Publications by authors named "Fausto Cossu"

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Long term longitudinal follow-up of an AD-HIES cohort: the impact of early diagnosis and enrollment to IPINet centers on the natural history of Job's syndrome.
Maria Carrabba, Rosa Maria Dellepiane, Manuela Cortesi, Lucia Augusta Baselli, Annarosa Soresina, Fausto Cossu

Allergy Asthma Clin Immunol· April 2023

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Metabolomic Characterization of Pediatric Acute-Onset Neuropsychiatric Syndrome (PANS).
Federica Murgia, Antonella Gagliano, Marcello G Tanca, Noga Or-Geva, Aran Hendren, Fausto Cossu

Front Neurosci· May 2021

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The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999-2019).
Vassilios Lougaris, Andrea Pession, Manuela Baronio, Annarosa Soresina, Roberto Rondelli, Fausto Cossu

J Clin Immunol· October 2020

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Autosomal-dominant hyper-IgE syndrome is associated with appearance of infections early in life and/or neonatal rash: Evidence from the Italian cohort of 61 patients with elevated IgE.
Tiziana Lorenzini, Mauro Giacomelli, Omar Scomodon, Manuela Cortesi, Vanessa Rivellini, Fausto Cossu

J Allergy Clin Immunol Pract· September 2020

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Long-term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality.
Vassilios Lougaris, Annarosa Soresina, Manuela Baronio, Davide Montin, Silvana Martino, Fausto Cossu

J Allergy Clin Immunol· August 2020

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RP-HPLC-ESI-IT Mass Spectrometry Reveals Significant Variations of the Human Salivary Protein Profile Associated with Predominantly Antibody Deficiencies.
Cristina Contini, Davide Firinu, Simone Serrao, Barbara Manconi, Alessandra Olianas, Fausto Cossu

J Clin Immunol· February 2020

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Genetics of SCID.
Fausto Cossu

Ital J Pediatr· November 2010

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Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome.
Cristina Woellner, E Michael Gertz, Alejandro A Schäffer, Macarena Lagos, Mario Perro, Fausto Cossu

J Allergy Clin Immunol· February 2010

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Molecular characterization of a large cohort of patients with Chronic Granulomatous Disease and identification of novel CYBB mutations: an Italian multicenter study.
Gigliola Di Matteo, Lucia Giordani, Andrea Finocchi, Annamaria Ventura, Maria Chiriaco, Fausto Cossu

Mol Immunol· June 2009

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Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: an Italian multicenter study.
Baldassarre Martire, Roberto Rondelli, Annarosa Soresina, Claudio Pignata, Teresa Broccoletti, Fausto Cossu

Clin Immunol· February 2008

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A novel DKC1 mutation, severe combined immunodeficiency (T+B-NK- SCID) and bone marrow transplantation in an infant with Hoyeraal-Hreidarsson syndrome.
Fausto Cossu, Tom J Vulliamy, Anna Marrone, Manuela Badiali, Antonio Cao

Br J Haematol· December 2002

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Autosomal recessive hypercholesterolaemia in Sardinia, Italy, and mutations in ARH: a clinical and molecular genetic analysis.
Marcello Arca, Giovanni Zuliani, Kenneth Wilund, Filomena Campagna, Renato Fellin, Fausto Cossu

Lancet· March 2002

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