2010, Number 3
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Gac Med Mex 2010; 146 (3)
Lactante de sexo femenino de siete meses de edad con hepatomegalia, hipoglucemia y talla baja
Ridaura-Sanz C, Sánchez-Márquez P
Language: Spanish
References: 12
Page: 207-211
PDF size: 93.87 Kb.
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No abstract
REFERENCES
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Cederbaum S. Molecular diagnosis and inborn errors of metabolism: a practitioner’s view. Genet Med 2000;2:345-349.
Rake JP, Visser G, Labrune P, Leonard JV, Ullrich K, Smit GP. Glycogen storage disease type I. Diagnosis, management, clinical course and outcome. Results of the European Study on Glycogen Storage Disease Type I (ESGSDI). Eur J Pediatr 2002;161:S20-S34.
Ozen H. Glycogen storage disease. New perspectives. World J Gastroenterol 2007:13:2541-2553.
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Göðüþ S, Koçak N, Ciliv G, Karabulut E, Akçören Z, Kale G, Caðlar M. Histologic features of the liver in type Ia glycogen storage disease: comparative study between different age groups and consecutive biopsies. Pediatr Dev Pathol 2002;5:299-304.
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Iyer SG, Chen CL, Wang CC, Wang SH, Concejero AM, Liu YW, et al. Long term results of living donor liver transplantation for glycogen disorders in children. Liver Transplantation 2007;13:848-852.
Jiménez-Forero SJ, Roa-Saavedra DX, Villalba MC. Pancreatitis aguda secundaria a hipertrigliceridemia. Presentación de dos casos clínicos. Rev Esp Enferm Dig 2008;100:367-371.
IanGan S, Edwards AL, Symonds CJ. Bech PL. Hypertriglyceridemiainduced pancreatitis: a case-based review. World J Gastroenterol 2006;12:7197- 7202.
Yadad D, Pitchumoni CS. Issues in hyperlipidemic pancreatitis. J Clin Gastroenterol 2003;26:54-62.