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Publications by Cecilia K. Björkvall
Polyneuropathy in Gaucher Disease Type 1 and 3 – A Descriptive Case Series
Scientific Reports
Multidisciplinary
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Multiple Glycosidase Deficiencies in a Case of Juvenile (Type 3) Gaucher Disease.
Proceedings of the National Academy of Sciences of the United States of America
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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
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Case Report Serious Pulmonary Infection in a Splenectomized Patient With Adult Type 1 Gaucher Disease
Genetics and Molecular Research
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Endocrine and Metabolic Disorders in Patients With Gaucher Disease Type 1: A Review
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Glucocerebrosidase 2 Gene Deletion Rescues Type 1 Gaucher Disease
Proceedings of the National Academy of Sciences of the United States of America
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Abnormal Saccadic Eye Movements and Esotropia in a Patient With Type 3 Gaucher Syndrome: Case Report
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Management of Neutralizing Antibody to Ceredase in a Patient With Type 3 Gaucher Disease
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Elevated Levels of M-Csf, sCD14 and IL8 in Type 1 Gaucher Disease
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Long-Term Follow Up and Sudden Unexpected Death in Gaucher Disease Type 3 in Egypt
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