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Referencias para el artículo
- Beers MH, Berkow R (eds). The Merck Manual, 17th ed. Whitehouse
Station, NJ: Merck and Co., Inc., 1999, 372–4.
- Lochs H, Plauth M. Liver cirrhosis: rationale and modalities for nutritional
support—the European Society of Parenteral and Enteral Nutrition consensus and beyond.
Curr Opin Clin Nutr Metab Care 1999;2:345–9.
- Lieber CS. Nutrition in liver disorders. In: Shils ME, Olson JA, Shike M, Ross
AC (eds). Modern Nutrition in Health and Disease, 9th ed. Baltimore, MD: Williams and
Wilkins, 1999, 1179–80.
- Rodriguez-Moreno F, Gonzalez-Reimers E, Santolaria-Fernandez F, et al. Zinc,
copper, manganese, and iron in chronic alcoholic liver disease. Alcohol
1997;14:39–44.
- Gibbs K, Walshe JM. Studies with radioactive copper (64 Cu and 67 Cu); the
incorporation of radioactive copper into caeruloplasmin in Wilson’s disease and in
primary biliary cirrhosis. Clin Sci 1971;41:189–202.
- Lieber CS. Nutrition in liver disorders. In: Shils ME, Olson JA, Shike M, Ross
AC (eds). Modern Nutrition in Health and Disease, 9th ed. Baltimore, MD: Williams and
Wilkins, 1999:1179–80.
- Halsted CH. Alcohol: medical and nutritional effects. In Ziegler EE, Filer LJ
(eds). Present Knowledge in Nutrition, 7th ed. ILSI Press, Washington, DC, 1996,
553.
- Roggin GM, Iber FL, Kater RM, Tabon F. Malabsorption in the chronic alcoholic.
Johns Hopkins Med J 1969;125:321–30.
- Roggin GM, Iber FL, Linscheer WG. Intraluminal fat digestion in the chronic
alcoholic. Gut 1972;13:107–11.
- Luca A, Garcia-Pagan JC, Bosch J, et al. Effects of ethanol consumption on
hepatic hemodynamics in patients with alcoholic cirrhosis. Gastroenterology
1997;112:1284–9.
- Mato JM, Camara J, Fernandez de Paz J, et al. S-adenosylmethionine in
alcoholic liver cirrhosis: a randomized, placebo-controlled, double-blind, multicenter
clinical trial. J Hepatol 1999;30:1081–9.
- Miglio F, Stefanini GF, Corazza GR, et al. Double-blind studies of the
therapeutic action of S-Adenosylmethionine (SAMe) in oral administration, in liver cirrhosis
and other chronic hepatitides. Minerva Med 1975;66:1595–9 [In Italian].
- Gorbakov VV, Galik VP, Kirillov SM. Experience in heptral treatment of diffuse
liver diseases. Ter Arkh 1998;70:82–6 [in Russian].
- Loguercio C, Nardi G, Argenzio F, et al. Effect of S-adenosyl-L-methionine
administration on red blood cell cysteine and glutathione levels in alcoholic patients with
and without liver disease. Alcohol Alcohol 1994;29:597–604.
- Frezza M, Centini G, Cammareri G, et al. S-adenosylmethionine for the
treatment of intrahepatic cholestasis of pregnancy. Results of a controlled clinical trial.
Hepatogastroenterology 1990;37 Suppl 2:122–5.
- Frezza M, Surrenti C, Manzillo G, et al. Oral S-adenosylmethionine in the
symptomatic treatment of intrahepatic cholestasis. A double-blind, placebo-controlled study.
Gastroenterology 1990;99:211–5.
- Lieber CS. Nutrition in liver disorders. In: Shils ME, Olson JA, Shike M, Ross
AC (eds). Modern Nutrition in Health and Disease, 9th ed. Baltimore, MD: Williams and
Wilkins, 1999, 1179–80.
- Beers MH, Berkow R (eds). The Merck Manual, 17th ed. Whitehouse
Station, NJ: Merck and Co., Inc., 1999, 362–4.
- Nompleggi DJ, Bonkovsky HL. Nutritional supplementation in chronic liver
disease: an analytical review. Hepatology 1994;19:518–33 [review].
- Horst D, Grace ND, Conn HO, et al. Comparison of dietary protein with an oral,
branched chain-enriched amino acid supplement in chronic portal-systemic encephalopathy: a
randomized controlled trial. Hepatology 1984;4:279–87.
- Okita M, Watanabe A, Nagashima H. Treatment of liver cirrhosis with branched
chain amino acid-supplemented diet. Gastroenterol Jpn 1981;16:389–92.
- Maddrey WC. Branched chain amino acid therapy in liver disease. J Am Coll
Nutr 1985;4:639–50 [review].
- Wahren J, Denis J, Desurmont P, et al. Is intravenous administration of
branched chain amino acids effective in the treatment of hepatic encephalopathy? A multicenter
study. Hepatology 1983;3(4):475–80.
- Egberts E-H, Schomerus H, Hamster W, Jürgens P. Branched chain amino
acids in the treatment of latent portosystemic encephalopathy. Gastroenterol
1985;88:887–95.
- Dioguardi FS, Brigatti M, Dell’Oca M, et al. Effects of chronic oral
branched-chain amino acid supplementation in a subpopulation of cirrhotics. Clin Physiol
Biochem 1990;8:101–7.
- Marchesini G, Dioguardi FS, Bianchi GP, et al. Long-term oral branched-chain
amino acid treatment in chronic hepatic encephalopathy. A randomized double-blind
casein-controlled trial. The Italian Multicenter Study Group. J Hepatol
1990;11:92–101.
- Chin SE, Shepherd RW, Thomas BJ, et al. Nutritional support in children with
end-stage liver disease: a randomized crossover trial of a branched-chain amino acid
supplement. Am J Clin Nutr 1992;56:158–63.
- Kato M, Miwa Y, Tajika M, et al. Preferential use of branched-chain amino
acids as an energy substrate in patients with liver cirrhosis. Internal Med
1998;37:429–34.
- Ma X, Zhao J, Lieber CS. Polyenylphosphatidylcholine attenuates non-alcoholic
hepatic fibrosis and accelerates its regression. J Hepatol 1996;24:604–13.
- Lieber CS, Robins SJ, Leo MA. Hepatic phosphatidylethanolamine
methyltransferase activity is decreased by ethanol and increased by phosphatidylcholine.
Alcohol Clin Exp Res 1994;18:592–5.
- Lieber CS, Robins SJ, Li J, et al. Phosphatidylcholine protects against
fibrosis and cirrhosis in the baboon. Gastroenterology 1994;106:152–9.
- Lieber CS, DeCarli LM, Mak KM, et al. Attenuation of alcohol-induced hepatic
fibrosis by polyunsaturated lecithin. Hepatology 1990;12:1390–8.
- Fassati P, Horejsi J, Fassati M, et al. Essential choline phospholipids and
their effect on HBsAg and selected biochemical tests in cirrhosis of the liver. Cas Lek
Cesk 1981 22;120:56–60 [in Czech].
- Taniguchi S, Kaneto K, Hamada T. Acquired zinc deficiency associated with
alcoholic liver cirrhosis. Int J Dermatol 1995;34:651–2.
- Scholmerich J, Lohle E, Kottgen E, Gerok W. Zinc and vitamin A deficiency in
liver cirrhosis. Hepatogastroenterology 1983;30:119–25.
- Reding P, Duchateau J, Bataille C. Oral zinc supplementation improves hepatic
encephalopathy. Results of a randomised controlled trial. Lancet
1984;2(8401):493–5.
- Marchesini G, Fabbri A, Bianchi G, et al. Zinc supplementation and amino
acid-nitrogen metabolism in patients with advanced cirrhosis. Hepatology
1996;23:1084–92.
- Sturniolo GC, D’Inca R, Parisi G, et al. Taste alterations in liver
cirrhosis: are they related to zinc deficiency? J Trace Elem Electrolytes Health Dis
1992;6:15–9.
- Weismann K, Christensen E, Dreyer V. Zinc supplementation in alcoholic
cirrhosis. A double-blind clinical trial. Acta Med Scand
1979;205(5):361–6.
- Vlahcevic ZR, Miller JR, Farrar JT, Swell L. Kinetics and pool size of primary
bile acids in man. Gastroenterology 1971;61:85–90.
- Angulo P, Batts KP, Therneau TM, et al. Long-term ursodeoxycholic acid delays
histological progression in primary biliary cirrhosis. Hepatology
1999;29:644–7.
- Larghi A, Crosignani A, Battezzati PM, et al. Ursodeoxycholic and
tauro-ursodeoxycholic acids for the treatment of primary biliary cirrhosis: a pilot crossover
study. Aliment Pharmacol Ther. 1997;11:409–14.
- Crosignani A, Battezzati PM, Setchell KD, et al. Tauroursodeoxycholic acid for
treatment of primary biliary cirrhosis. A dose-response study. Dig Dis Sci
1996;41:809–15.
- Setchell KD, Rodrigues CM, Podda M, Crosignani A. Metabolism of orally
administered tauroursodeoxycholic acid in patients with primary biliary cirrhosis.
Gut 1996;38:439–46.
- Ferri F, Bernocchi P, Fedeli S. Taurodeoxycholic acid in the treatment of
primary biliary cirrhosis. A controlled study in comparison to ursodeoxycholic acid. Clin
Ter 1993;143:321–6 [in Italian].
- Pares A, Caballeria L, Rodes J, et al. Long-term effects of ursodeoxycholic
acid in primary biliary cirrhosis: results of a double-blind controlled multicentric trial.
UDCA-Cooperative Group from the Spanish Association for the Study of the Liver. J
Hepatol 2000;32:561–6.
- Stauch S, Kircheis G, Adler G, et al. Oral L-ornithine-L-aspartate therapy of
chronic hepatic encephalopathy: results of a placebo-controlled double-blind study. J
Hepatol 1998;28:856–64.
- Kircheis G, Nilius R, Held C, et al. Therapeutic efficacy of
L-ornithine-L-aspartate infusions in patients with cirrhosis and hepatic encephalopathy:
results of a placebo-controlled, double-blind study. Hepatology
1997;25:1351–60.
- Staedt U, Leweling H, Gladisch R, et al. Effects of ornithine aspartate on
plasma ammonia and plasma amino acids in patients with cirrhosis. A double-blind, randomized
study using a four-fold crossover design. J Hepatol 1993;19:424–30.
- Pugliese D, Sabba C, Ettorre G et al. Acute systemic and splanchnic
haemodynamic effects of l-carnitine in patients with cirrhosis. Drugs Exp Clin Res
1992;18:147–53.
- Ferro D, Basili S, Practico D, et al. Vitamin E reduces monocyte tissue factor
expression in cirrhotic patients. Blood 1999;93:2945–50.
- de la Maza MP, Petermann M, Bunout D, Hirsch S. Effects of long-term vitamin E
supplementation in alcoholic cirrhotics. J Am Coll Nutr 1995;14:192–6.
- Burk RF, Early DS, Hill KE, et al. Plasma selenium in patients with cirrhosis.
Hepatology 1998;27:794–8.
- Feher J, Lengyel G, Blazovics A. Oxidative stress in the liver and biliary
tract diseases. Scand J Gastroenterol Suppl 1998;228:38–46.
- Van Gossum A, Neve J. Low selenium status in alcoholic cirrhosis is correlated
with aminopyrine breath test. Preliminary effects of selenium supplementation. Biol Trace
Elem Res 1995;47:201–7.
- Shiomi S, Masaki K, Habu D, et al. Calcitriol for bone loss in patients with
primary biliary cirrhosis. J Gastroenterol 1999;34:241–5.
- Yamamoto M, Oka H, Kanno T, et al. Controlled prospective trial to evaluate
sho-saiko-to for the prevention of hepatotcellular carcinoma in patients with cirrhosis of the
liver. Gan To Kagaku Ryoho (Jpn J Cancer Chemother) 1989;16:1519–24
[in Japanese].
- Kumada T, et al. Effect of shakuyaku-kanzo-to (Tsumura TJ-68) on muscle cramps
accompanying cirrhosis in a placebo-controlled double-blind parallel study. J Clin Ther
Med 1999;15:499–523.
- Salmi HA, Sarna S. Effect of silymarin on chemical, functional and
morphological alterations of the liver. A double-blind controlled study. Scand J
Gastroenterol 1982;17:517–21.
- Feher J, Deak G, Muzes G, et al. Liver-protective action of silymarin therapy
in chronic alcoholic liver diseases. Orv Hetil 1989;130:2723–7 [in
Hungarian].
- Muzes G, Deak G, Lang I, et al. Effect of silymarin (Legalon) therapy on the
antioxidant defense mechanism and lipid peroxidation in alcoholic liver disease (double blind
protocol.) Orv Hetil 1990:131:863–6 [in Hungarian].
- Velussi M, Cernigoi AM, De Monte A, et al. Long-term (12 months) treatment
with an anti-oxidant drug (silymarin) is effective on hyperinsulinemia, exogenous insulin need
and malondialdehyde levels in cirrhotic diabetic patients. J Hepatol
1997;26:871–9.
- Ferenci P, Dragosics B, Dittrich H, et al. Randomized controlled trial of
silymarin treatment in patients with cirrhosis of the liver. J Hepatol
1989;9:105–13.
- Velussi M, Cernogoi AM, De Monte A, et al. Long-term (12 months) treatment
with an antioxidant drug (silymarin) is effective on hyperinsulinemia, exogenous insulin need
and malondialdehyde levels in cirrhotic diabetic patients. J Hepatology
1997;26:871–9.
- Pares A, Planas R, Torres M, et al. Effects of silymarin in alcoholic patients
with cirrhosis of the liver: results of a double-blind, randomized and multicenter trial.
J Hepatol 1998;28:731–3.