Fabry disease: recent advances in pathology, diagnosis, treatment and monitoring
about
Prediction of the responsiveness to pharmacological chaperones: lysosomal human alpha-galactosidase, a case of studyHypertrophic cardiomyopathy and sudden cardiac deathPersistent increase in cardiac troponin I in Fabry disease: a case report.Multi-system disorders of glycosphingolipid and ganglioside metabolismEndomyocardial biopsies in patients with left ventricular hypertrophy and a common Chinese later-onset Fabry mutation (IVS4 + 919G > A).Heart failure in a woman with SLE, anti-phospholipid syndrome and Fabry's diseaseGenetic screening of Fabry patients with EcoTILLING and HRM technology.Update on role of agalsidase alfa in management of Fabry disease.The Large Phenotypic Spectrum of Fabry Disease Requires Graduated Diagnosis and Personalized Therapy: A Meta-Analysis Can Help to Differentiate Missense MutationsDescriptive epidemiology of Fabry disease among beneficiaries of the Specified Disease Treatment Research Program in Japan.Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it allClinical observation of patients with Fabry disease after switching from agalsidase beta (Fabrazyme) to agalsidase alfa (Replagal).NKT cell ligand recognition logic: molecular basis for a synaptic duet and transmission of inflammatory effectors.Animal models for metabolic, neuromuscular and ophthalmological rare diseases.When rare illuminates common: how cardiocutaneous syndromes transformed our perspective on arrhythmogenic cardiomyopathy.Electrochemical characterization of globotriose-containing self-assembled monolayers on nanoporous gold and their binding of soybean agglutininEnzyme replacement therapy in a patient with Fabry disease and the development of IgE antibodies against agalsidase beta but not agalsidase alpha.Fabry disease and incidence of cancerMolecular damage in Fabry disease: characterization and prediction of alpha-galactosidase A pathological mutations.Enzyme replacement therapy in a patient of heterozygous Fabry disease: clinical and pathological evaluations by repeat kidney biopsy and a successful pregnancy.
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P2860
Fabry disease: recent advances in pathology, diagnosis, treatment and monitoring
description
2009 nî lūn-bûn
@nan
2009 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
name
Fabry disease: recent advances in pathology, diagnosis, treatment and monitoring
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Fabry disease: recent advances in pathology, diagnosis, treatment and monitoring
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Fabry disease: recent advances in pathology, diagnosis, treatment and monitoring
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Fabry disease: recent advances in pathology, diagnosis, treatment and monitoring
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Fabry disease: recent advances in pathology, diagnosis, treatment and monitoring
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Fabry disease: recent advances in pathology, diagnosis, treatment and monitoring
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Fabry disease: recent advances in pathology, diagnosis, treatment and monitoring
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Fabry disease: recent advances in pathology, diagnosis, treatment and monitoring
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Fabry disease: recent advances in pathology, diagnosis, treatment and monitoring
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Fabry disease: recent advances in pathology, diagnosis, treatment and monitoring
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Fabry disease: recent advances in pathology, diagnosis, treatment and monitoring
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Fabry disease: recent advances in pathology, diagnosis, treatment and monitoring
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Fabry disease: recent advances in pathology, diagnosis, treatment and monitoring
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Björn Hoffmann
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10.1186/1750-1172-4-21
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P5008
P577
2009-10-11T00:00:00Z
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P6179
1030194226