Zobrazeno 1 - 6 of 6 pro vyhledávání: '"Valentina Ferrucci"'
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Sostenere la rete, sostenere l'inclusione: analisi dei bisogni dei servizi di accoglienza per minori stranieri non accompagnati
Autor: Cristina Cecchini, Moira Chiodini, Camillo Donati, Valentina Ferrucci, Elisa Guidi
Publikováno v: PSICOLOGIA DI COMUNITA'. :60-78
Nell'ambito del sistema di accoglienza dei MSNA, la capacità dei servizi di una comunità di lavorare in una rete strutturata e formalizzata appare cruciale per rispondere efficacemente ai bisogni emergenti. Questo contributo si inserisce all'intern
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::79b3a707f49437efd282b7f51fb69fa2
https://doi.org/10.3280/psc2022-001004
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3
Absence of severe recurrent infections in glycogen storage disease type Ib with neutropenia and neutrophil dysfunction
Autor: Martina Tetti, Mauro Celli, Anna Zambrano, R. Finocchiaro, Valentina Ferrucci, L. Lenti, Patrizia D'Eufemia
Publikováno v: Journal of inherited metabolic disease. 30(1)
We describe a 10-year-old boy with glycogen storage disease type Ib (GSD Ib) with neutropenia and neutrophil dysfunction who never suffered from severe recurrent infections. Lymphocyte subpopulations and assay of intracellular cytokines (IL-2, IL-4 a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::641b5b7c8037246d6712e136aa295245
https://pubmed.ncbi.nlm.nih.gov/17187242
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4
Reduction of plasma taurine level in children affected by osteogenesis imperfecta during bisphosphonate therapy
Autor: Martina Tetti, Anna Zambrano, Valentina Ferrucci, Patrizia D'Eufemia, Mauro Celli, R. Finocchiaro
Publikováno v: Biomedicinepharmacotherapy = Biomedecinepharmacotherapie. 61(4)
Osteogenesis imperfecta (OI) is a heritable disease of connective tissue characterized by increased bone fragility. To date, bisphosphonates seem to be the most promising therapy, at least for children. In the last decade experimental and clinical st
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06049247352938fca21cb64ebd73ebca
https://pubmed.ncbi.nlm.nih.gov/17275249
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5
Neutrophil glutamine deficiency in relation to genotype in children with cystic fibrosis
Autor: R. Finocchiaro, Julia Tote, Patrizia Troiani, Patrizia D'Eufemia, Serena Quattrucci, Anna Zambrano, Valentina Ferrucci, Mauro Celli
Publikováno v: Pediatric research. 59(1)
Pulmonary disease in cystic fibrosis (CF) is characterized by a chronic neutrophil-dominated inflammation of lung tissue. Inasmuch as some amino acids (AA) play a pivotal role in various aspects of neutrophil metabolism, the aim of this study was to
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebe72020e853483f26fc9f9044b06be1
https://pubmed.ncbi.nlm.nih.gov/16327011
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6
Premessa .Come e diversamente da Pollicino
Autor: TAGLIAVENTI, MARIA TERESA
Si tratta di una premessa relativa ai tre anni di attuazione del Progetto nazionale per l'inclusione e l'integrazione dei bambini Rom, Sinti e Caminanti promosso dal Ministero del Lavoro e delle Politiche sociali (la scrivente è membro del Comitato
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______4094::0444d9ef3acccf4eed665e573861eb01
http://hdl.handle.net/11585/598509
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