Special issue on Fabry disease - book 1: editorial

Derralynn Hughes , Guillem Pintos-Morell

Rare Disease and Orphan Drugs Journal ›› 2024, Vol. 3 ›› Issue (4) : 29

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Rare Disease and Orphan Drugs Journal ›› 2024, Vol. 3 ›› Issue (4) :29 DOI: 10.20517/rdodj.2024.30
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Special issue on Fabry disease - book 1: editorial

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Derralynn Hughes, Guillem Pintos-Morell. Special issue on Fabry disease - book 1: editorial. Rare Disease and Orphan Drugs Journal, 2024, 3(4): 29 DOI:10.20517/rdodj.2024.30

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References

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Anderson W.A case of “ANGEIO-KERATOMA”.Br J Dermatol1898;10:113-7

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Fabry J.Ein Beitrag zur Kenntniss der Purpura haemorrhagica nodularis (Purpura papulosa haemorrhagica Hebrae) Arch Dermatol Syph 1898;43:187-200.

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de Duve C. Tissue fraction-past and present.J Cell Biol1971;50:20.

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Brady RO,Bradley RM,Warshaw AL.Enzymatic defect in Fabry's disease. Ceramidetrihexosidase deficiency.N Engl J Med1967;276:1163-7

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Desnick RJ,Barranger J.Fabry disease, an under-recognized multisystemic disorder: expert recommendations for diagnosis, management, and enzyme replacement therapy.Ann Intern Med2003;138:338-46

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Schiffmann R.Investigating Fabry disease - some lessons learned.Rare Dis Orphan Drugs J2024;3:4

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Feriozzi S.The inflammatory pathogenetic pathways of Fabry nephropathy.Rare Dis Orphan Drugs J2024;3:11

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Aguiar P.Biomarkers in anderson-Fabry disease: what should we use in the clinical practice?.Rare Dis Orphan Drugs J2024;3:13

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West ML,Bichet DG.Fabry nephropathy: a treatable cause of chronic kidney disease.Rare Dis Orphan Drugs J2024;3:22

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Politei JM.Gastrointestinal involvement in Fabry disease.Rare Dis Orphan Drugs J2024;3:10

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Moreno-Martínez D,Reisin R.Cerebrovascular disorders and Fabry disease.Rare Dis Orphan Drugs J2024;3:9

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