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45. Intermittent maple syrup urine disease: two case reports. Axler O; Holmquist P Pediatrics; 2014 Feb; 133(2):e458-60. PubMed ID: 24394677 [TBL] [Abstract][Full Text] [Related]
46. Maple syrup urine disease variant form: presentation with psychomotor retardation and CT scan abnormalities. Verdu A; Lopez-Herce J; Pascual-Castroviejo I; Martinez-Bermejo A; Ugarte M; Garcia MJ Acta Paediatr Scand; 1985 Sep; 74(5):815-8. PubMed ID: 4050430 [TBL] [Abstract][Full Text] [Related]
47. Chloride-dependent inhibition of vesicular glutamate uptake by alpha-keto acids accumulated in maple syrup urine disease. Reis M; Farage M; Wolosker H Biochim Biophys Acta; 2000 Jul; 1475(2):114-8. PubMed ID: 10832024 [TBL] [Abstract][Full Text] [Related]
48. Maple syrup urine disease. LANE MR J Pediatr; 1961 Jan; 58():80-5. PubMed ID: 13758724 [No Abstract] [Full Text] [Related]
49. Maple syrup urine disease. PATRICK AD Arch Dis Child; 1961 Jun; 36(187):269-72. PubMed ID: 13733337 [No Abstract] [Full Text] [Related]
51. Reduction of plasma concentrations of large neutral amino acids in patients with maple syrup urine disease during crises. Wajner M; Vargas CR Arch Dis Child; 1999 Jun; 80(6):579. PubMed ID: 10523253 [No Abstract] [Full Text] [Related]
53. Intermediate maple syrup urine disease: neuroimaging observations in 3 patients from South India. Bindu PS; Shehanaz KE; Christopher R; Pal PK; Ravishankar S J Child Neurol; 2007 Jul; 22(7):911-3. PubMed ID: 17715290 [TBL] [Abstract][Full Text] [Related]
54. A rapid method for assay of branched-chain keto acid decarboxylation in cultured cells and its application to prenatal diagnosis of maple syrup urine disease. Fensom AH; Benson PF; Baker JE Clin Chim Acta; 1978 Jul; 87(1):169-74. PubMed ID: 668138 [TBL] [Abstract][Full Text] [Related]
55. Morphological alterations and induction of oxidative stress in glial cells caused by the branched-chain alpha-keto acids accumulating in maple syrup urine disease. Funchal C; Latini A; Jacques-Silva MC; Dos Santos AQ; Buzin L; Gottfried C; Wajner M; Pessoa-Pureur R Neurochem Int; 2006 Dec; 49(7):640-50. PubMed ID: 16822590 [TBL] [Abstract][Full Text] [Related]
56. Branched-chain alpha-keto acids for the diagnosis of maple-syrup-urine disease. Parsons H; Fung E; Snyder FF N Engl J Med; 1987 Apr; 316(15):951. PubMed ID: 3821846 [No Abstract] [Full Text] [Related]
57. Determination of (S)- and (R)-2-oxo-3-methylvaleric acid in plasma of patients with maple syrup urine disease. Wendel U; Even G; Langenbeck U; Schadewaldt P; Hummel W Clin Chim Acta; 1992 Jun; 208(1-2):85-91. PubMed ID: 1638756 [TBL] [Abstract][Full Text] [Related]
58. Definition of the mutation responsible for maple syrup urine disease in Poll Shorthorns and genotyping Poll Shorthorns and Poll Herefords for maple syrup urine disease alleles. Dennis JA; Healy PJ Res Vet Sci; 1999 Aug; 67(1):1-6. PubMed ID: 10425233 [TBL] [Abstract][Full Text] [Related]
59. Maple syrup disease and other disorders of keto acid metabolism. MENKES JH Res Publ Assoc Res Nerv Ment Dis; 1962; 40():69-93. PubMed ID: 13934868 [No Abstract] [Full Text] [Related]
60. Dietary treatment of maple sirup urine disease (branched-chain ketoaciduria). Noel MB; Stanley PB; Girz JC; Allen RJ J Am Diet Assoc; 1976 Jul; 69(1):62-8. PubMed ID: 932376 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]