Evidence-Based Management of Patients with Fabry Disease | National Kidney Foundation
Patterns
Reduced α-galactosidase A activity in zebrafish (Danio rerio) mirrors distinct features of Fabry nephropathy phenotype - ScienceDirect
Fabry disease | Orphanet Journal of Rare Diseases | Full Text
Chapter 10 – Metabolic and Storage Disease | Thoracic Key
IJMS | Free Full-Text | α-Galactosidase a Deficiency in Fabry Disease Leads to Extensive Dysregulated Cellular Signaling Pathways in Human Podocytes
Fibrosis: a key feature of Fabry disease with potential therapeutic implications | Orphanet Journal of Rare Diseases | Full Text
GLA-mutant kidney organoids recapitulated human renal Fabry disease. a... | Download Scientific Diagram
Fabry Disease Associated With Antiglomerular Basement Membrane Disease: Chance or Consequence - Kidney International Reports
Final Diagnosis -- Case 662
Human kidney organoids reveal the role of glutathione in Fabry disease | Experimental & Molecular Medicine
Fabry Disease that Phenocopies Hypertrophic Cardiomyopathy: a thorough Genetic 'Detective' Identifies the 'Rogue' Hidden in the GLA Gene
Periodic Acid-Schiff (PAS) Staining
Screening for Fabry Disease in patients with unexplained left ventricular hypertrophy | PLOS ONE
Lysosomal storage disease - Wikipedia
Evolution of cardiac pathology in classic Fabry disease: Progressive cardiomyocyte enlargement leads to increased cell death and fibrosis, and correlates with severity of ventricular hypertrophy - ScienceDirect
Evidence-Based Management of Patients with Fabry Disease | National Kidney Foundation
Pregnancy Outcome after Exposure to Migalastat for Fabry Disease: A Clinical Report
Histologic and electron microscopy findings in myocardium of treated Fabry disease - ScienceDirect
Anderson-Fabry Disease and Other Lysosomal Storage Disorders | Circulation
Pathology Outlines - PAS (Periodic acid-Schiff)
Periodic acid Schiff (PAS) staining. Periodic acid Schiff (PAS) stained... | Download Scientific Diagram
Expert opinion on the recognition, diagnosis and management of children and adults with Fabry disease: a multidisciplinary Turkey perspective | Orphanet Journal of Rare Diseases | Full Text
Fabry disease associated with multiple myeloma: a case report | CEN Case Reports
Glomerular podocyte vacuolar degeneration (PAS stain, ×400). PAS,... | Download Scientific Diagram
JCM | Free Full-Text | Downregulation of Mannose-6-Phosphate Receptors in Fabry Disease Cardiomyopathy: A Potential Target for Enzyme Therapy Enhancement
