Referências Bibliográficas


E-m@il
 

Martins AM. Inborn Errors of Metabolism: a clinical purview. São Paulo Medical Journal/Rev Paul Med. 1999. 117(6): 251-65.
Scriver CR. Foreword IN: Blau N, Duran M, Blaskovics ME. Physician's Guide to the Laboratory Diagnosis of Metabolic Diseases. 3rd ed. Great Britain 1996.
Wilcox WR. Inborn Errors of Metabolism. Online Copyright (C) 1995 World Wide
Web URL: http://www.neonatology.org/syllabus/iem.01.html
Online Mendelian Inheritance in Man, OMIM ™. Center for Medical Genetics, Johns Hopkins University (Baltimore, MD) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD), 1997. World Wide Web URL:http://www.ncbi.nlm.nih.gov/omim/
Martins AM, D'Almeida V; Tavares FM; Oliveira RB; Macedo DM*, Aoki M et al. Características de um ambulatório geral de doenças metabólicas hereditárias. Artigo eletrônico, 1(4) - Online 1999 - World Wide Web URL: http://www.brazilpednews.org.br
Burton, BK - Inborn Errors of Metabolism: A Guide to Diagnosis. Pediatrics, 102 (6)e69, 1998
Fernandes, J; Saudubray, J-M; van den Berghe, G - Clinical Approach to Inherited Metabolic Diseases. IN: Inborn Metabolic Diseases - diagnosis and treatment,chapter 1, pp. 3-41,3rd ed., Springer, 2000.
Buist, N. Set of simple side-room urine tests for detection of inborn errors of metabolism. British Med.J., 2: 745-9, 1968.
Efron, M.L. Young, D.; Moser, H.W. & Mac Cready, R.A. - A simple chromatographic screening test for the detection of disorders of amino acid metabolism: a technique using whole blood or urine collected on filter paper. N.Engl.J.Med, 270: 1378-83, 1964.
Hommes, F.A. Techiniques in Diagnostic Human Biochemical Genetics - A laboratory manual. Nova York, Wiley-Liss, 1991.
Thomas, G.H. & Howell, R.R. Selected screening tests for genetic metabolic diseases. Chicago, Year Book Medical Publishers, 1973


Coordenação: Profa.Dra. Ana Maria Martins
End.: Rua Coronel Lisboa, 957- Vila Clementino
CEP 04020-041 - São Paulo, SP
fone: 11 5081 9620
fax: 11 5081 9624