Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mattassi, R E"'
Autor:
Kiani, A K, Paolacci, S, Amato, B, Mattassi, R E, Tassi, V, Falsini, B, Di Renzo, G, Guda, T, Kallazi, M, Dautaj, A, Dhuli, K, Morrone, A, Bellinato, F, Gisondi, P, Bertelli, M
Publikováno v:
European review for medical and pharmacological sciences. 25
The amniotic fluid contains a large population of stem keratinocytes demonstrating minimal immunological rejection. Recent evidence suggests that stem cells from the amniotic fluid can be employed in the field of tissue engineering. In this work we i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::29c5e33ec59d17b9653e5e25834b1c0c
https://pubmed.ncbi.nlm.nih.gov/34890034
https://pubmed.ncbi.nlm.nih.gov/34890034
Autor:
Albokhari, Daniah, Bailey, Christopher R., Hwang, Francis, Weiss, Clifford R., Forsberg, Jonathan, Sobreira, Nara
Publikováno v:
American Journal of Medical Genetics. Part A; Jun2023, Vol. 191 Issue 6, p1570-1575, 6p
Autor:
Raul Mattassi, Elena Manara, Alice Bruson, Byung-Boong Lee, Sandro Michelini, Stefano Paolacci, Alessandra Zulian, Matteo Bertelli, Bruno Amato
INTRODUCTION Vascular anomalies encompass an extremely heterogeneous group of congenital abnormalities of the vascular system. They include vascular tumors and malformations and have a prevalence of 4.5%. Vascular anomalies are frequently sporadic an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3819593b54eb64c0c39d3606228cb53
http://hdl.handle.net/11588/781514
http://hdl.handle.net/11588/781514
Autor:
Paolo Enrico Maltese, Francesca Fanelli, Matteo Bertelli, Bruno Amato, Stefano Paolacci, Yeltay Rakhmanov, Raul Mattassi
Publikováno v:
The EuroBiotech Journal, Vol 2, Iss s1, Pp 26-31 (2018)
Vascular anomalies (VAs) have phenotypic variability within the same entity, overlapping clinical features between different conditions, allelic and locus heterogeneity and the same disorder can be inherited in different ways. Most VAs are sporadic (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46a5afbb5c52ee2e6fe92d4e69abb5a4
http://hdl.handle.net/11588/724629
http://hdl.handle.net/11588/724629
Autor:
Stefano Paolacci, Raul Mattassi, Yeltay Rakhmanov, Munis Dundar, Matteo Bertelli, Bruno Amato, Carla Marinelli, Paolo Enrico Maltese, Tommaso Beccari
Publikováno v:
The EuroBiotech Journal, Vol 2, Iss s1, Pp 32-34 (2018)
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant vascular dysplasia characterized by telangiectases and arteriovenous malformations. These lesions cause bleeding, particularly in the nose, gastrointestinal tract and brain. HHT has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::564bbe66461e257fcfc124b361fde0f3
http://hdl.handle.net/11588/724641
http://hdl.handle.net/11588/724641