Enfermedad de Fabry: reconocimiento en la edad pediátrica
- 1 January 2002
- journal article
- Published by Elsevier in Anales de Pediatría
- Vol. 57 (1) , 45-50
- https://doi.org/10.1016/s1695-4033(02)77891-0
Abstract
No abstract availableThis publication has 41 references indexed in Scilit:
- Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous malesJournal of Medical Genetics, 2001
- Lower limb cold exposure induces pain and prolonged small fiber dysfunction in Fabry patientsPain, 2000
- The frequency of lysosomal storage diseases in The NetherlandsHuman Genetics, 1999
- Prevalence of Lysosomal Storage DisordersJAMA, 1999
- Painful Fingers, Heat Intolerance, and Telangiectases of the Ear: Easily Ignored Childhood Signs of Fabry DiseasePediatric Dermatology, 1995
- The arthropathy of fabry diseaseArthritis & Rheumatism, 1979
- Ophthalmologic Aspects of Lipid Storage DiseasesOphthalmology, 1978
- Enzymatic Defect in Fabry's DiseaseNew England Journal of Medicine, 1967
- Ein Beitrag zur Kenntniss der Purpura haemorrhagica nodularis (Purpura papulosa haemorrhagica Hebrae)Archives of Dermatological Research, 1898
- A CASE OF “ANGEIO-KERATOMA.”British Journal of Dermatology, 1898