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8. 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]
9. 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]
10. 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]
11. [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]
12. Potential urinary biomarkers of nephrotoxicity in cyclophosphamide-treated rats investigated by NMR-based metabolic profiling. Lim SR; Hyun SH; Lee SG; Kim JY; Kim SH; Park SJ; Moon KS; Sul D; Kim DH; Choi HK J Biochem Mol Toxicol; 2017 Mar; 31(3):. PubMed ID: 27870266 [TBL] [Abstract][Full Text] [Related]
13. The recovery of amino acids from acid hydrolysates of whole urine from patients with thermal burns. Estes FL; Wetzel RL Clin Chim Acta; 1967 Mar; 15(3):421-7. PubMed ID: 6034418 [No Abstract] [Full Text] [Related]
14. Evaluation of circulating levels and renal clearance of natural amino acids in patients with Cushing's disease. Faggiano A; Pivonello R; Melis D; Alfieri R; Filippella M; Spagnuolo G; Salvatore F; Lombardi G; Colao A J Endocrinol Invest; 2002 Feb; 25(2):142-51. PubMed ID: 11929085 [TBL] [Abstract][Full Text] [Related]
15. Dietary branched-chain amino acid valine, isoleucine and leucine requirements of fingerling Indian major carp, Cirrhinus mrigala (Hamilton). Ahmed I; Khan MA Br J Nutr; 2006 Sep; 96(3):450-60. PubMed ID: 16925849 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Urinary amino acid excretion in patients with scleroderma. Winkelmann RK; Jones JD; Ulrich JA Mayo Clin Proc; 1971 Feb; 46(2):114-8. PubMed ID: 5546411 [No Abstract] [Full Text] [Related]
18. Valine, isoleucine, and leucine. A new treatment for phenylketonuria. Berry HK; Brunner RL; Hunt MM; White PP Am J Dis Child; 1990 May; 144(5):539-43. PubMed ID: 2184659 [TBL] [Abstract][Full Text] [Related]
19. Isoleucine, a potent plasma glucose-lowering amino acid, stimulates glucose uptake in C2C12 myotubes. Doi M; Yamaoka I; Fukunaga T; Nakayama M Biochem Biophys Res Commun; 2003 Dec; 312(4):1111-7. PubMed ID: 14651987 [TBL] [Abstract][Full Text] [Related]
20. The need of essential amino acids in children. An evaluation based on the intake of phenylalanine, tyrosine, leucine, isoleucine, and valine in children with phenylketonuria, tyrosine amino transferase defect, and maple syrup urine disease. Kindt E; Halvorsen S Am J Clin Nutr; 1980 Feb; 33(2):279-86. PubMed ID: 6101930 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]