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PUBMED FOR HANDHELDS

Journal Abstract Search


428 related items for PubMed ID: 108196

  • 21. The biochemical basis of gangliosidoses.
    Sandhoff K, Conzelmann E.
    Neuropediatrics; 1984 Sep; 15 Suppl():85-92. PubMed ID: 6242704
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  • 22. [Enzyme diagnostics in lysosomal diseases with emphasis on sphingolipidoses].
    Dreyfus JC, Poenaru L.
    Arch Fr Pediatr; 1975 Sep; 32(6):503-14. PubMed ID: 810108
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  • 30. LIPID CLASS COMPOSITION OF NORMAL HUMAN BRAIN AND VARIATIONS IN METACHROMATIC LEUCODYSTROPHY, TAY-SACHS, NIEMANN-PICK, CHRONIC GAUCHER'S AND ALZHEIMER'S DISEASES.
    ROUSER G, GALLI C, KRITCHEVSKY G.
    J Am Oil Chem Soc; 1965 May; 42():404-10. PubMed ID: 14324330
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  • 34. Gene Therapy of Sphingolipid Metabolic Disorders.
    Shaimardanova AA, Solovyeva VV, Issa SS, Rizvanov AA.
    Int J Mol Sci; 2023 Feb 11; 24(4):. PubMed ID: 36835039
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  • 36. Clinical and biochemical pathophysiology of ataxia in the sphingolipidoses.
    Philippart M.
    Adv Neurol; 1978 Feb 11; 21():131-49. PubMed ID: 104554
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  • 40. Sphingolipidoses in Turkey.
    Ozkara HA, Topçu M.
    Brain Dev; 2004 Sep 11; 26(6):363-6. PubMed ID: 15275696
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