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2. [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]
3. 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]
4. 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]
5. 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]
6. [On the clinical picture and pathological anatomy of the maple syrup disease ("branded chain ketoaciduria"). Report on 2 cases in 1 family]. Sander C; Clotten R; Noetzel H; Wehinger H Dtsch Med Wochenschr; 1968 May; 93(18):895-903 passim. PubMed ID: 5650843 [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. 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]
10. [Neonatal leucinosis with favourable course. Therapeutic problems]. Astruc J; Froye E; Luciani JM; Bellet H; Magnan de Bornier P; Brunel D Ann Pediatr (Paris); 1977 Sep; 24(8-9):605-10. PubMed ID: 16211914 [No Abstract] [Full Text] [Related]
11. [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]
12. Semiquantitation of leucine, isoleucine, and valine by thin-layer chromatography in management of maple-syrup urine diseases. Allen RJ; Frey HJ; Fleming LM; Owings CL Clin Chem; 1972 May; 18(5):413-6. PubMed ID: 5019114 [No Abstract] [Full Text] [Related]
13. Maple syrup urine disease: coenzyme function and prenatal monitoring. Elsas LJ; Priest JH; Wheeler FB; Danner DJ; Pask BA Metabolism; 1974 Jun; 23(6):569-79. PubMed ID: 4857216 [No Abstract] [Full Text] [Related]
14. Maple syrup urine disease. Four years' experience with dietary treatment of a case. Dickinson JP; Holton JB; Lewis GM; Littlewood JM; Steel AE Acta Paediatr Scand; 1969 Jul; 58(4):341-51. PubMed ID: 5824823 [No Abstract] [Full Text] [Related]
15. Prospective study of maple-syrup-urine disease for the first four days of life. DiGeorge AM; Rezvani I; Garibaldi LR; Schwartz M N Engl J Med; 1982 Dec; 307(24):1492-5. PubMed ID: 7144815 [No Abstract] [Full Text] [Related]
16. Maple syrup urine disease. Two cases in Israel. Chemke J; Levin S Isr J Med Sci; 1975 Aug; 11(8):809-16. PubMed ID: 1165176 [TBL] [Abstract][Full Text] [Related]
17. Biochemical studies on a variant of branched chain ketoaciduria in a 19-year-old female. Fischer MH; Gerritsen T Pediatrics; 1971 Nov; 48(5):795-801. PubMed ID: 5125877 [No Abstract] [Full Text] [Related]