4.6 Review

Effects of enzyme replacement therapy in Fabry disease-A comprehensive review of the medical literature

Related references

Note: Only part of the references are listed.
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Fabry disease: Baseline medical characteristics of a cohort of 1765 males and females in the Fabry Registry

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Improvement of sympathetic skin responses under enzyme replacement therapy in Fabry disease

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White matter lesions in Fabry disease before and after enzyme replacement therapy - A 2-year follow-up

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Improvement in serial cardiopulmonary exercise testing following enzyme replacement therapy in Fabry disease

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Impact of enzyme replacement therapy on cardiac morphology and function and late enhancement in Fabry's cardiomyopathy

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Clinical benefit of enzyme replacement therapy in Fabry disease

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The effect of 12-month enzyme replacement therapy on myocardial perfusion in patients with Fabry disease

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Enzyme replacement therapy in Japanese Fabry disease patients: The results of a phase 2 bridging study

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Is globotriaosylceramide a useful biomarker in Fabry disease?

E Young et al.

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Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome Survey

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Long-term safety and efficacy of enzyme replacement therapy for Fabry disease

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Enzyme therapy for Fabry disease: Neutralizing antibodies toward agalsidase alpha and beta

GE Linthorst et al.

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CNS involvement in Fabry disease: Clinical and imaging studies before and after 12 months of enzyme replacement therapy

L Jardim et al.

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Relief of gastrointestinal symptoms under enzyme replacement therafpy in patients with Fabry disease

F Dehout et al.

JOURNAL OF INHERITED METABOLIC DISEASE (2004)

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Hearing loss in Fabry disease: The effect of agalsidase alfa replacement therapy

D Hajioff et al.

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Enzyme replacement therapy in heterozygous females with Fabry disease: Results of a phase IIIB study

F Baehner et al.

JOURNAL OF INHERITED METABOLIC DISEASE (2003)

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Quality of life of patients with Fabry disease

KF Gold et al.

QUALITY OF LIFE RESEARCH (2002)

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Patients with Fabry disease on dialysis in the United States

R Thadhani et al.

KIDNEY INTERNATIONAL (2002)

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Assessment of health-related quality-of-life in males with Anderson Fabry Disease before therapeutic intervention

AH Miners et al.

QUALITY OF LIFE RESEARCH (2002)

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Anderson-Fabry disease:: Clinical manifestations of disease in female heterozygotes

C Whybra et al.

JOURNAL OF INHERITED METABOLIC DISEASE (2001)

Article Genetics & Heredity

Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males

KD MacDermot et al.

JOURNAL OF MEDICAL GENETICS (2001)

Article Medicine, General & Internal

Safety and efficacy of recombinant human α-galactosidase a replacement therapy in Fabry's disease.

CM Eng et al.

NEW ENGLAND JOURNAL OF MEDICINE (2001)

Article Medicine, General & Internal

Enzyme replacement therapy in Fabry disease - A randomized controlled trial

R Schiffmann et al.

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2001)

Article Multidisciplinary Sciences

Infusion of α-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease

R Schiffmann et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)