These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. [Maple syrup urine disease with an intermittent relatively benign course]. Müller H; Bickel H; Feist D; Lutz P Dtsch Med Wochenschr; 1971 Oct; 96(40):1552-7. PubMed ID: 5093339 [No Abstract] [Full Text] [Related]
6. M aple syrup urine disease. A review with a report of an additional case. Schwartz JF; Kolendrianos ET Dev Med Child Neurol; 1969 Aug; 11(4):460-70. PubMed ID: 5805351 [No Abstract] [Full Text] [Related]
7. Plasma amino acid analyses in two cases of maple syrup urine disease. Surarit R; Srisomsap C; Wasant P; Svasti J; Suthatvoravut U; Chokchaichamnankit D; Liammongkolkul S Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():138-9. PubMed ID: 11400750 [TBL] [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. Maple syrup urine disease variant: report on an infant. Koepp P; Rybak C; Rüdiger HW; Wendel U Z Kinderheilkd; 1974 Feb; 116(3):177-84. PubMed ID: 4813457 [No Abstract] [Full Text] [Related]
10. 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]
11. Leucine equivalency system in managing branched chain ketoaciduria. Smith BA; Waisman HA J Am Diet Assoc; 1971 Oct; 59(4):342-6. PubMed ID: 5095277 [No Abstract] [Full Text] [Related]
12. DIETARY TREATMENT OF A CHILD WITH MAPLE SYRUP URINE DISEASE (BRANCHED-CHAIN KETOACIDURIA). WESTALL RG Arch Dis Child; 1963 Oct; 38(201):485-91. PubMed ID: 14065992 [No Abstract] [Full Text] [Related]
13. 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]
14. [Metabolic study of the classic form of leucinosis during exchange transfusion therapy]. Zeman J; Hyánek J; Houstková H; Rubín A; Verner P; Pehal F; Konecná L; Zapadlo M; Plavka R; Wendel U Cesk Pediatr; 1987 Apr; 42(4):219-22. PubMed ID: 3594613 [No Abstract] [Full Text] [Related]
15. The therapy of maple syrup urine disease. Snyderman SE Am J Dis Child; 1967 Jan; 113(1):68-73. PubMed ID: 6015908 [No Abstract] [Full Text] [Related]
16. A variant form of branched-chain keto aciduria. van der Horst JL; Wadman SK Acta Paediatr Scand; 1971 Sep; 60(5):594-9. PubMed ID: 5125167 [No Abstract] [Full Text] [Related]
18. Electroencephalograms in a case of maple syrup urine disease: their relation to serum levels of branched-chain amino acids. Iinuma K; Saito T; Wada Y; Onuma A; Takamatsu N Tohoku J Exp Med; 1976 Oct; 120(2):191-5. PubMed ID: 982436 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Maple syrup urine disease (branched-chain keto-aciduria) variant type manifesting as hyperkinetic behaviour and mental retardation. Report of two cases. Kalyanaraman K; Chamukuttan S; Arjundas G; Gajanan N; Ramamurthi B J Neurol Sci; 1972 Feb; 15(2):209-17. PubMed ID: 5010106 [No Abstract] [Full Text] [Related] [Next] [New Search]