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Publications by Catherine Groden

The Clinical Management of Type 2 Gaucher Disease

Molecular Genetics and Metabolism

Molecular Biology

English

Related publications

Glucocerebrosidase 2 Gene Deletion Rescues Type 1 Gaucher Disease

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

Neonatal Cholestasis as Initial Manifestation of Type 2 Gaucher Disease: A Continuum in the Spectrum of Early Onset Gaucher Disease

Internal Medicine

Molecular Biology

English

High Incidence of Cholesterol Gallstone Disease in Type 1 Gaucher Disease: Characterizing the Biliary Phenotype of Type 1 Gaucher Disease

Journal of Inherited Metabolic Disease

English

Glucosylsphingosine Accumulation in Type 2 Gaucher Disease Begins Early in Gestation

Pediatric Research

English

Management of Neutralizing Antibody to Ceredase in a Patient With Type 3 Gaucher Disease

English

Long-Term Clinical Outcomes in Type 1 Gaucher Disease Following 10 Years of Imiglucerase Treatment

Journal of Inherited Metabolic Disease

English

Gaucher Disease Type I Complicated With Parkinson's Syndrome

English

Impact of Imiglucerase Supply Constraint on the Therapeutic Management and Course of Disease in French Patients With Gaucher Disease Type 1

Orphanet Journal of Rare Diseases

English

Psy51 - Clinical and Economic Aspects of Enzyme Replacement Therapy in Russian Patients With Gaucher Disease Type 1

Value in Health

Occupational Health

English