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Results: 1-25 | 26-50 | 51-75 | 76-86
Results: 1-25/86
EXPRESSION OF INDUCIBLE NITRIC-OXIDE SYNTHASE (INOS) IN MONOCYTIC CELLS FROM CHILDREN WITH INFECTIONS BY INTRACELLULAR PATHOGENS
Authors: BADOLATO R FIORENTINI S CARUSO A UGAZIO AG ALEBARDI O NOTARANGELO LD DUSE M FACCHETTI F
Citation: R. Badolato et al., EXPRESSION OF INDUCIBLE NITRIC-OXIDE SYNTHASE (INOS) IN MONOCYTIC CELLS FROM CHILDREN WITH INFECTIONS BY INTRACELLULAR PATHOGENS, The FASEB journal, 12(5), 1998, pp. 5349-5349
PRENATAL-DIAGNOSIS IN 26 FETUSES AT-RISK FOR SEVERE PRIMARY IMMUNE DEFICIENCIES
Authors: COMINOTTI A GILIANI S ZUCCA S BRUGNONI D AIRO P CANDOTTI F FIORINI M MELLA P BADOLATO R SCHUMACHER RF GUANDALINI F BELLOTTI D LALATTA F TORCOLI D NOTARANGELO LD
Citation: A. Cominotti et al., PRENATAL-DIAGNOSIS IN 26 FETUSES AT-RISK FOR SEVERE PRIMARY IMMUNE DEFICIENCIES, Rivista italiana di pediatria, 24(1), 1998, pp. 117-121
GENETICS AND TREATMENT OF PRIMARY IMMUNODEFICIENCIES - INTRODUCTION
Authors: NOTARANGELO LD
Citation: Ld. Notarangelo, GENETICS AND TREATMENT OF PRIMARY IMMUNODEFICIENCIES - INTRODUCTION, Perspectives in mathematical logic, 19(4), 1998, pp. 363-367
THE HYPER-IGM (HIM) SYNDROME
Authors: RAMESH N SEKI M NOTARANGELO LD GEHA RS
Citation: N. Ramesh et al., THE HYPER-IGM (HIM) SYNDROME, Perspectives in mathematical logic, 19(4), 1998, pp. 383-399
URETERAL OBSTRUCTION IN A PATIENT WITH CHRONIC GRANULOMATOUS-DISEASE,RECEIVING COMBINED PROPHYLAXIS WITH IFN-GAMMA AND ANTIBIOTICS
Authors: SCHUMACHER RF ARRIGHINI A ALBERTI D BADOLATO R FIORINI M NOTARANGELO L NOTARANGELO LD UGAZIO AG
Citation: Rf. Schumacher et al., URETERAL OBSTRUCTION IN A PATIENT WITH CHRONIC GRANULOMATOUS-DISEASE,RECEIVING COMBINED PROPHYLAXIS WITH IFN-GAMMA AND ANTIBIOTICS, European journal of pediatrics, 157(4), 1998, pp. 352-353
IN-UTERO TRANSPLANTATION (IUT) OF PARENTAL CD34+ CELLS IN 3 PATIENTS AFFECTED BY PRIMARY IMMUNODEFICIENCIES
Authors: LANFRANCHI A NEVA A TETTONI K VERARDI R MAZZOLARI E WENGLER G FRUSCA T ZUCCA A CARLOSTELLA C NOTARANGELO LD UGAZIO AG ALBERTINI A PORTA F
Citation: A. Lanfranchi et al., IN-UTERO TRANSPLANTATION (IUT) OF PARENTAL CD34+ CELLS IN 3 PATIENTS AFFECTED BY PRIMARY IMMUNODEFICIENCIES, Bone marrow transplantation, 21, 1998, pp. 443-443
REPORT OF THE ESID COLLABORATIVE STUDY ON CLINICAL-FEATURES AND MOLECULAR ANALYSIS IN X-LINKED HYPER-IGM SYNDROME
Authors: NOTARANGELO LD GILIANI S JONES A DESAINTBASILE G FLORINI M TONIATI P MELLA P VIHINEN M
Citation: Ld. Notarangelo et al., REPORT OF THE ESID COLLABORATIVE STUDY ON CLINICAL-FEATURES AND MOLECULAR ANALYSIS IN X-LINKED HYPER-IGM SYNDROME, Molecular immunology, 35(11-12), 1998, pp. 665-665
MUTATIONS IN THE JAK3-GENE IN CHILDREN WITH AUTOSOMAL RECESSIVE T-B-GENE IN CHILDREN WITH AUTOSOMAL RECESSIVE T-B+ SCID( SCID IN THE JAK3)
Authors: SCHUMACHER RF MELLA P BADOLATO R FIORINI M GILIANI S VILLA A CANDOTTI F VEZZONI P NOTARANGELO LD
Citation: Rf. Schumacher et al., MUTATIONS IN THE JAK3-GENE IN CHILDREN WITH AUTOSOMAL RECESSIVE T-B-GENE IN CHILDREN WITH AUTOSOMAL RECESSIVE T-B+ SCID( SCID IN THE JAK3), Molecular immunology, 35(11-12), 1998, pp. 713-713
BIOCHEMICAL, IMMUNOLOGICAL AND MOLECULAR STUDIES IN 2 PATIENTS WITH ATYPICAL SCIDX1
Authors: MELLA P GILIANI S BRUGNONI D CANDOTTI F MARTIRE B DEMATIA D PENNACCHIO M PORTA F IMBERTI L NOTARANGELO LD
Citation: P. Mella et al., BIOCHEMICAL, IMMUNOLOGICAL AND MOLECULAR STUDIES IN 2 PATIENTS WITH ATYPICAL SCIDX1, Molecular immunology, 35(11-12), 1998, pp. 713-713
MOLECULAR, BIOCHEMICAL AND IMMUNO-CYTOCHEMICAL ANALYSIS IN FAMILIES WITH WAS XLT/
Authors: GILIANI S FIORINI M MELLA P VERMI W FRANCESCHINI R IMBERTI L SCHUMACHER RF BOE F FACCHETTI F NOTARANGELO LD
Citation: S. Giliani et al., MOLECULAR, BIOCHEMICAL AND IMMUNO-CYTOCHEMICAL ANALYSIS IN FAMILIES WITH WAS XLT/, Molecular immunology, 35(11-12), 1998, pp. 718-718
MOLECULAR ANALYSIS IN X-LINKED AGAMMAGLOBULINEMIA - RESULTS OF AN ITALIAN MULTICENTER STUDY
Authors: MOSCHESE V ORLANDI P RITIS K MELLA P FIORINI M NOTARANGELO LD PLEBANI A
Citation: V. Moschese et al., MOLECULAR ANALYSIS IN X-LINKED AGAMMAGLOBULINEMIA - RESULTS OF AN ITALIAN MULTICENTER STUDY, Molecular immunology, 35(11-12), 1998, pp. 719-719
INDUCIBLE NITRIC-OXIDE SYNTHASE EXPRESSION ON HUMAN MONOCYTE-DERIVED CELLS IN GRANULOMATOUS REACTIONS
Authors: FACCHETTI F VERMI W ALEBARDI O SOLFRINI C FIORENTINI S CARUSO A DUSE M CHILOSI M NOTARANGELO LD BADOLATO R
Citation: F. Facchetti et al., INDUCIBLE NITRIC-OXIDE SYNTHASE EXPRESSION ON HUMAN MONOCYTE-DERIVED CELLS IN GRANULOMATOUS REACTIONS, Molecular immunology, 35(11-12), 1998, pp. 723-723
THE SPLEEN IN THE WISKOTT-ALDRICH-SYNDROME - WHITE PULP CHANGES CORRELATE WITH THE CLINICAL PHENOTYPE OF THE DISEASE
Authors: FACCHETTI F VERMI W BLANZUOLI L GRIGOLATO PG DONATO F GILIANI S NOTARANGELO LD
Citation: F. Facchetti et al., THE SPLEEN IN THE WISKOTT-ALDRICH-SYNDROME - WHITE PULP CHANGES CORRELATE WITH THE CLINICAL PHENOTYPE OF THE DISEASE, Molecular immunology, 35(11-12), 1998, pp. 733-733
DEFECTIVE ACTIN POLYMERIZATION IN PATIENTS WITH THE WISKOTT-ALDRICH-SYNDROME
Authors: FACCHETTI F BLANZUOLI L VERMI W NOTARANGELO LD NELSON DL
Citation: F. Facchetti et al., DEFECTIVE ACTIN POLYMERIZATION IN PATIENTS WITH THE WISKOTT-ALDRICH-SYNDROME, Molecular immunology, 35(11-12), 1998, pp. 734-734
PRIMARY IMMUNODEFICIENCY WITH MICROCEPHALIA - REPORT OF 8 CASES
Authors: RESNICK IB KONDRATENKO IV NOTARANGELO LD NOTARANGELO LD
Citation: Ib. Resnick et al., PRIMARY IMMUNODEFICIENCY WITH MICROCEPHALIA - REPORT OF 8 CASES, Molecular immunology, 35(11-12), 1998, pp. 743-743
SUCCESSFUL HAPLOIDENTICAL TRANSPLANT IN A SCID T-B-NK+ BY COINFUSION OF PURIFIED CD34+ AND STROMAL CELLS
Authors: PORTA F LANFRANCHI A VERARDI R VERZERI U MAZZOLARI E CARLOSTALLA C NOTARANGELO LD UGAZIO AG
Citation: F. Porta et al., SUCCESSFUL HAPLOIDENTICAL TRANSPLANT IN A SCID T-B-NK+ BY COINFUSION OF PURIFIED CD34+ AND STROMAL CELLS, Molecular immunology, 35(11-12), 1998, pp. 771-771
RESOLUTION OF PULMONARY AND VERTEBRAL ASPERGILLOSIS IN A CHILD WITH CGD FOLLOWING COMBINED USE OF GRANULOCYTE TRANSFUSIONS AND VORICONAZOLE
Authors: NOTARANGELO LD CASA C FERRARI E PLUCK N BADOLATO R SCHUMACHER RF CABONA MG FERREMI P TAFURI C UGAZIO AG
Citation: Ld. Notarangelo et al., RESOLUTION OF PULMONARY AND VERTEBRAL ASPERGILLOSIS IN A CHILD WITH CGD FOLLOWING COMBINED USE OF GRANULOCYTE TRANSFUSIONS AND VORICONAZOLE, Molecular immunology, 35(11-12), 1998, pp. 786-786
REPORT OF THE ESID COLLABORATIVE STUDY ON CLINICAL-FEATURES AND MOLECULAR ANALYSIS IN X-LINKED HYPER-IGM SYNDROME
Authors: NOTARANGELO LD GILIANI S JONES A DESAINTBASILE G FIORINI M TONIATI P MELLA P VIHINEN M
Citation: Ld. Notarangelo et al., REPORT OF THE ESID COLLABORATIVE STUDY ON CLINICAL-FEATURES AND MOLECULAR ANALYSIS IN X-LINKED HYPER-IGM SYNDROME, Molecular immunology, 35(11-12), 1998, pp. 796-796
PARTIAL V(D)J RECOMBINATION ACTIVITY LEADS TO OMENN-SYNDROME
Authors: VILLA A SANTAGATA S BOZZI F GILIANI S FRATTINI A IMBERTI L GATTA LB OCHS HD SCHWARZ K NOTARANGELO LD VEZZONI P SPANOPOULOU E
Citation: A. Villa et al., PARTIAL V(D)J RECOMBINATION ACTIVITY LEADS TO OMENN-SYNDROME, Cell, 93(5), 1998, pp. 885-896
SPECTRUM OF THE X-LINKED HYPER IGM SYNDROME - REPLY
Authors: LEVY J NOTARANGELO LD
Citation: J. Levy et Ld. Notarangelo, SPECTRUM OF THE X-LINKED HYPER IGM SYNDROME - REPLY, The Journal of pediatrics, 132(3), 1998, pp. 561-562
DEFECTIVE ACTIN POLYMERIZATION IN EBV-TRANSFORMED B-CELL LINES FROM PATIENTS WITH THE WISKOTT-ALDRICH-SYNDROME
Authors: FACCHETTI F BLANZUOLI L VERMI W NOTARANGELO LD GILIANI S FIORINI M FASTH A STEWART DM NELSON DL
Citation: F. Facchetti et al., DEFECTIVE ACTIN POLYMERIZATION IN EBV-TRANSFORMED B-CELL LINES FROM PATIENTS WITH THE WISKOTT-ALDRICH-SYNDROME, Journal of pathology, 185(1), 1998, pp. 99-107
MONOCYTES FROM WISKOTT-ALDRICH PATIENTS DISPLAY REDUCED CHEMOTAXIS AND LACK OF CELL POLARIZATION IN RESPONSE TO MONOCYTE CHEMOATTRACTANT PROTEIN-1 AND FORMYL-METHIONYL-LEUCYL-PHENYLALANINE
Authors: BADOLATO R SOZZANI S MALACARNE F BRESCIANI S FIORINI M BORSATTI A ALBERTINI A MANTOVANI A UGAZIO AG NOTARANGELO LD
Citation: R. Badolato et al., MONOCYTES FROM WISKOTT-ALDRICH PATIENTS DISPLAY REDUCED CHEMOTAXIS AND LACK OF CELL POLARIZATION IN RESPONSE TO MONOCYTE CHEMOATTRACTANT PROTEIN-1 AND FORMYL-METHIONYL-LEUCYL-PHENYLALANINE, The Journal of immunology (1950), 161(2), 1998, pp. 1026-1033
CHARACTERIZATION OF A CD38-LIKE 78-KILODALTON SOLUBLE-PROTEIN RELEASED FROM B-CELL LINES DERIVED FROM PATIENTS WITH X-LINKED AGAMMAGLOBULINEMIA
Authors: MALLONE R FERRUA S MORRA M ZOCCHI E MEHTA K NOTARANGELO LD MALAVASI F
Citation: R. Mallone et al., CHARACTERIZATION OF A CD38-LIKE 78-KILODALTON SOLUBLE-PROTEIN RELEASED FROM B-CELL LINES DERIVED FROM PATIENTS WITH X-LINKED AGAMMAGLOBULINEMIA, The Journal of clinical investigation, 101(12), 1998, pp. 2821-2830
MOLECULAR AND BIOCHEMICAL-CHARACTERIZATION OF JAK3 DEFICIENCY IN A PATIENT WITH SEVERE COMBINED IMMUNODEFICIENCY OVER 20 YEARS AFTER BONE-MARROW TRANSPLANTATION - IMPLICATIONS FOR TREATMENT
Authors: BOZZI F LEFRANC G VILLA A BADOLATO R SCHUMACHER RF KHALIL G LOISELET J BRESCIANI S OSHEA JJ VEZZONI P NOTARANGELO LD CANDOTTI F
Citation: F. Bozzi et al., MOLECULAR AND BIOCHEMICAL-CHARACTERIZATION OF JAK3 DEFICIENCY IN A PATIENT WITH SEVERE COMBINED IMMUNODEFICIENCY OVER 20 YEARS AFTER BONE-MARROW TRANSPLANTATION - IMPLICATIONS FOR TREATMENT, British Journal of Haematology, 102(5), 1998, pp. 1363-1366
MUTATION ANALYSIS BY A NONRADIOACTIVE SINGLE-STRAND CONFORMATION POLYMORPHISM ASSAY IN 9 FAMILIES WITH X-LINKED SEVERE COMBINED IMMUNODEFICIENCY (SCIDX1)
Authors: WENGLER GS GILIANI S FIORINI M MELLA P MANTUANO E ZANOLA A POLLONINI G EIBL MM UGAZIO AG NOTARANGELO LD PAROLINI O
Citation: Gs. Wengler et al., MUTATION ANALYSIS BY A NONRADIOACTIVE SINGLE-STRAND CONFORMATION POLYMORPHISM ASSAY IN 9 FAMILIES WITH X-LINKED SEVERE COMBINED IMMUNODEFICIENCY (SCIDX1), British Journal of Haematology, 101(3), 1998, pp. 586-591
Risultati: 1-25 | 26-50 | 51-75 | 76-86