Výsledky vyhledávání

High membrane expression of CD163 by bone marrow cells is not a specific marker of macrophage activation syndrome (MAS)

Autor: Paola Sabrina Buonuomo, AG Ugazio, Antonella Insalaco, R Devito, Andrea Campana, Elisabetta Cortis, Claudia Bracaglia

Publikováno v: Pediatric Rheumatology Online Journal
Pediatric Rheumatology Online Journal, Vol 6, Iss Suppl 1, p P17 (2008)

Background MAS is a life-threatening complication seen predominantly in children with SoJIA, often difficult to recognize because specific diagnostic criteria for MAS have not yet been devised. MAS is characterized by an overwhelming inflammatory rea

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a6c2e8c7730cab50b841433f5f6c486
https://doi.org/10.1186/1546-0096-6-s1-p17

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Pyomyositis: a difficult diagnosis of an emerging disease in Italian immunocompetent children

Autor: AG Ugazio, Loredana Lepore, Paola Sabrina Buonuomo, Elisabetta Cortis, A De Cunto, S Colafati, Claudia Bracaglia, P Salierno, L Lancella

Publikováno v: Pediatric Rheumatology Online Journal
Pediatric Rheumatology Online Journal, Vol 6, Iss Suppl 1, p P142 (2008)

Seven male and 1 female child with primary pyomyositis (mean age 11,4 years, range 3 – 1), were diagnosed in 2 Italian Pediatric Hospitals since 2005. The most frequently reported symptoms were fever, increasing hip pain with functional impairment,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72f977fadd7cba8aabec949b4d643d31
http://europepmc.org/articles/PMC3333940

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Akademický článek

Different immunological patterns of Down syndrome patients with and without recurrent infections.

Autor: Martins, Kamila Rosa, Araujo Alves, Flavia, Roberto da Silva, Luiz, Alves da Silva, Lauren Olivia, Silva Segundo, Gesmar Rodrigues

Publikováno v: Jornal de Pediatria; Nov/Dec2024, Vol. 100 Issue 6, p653-659, 7p

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Staphylocidal defect of polymorphonuclear leukocytes in a patient with leprechaunism

Autor: Siccardi Ag, Sacchi F, Gian Luigi Marseglia, E. Bianchi, Giuseppe Maggiore, M. Marconi, Ag Ugazio

A patient with the features of Leprechaunism had a severe and constant defect of bactericidal activity of his phagocytes. We suggest this abnormality might be the basis of the well known recurrence of infections in this syndrome.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c85e62b5b16060674920aa6f4fcb8ef3
http://hdl.handle.net/11568/6111

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Structural and functional basis for JAK3-deficient severe combined immunodeficiency

Autor: Candotti F, Sa, Oakes, Ja, Johnston, Giliani S, Rf, Schumacher, Mella P, Fiorini M, Ag, Ugazio, Badolato R, Ld, Notarangelo, Fabio Bozzi, Macchi P, Strina D, Vezzoni P, Rm, Blaese, Shea Jj, O., Villa A

Publikováno v: Europe PubMed Central

Mutations of the Janus family kinase JAK3 have been found to be responsible for autosomal recessive severe combined immunodeficiency (SCID) in humans. We report here the analysis of four new unrelated patients affected by JAK3-deficient SCID. The gen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f1c0ab852281738f6a13205f2938ea91
http://europepmc.org/abstract/med/9354668

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