Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Giulia Forzano"'
Autor:
Angelica Pagliazzi, Giorgia Mancano, Giulia Forzano, Fabiana diGiovanni, Giulia Gori, Giovanna Traficante, Achille Iolascon, Sabrina Giglio
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Abstract Background COVID‐19 outbreak prompted health centres to reorganize their clinical and surgical activity. In this paper, we show how medical genetics department's activity, in our tertiary pediatric hospital, has changed due to pandemic. Me
Externí odkaz:
https://doaj.org/article/291f298d144640b89d5c92f0074fb0b0
Autor:
Silvia Ricci, Lorenzo Lodi, Daniele Serranti, Marco Moroni, Gilda Belli, Giorgia Mancano, Andrea La Barbera, Giulia Forzano, Giusi Mangone, Giuseppe Indolfi, Chiara Azzari
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
This is the first case of NBAS disease detected by NBS for primary immunodeficiency. NBS with KRECs is revealing unknown potentialities detecting conditions that benefit from early recognition like NBAS deficiency. Immune phenotyping should be mandat
Externí odkaz:
https://doaj.org/article/eb6d3df20c0f428d83b358a7395f1567
Autor:
Flavio Giordano, Viviana Palazzo, Silvia Guarducci, Livia Garavelli, Mirko Scagnet, Angelica Pagliazzi, Marzia Mortilla, Rosangela Artuso, Sabrina Giglio, Daniele di Feo, Orsetta Zuffardi, Giulia Forzano, Gianluca Mattei, Giovanna Traficante, Lucia Tiberi, Betti Giusti, Aldesia Provenzano, Andrea La Barbera, Lorenzo Genitori, Claudio De Filippi, Ada Kura, Nehir Edibe Kurtas, Debora Vergani, Marilena Pantaleo, Sara Bargiacchi
Publikováno v:
Human Genetics
Type 1 Chiari malformation (C1M) is characterized by cerebellar tonsillar herniation of 3–5 mm or more, the frequency of which is presumably much higher than one in 1000 births, as previously believed. Its etiology remains undefined, although a gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eef7b265e29d98ef94ded04a2e328ebe
https://doi.org/10.1007/s00439-020-02231-6
https://doi.org/10.1007/s00439-020-02231-6
Autor:
Sabrina Giglio, Angelica Pagliazzi, Giovanna Traficante, Achille Iolascon, Fabiana di Giovanni, Giulia Gori, Giorgia Mancano, Giulia Forzano
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background COVID‐19 outbreak prompted health centres to reorganize their clinical and surgical activity. In this paper, we show how medical genetics department's activity, in our tertiary pediatric hospital, has changed due to pandemic. Methods We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b88d15f29b2754d067d4d8ac5953bbe
https://lirias.kuleuven.be/handle/20.500.12942/691217
https://lirias.kuleuven.be/handle/20.500.12942/691217
Autor:
Gilda Belli, Lorenzo Lodi, Andrea La Barbera, Marco Moroni, Giuseppe Indolfi, Giulia Forzano, Silvia Ricci, Giorgia Mancano, Daniele Serranti, Chiara Azzari, Giusi Mangone
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Frontiers in Immunology
Frontiers in Immunology
This is the first case of NBAS disease detected by NBS for primary immunodeficiency. NBS with KRECs is revealing unknown potentialities detecting conditions that benefit from early recognition like NBAS deficiency. Immune phenotyping should be mandat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dccb9b189c007981c8fe615b6d397137
https://doi.org/10.3389/fimmu.2019.01955
https://doi.org/10.3389/fimmu.2019.01955