Zobrazeno 1 - 10
of 10
pro vyhledávání: '"M. P. Cicini"'
Publikováno v:
European review for medical and pharmacological sciences. 26(21)
Treatment choices for patients with advanced-stage mycosis fungoides (MF) or Sézary syndrome (SS) who have failed first-line systemic therapies can be challenging, as several options are available. However, most evidence is based on observational an
Autor:
Salvatore Giannico, M. P. Cicini, Fiore S. Iorio, Carlo Marcelletti, Bruno Marino, Antonio F. Corno
Publikováno v:
Chest. 101:115-118
Of 353 children who underwent surgical repair of a congenital heart defect, including closure of a ventricular septal defect (VSD), 12 patients (four with tetralogy of Fallot, five with a VSD, and three with a double-outlet right ventricle) developed
Autor:
M. P. Cicini, Luciano Pasquini, P. Ragonese, Fabrizio Drago, Roberto M. Di Donato, Bruno Marino, Paolo Guccione, Carlo Marcelletti
Publikováno v:
American Heart Journal. 122:1022-1027
The use of oral propafenone was assessed in 57 children. Mean age was 4.8 +/- 5.2 years (range 1 day to 17 years). Twenty-three patients were less than 1 year of age (40%) and 10 were less than 1 month of age (18%). Arrhythmias included supraventricu
Publikováno v:
Scopus-Elsevier
From November 1985 to 31 July 1997, 65 pediatric patients underwent heart transplantation at Bambino Gesù Hospital in Rome. Two of them underwent retransplantation, both 6 years after the first transplant. The 67 transplant patients had a mean age o
Publikováno v:
Giornale italiano di cardiologia. 24(12)
A 7-year-old boy had undergone heart transplantation (HT) at 1 year of age. The immunosuppressive regimen consisted of cyclosporine and azathioprine (Cy+Aza). During the follow-up there were 7 episodes of moderate rejection: 4 of them occurred during
Autor:
M P, Cicini, C, Marcelletti
Publikováno v:
Rays. 19(3)
Autor:
S, Giannico, A, Corno, B, Marino, M P, Cicini, M G, Gagliardi, A, Amodeo, S, Picardo, C, Marcelletti
Publikováno v:
Circulation. 86
Total cavopulmonary connection has been proposed as a rational alternative to atriopulmonary connection for complex Fontan operations. In addition to fluid dynamic advantages proposed by de Leval, total right heart bypass may address an emerging impo
Bidirectional cavopulmonary anastomosis in congenital heart disease. Functional and clinical outcome
Publikováno v:
Herz. 17(4)
The bidirectional cavopulmonary anastomosis is a surgical procedure suitable for patients with cyanotic congenital heart disease and univentricular physiology. This operation is able to increase the effective pulmonary blood flow without any addition
Autor:
U, Vairo, B, Marino, D, Parretti di Iulio, M, Papa, C, Donfrancesco, M P, Cicini, S, Grazioli, R M, Di Donato
Publikováno v:
Giornale italiano di cardiologia. 21(6)
The patterns of pulmonary circulation were assessed by angiography in a series of 24 patients with right atrial isomerism (asplenia syndrome) and pulmonary atresia. Mean age at catheterization was 21.5 days (range 1 day-11 months). The pulmonary arte
Autor:
M, Papa, B, Marino, U, Vairo, S, Nava, D, Parretti Di Iulio, C, Donfrancesco, M P, Cicini, S, Grazioli, E, Mazzera, C, Marcelletti
Publikováno v:
Giornale italiano di cardiologia. 20(9)
The muscular ventricular septal defect associated with the atrioventricular canal is a malformation which has not yet been extensively studied. Between June 1982 and December 1989, 151 patients with atrioventricular canal underwent echocardiography a