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2. Inborn errors of metabolism in children referred with Reye's syndrome. A changing pattern. Rowe PC; Valle D; Brusilow SW JAMA; 1988 Dec; 260(21):3167-70. PubMed ID: 3184395 [TBL] [Abstract][Full Text] [Related]
3. 3-Hydroxy-3-methylglutaric aciduria: a possible pitfall in diagnosis. Mills GA; Hill MA; Buchanan R; Corina DL; Walker V Clin Chim Acta; 1991 Dec; 204(1-3):131-6. PubMed ID: 1726424 [No Abstract] [Full Text] [Related]
6. The metabolic crisis: a diagnostic challenge [editoria; comment]. Bove KE J Pediatr; 1997 Aug; 131(2):181-2. PubMed ID: 9290601 [No Abstract] [Full Text] [Related]
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10. [Do defects in fatty acid oxidation cause sudden infant death?]. Hagenfeldt L; von Döbeln V Lakartidningen; 1989 Apr; 86(17):1575-6. PubMed ID: 2725141 [No Abstract] [Full Text] [Related]
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12. Recurrent myoglobinuria as a presenting manifestation of very long chain acyl coenzyme A dehydrogenase deficiency. Straussberg R; Harel L; Varsano I; Elpeleg ON; Shamir R; Amir J Pediatrics; 1997 Jun; 99(6):894-6. PubMed ID: 9164788 [No Abstract] [Full Text] [Related]
13. Medicine. Fast technology drives new world of newborn screening. Marshall E Science; 2001 Dec; 294(5550):2272-4. PubMed ID: 11743177 [No Abstract] [Full Text] [Related]
14. [Carnitine deficiency in inborn errors of metabolism]. Sela BA; Lerman-Sagie T; Berkovitz M Harefuah; 1997 Nov; 133(10):419-23, 504. PubMed ID: 9418309 [TBL] [Abstract][Full Text] [Related]
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