Eva Maria Rivas
Overview
Explore the profile of Eva Maria Rivas including associated specialties, affiliations and a list of published articles.
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Articles
6
Citations
34
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Recent Articles
1.
Barese C, Copelli S, De Matteo E, Zandomeni R, Salgueiro F, Di Giovanni D, et al.
Pediatr Blood Cancer
. 2004 Oct;
44(4):420-2.
PMID: 15468310
Chronic granulomatous disease (CGD) is a primary immunodeficiency that affects the oxidative mechanism of microbial killing of phagocytic cells. The defect is characterized by a lack or severely reduced superoxide...
2.
Barese C, Copelli S, Zandomeni R, Oleastro M, Zelazko M, Rivas E
J Pediatr Hematol Oncol
. 2004 Oct;
26(10):656-660.
PMID: 27811607
Background: Chronic granulomatous disease (CGD) is a primary immunodeficiency due to absent or decreased NADPH oxidase activity in phagocytic cells. The X-linked form of the disease (X-CGD) arises from mutations...
3.
Barese C, Copelli S, Zandomeni R, Oleastro M, Zelazko M, Rivas E
J Pediatr Hematol Oncol
. 2004 Sep;
26(10):656-60.
PMID: 15454837
Background: Chronic granulomatous disease (CGD) is a primary immunodeficiency due to absent or decreased NADPH oxidase activity in phagocytic cells. The X-linked form of the disease (X-CGD) arises from mutations...
4.
Barese C, Podesta M, Litvak E, Villa M, Rivas E
J Pediatr Hematol Oncol
. 2004 May;
26(3):209-12.
PMID: 15125617
Eosinophilic cystitis is an uncommon disease in children, and its association with chronic granulomatous disease (CGD) has been previously reported in only five patients. In all those patients the disease...
5.
Danielian S, El-Hakeh J, Basilico G, Oleastro M, Rosenzweig S, Feldman G, et al.
Hum Mutat
. 2003 Mar;
21(4):451.
PMID: 12655572
The block in differentiation from pro-B to pre-B cells results in a selective defect in the humoral immune response characteristic of human X-linked agammaglobulinemia (XLA). Mutations of Bruton tyrosine kinase...
6.
El-Hakeh J, Rosenzweig S, Oleastro M, Basack N, Berozdnik L, Molina F, et al.
Hum Mutat
. 2002 Jan;
19(2):186-7.
PMID: 11793485
Wiskott-Aldrich syndrome (WAS), is an X-linked immunodeficiency disease caused by mutations of the WAS protein (WASP) gene, characterized by thrombocytopenia, eczema and recurrent infections. X-linked thrombocytopenia (XLT) is a milder...