Prenatal counseling and diagnosis of Gaucher disease in Egypt: an 18-year experience

Beta-glucocerebrosidase gene mutation in a sample of Egyptian patients with Gaucher disease

Genotype phenotype relationship in gaucher's disease

Biochemical diagnosis of Wolman disease among patients with suspected lysosomal storage diseases

Skeletal involvement in pediatric patients with Gaucher disease and its response to enzyme replacement therapy

Bony and Dental Radiographic Features of Type I and Type III Gaucher Diseased Children

IN-SILICO STUDY OF CASSIA TORA LINN IN THE TREATMENT OF GAUCHER DISEASE: A SCIENTIFIC ETHNOMEDICAL STUDY

Characterization of 42 Egyptian Children with Lysosomal Storage Disorders

Cardiac Affection in Lysosomal Storage Disorders: Review Article

AUTOPHAGY; Recent Advances in Health and Disease