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PUBMED FOR HANDHELDS

Journal Abstract Search


176 related items for PubMed ID: 5687137

  • 1. [A case of neurovisceral gangliosidosis].
    Hooghwinkel GJ, Bots GT.
    Ned Tijdschr Geneeskd; 1968 Oct 26; 112(43):1952-8. PubMed ID: 5687137
    [No Abstract] [Full Text] [Related]

  • 2. A case of GM2-gangliosidosis with total hexosaminidase deficiency.
    Suzuki Y, Jacob JC, Suzuki K, Suzuki K.
    Neurology; 1970 Apr 26; 20(4):388. PubMed ID: 5535009
    [No Abstract] [Full Text] [Related]

  • 3. [GM1- and GM2-gangliosidosis. First cases in Finland].
    Palo J, Haltia M, Amnell G.
    Duodecim; 1975 Apr 26; 91(6):354-61. PubMed ID: 1140115
    [No Abstract] [Full Text] [Related]

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  • 5. [A new form of neurovisceral thesaurismosis with abnormality of ganglioside distribution].
    Allegranza A, Grisoni R, Tettamanti G, Cescon I, Bruno S.
    Acta Neurol (Napoli); 1970 Apr 26; 25(2):197-205. PubMed ID: 5422846
    [No Abstract] [Full Text] [Related]

  • 6. [Early diagnosis and place in the body of lipidosis, of the generalized Norman-Landing, GM1, type, gangliosidosis].
    Seringe P, Plainfosse B, Lautmann F, Lorilloux J, Calamy G, Berry JP, Watchi JM.
    Bull Mem Soc Med Hop Paris; 1968 Apr 26; 119(2):179-96. PubMed ID: 5670366
    [No Abstract] [Full Text] [Related]

  • 7. Infantile GM1 gangliosidosis. Histochemical, ultrastructural and biochemical studies.
    Severi F, Magrini U, Tettamanti G, Bianchi E, Lanzi G.
    Helv Paediatr Acta; 1971 Jun 26; 26(2):192-209. PubMed ID: 4257921
    [No Abstract] [Full Text] [Related]

  • 8. [Cutaneous manifestations during a generalized, landing type of gangliosidosis with GM 1].
    Vissian L, Manassero J, Vaillaud JC, Kermarec J, Duplay H.
    Bull Soc Fr Dermatol Syphiligr; 1969 Jun 26; 76(4):631-3. PubMed ID: 5368316
    [No Abstract] [Full Text] [Related]

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  • 10. Studies on neuronal lipid dystrophies.
    Seitelberger F, Sluga E, Bernhelmer H.
    Pathol Eur; 1968 Jun 26; 3(2):230-47. PubMed ID: 5688460
    [No Abstract] [Full Text] [Related]

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  • 15. Leukocyte beta-galactosidase activity in the diagnosis of generalized GM 1 gangliosidosis.
    Singer HS, Nankervis GA, Schafer IA.
    Pediatrics; 1972 Mar 26; 49(3):352-61. PubMed ID: 4258708
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  • 18. Clinical neuropathological conference.
    Dis Nerv Syst; 1967 Dec 26; 28(12):828-35. PubMed ID: 6074336
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  • 20. [GM2 gangliosidosis with total beta-N-acetyl-hexosaminidase deficit or Sandhoff's disease].
    Juif JG, Luckel JC, Nussbaum JL, Stoebner R, Kapps R.
    Arch Fr Pediatr; 1973 Jan 26; 30(1):29-43. PubMed ID: 4721586
    [No Abstract] [Full Text] [Related]


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