4.6 Article

A 4-year study of the efficacy and tolerability of enzyme replacement therapy with agalsidase alfa in 36 women with Fabry disease

Related references

Note: Only part of the references are listed.
Article Pediatrics

Cardiac manifestations of Anderson-Fabry disease in children and adolescents

Christoph Kampmann et al.

ACTA PAEDIATRICA (2008)

Article Cardiac & Cardiovascular Systems

Onset and progression of the Anderson-Fabry disease related cardiomyopathy

Christoph Kampmann et al.

INTERNATIONAL JOURNAL OF CARDIOLOGY (2008)

Article Endocrinology & Metabolism

Females with Fabry disease frequently have major organ involvement: Lessons from the Fabry Registry

William R. Wilcox et al.

MOLECULAR GENETICS AND METABOLISM (2008)

Article Pediatrics

Characterization of Fabry Disease in 352 Pediatric Patients in the Fabry Registry

Robert J. Hopkin et al.

PEDIATRIC RESEARCH (2008)

Article Urology & Nephrology

Weekly enzyme replacement therapy may slow decline of renal function in patients with Fabry disease who are on long-term biweekly dosing

Raphael Schiffmann et al.

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2007)

Article Urology & Nephrology

Sustained, long-term renal stabilization after 54 months of agalsidase β therapy in patients with Fabry disease

Dominique P. Germain et al.

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2007)

Article Endocrinology & Metabolism

Fabry disease: Baseline medical characteristics of a cohort of 1765 males and females in the Fabry Registry

C. M. Eng et al.

JOURNAL OF INHERITED METABOLIC DISEASE (2007)

Article Endocrinology & Metabolism

The Dutch Fabry cohort:: Diversity of clinical manifestations and Gb3 levels

A. C. Vedder et al.

JOURNAL OF INHERITED METABOLIC DISEASE (2007)

Article Medicine, General & Internal

Agalsidase-beta therapy for advanced Fabry disease - A randomized trial

Maryam Banikazemi et al.

ANNALS OF INTERNAL MEDICINE (2007)

Article Pharmacology & Pharmacy

Stroke and brain structural alterations in Fabry disease

Andreas Fellgiebel

CLINICAL THERAPEUTICS (2007)

Article Genetics & Heredity

High incidence of later-onset Fabry disease revealed by newborn screening

Marco Spada et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2006)

Article Genetics & Heredity

Natural history of Fabry disease in females in the Fabry outcome survey

PB Deegan et al.

JOURNAL OF MEDICAL GENETICS (2006)

Article Pediatrics

Pediatric Fabry disease

M Ries et al.

PEDIATRICS (2005)

Article Medicine, General & Internal

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

A Mehta et al.

EUROPEAN JOURNAL OF CLINICAL INVESTIGATION (2004)

Article Medicine, General & Internal

Fabry disease: overall effects of agalsidase alfa treatment

M Beck et al.

EUROPEAN JOURNAL OF CLINICAL INVESTIGATION (2004)

Article Genetics & Heredity

Clinical presentation in female patients with Fabry disease

N Guffon

JOURNAL OF MEDICAL GENETICS (2003)

Article Medicine, General & Internal

Functional class in patients with heart failure is associated with the development of diabetes

A Tenenbaum et al.

AMERICAN JOURNAL OF MEDICINE (2003)

Article Endocrinology & Metabolism

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)

Article Medicine, General & Internal

Nondiabetic kidney disease

AS Levey

NEW ENGLAND JOURNAL OF MEDICINE (2002)

Article Cardiac & Cardiovascular Systems

Cardiac manifestations of Anderson-Fabry disease in heterozygous females

C Kampmann et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2002)

Review Cardiac & Cardiovascular Systems

The heart in Anderson Fabry disease

C Kampmann et al.

ZEITSCHRIFT FUR KARDIOLOGIE (2002)

Article Health Care Sciences & Services

Quality of life of patients with Fabry disease

KF Gold et al.

QUALITY OF LIFE RESEARCH (2002)

Article Health Care Sciences & Services

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)

Article Endocrinology & Metabolism

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 Pharmacology & Pharmacy

Neuropathic pain in Anderson-Fabry disease: pathology and therapeutic options

J MacDermot et al.

EUROPEAN JOURNAL OF PHARMACOLOGY (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)