Zobrazeno 1 - 10
of 55
pro vyhledávání: '"C. Comparato"'
Publikováno v:
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-4 (2019)
Abstract Background There are reports of the familial occurrence of Kawasaki disease but only a few reports described Kawasaki disease in siblings. However, the familial cases were not simultaneous. In these patients the idea of infective agents as t
Externí odkaz:
https://doaj.org/article/4e8e9367b5394cf5a47705579ab497c2
Publikováno v:
European Heart Journal Supplements. 25:D60-D60
DORV accounts for 2–3% of congenital heart disease (prevalence of 1/10,000). It is a cono–truncal anomaly with variable clinic. In 25–42.5% of cases there are chromosomal anomalies such as trisomy 13, 18, 22q11 microdeletion and possible associ
Publikováno v:
European Heart Journal Supplements. 25:D97-D97
Sacubitril/Valsartan (S/V) is used with optimal results in the therapy of heart failure (HF); reduces mortality and hospitalizations by 20% compared to ACE inhibitor therapy. There is a little data on the use of S/V in adult patients with congenital
Autor:
C. Cavallaro, M. Cunsolo, F. Cardella, C. Comparato, F. Sanfilippo, G. Ottoveggio, M. Lapi, S. Amato, V. Sicilano, M. C. Maggio
Introduzione La Malattia di Kawasaki (MK) è una vasculite acuta sistemica dei vasi di medio calibro, con interesse elettivo per le arterie coronarie, auto-limitantesi. La diagnosi è clinica, complicanze cardiovascolari quali aneurismi delle coronar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3658::db6d6d38b31baf9ffca3d1ebf97ccabf
http://hdl.handle.net/10447/528737
http://hdl.handle.net/10447/528737
Akademický článek
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L’infezione da Parvovirus B19, responsabile del “megaloeritema infettivo”, può determinare conseguenze cliniche gravi, tra le quali: la miocardite acuta, la crisi aplastica del midollo osseo e l’artrite. Esponiamo tre casi clinici di miocard
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3658::43fd353d6494c26215df945a4e3f4a88
http://hdl.handle.net/10447/368219
http://hdl.handle.net/10447/368219
Autor:
G. M. Sciarrabone, L. Alessi, L. A. Canduscio, L. Campa, A. Alaimo, E. Caruso, D. Di Lisi, S. Spoto, F. Cardella, M. C. Maggio, C. Comparato, G. Corsello
Presentiamo il caso di Nicolas, un lattante di 3 mesi giunto alla nostra osservazione per febbre elevata da 3 giorni poco responsiva al paracetamolo. Secondogenito, nato da gravidanza normodecorsa, genitori non consanguinei. In anamnesi un precedente
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3658::f115d67b84ed7cc1ed4593de465a7e5f
http://hdl.handle.net/10447/368585
http://hdl.handle.net/10447/368585
Autor:
M. C. Maggio, A. Alaimo, R. Cimaz, C. Comparato, D. Di Lisi, C. G. Alizzi, S. Spoto, M. A. Garofalo, G. Corsello
E' rara la descrizione della Malattia di Kawasaki (MK) in fratelli, ma -se presente- è necessario escludere un trigger infettivo. Riportiamo il caso di due fratelli affetti da MK esordita contemporaneamente in seguito ad un’infezione da Parvovirus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3658::1a3271d264eeddfe4263ba6569388626
http://hdl.handle.net/10447/368868
http://hdl.handle.net/10447/368868
Publikováno v:
Advancements in Cardiovascular Research. 2
Hypertrophic cardiomiopathy (HCM) is the most common cardiac disease affecting the cardiac muscle and is characterized by heterogeneous genetic, morphological, functional, and clinical features. It is also one of the main causes of sudden cardiac dea
Autor:
Giovanni Corsello, Maria Cristina Maggio, Daniela Di Lisi, C Comparato, Rolando Cimaz, A. Alaimo
Publikováno v:
Journal of Medical Case Reports
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-4 (2019)
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-4 (2019)
Background There are reports of the familial occurrence of Kawasaki disease but only a few reports described Kawasaki disease in siblings. However, the familial cases were not simultaneous. In these patients the idea of infective agents as trigger mu