P. G. Sido

Outcome of enzyme replacement therapy in patients with Gaucher disease type I. The Romanian experience

C. Coldéa, C. Drugan, A. Zimmermann, 2007, Journal of Inherited Metabolic Disease.

Early clinical signs in lysosomal diseases

C. Lazea, Ioana Nașcu, Simona Bucerzan, 2021, Medicine and pharmacy reports.

BRIEF REPORT 21-Hydroxylase and 11-Hydroxylase Mutations in Romanian Patients with Classic Congenital Adrenal Hyperplasia

S. Clausmeyer, U. Heinrich, E. Schulze, 2005 .

CRANIO-FACIAL DYSMORPHISM AND DEVELOPMENTAL DELAY IN ROMANIAN CHILDREN WITH TRISOMY 21

C. Davila, E. Ciofu, C. Al-Khzouz, 2013 .

Bone mineral density and bone turnover in Romanian children and young adults with classical 21‐hydroxylase deficiency are influenced by glucocorticoid replacement therapy

C. Coldéa, C. Lazea, A. Zimmermann, 2009, Clinical endocrinology.