Literature DB >> 5763858

Urinary glycolipids in Fabry's disease. Their examination in the detection of atypical variants and the pre-symptomatic state.

M Philippart, L Sarlieve, A Manacorda.   

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Year:  1969        PMID: 5763858

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


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  6 in total

1.  Angiokeratoma corporis diffusum (Anderson-Fabry disease) in a single large family in Nova Scotia.

Authors:  M W Spence; J T Clarke; D M D'Entremont; G A Sapp; E R Smith; A L Goldbloom; G Davar
Journal:  J Med Genet       Date:  1978-12       Impact factor: 6.318

2.  Kidney transplantation in Fabry's disease.

Authors:  F R Bühler; G Thiel; U C Dubach; F Enderlin; F Gloor; H Thölen
Journal:  Br Med J       Date:  1973-07-07

3.  Gut lesions in Fabry's disease without a rash.

Authors:  D M Flynn; B D Lake; C B Boothby; E P Young
Journal:  Arch Dis Child       Date:  1972-02       Impact factor: 3.791

4.  Increased glycosphingolipid excretion associated with proteinuria.

Authors:  R R Townsend; R M Orth; C M Clawson; S C Li; Y T Li
Journal:  J Clin Invest       Date:  1978-07       Impact factor: 14.808

5.  Urinary lysosomal hydrolases in mucolipidosis II and mucolipidosis III.

Authors:  B C Kress; A L Miller
Journal:  Biochem J       Date:  1979-02-01       Impact factor: 3.857

6.  Heterozygote detection in angiokeratoma corporis diffusum (Anderson-Fabry disease). Studies on plasma, leucocytes, and hair follicles.

Authors:  M W Spence; A L Goldbloom; J K Burgess; D D'entremont; B A Ripley; K L Weldon
Journal:  J Med Genet       Date:  1977-04       Impact factor: 6.318

  6 in total

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