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Akademický článek

Fatal complication of sickle cell anemia in an immigrant patient rescued from the mediterranean sea.

Autor: Alongi, A., Spagnolo, E. Ventura, Zerbo, S., Aronica, G. L., Korte, F., Maresi, E., Argo, A.

Publikováno v: Clinica Terapeutica; Jul/Aug2020, Vol. 171 Issue 4, pe291-e294, 4p

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Akademický článek

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Anatomical features and clinical correlations in Caucasian patients with definite arrhythmogenic right ventricular dysplasia/cardiomyopathy

Autor: Inciardi, R. M., Maresi, E., Coppola, G., Rotolo, A., Clemenza, F., Giordano, U., Lombardo, E., Schicchi, R., Torcivia, R., Arrotti, S., Iacona, R., Minacapelli, A. A., Assennato, P., Salvatore Novo

Publikováno v: Scopus-Elsevier

AIM: Arrhythmogenic right ventrticular dysplasia/cardiomyopathy (ARVD/C) is an inherited cardiomyopathy characterized by fibrofatty replacement and a high risk of ventricular arrhythmias (VA) and sudden cardiac death (SCD). The aim of the present inv

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e7b2be8bbd280b2625cf51cda28e497c
https://pubmed.ncbi.nlm.nih.gov/25295491

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ANTITHROMBOTIC PROPHYLAXIS IN LAPAROSCOPIC CHOLECYSTECTOMY

Autor: Triolo, V., Zerbo, S., Maresi, E., Grassi, N., Inguglia, R.

Pulmonary thromboembolism is a common cause of in-hospital death. In moderate or high risk patients undergoing laparotomy, acute and long-term mortality can be effec-tively reduced with an appropriate prophylactic drug treatment, while in low-risk pa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0d98f64928f6273dbe0806369d81a74e
http://hdl.handle.net/10447/100597

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Akademický článek

Death of a 23-year-old man from cardiac conduction system injury through a blunt chest impact after a car accident

Autor: Zerbo, S., Maresi, E., Portelli, F., Sortino, C., Ventura Spagnolo, E., Procaccianti, P., Argo, A.

Publikováno v: In Egyptian Journal of Forensic Sciences December 2014 4(4):137-139

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Oral necrotizing microvasculitis in a patient affected by Kawasaki disease

Autor: Scardina, G. A., Fucà, G., Carini, F., Valenza, V., Spicola, M., Procaccianti, P., Pietro MESSINA, Maresi, E.

Publikováno v: Scardina, G.A. ; Fucà, Gerlandina ; Carini, F. ; Valenza, Vincenzo ; Spicola, Michele ; Procaccianti, Paolo ; Messina, P. ; Maresi, Emiliano. Oral necrotizing microvasculitis in a patient affected by Kawasaki disease. En: Medicina oral, patología oral y cirugía bucal. Ed. inglesa, 12 8 2007: 4
Scopus-Elsevier
Medicina Oral, Patología Oral y Cirugía Bucal (Internet) v.12 n.8 2007
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
instname
RODERIC. Repositorio Institucional de la Universitat de Valéncia
Medicina Oral, Patología Oral y Cirugía Bucal (Internet), Volume: 12, Issue: 8, Pages: 560-564, Published: DEC 2007

Kawasaki disease (KD) was first described in 1967 by Kawasaki, who defined it as ?mucocutaneous lymph node syndrome?. KD is an acute systemic vasculitis, which mainly involves medium calibre arteries; its origin is unknown, and it is observed in chil

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::289bcd70dea50155ce550631d7039327
http://hdl.handle.net/10550/63104

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Prevalence of vulval lichen planus in a cohort of women with oral lichen planus:an interdisciplinary study

Autor: Belfiore, P., DI FEDE, O., Cabibi, D., Campisi, G., Amaru', G., DE CANTIS, S., Maresi, E.

BACKGROUND: Lichen planus (LP) is a mucocutaneous inflammatory dermatosis that frequently involves the oral and genital mucosae. Patients with LP affecting these sites are often seen by oral medicine specialists or gynaecologists who work in isolatio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5244bfe0110bd2eba66efd5760fddb12
http://hdl.handle.net/10447/22101

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An interesting question of Pompe disease. A case report

Autor: Accomando, S., Montaperto, D., Fragapane, M. L., Amato, G. M., Corsello, G., Francesco Cappello, Maresi, E.

Publikováno v: Scopus-Elsevier
Europe PubMed Central

Glycogenosis type II or Pompe disease is an inherited autosomal recessive disorder known in 3 different clinical forms (infantile, juvenile and adult). We report on a case diagnosed as a classic infantile form with the worst outcome of all 3 describe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d8185d33d9a12c05128dd11d2f7b8bb5
http://hdl.handle.net/10447/13276

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