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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

219 related items for PubMed ID: 6810572

  • 41. Recent progress of lysosomal diseases.
    Durand P.
    Enzyme; 1987; 38(1-4):256-61. PubMed ID: 3326733
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  • 42.
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  • 44. [Use of an information-search diagnostic system for recognizing acute hereditary metabolic diseases with early lethal outcomes].
    Krasnopol'skaia KD, Sakhibzadaeva KK, Goncharova IA, Chebotarev AN.
    Genetika; 1994 Nov; 30(11):1563-5. PubMed ID: 7883163
    [Abstract] [Full Text] [Related]

  • 45. [Arginase deficiency].
    Uchino T, Matsuda I.
    Ryoikibetsu Shokogun Shirizu; 1998 Nov; (18 Pt 1):182-4. PubMed ID: 9590022
    [No Abstract] [Full Text] [Related]

  • 46. An approach to the diagnosis of metabolic diseases.
    Barness LA.
    Fetal Pediatr Pathol; 2004 Jan; 23(1):3-10. PubMed ID: 15371119
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  • 48. Letter: Phenotypic variation in alpha-L-iduronidase deficiency.
    Leisti J, Rimoin DL, Kaback MM, Hollister DW, DEn Tandt W, Neufeld E, Matalon R, Philippart M.
    Lancet; 1975 Jun 14; 1(7920):1344. PubMed ID: 49545
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  • 51. The biochemical diagnosis of lysosomal storage diseases--a review of five years experience.
    Wallace IJ, McCusker CA, McCormick D.
    Ir J Med Sci; 1990 Jul 14; 159(7):203-9. PubMed ID: 2283277
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  • 52. [Protocol of metabolic investigations in hereditary metabolic diseases].
    Poggi F, Rabier D, Vassault A, Charpentier C, Kamoun P, Saudubray JM.
    Arch Pediatr; 1994 Jul 14; 1(7):667-73. PubMed ID: 7987467
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  • 54. Deficiency of beta-galactosidase and alpha-mannosidase--primary enzyme defects in gargoylism and a new generalized disease?
    Ockerman PA.
    Acta Paediatr Scand; 1967 Jul 14; ():Suppl 177:35-6. PubMed ID: 4967547
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  • 56. [Mucopolysaccharidoses. V. Lysosomal pathology and mucopolysaccharidosis].
    Tettamanti G.
    Minerva Pediatr; 1972 Oct 06; 24(34):1629-33. PubMed ID: 4264144
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