Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sarah Catalano"'
Autor:
Barbara Fiorini, Sarah Catalano
Publikováno v:
RUC. Repositorio da Universidade da Coruña
instname
instname
[Resumen] La intervención tiene como objetivo investigar la figura de Lina Bo Bardi, una arquitecta italiana que se trasladó a Brasil en 1946, al final de la Segunda Guerra Mundial, y que durante sus años de actividad en Italia fue también colabo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88848eb3d21fb99945aad6b7d859582b
https://doi.org/10.17979/aarc.2015.4.0.5133
https://doi.org/10.17979/aarc.2015.4.0.5133
Autor:
Sarah Catalano
Publikováno v:
Risco Revista de Pesquisa em Arquitetura e Urbanismo (Online). :65-73
This paper shows that the years Lina Bo Bardi spent in Italy deserve further examination. In fact, bibliographical and archival research, which should be carried out in Italy and also at Lina Bo and P.M. Bardi Institute, can still reveal previously u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::079174e9d12afab93a06e771191cb41c
https://doi.org/10.11606/issn.1984-4506.v0i20p65-73
https://doi.org/10.11606/issn.1984-4506.v0i20p65-73
Publikováno v:
Pediatric Dermatology. 32:e95-e97
A blue patch on the vertex scalp of an infant has a broad differential diagnosis, including vascular malformations, melanocytic lesions, trauma, and exogenous or endogenous pigmentation. We present two cases of infants who developed blue patches on t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61ce7311f0447eef28eb323356885461
https://doi.org/10.1111/pde.12528
https://doi.org/10.1111/pde.12528
Autor:
Elizabeth M. McCormick, Jobayer Hossain, Deborah L. Stabley, Karen W. Gripp, Elizabeth Hopkins, Laura Conway, Sarah Catalano, Katia Sol-Church
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 15(7)
Costello syndrome, a rare genetic disorder with multisystemic involvement, is caused by germline HRAS mutations. Because several different missense mutations have been reported, a severity scoring system was developed to assess a possible genotype–
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ea25aa85d0d9530a47830e4ac154b3f
https://pubmed.ncbi.nlm.nih.gov/23429430
https://pubmed.ncbi.nlm.nih.gov/23429430
Autor:
Jillian S. Parboosingh, Karen W. Gripp, Tanya L. Gillan, Linda Nicholson, Sarah Catalano, A. Micheil Innes, Marni E. Axelrad, Daniel Doyle, Deborah L. Stabley, Katia Sol-Church, Christine Davies, Monique Lapointe, Norma Leonard
Publikováno v:
American journal of medical genetics. Part A. (6)
Costello syndrome is a rare congenital disorder typically characterized by severe failure-to-thrive, cardiac abnormalities including tachyarrhythmia and hypertrophic cardiomyopathy, distinctive facial features, a predisposition to papillomata and mal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::728a0ce49debcabfedef3143358fc3e1
https://pubmed.ncbi.nlm.nih.gov/18247425
https://pubmed.ncbi.nlm.nih.gov/18247425