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Cutaneous manifestations as presenting sign of autoimmune lymphoproliferative syndrome in childhoodAURICCHIO, Luigi; VITIELLO, Laura; ADRIANI, Marsilio et al.Dermatology (Basel). 2005, Vol 210, Num 4, pp 336-340, issn 1018-8665, 5 p.Article

First use of thymus transplantation therapy for FOXN1 deficiency (nude/SCID): a report of 2 casesMARKERT, M. Louise; MARQUES, José G; VICTORINO, Rui M et al.Blood. 2011, Vol 117, Num 2, pp 688-696, issn 0006-4971, 9 p.Article

Hereditary Deficiency of gp91phox Is Associated With Enhanced Arterial Dilatation: Results of a Multicenter StudyVIOLI, Francesco; SANGUIGNI, Valerio; MARTINO, Silvana et al.Circulation (New York, N.Y.). 2009, Vol 120, Num 16, pp 1616-1622, issn 0009-7322, 7 p.Article

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndromeWOELLNER, Cristina; GERTZ, E. Michael; PIETRUCHA, Barbara et al.Journal of allergy and clinical immunology. 2010, Vol 125, Num 2, pp 424-432, issn 0091-6749, 9 p.Article

Search for poliovirus long-term excretors among patients affected by agammaglobulinemiaFIORE, Lucia; PLEBANI, Alessandro; CARDINALE, Fabio et al.Clinical immunology (Orlando, Fla. Print). 2004, Vol 111, Num 1, pp 98-102, issn 1521-6616, 5 p.Article

Human equivalent of the mouse Nude/SCID phenotype : long-term evaluation of immunologic reconstitution after bone marrow transplantationPIGNATA, Claudio; GAETANIELLO, Lucia; MASCI, Anna Maria et al.Blood. 2001, Vol 97, Num 4, pp 880-885, issn 0006-4971Article

High-content cytometry and transcriptomic biomarker profiling of human B-cell activationHENNIG, Christian; LLGINUS, Claudia; BAUMANN, Ulrich et al.Journal of allergy and clinical immunology. 2014, Vol 133, Num 1, pp 172-180, issn 0091-6749, 9 p.Article

De novo 13q12.3―q14.11 Deletion Involving BRCA2 Gene in a Patient With Developmental Delay, Elevated IgM Levels, Transient Ataxia, and Cerebellar Hypoplasia, Mimicking an A-T like PhenotypeCIRILLO, Emilia; ROMANO, Rosa; DEL VECCHIO, Luigi et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 10, pp 2571-2576, issn 1552-4825, 6 p.Article

Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndromeMAZZA, Cinzia; BUZI, Fabio; TADDIO, Andrea et al.Clinical immunology (Orlando, Fla. Print). 2011, Vol 139, Num 1, pp 6-11, issn 1521-6616, 6 p.Article

Simultaneous peripubertal onset of multireactive autoimmune diseases with an unusual long-lasting remission of type 1 diabetes mellitusVALERIO, Giuliana; FRANZESE, Adriana; LOVINO, Andrea et al.Clinical endocrinology (Oxford. Print). 2000, Vol 53, Num 5, pp 649-653, issn 0300-0664Article

Brain alteration in a Nude/SCID fetus carrying FOXN1 homozygous mutationAMOROSI, Stefania; VIGLIANO, Ilaria; PIGNATA, Claudio et al.Journal of the neurological sciences. 2010, Vol 298, Num 1-2, pp 121-123, issn 0022-510X, 3 p.Article

Abnormal GH receptor signaling in children with idiopathic short statureSALERNO, Mariacarolina; BALESTRIERI, Barbara; MATRECANO, Eliana et al.The Journal of clinical endocrinology and metabolism. 2001, Vol 86, Num 8, pp 3882-3888, issn 0021-972XArticle

Defective function of Fas in patients with type 1 diabetes associated with other autoimmune diseasesDEFRANCO, Simona; BONISSONI, Sara; PIGNATA, Claudio et al.Diabetes (New York, NY). 2001, Vol 50, Num 3, pp 483-488, issn 0012-1797Article

Phenotypic characterization and outcome of paediatric patients affected with haemophagocytic syndrome of unknown genetic causeGIARDINO, Giuliana; VEROPALUMBO, Claudio; PIGNATA, Claudio et al.British journal of haematology. 2013, Vol 162, Num 5, pp 713-717, issn 0007-1048, 5 p.Article

X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the diseaseBOOTH, Claire; GILMOUR, Kimberly C; KERRIGAN, Hilary et al.Blood. 2011, Vol 117, Num 1, pp 53-62, issn 0006-4971, 10 p.Article

Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease : An Italian multicenter studyMARTIRE, Baldassarre; RONDELLI, Roberto; DELLEPIANE, Rosa M et al.Clinical immunology (Orlando, Fla. Print). 2008, Vol 126, Num 2, pp 155-164, issn 1521-6616, 10 p.Article

Atypical features of familial hemophagocytic lymphohistiocytosisBUSIELLO, Rosanna; ADRIANI, Marsilio; LOCATELLI, Franco et al.Blood. 2004, Vol 103, Num 12, pp 4610-4612, issn 0006-4971, 3 p.Article

Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: An Italian multicenter studyPLEBANI, Alessandro; SORESINA, Annarosa; DUSE, Marzia et al.Clinical immunology (Orlando, Fla. Print). 2002, Vol 104, Num 3, pp 221-230, issn 1521-6616, 10 p.Article

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