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Journal Abstract Search
103 related items for PubMed ID: 5730703
1. [Biochemical-genetic studies in maple syrup disease]. Goedde HW, Blume KG. Med Welt; 1968 Dec; 49():2699-703. PubMed ID: 5730703 [No Abstract] [Full Text] [Related]
2. [Disorders of leucine, isoleucine and valine metabolism (maple syrup urine disease)]. Vulović D, Vilhar N, Hajduković R, Marjanović B, Stojanović Lj. Srp Arh Celok Lek; 1975 May; 103(5):419-36. PubMed ID: 1188483 [No Abstract] [Full Text] [Related]
3. [Studies on "branched chain oxoacid aciduria" (maple syrup diseases)]. Goedde HW, Blume KG, Möhlenbeck F, Rotthauwe HW, Simon HA, Lang K. Med Klin; 1966 Dec 30; 61(52):2063-7. PubMed ID: 4385693 [No Abstract] [Full Text] [Related]
4. Proceedings: Neonatal diagnosis of maple syrup urine disease and the influence of exchange blood transfusion. Russell A, Statter M, Shina A, Perlman M. Isr J Med Sci; 1975 Nov 30; 11(11):1218-9. PubMed ID: 1205813 [No Abstract] [Full Text] [Related]
14. M aple syrup urine disease. A review with a report of an additional case. Schwartz JF, Kolendrianos ET. Dev Med Child Neurol; 1969 Aug 30; 11(4):460-70. PubMed ID: 5805351 [No Abstract] [Full Text] [Related]
16. [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 30; 46():339-65. PubMed ID: 14122039 [No Abstract] [Full Text] [Related]
17. Maple syrup urine disease: branched-chain amino acid concentrations and metabolism in cultured human lymphoblasts. Skaper SD, Molden DP, Seegmiller JE. Biochem Genet; 1976 Aug 30; 14(7-8):527-39. PubMed ID: 985377 [Abstract] [Full Text] [Related]