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Publications by Jay A Barth
Reduction of Podocyte Globotriaosylceramide Content in Adult Male Patients With Fabry Disease With Amenable GLA Mutations Following 6 Months of Migalastat Treatment
Journal of Medical Genetics
Genetics
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Progressive Podocyte Injury and Globotriaosylceramide (GL-3) Accumulation in Young Patients With Fabry Disease
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Mosaicism of Podocyte Involvement Is Related to Podocyte Injury in Females With Fabry Disease
Molecular Genetics and Metabolism
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Mutations of the GLA Gene in Young Patients With Stroke
Stroke
Cardiology
Neurology
Cardiovascular Medicine
Advanced
Medicine
Neuroscience
Specialized Nursing
A Classical Phenotype of Anderson-Fabry Disease in a Female Patient With Intronic Mutations of the GLA Gene: A Case Report
BMC Cardiovascular Disorders
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Strong Increase of Leukocyte Apha‐galactosidase a Activity in Two Male Patients With Fabry Disease Following Oral Chaperone Therapy
Molecular genetics & genomic medicine
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Prevalence of Fabry Disease and GLA C.196G>C Variant in Japanese Stroke Patients
Journal of Human Genetics
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Sustained, Long-Term Renal Stabilization After 54 Months of Agalsidase Beta Therapy in Patients With Fabry Disease
Journal of the American Society of Nephrology : JASN
Medicine
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Clinical Presentation in Female Patients With Fabry Disease
Journal of Medical Genetics
Genetics
Epidemiological and Clinical Profile of Patients With Fabry Disease
Revista de Enfermagem UFPE on line