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 PDF
(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 PDF
(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 PDF
(Rus)

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