS WITH X-LINKED HYPER IGM SYNDROME OF VARIOUS ANCESTRY, American journal of human genetics, 56(4), 1995, pp. 898-906
C TO T MUTATION CAUSING PREMATURE TERMINATION OF CD40 LIGAND AT AMINO-ACID 221 IN A PATIENT AFFECTED BY HYPER IGM SYNDROME
Authors: VILLA A STRINA D MACCHI P PATROSSO MC VEZZONI P TOVO PA GILIANI S UGAZIO AG NOTARANGELO LD
Citation: A. Villa et al., C TO T MUTATION CAUSING PREMATURE TERMINATION OF CD40 LIGAND AT AMINO-ACID 221 IN A PATIENT AFFECTED BY HYPER IGM SYNDROME, Human mutation, 3(1), 1994, pp. 73-75
HUMAN SOMATIC-CELL GENE-THERAPY FOR CONGENITAL AND ACQUIRED IMMUNODEFICIENCIES
Authors: FERRARI G SMITH CA ROSSINI S NOTARANGELO LD GIAVAZZI R SERVIDA P SICCARDI A BONHLEIN E UGAZIO AG GILBOA E MAVILIO F BORDIGNON C
Citation: G. Ferrari et al., HUMAN SOMATIC-CELL GENE-THERAPY FOR CONGENITAL AND ACQUIRED IMMUNODEFICIENCIES, AIDS research and human retroviruses, 10, 1994, pp. 190000019-190000019
ISOLATION OF COSMID AND CDNA CLONES IN THE REGION SURROUNDING THE BTKGENE AT XQ21.3-Q22
Authors: VORECHOVSKY I VETRIE D HOLLAND J BENTLEY DR THOMAS K ZHOU JN NOTARANGELO LD PLEBANI A FONTAN G OCHS HD HAMMARSTROM L SIDERAS P SMITH CIE
Citation: I. Vorechovsky et al., ISOLATION OF COSMID AND CDNA CLONES IN THE REGION SURROUNDING THE BTKGENE AT XQ21.3-Q22, Genomics, 21(3), 1994, pp. 517-524
Risultati: 1-25 | 26-50 | 51-75 | 76-86