Zobrazeno 1 - 10
of 34
pro vyhledávání: '"R A Costantini"'
Autor:
Silvio H. Barberato, Sérgio G. E. Bucharles, Admar M. Sousa, Costantino O. Costantini, Costantino R. F. Costantini, Roberto Pecoits-Filho
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 94, Iss 4, Pp 457-462 (2010)
FUNDAMENTO: Disfunção diastólica é frequente em pacientes de hemodiálise, mas seu impacto na evolução clínica é incerto. OBJETIVO: Avaliar a prevalência e o impacto prognóstico da disfunção diastólica (DD) avançada (DDA) do ventrículo
Externí odkaz:
https://doaj.org/article/f7855e725e814ba69c64788073ea1396
Publikováno v:
European Heart Journal. 42
Background In lower limbs deep venous thrombosis (DVT) scenario there is evidence that favours catheter guided invasive treatment. The treatment with stenting in the common femoral vein could be related with a diminished permeability in the inflow of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78595d85f83cc629c57ec04e116e561e
https://doi.org/10.1093/eurheartj/ehab724.2044
https://doi.org/10.1093/eurheartj/ehab724.2044
Autor:
S. Toracchio, F. Verginelli, P. Battista, C. Di Bella, A. Cama, L. Rigoli, R. A. Caruso, R. Mariani Costantini, ROCCO, ALBA, NARDONE, GERARDO ANTONIO PIO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::41ddf71de95c0b801cb4d0fc646835c7
http://hdl.handle.net/11588/414286
http://hdl.handle.net/11588/414286
Autor:
R. Mariani Costantini, Annalisa Ranieri, P Battista, Alfredo Pontecorvi, Alessandro Cama, G Colletta, Salvatore Sciacchitano, E Zanella, Raffaele Palmirotta
Publikováno v:
British Journal of Cancer
Familial adenomatous polyposis (FAP) is known to be associated with neoplasia of various tissues, including thyroid carcinoma. Germline mutations of the tumour-suppressor gene APC, responsible for the predisposition to FAP, may therefore be involved
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01daad3281ccbf3177cd126965533f1c
https://doi.org/10.1038/bjc.1994.452
https://doi.org/10.1038/bjc.1994.452
Autor:
Silvio Henrique, Barberato, Sérgio G E, Bucharles, Admar M, Sousa, Costantino O, Costantini, Costantino R F, Costantini, Roberto, Pecoits-Filho
Publikováno v:
Arquivos brasileiros de cardiologia. 94(4)
Diastolic dysfunction (DD) is frequent in patients on hemodialysis (HD), but its impact on the clinical evolution is yet to be established.To evaluate the prevalence and prognostic impact of left ventricular (LV) advanced diastolic dysfunction (ADD)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::67f1de049d8901c2d6558a4020e84371
https://pubmed.ncbi.nlm.nih.gov/20339814
https://pubmed.ncbi.nlm.nih.gov/20339814
Autor:
A. Contegiacomo, R. Mariani Costantini, R. Muraro, P. Battista, C. Valli, L. Frati, R. Calderopoli, N. Zilembo, I. Falco, G. Petrella, A.R. Bianco
Publikováno v:
Scopus-Elsevier
Twenty-six primary breast carcinomas were studied to evaluate cell proliferation as assessed by thymidine labeling index (TLI), and antigenic phenotype, as defined by immunohistochemistry using eight monoclonal antibodies (MAbs) to tumor-associated a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd88441bd6784b59946a7ca0de3825dc
https://doi.org/10.1177/172460089100600304
https://doi.org/10.1177/172460089100600304
Autor:
M C, Curia, R, Palmirotta, G, Aceto, L, Messerini, M C, Verì, S, Crognale, R, Valanzano, F, Ficari, P, Fracasso, V, Stigliano, F, Tonelli, V, Casale, F, Guadagni, P, Battista, R, Mariani-Costantini, A, Cama
Publikováno v:
Cancer research. 59(15)
We analyzed the hMLH1 and hMSH2 genes in 30 unrelated hereditary nonpolyposis colorectal cancer (HNPCC) patients using mutational and immunohistochemical analyses combined whenever possible with primer extension assays, designed to estimate hMLH1 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a5f34cbd8c2b7d2b70c4864526b000d5
https://pubmed.ncbi.nlm.nih.gov/10446963
https://pubmed.ncbi.nlm.nih.gov/10446963
Autor:
S, Mammarella, B, Creati, D L, Esposito, P, Arcuri, F, Della Loggia, F, Capani, R, Mariani-Costantini, F G, Caramia, P, Battista, A, Cama
Publikováno v:
Human mutation. 11(5)
We analyzed by SSCP the complete IRS-1 coding sequence in NIDDM patient #25 D. Unique conformers corresponding to a Ser to Tyr substitution at codon 1043 (S1043Y), and to a Cys to Tyr substitution at codon 1095 (C1095Y) were detected in this patient.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::35fae2643188f37f032cbc66a60fb00f
https://pubmed.ncbi.nlm.nih.gov/10206679
https://pubmed.ncbi.nlm.nih.gov/10206679