Desenvolvimento de poli(cloreto de vinila)-PVC para utilização no tratamento radioterapico de pacientes com cancer

Autor: Salman, Karin Dias

Publikováno v: Biblioteca Digital de Teses e Dissertações da Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP

Orientador: Lucia H. Innocentini Mei Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Engenharia Quimica Resumo: No tratamento radioterápico, tem-se comumente utilizado altas energias de raios X (como as produzidas por acel

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49f59a2af7f988eea6dca2e9a9905de0
https://doi.org/10.47749/t/unicamp.1995.109826

Neurofibromatosis Type1 - Proposal of and Follow Up Guidelines

Autor: Marisol Anselmo, Eulália Calado, José P. Vieira, Ana I. Dias, Ana Moreira, Karin Dias

Publikováno v: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Acta Pediátrica Portuguesa; v. 36, n. 2/3 (2005); Pag. 115-120
Portuguese Journal of Pediatrics (former Acta Pediátrica Portuguesa); Vol. 36 No. 2/3 (2005); Pag. 115-120
Portuguese Journal of Pediatrics; vol. 36 n.º 2/3 (2005); Pag. 115-120
Portuguese Journal of Pediatrics, Vol 36, Iss 2/3 (2014)

Resumo A Neurofibromatose tipo 1 (NF1) é uma doença multissistémica de carácter progressivo. Tem uma expressão fenotípica muito variada, sem factores preditivos de gravidade. Objectivos: caracterizar a população pediátrica com NF1 seguida na

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efd68d48b87ac09d234ae5d94c7ef6a3

Movement disorders in Rett syndrome: an analysis of 60 patients with detected MECP2 mutation and correlation with mutation type

Autor: Teresa, Temudo, Elisabete, Ramos, Karin, Dias, Clara, Barbot, Jose P, Vieira, Ana, Moreira, Eulalia, Calado, Ines, Carrilho, Guiomar, Oliveira, Antonio, Levy, Maria, Fonseca, Alexandra, Cabral, Pedro, Cabral, Joao P, Monteiro, Luis, Borges, Roseli, Gomes, Manuela, Santos, Jorge, Sequeiros, Patricia, Maciel

Publikováno v: Movement disorders : official journal of the Movement Disorder Society. 23(10)

Rett syndrome (RS) is one of the best human models to study movement disorders. Patients evolve from a hyperkinetic to a hypokinetic state, and a large series of abnormal movements may be observed along their lives such as stereotypies, tremor, chore

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1ffc1ad45b8d3e7708ca301d6e5227a1
https://pubmed.ncbi.nlm.nih.gov/18512755

AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders

Autor: Valente, Em, Brancati, F, Silhavy, Jl, Castori, M, Marsh, Se, Barrano, G, Bertini, E, Boltshauser, E, Zaki, Ms, Abdel Aleem, A, Abdel Salam GM, Bellacchio, E, Battini, R, Cruse, Rp, Dobyns, Wb, Krishnamoorthy, Ks, Lagier Tourenne, C, Magee, A, Pascual Castroviejo, I, SALPIETRO DAMIANO, Carmelo, Sarco, D, Richard, Leventer, Padraic Grattan Smith, Andreas, Janecke, Marc, D’Hooghe, Rudy Van Coster, Karin, Dias, Carla, Moco, Ana, Moreira, Chong Ae Kim, Gustavo, Maegawa, Itxaso, Marti, Susana Quijano Roy, Alain, Verloes, Renaud, Touraine, Miche, Bernard, Stuart, Dorit, Lev, Bruria Ben Zeev, Rita, Fischetto, Mattia, Gentile, Lucio, Giordano, Loredana, Boccone, Martino, Ruggieri, Stefania, Bigoni, Maria Alide Donati, Elena, Procopio, Gianluca, Caridi, Francesca, Faravelli, Gianmarco, Ghiggeri, Briuglia, Silvana, Gaetano, Tortorella, Stefano, D’Arrigo, Chiara, Pantaleoni, Daria, Riva, Graziella, Uziel, Stefania, Bova, Elisa, Fazzi, Sabrina, Signorini, Maria Roberta Cilio, Marilu` Di Sabato, Francesco, Emma, Vincenzo, Leuzzi, Pasquale, Parisi, Alessandro, Simonati, de Jong, Mirjam M., Matloob, Azam, Berta, Rodriguez, Hulya, Kayserili, Lihadh Al Gazali, Laszlo, Sztriha, David, Nicholl, Geoffrey Woods, C., Raoul, Hennekam, Saunder, Bernes, Henry, Sanchez, Clark, Aldon E., Elysa, Demarco, Clement, Donahue, Elliot, Sherr, Jin, Hahn, Terence, D, Sanger, Gallager H, Tomas E., Cynthia, Daugherty, Walsh, Christopher A., Trudy, Mckanna, Joanne, Milisa, Chung, Wendy K., De Vivo, Darryl C., Hillary, Raynes, Romaine, Schubert, Alison, Seward, Brooks, David G., Amy, Goldstein, James, Caldwell, Eco, Finsecke, Kenton, Holden, Swobod, Kathryn J., Dave Viskochil, Dallapiccola, B, Gleeson, Jg

Publikováno v: Valente, E M; Brancat, F; Silhavy, J L; Castori, M; March, S E; Barrano, G; et al.(2006). AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders. Annals of Neurology, 59(3), 527-534. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/4jp5t97n

Author(s): Valente, E M; Brancat, F; Silhavy, J L; Castori, M; March, S E; Barrano, G; Bertini, E; Boltshauser, E; Zaki, M S; Abdel-Aleem, A; Abdel-Salam, GMH; Bellacchlo, E; Battini, R; Cruse, R P; Dobyns, W B; Krishnamoorthy, K S; Lagier-Tourenne,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3243eb573c5d84d0efe6229042b9a7cb
https://pubmed.ncbi.nlm.nih.gov/16453322

Recessive ataxia with ocular apraxia: review of 22 Portuguese patients

Autor: I. Fineza, P. Mendonça, A. Guimarães, R. Chorão, Clara Barbot, José Barros, Carla Ferreira, Karin Dias, José P. Monteiro, Paula Coutinho, Jorge Sequeiros, Maria do Céu Moreira

Publikováno v: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Scopus-Elsevier

BACKGROUND: The recessive ataxias are a heterogeneous group of neurodegenerative disorders characterized by cerebellar ataxia associated with a number of different neurologic, ophthalmologic, or general signs. They are often difficult to classify in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6427700ea30329c206a5a49bc8765b05
https://hdl.handle.net/10400.16/718