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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

284 related items for PubMed ID: 4882505

  • 21.
    ; . PubMed ID:
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  • 22. [A case of porphyria variegata. Severe neurologic syndrome following surgery. 2 normal pregnancies and labors].
    Gajdos A, Gajdos-Torok M, Guillard A, Nouailhat F.
    Presse Med (1893); 1969 Mar 29; 77(16):589-90. PubMed ID: 5783381
    [No Abstract] [Full Text] [Related]

  • 23. Clinical use of porphyrin ester cromatography of urine and feces.
    With TK.
    Dan Med Bull; 1975 Feb 29; 22(2):74-80. PubMed ID: 1132256
    [No Abstract] [Full Text] [Related]

  • 24. Hereditary hepatic prophyrias. Gene penetration, drug sensitivity and subdivision in the light of systematic family studies.
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    Acta Med Scand; 1969 Feb 29; 186(1-2):117-24. PubMed ID: 5807639
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  • 28. [Porphyria diagnosis in urine with special reference to simple search tests].
    Köstler E, Bergmann P, Haubold E.
    Z Arztl Fortbild (Jena); 1985 Feb 29; 79(18):787-9. PubMed ID: 4072285
    [No Abstract] [Full Text] [Related]

  • 29. [Modification of perpyrin metabolism by griseofulvin. II. Clinical and experimental studies].
    Schlenzka K, Tannous J.
    Dermatol Monatsschr; 1971 Feb 29; 157(2):88-98. PubMed ID: 5557964
    [No Abstract] [Full Text] [Related]

  • 30.
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  • 31. The first Swedish case of congenital erythropoietic porphyria, with a revised view of the porphyrin excretion pattern in this disease.
    Stenberg B, With TK.
    Acta Derm Venereol Suppl (Stockh); 1982 Feb 29; 100():87-90. PubMed ID: 6962640
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  • 32.
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  • 34. [Hereditary coproporphyria in 2 Dutch families].
    te Velde K, Noordhoek KH.
    Ned Tijdschr Geneeskd; 1984 May 12; 128(19):892-5. PubMed ID: 6728057
    [No Abstract] [Full Text] [Related]

  • 35. The diagnostic importance of faecal porphyrins in the differentiation of the porphyrias. 3. South African genetic porphyria (variegcte porphyria)--the acute attack.
    Eales L, Dowdle EB, Levey MJ, Sweeney GD.
    S Afr Med J; 1966 May 07; 40(17):380-2. PubMed ID: 5943748
    [No Abstract] [Full Text] [Related]

  • 36. Hepatic delta-aminolaevulinic acid synthetase in an attack of hereditary coproporphyria and during remission.
    McIntyre N, Pearson AJ, Allan DJ, Craske S, West GM, Moore MR, Beattie AD, Paxton J, Goldberg A.
    Lancet; 1971 Mar 20; 1(7699):560-4. PubMed ID: 4100900
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  • 40. Porphyrin distribution and porphyrin excretion in human congenital erythropoietic porphyria.
    Eriksen L, Eriksen N.
    Scand J Clin Lab Invest; 1974 Jun 20; 33(4):323-32. PubMed ID: 4853698
    [No Abstract] [Full Text] [Related]

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