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Fabry disease
Sphingolipid Metabolism Diseases ⁎ Thomas Kolter, Konrad Sandhoff
Management of Patients with Cardiac Manifestations
Correction of the Enzymic Defect in Cultured Fibroblasts from Patients with Fabry's Disease: Treatment with Purified A-Galactosidase from Ficin
Short PR Intervals and Tachyarrhythmias in Fabry's Disease
The Clinical Landscape for AAV Gene Therapies
Enzyme Defects in the Sphingolipidoses and Their Application to Diagnosis*
Testing Options for Fabry Disease
Low Frequency of Fabry Disease in Patients with Common Heart Disease
Fabry Disease: Developing Drugs for Treatment Guidance for Industry
The Challenge of Diagnosis and Indication for Treatment in Fabry
Fabry Disease: Molecular Basis, Pathophysiology, Diagnostics and Potential Therapeutic Directions
Newborn Screening Act Sheet Fabry Disease
Study of Indications for Cardiac Device Implantation and Utilisation in Fabry
Anderson-Fabry Disease: a Cardiomyopathy That Can Be Cured
Cardiomyopathy Associated with the Ala143thr Variant of the Α
A Surgical Case of Mitral Valve Replacement for a Patient with Fabry Disease Complicated with Hemodialysis
Fabry Disease Community Landscape
Expanded Carrier Screening
Top View
Fabry Disease and the Heart: a Comprehensive Review
X02010;Galactosidase a Mutations in Fabry Disease
38 Disorders of Sphingolipid Metabolism
X Chromosome Inactivation in Carriers of Fabry Disease: Review and Meta-Analysis
Anderson-Fabry Disease
Gastrointestinal Involvement in Anderson-Fabry Disease: a Narrative Review
Inherited Neuromuscular Disorders: Which Role Forserum Biomarkers?
Fabry Disease Screening in High-Risk Populations in Japan
Fabry Disease
The Efficacy of Gene Therapy to Treat Fabry Disease
Predictors of Fabry Disease in Patients with Hypertrophic Cardiomyopathy
Non-Homologous Recombination Between Alu and LINE-1 Repeats Caused a 430-Kb Deletion in the Dystrophin Gene: a Novel Source of Genomic Instability
Fabry Disease Test Information Sheet
Rare Disease Registries in Europe - June 2020 2
Fabry Cardiomyopathy: Current Treatment and Future Options
Fabry Disease Under Enzyme Replacement Therapy
Fabry Cardiomyopathy: Current Practice and Future Directions
Sphingolipidoses
A Guide for Women Living with Fabry Disease
Cardiac Challenges in Patients with Fabry Disease
Annotation: Fabry's Disease: the Search for a Regulator Gene Mutation in Man
Disease Gene Mapping in Isolated Human Populations: the Example of Finland
Fabry Disease: a Mimic for Obstructive Hypertrophic Cardiomyopathy? S R Ommen, R a Nishimura, W D Edwards
Dosage Compensation in Females with X-Linked Metabolic Disorders
Invitae Carrier Screening (Continued)
4D Molecular Therapeutics Announces First Patient Dosed in Phase 1/2 Clinical Trial of 4D-310 for the Treatment of Fabry Disease
PGT-M Disease List
Gene Therapy for Inherited Muscle Diseases: Where Genetics Meets Rehabilitation Medicine
Oreana Panel
Fabry Disease