Belaya, Zhanna E., Endocrinology Research Centre, Russian Federation
| Issue | Section | Title | Abstract | File |
| Vol 22, No 1 (2019) | Case report | Clinical application experience of asfotase alfa for a young patient with childhood hypophosphatasia | Abstract |
 (Rus) |
| Vol 22, No 1 (2019) | Original study | Evaluation of diagnostic potential of the collagen osteogenesis marker (P1NP) compared with osteocalcin in Cushing’s disease | Abstract |
(Rus) |
| Vol 22, No 2 (2019) | Case report | First description of a type v osteogenesis imperfecta clinical case with severe skeletal deformities caused by a mutation p.119C> T in IFITM5 gene in Russia | Abstract |
(Rus) |