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655 related items for PubMed ID: 11400750
1. 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 [Abstract] [Full Text] [Related]
2. Amino acids levels and lipid peroxidation in maple syrup urine disease patients. Barschak AG, Sitta A, Deon M, Busanello EN, Coelho DM, Cipriani F, Dutra-Filho CS, Giugliani R, Wajner M, Vargas CR. Clin Biochem; 2009 Apr; 42(6):462-6. PubMed ID: 19121297 [Abstract] [Full Text] [Related]
3. 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 09; 307(24):1492-5. PubMed ID: 7144815 [No Abstract] [Full Text] [Related]
4. The relationship between the branched chain amino acids and their alpha-ketoacids in maple syrup urine disease. Snyderman SE, Goldstein F, Sansaricq C, Norton PM. Pediatr Res; 1984 Sep 09; 18(9):851-3. PubMed ID: 6483508 [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 03; 93(18):895-903 passim. PubMed ID: 5650843 [No Abstract] [Full Text] [Related]
7. Clearance of branched chain amino acids by peritoneal dialysis in maple syrup urine disease. McMahon Y, MacDonnell RC. Adv Perit Dial; 1990 May 03; 6():31-4. PubMed ID: 1982835 [Abstract] [Full Text] [Related]
8. Maple syrup urine disease. Two cases in Israel. Chemke J, Levin S. Isr J Med Sci; 1975 Aug 03; 11(8):809-16. PubMed ID: 1165176 [Abstract] [Full Text] [Related]
9. [Maple syrup urine disease with an intermittent relatively benign course]. Müller H, Bickel H, Feist D, Lutz P. Dtsch Med Wochenschr; 1971 Oct 03; 96(40):1552-7. PubMed ID: 5093339 [No Abstract] [Full Text] [Related]
10. [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 03; 42(4):219-22. PubMed ID: 3594613 [No Abstract] [Full Text] [Related]
11. M aple syrup urine disease. A review with a report of an additional case. Schwartz JF, Kolendrianos ET. Dev Med Child Neurol; 1969 Aug 03; 11(4):460-70. PubMed ID: 5805351 [No Abstract] [Full Text] [Related]
12. Diagnosis and treatment of maple syrup disease: a study of 36 patients. Morton DH, Strauss KA, Robinson DL, Puffenberger EG, Kelley RI. Pediatrics; 2002 Jun 03; 109(6):999-1008. PubMed ID: 12042535 [Abstract] [Full Text] [Related]
15. Biochemical studies on a variant of branched chain ketoaciduria in a 19-year-old female. Fischer MH, Gerritsen T. Pediatrics; 1971 Nov 03; 48(5):795-801. PubMed ID: 5125877 [No Abstract] [Full Text] [Related]
16. Leucine equivalency system in managing branched chain ketoaciduria. Smith BA, Waisman HA. J Am Diet Assoc; 1971 Oct 03; 59(4):342-6. PubMed ID: 5095277 [No Abstract] [Full Text] [Related]
18. Clinical consequences of disorders in the intermediate metabolism of branched chain amino acids (valine, leucine and isoleucine). Mogoş T, Cheţa CP, Mincu IT. Rom J Intern Med; 1994 May 07; 32(1):57-61. PubMed ID: 8081313 [Abstract] [Full Text] [Related]
19. Multiple exchange transfusions as treatment during the acute period in maple syrup urine disease. Schuchmann L, Witt I, Schulz P, Schumacher H, Rüdiger H. Helv Paediatr Acta; 1972 Sep 07; 27(4):449-56. PubMed ID: 4644280 [No Abstract] [Full Text] [Related]
20. [Experiences with a new amino acid analyzer for a rapid analysis]. Irtel von Brenndorff A, Hagge W. Monatsschr Kinderheilkd (1902); 1970 Jun 07; 118(6):417-9. PubMed ID: 5523694 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]