Mulberries in the urine: a tell-tale sign of Fabry disease
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/article/10.1007/s10545-018-0155-6/fulltext.html
Reference3 articles.
1. Becker GJ, Nicholls K (2015) Lipiduria — with special relevance to Fabry disease. Clin Chem Lab Med 53:s1465–s1470
2. Dobrovolny R, Dvorakova L, Ledvinova J et al (2005) Relationship between X-inactivation and clinical involvement in Fabry heterozygotes. Eleven novel mutations in the alpha-galactosidase A gene in the Czech and Slovak population. J Mol Med 83:647–654
3. Selvarajah M, Nicholls K, Hewitson TD, Becker GJ (2011) Targeted urine microscopy in Anderson-Fabry disease: a cheap, sensitive and specific diagnostic technique. Nephrol Dial Transplant 26:3195–3202
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1. Fabry nephropathy: a treatable cause of chronic kidney disease;Rare Disease and Orphan Drugs Journal;2024-07-11
2. Mulberry body in a patient with Fabry disease;QJM: An International Journal of Medicine;2022-05-14
3. A morphological classification of the fat particles found in the urinary sediment of patients with Fabry disease;Clinical Chemistry and Laboratory Medicine (CCLM);2021-07-06
4. Fabry disease in two brothers with proteinuria: A case report and Fabry disease review;Clinical Nephrology;2020-06-01
5. Urinary Mulberry Cells as a Biomarker of the Efficacy of Enzyme Replacement Therapy for Fabry Disease;Internal Medicine;2020-04-01
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