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5. Maple syrup urine disease in an infant with microgyria. Martin JK; Norman RM Dev Med Child Neurol; 1967 Apr; 9(2):152-9. PubMed ID: 6059316 [No Abstract] [Full Text] [Related]
6. Maple syrup urine disease; an inborn error of the metabolism of valine, leucine, and isoleucine associated with gross mental deficiency. MACKENZIE DY; WOOLF LI Br Med J; 1959 Jan; 1(5114):90-1. PubMed ID: 13608087 [No Abstract] [Full Text] [Related]
7. An 11-day-old boy with lethargy, poor feeding, vomiting. Maple syrup urine disease. Charrow J Pediatr Ann; 2005 Oct; 34(10):772-4. PubMed ID: 16285630 [No Abstract] [Full Text] [Related]
8. Intermittent branched chain ketonuria (variant of maple syrup urine disease). Irwin WC; Martel SB; Goluboff N Clin Biochem; 1971 Jun; 4(2):52-8. PubMed ID: 5128296 [No Abstract] [Full Text] [Related]
9. A new variant of maple syrup urine disease (branched chain ketoaciduria). Clinical and biochemical evaluation. Schulman JD; Lustberg TJ; Kennedy JL; Museles M; Seegmiller JE Am J Med; 1970 Jul; 49(1):118-24. PubMed ID: 5431474 [No Abstract] [Full Text] [Related]
17. MAPLE-SYRUP-URINE DISEASE. REPORT OF A CASE, WITH A PEDIGREE. LONSDALE D; BARBER DH N Engl J Med; 1964 Dec; 271():1338-41. PubMed ID: 14214646 [No Abstract] [Full Text] [Related]
18. A new finding in maple-syrup-urine disease. NORTON PM; ROITMAN E; SNYDERMAN SE; HOLT LE Lancet; 1962 Jan; 1(7219):26-7. PubMed ID: 14480431 [No Abstract] [Full Text] [Related]
19. [CLINICAL, BIOCHEMICAL, AND NEUROPATHOLOGIC ASPECTS OF MAPLE SYRUP URINE DISEASE. A KETOACIDURIA OF THE OPEN CHAIN AMINOACIDS LEUCINE, ISOLEUCINE AND VALINE]. SILBERMANSCHWARTZMAN J An Fac Med Lima; 1963 Sep; 46():339-65. PubMed ID: 14122039 [No Abstract] [Full Text] [Related]
20. MAPLE SYRUP URINE DISEASE. SNYDERMAN SE; HOLT LE J Maine Med Assoc; 1964 Jan; 55():3-5. PubMed ID: 14109847 [No Abstract] [Full Text] [Related] [Next] [New Search]