These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 4697756)

  • 1. Intermittent ataxia and biochemical disorders.
    Gordon N
    Dev Med Child Neurol; 1973 Apr; 15(2):208-10. PubMed ID: 4697756
    [No Abstract]   [Full Text] [Related]  

  • 2. Hyperalaninemia with pyruvicemia in a patient suggestive of Leigh's encephalomyelopathy.
    Tada K; Sugita K; Fujitani K; Uesaki T; Takada G
    Tohoku J Exp Med; 1973 Jan; 109(1):13-8. PubMed ID: 4717261
    [No Abstract]   [Full Text] [Related]  

  • 3. Family with intermittent maple syrup urine disease.
    Valman HB; Patrick AD; Seakins JW; Platt JW; Gompertz D
    Arch Dis Child; 1973 Mar; 48(3):225-8. PubMed ID: 4693464
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Biochemical studies and therapy in subacute necrotizing encephalomyelopathy (Leigh's syndrome).
    Grover WD; Auerbach VH; Patel MS
    J Pediatr; 1972 Jul; 81(1):39-44. PubMed ID: 4556192
    [No Abstract]   [Full Text] [Related]  

  • 5. Letter: Leigh's disease and failure of automatic respiration.
    Kissach AW; Currie S; Harriman DG; Littlewood JM; Payne RB; Walker BE
    Lancet; 1974 Sep; 2(7881):662. PubMed ID: 4137785
    [No Abstract]   [Full Text] [Related]  

  • 6. Letter: Biochemical abnormalities in Leigh's disease.
    Blass JP; Cederbaum SD; Dunn HG
    Lancet; 1976 Jun; 1(7971):1237-8. PubMed ID: 58277
    [No Abstract]   [Full Text] [Related]  

  • 7. Subacute necrotizing encephalomyelopathy associated with renal and arterial lesions.
    Crome L
    Brain; 1970; 93(4):709-14. PubMed ID: 5490272
    [No Abstract]   [Full Text] [Related]  

  • 8. Leigh's subacute necrotizing encephalomyelopathy in a child with infantile spasms and hypsarrhythmia.
    Kamoshita S; Mizutani I; Fukuyama Y
    Dev Med Child Neurol; 1970 Aug; 12(4):430-5. PubMed ID: 5457538
    [No Abstract]   [Full Text] [Related]  

  • 9. Crib-death syndrome.
    Murphy JV; Perper JA
    Lancet; 1973 Mar; 1(7803):614. PubMed ID: 4120686
    [No Abstract]   [Full Text] [Related]  

  • 10. Ocular findings in subacute necrotizing encephalomyelitis.
    Grover WD; Green WR; Pileggi AJ
    Am J Ophthalmol; 1970 Oct; 70(4):599-603. PubMed ID: 5505478
    [No Abstract]   [Full Text] [Related]  

  • 11. Further observations on the biochemical lesion in maple syrup urine disease.
    Dreyfus PM; Prensky AL
    Nature; 1967 Apr; 214(5085):276. PubMed ID: 6034241
    [No Abstract]   [Full Text] [Related]  

  • 12. Ocular manifestations in aminoacidopathies.
    François J
    Adv Ophthalmol; 1972; 25():28-103. PubMed ID: 4560371
    [No Abstract]   [Full Text] [Related]  

  • 13. [Intermittent maple syrup urine disease in a 12-year-old boy: clinical aspects, diagnosis and treatment].
    Fritsch G; Langenbeck U; Wendel U; Lehnert W; Palm W; Steger W
    Klin Padiatr; 1983; 195(5):351-4. PubMed ID: 6632715
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Intermittent ataxia with pyruvate-decarboxylase deficiency.
    Blass JP; Lonsdale D; Uhlendorf BW; Hom E
    Lancet; 1971 Jun; 1(7712):1302. PubMed ID: 4104759
    [No Abstract]   [Full Text] [Related]  

  • 15. Maple syrup urine disease.
    DANCIS J; LEVITZ M; MILLER S; WESTALL RG
    Br Med J; 1959 Jan; 1(5114):91-3. PubMed ID: 13608088
    [No Abstract]   [Full Text] [Related]  

  • 16. Maple syrup urine disease (branched-chain keto-aciduria) variant type manifesting as hyperkinetic behaviour and mental retardation. Report of two cases.
    Kalyanaraman K; Chamukuttan S; Arjundas G; Gajanan N; Ramamurthi B
    J Neurol Sci; 1972 Feb; 15(2):209-17. PubMed ID: 5010106
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. THE METABOLISM OF LEUCINE IN TISSUE CULTURE OF SKIN FIBROBLASTS OF MAPLE-SYRUP-URINE DISEASE.
    DANCIS J; JANSEN V; HUTZLER J; LEVITZ M
    Biochim Biophys Acta; 1963 Nov; 77():523-4. PubMed ID: 14089436
    [No Abstract]   [Full Text] [Related]  

  • 19. Necrotizing encephalomyelopathy (Leigh).
    David RB; Gomez MR; Okazaki H
    Dev Med Child Neurol; 1970 Aug; 12(4):436-45. PubMed ID: 5457539
    [No Abstract]   [Full Text] [Related]  

  • 20. [Mental retardation and hereditary enzymopathy (review)].
    D'iachkova AIa; Lebedev BV
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(10):1588-93. PubMed ID: 5003148
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.