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Dysregulated miR-155 and miR-125b Are Related to Impaired B-cell Responses in Down Syndrome

Frontiers in immunology, 2018-11, Vol.9, p.2683-2683

2018

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Gene Therapy in Peripheral Blood Lymphocytes and Bone Marrow for ADA$^-$ Immunodeficient Patients

Science (American Association for the Advancement of Science), 1995-10, Vol.270 (5235), p.470-475

1995

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Reduced numbers of switched memory B cells with high terminal differentiation potential in Down syndrome

European journal of immunology, 2015-03, Vol.45 (3), p.903-914

2015

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Low serum levels of mannose binding lectin are a risk factor for neonatal sepsis

Pediatric research, 2007-03, Vol.61 (3), p.325-328

2007

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Use of the internet by Italian pediatricians: habits, impact on clinical practice and expectations

BMC medical informatics and decision making, 2012-03, Vol.12 (1), p.23-23, Article 23

2012

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Mechanistic Associations of a Mild Phenotype of Immunodysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome

Clinical gastroenterology and hepatology, 2006-05, Vol.4 (5), p.653-659

2006

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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), 1998-07, Vol.161 (2), p.1026-1033

1998

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Mutations of CD40 Gene Cause an Autosomal Recessive Form of Immunodeficiency with Hyper IgM

Proceedings of the National Academy of Sciences - PNAS, 2001-10, Vol.98 (22), p.12614-12619

2001

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Attitudes towards HPV immunization of Italian mothers of adolescent girls and potential role of health professionals in the immunization program

Vaccine, 2009-04, Vol.27 (19), p.2625-2629

2009

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Parental perception of influenza in Italy: A web survey

Vaccine, 2012-03, Vol.30 (12), p.2041-2041

2012

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Defective migration of monocyte-derived dendritic cells in LAD-1 immunodeficiency

Journal of leukocyte biology, 2002-10, Vol.72 (4), p.650-656

2002

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Radiation risks knowledge in resident and fellow in paediatrics: a questionnaire survey

Italian journal of pediatrics, 2015-03, Vol.41 (1), p.21, Article 21

2015

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Infliximab therapy in pediatric Takayasu’s arteritis: report of two cases

Rheumatology international, 2011, Vol.31 (1), p.93-95

2011

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Mutations of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID)

Nature (London), 1995-09, Vol.377 (6544), p.65-68

1995

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Linezolid Therapy of Brain Abscess

The Pediatric infectious disease journal, 2010-11, Vol.29 (11), p.1063-1064

2010

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Abnormal production of the tumor necrosis factor inhibitor etanercept and clinical efficacy of tumor in a patient with PAPA syndrome

The Journal of pediatrics, 2004-12, Vol.145 (6), p.851-855

2004

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Longitudinal myelitis in systemic lupus erythematosus: a paediatric case

Rheumatology international, 2012-08, Vol.32 (8), p.2587-2588

2012

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Pediatric allergy and immunology in Italy

Pediatric allergy and immunology, 2011-05, Vol.22 (3), p.267-276

2011

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Necrosis of the tongue as first symptom of Polyarteritis Nodosa (PAN): unusual presentation of a rare disease in children

Rheumatology international, 2013-04, Vol.33 (4), p.1071-1073

2013

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Defective expression of T-cell CD40 ligand causes X-linked immunodeficiency with hyper-IgM

Nature (London), 1993-02, Vol.361 (6412), p.539-541

1993

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Relapsing polychondritis: new therapeutic strategies with biological agents

Rheumatology international, 2010-03, Vol.30 (5), p.691-693

2010

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Pigmented villonodular synovitis in a patient with Noonan syndrome and SOS1 gene mutation

American journal of medical genetics. Part A, 2008-11, Vol.146A (22), p.2966-2967

2008

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Reconstitution of T-cell compartment after in utero stem cell transplantation: analysis of T-cell repertoire and thymic output

Haematologica (Roma), 2004-04, Vol.89 (4), p.450

2004

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Of genes and phenotypes : the immunological and molecular spectrum of combined immune deficiency. Defects of the γc-JAK3 signaling pathway as a model

Immunological reviews, 2000, Vol.178, p.39-48

2000

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Dysregulated miR-155 and miR-125b Are Related to Impaired B-cell Responses in Down Syndrome

Activation-Induced Cytidine Deaminase (AID) Deficiency Causes the Autosomal Recessive Form of the Hyper-IgM Syndrome (HIGM2)

Gene Therapy in Peripheral Blood Lymphocytes and Bone Marrow for ADA$^-$ Immunodeficient Patients

Reduced numbers of switched memory B cells with high terminal differentiation potential in Down syndrome

Low serum levels of mannose binding lectin are a risk factor for neonatal sepsis

Use of the internet by Italian pediatricians: habits, impact on clinical practice and expectations

Mechanistic Associations of a Mild Phenotype of Immunodysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome

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

Mutations of CD40 Gene Cause an Autosomal Recessive Form of Immunodeficiency with Hyper IgM

Attitudes towards HPV immunization of Italian mothers of adolescent girls and potential role of health professionals in the immunization program

Parental perception of influenza in Italy: A web survey

Defective migration of monocyte-derived dendritic cells in LAD-1 immunodeficiency

Radiation risks knowledge in resident and fellow in paediatrics: a questionnaire survey

Infliximab therapy in pediatric Takayasu’s arteritis: report of two cases

Mutations of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID)

Linezolid Therapy of Brain Abscess

Abnormal production of the tumor necrosis factor inhibitor etanercept and clinical efficacy of tumor in a patient with PAPA syndrome

Longitudinal myelitis in systemic lupus erythematosus: a paediatric case

Pediatric allergy and immunology in Italy

Necrosis of the tongue as first symptom of Polyarteritis Nodosa (PAN): unusual presentation of a rare disease in children

Defective expression of T-cell CD40 ligand causes X-linked immunodeficiency with hyper-IgM

Relapsing polychondritis: new therapeutic strategies with biological agents

Pigmented villonodular synovitis in a patient with Noonan syndrome and SOS1 gene mutation

Reconstitution of T-cell compartment after in utero stem cell transplantation: analysis of T-cell repertoire and thymic output

Of genes and phenotypes : the immunological and molecular spectrum of combined immune deficiency. Defects of the γc-JAK3 signaling pathway as a model

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