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PUBMED FOR HANDHELDS

Journal Abstract Search


166 related items for PubMed ID: 818606

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  • 2. [Clinical, preclinical and prenatal diagnosis of congenital sphingolipidoses by determining lysosomal hydrolases (author's transl)].
    Pilz H, Heipertz R, Seidel D.
    Fortschr Neurol Psychiatr Grenzgeb; 1978 Apr; 46(4):207-21. PubMed ID: 417009
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  • 3. Heritable catabolic and anabolic disorders of lipid metabolism.
    Brady RO.
    Metabolism; 1977 Mar; 26(3):329-45. PubMed ID: 13262
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  • 5. Cerebral degenerative disorders of infancy and childhood.
    Noronha MJ.
    Dev Med Child Neurol; 1974 Apr; 16(2):228-41. PubMed ID: 4209600
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  • 8. Progress in investigations of sphingolipidoses.
    Adachi M, Schneck L, Volk BW.
    Acta Neuropathol; 1978 Aug 07; 43(1-2):1-18. PubMed ID: 97916
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  • 12. [Enzyme diagnostics in lysosomal diseases with emphasis on sphingolipidoses].
    Dreyfus JC, Poenaru L.
    Arch Fr Pediatr; 1975 Aug 07; 32(6):503-14. PubMed ID: 810108
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  • 13. Basic findings and current developments in sphingolipidoses.
    Pilz H, Heipertz R, Seidel D.
    Hum Genet; 1979 Mar 12; 47(2):113-34. PubMed ID: 108196
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  • 16. Lipid storage disease: Part II. Ultrastructural pathology of lipid storage cells in sphingolipidoses.
    Takahashi K, Naito M.
    Acta Pathol Jpn; 1985 Mar 12; 35(2):385-408. PubMed ID: 2992227
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