Sfoglia per Autore
Lack of transmission of TT virus through immunoglobulins
2001 Azzari C; Resti M; Moriondo M; Gambineri E; Rossi ME; Novembre E; Vierucci A.
The molecular basis of Hyper IgM syndrome (HIM)
2002 Lee, WI; Zhu, QL; Sweetser, M; Torgerson, TR; Gambineri E; Ochs, HD
Mutations of FOXP3 causing IPEX syndrome.
2002 Gambineri E; Torgerson, TR; Bennett, CL; Amoroso, A; Barker, DF; Cunningham-Rundles, C; Notarangelo, L; Ronchetti, R; Sakiyama, Y; Ochs, HD
Inducible CO-stimulator molecule, a candidate gene for defective isotype switching, is normal in patients with hyper-IgM syndrome of unknown molecular diagnosis
2003 Lee W.-I.; Zhu Q.; Gambineri E.; Jin Y.; Welcher A.A.; Ochs H.D.
Immune dysregulation, polyendocrinopathy, enteropathy, and X-linked inheritance (IPEX), a syndrome of systemic autoimmunity caused by mutations of FOXP3, a critical regulator of T-cell homeostasis.
2003 E. GAMBINERI; T.R.TORGERSON; H.D.OCHS
INDUCIBLE CO-STIMULATOR MOLECULE (ICOS), A CANDIDATE GENE FOR DETECTIVE ISOTOPE SWITCHING, IS NORMAL IN PATIENTS WITH HYPER IGM SINDROME OF UNKNOWN MOLECULAR DIAGNOSIS.
2003 W.I. Lee; Q. ZHU; E. Gambineri;Y. Jin; A.A. Welcher AA; H.D. Ochs
LE IPER-IGE
2003 E. GAMBINERI; C. AZZARI; M. MORIONDO; A. ET
Clinical, laboratory and molecular analysis of 30 patients with the phenotype of IPEX syndrome.
2003 Torgerson, TR; Gambineri E; Vijay, S; Gersuk, V; Ziegler, SF; Ochs, HD
VACCINAZIONI NEGLI ALLERGICI
2003 E. GAMBINERI; C. AZZARI; L. BETTI; A. ET
Other Well-Defined Immunodeficiency Syndromes: IPEX-SYNDROME
2004 E. GAMBINERI; T. TORGERSON
RECENTI ACQUISIZIONI SULLA IMMUNO-PATOGENESI DELL' ASMA
2004 A. VIERUCCI; E. GAMBINERI; R. BERNARDINI
AN ATYPICAL CASE OF IPEX SINDROME WITH MULTIPLE FOXP3 MUTATIONS
2004 E. GAMBINERI; L. BIANCHI; A. ET
THE MOLECULAR BASIS OF PRIMARY IMMUNE DEFICIENCY DISEASES
2004 E. GAMBINERI; T. TORGERSON; H. OCHS; W. LEE; Q. ZHU; Y. JIN
Chronic granulomatous disease in two adolescent males: uncommon mild presentation
2005 Baccini A; Azzari C; Carbonella R; Gambineri E; Lippi F; Vierucci A; Indolfi G; de Martino M.
Identification of important functional domains of FOXP3 by analysis of mutations present in patients with IPEX syndrome.
2005 Torgerson, TR; Gambineri E; Vijay, S; Anover, S; Ochs, HD
A NEW CASE OF IPEX RECEIVING BONE MARROW TRANSPLANTATION.
2005 E. MAZZOLARI;C. FIORINO; M. FONTANA;C. D'IPPOLITO; A. LANFRANCHI; E. GAMBINERI; H. OCHS; R. BADOLATO; L.D. NOTARANGELO
A case of antibody deficiency: CVID or XLA?
2005 E. GAMBINERI
Safety and immunogenicity of measles-mumps-rubella vaccine in children with congenital immunodeficiency (DiGeorge syndrome).
2005 C.Azzari; E.Gambineri; M.Resti; M.Moriondo;L.Betti; L.R.Saldias; G. Gelli; A.Vierucci
Defective regulatory and effector T cell functions in patients with FOXP3 mutations.
2006 Bacchetta R;Passerini L;Gambineri E;Dai M;Allan SE;Perroni L;Dagna-Bricarelli F;Sartirana C;Matthes-Martin S;Lawitschka A;Azzari C;Ziegler SF;Levings MK;Roncarolo MG
OR.40. Foxp3 Mutations in Children: Different Degrees of Impairment in Regulatory and Effector T-Cell Functions in Patients with Distinct Genotypes and Phenotypes
2006 Rosa Bacchetta;Laura Passerini;Gambineri E;Sarah Allan;Lucia Perroni;Susan Matthes-Martin;Anita Lawitschka;Steven Ziegler;Megan Levings;Maria Grazia Roncarolo
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