Zobrazeno 1 - 6
of 6
pro vyhledávání: '"F Ciuccarelli"'
Autor:
V Carnielli, Carlo Polidori, V Moretti, E Andresciani, De Meo, F Ciuccarelli, Amf Garzone, A Pompilio, L Carloni, S Savini
Publikováno v:
European Journal of Hospital Pharmacy. 22:A27.2-A27
Background Intravenous (IV) drug treatment of preterm neonates is affected by: clinical status (i.e. sepsis/infections, immature physiology, pharmacokinetic/pharmacodynamic variation), shortage of ready-to-use formulations, small doses of drug requir
Autor:
D Marravalle, Amf Garzone, V Moretti, A Mannucci, E Andresciani, A Ficcadenti, De Meo, F Ciuccarelli, A Pompilio
Publikováno v:
European Journal of Hospital Pharmacy. 21:A19.2-A19
Background There are almost 8,000 rare diseases (RD) (80% are genetically based) and 50% of them affect children. They are often highly complex metabolic diseases (MD): factors include heterogeneity (age of occurrence, aetiopathogenesis and symptomat
Publikováno v:
European Journal of Hospital Pharmacy. 20:A23.1-A23
Background Our paediatric hospital ‘G. Salesi’ officially follows regional guidelines on the proper use of IVIG. Guidelines aim to improve the management of drug requests during times of shortage and to ensure IVIG supplies for critical situation
Autor:
A Pompilio, L Carloni, Amf Garzone, P Colonna, MC Cerlesi, P Marzioni, E Franchi, F Pinto, M Buccolini, E Andresciani, V Moretti, De Meo, F Ciuccarelli
Publikováno v:
European Journal of Hospital Pharmacy. 20:A177.1-A177
Background Clopidogrel is a thienopyridine drug that acts by binding selectively and irreversibly to the adenosine diphosphate P2Y12 receptor on platelets. Platelet aggregation is consequently inhibited. Clopidogrel is used to prevent ischemic events
Autor:
L Carloni, A Ficcadenti, A Mannucci, M De Meo, F Ciuccarelli, A Pompilio, V Moretti, M Buccolini, Amf Garzone, P Marzioni, E Andresciani, F Pinto
Publikováno v:
European Journal of Hospital Pharmacy. 20:A196.1-A196
Background GM1 gangliosidosis, a rare metabolic disease, is an autosomal recessive lysosomal storage disorder caused by a deficiency of beta-galactosidase, and characterised by the generalised accumulation of GM1 ganglioside. The most severe form, ca
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.