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| Issue |
Title |
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| Vol 28, No 2 (2025) |
X-linked osteoporosis/osteogenesis imperfecta due to a PLS3 mutation: the first description in Russia |
Abstract
PDF (Rus)
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E. O. Mamedova, E. S. Senyshkina, S. A. Buryakina, E. V. Tarasova, K. V. Smirnov, R. R. Salakhov, R. I. Khusainova, Zh. E. Belaya |
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| Vol 27, No 4 (2024) |
Familial hypocalciuric hypercalciemia: clinical case report |
Abstract
PDF (Rus)
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A. S. Sudnitsyna, A. I. Lyapunova, L. A. Suplotova |
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| Vol 27, No 4 (2024) |
A case report of autosomal dominant hypophosphatemic rickets due to a mutation in the FGF23 gene in an adult: diagnostic difficulties |
Abstract
PDF (Rus)
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E. E. Sakhnova, E. G. Przhiyalkovskaya, E. O. Mamedova, I. S. Chugunov |
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| Vol 27, No 4 (2024) |
Hypophosphatasia diagnosis in adults: clinical case and literature review |
Abstract
PDF (Rus)
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S. T. Magerramova, Yu. V. Tyutyugina, Zh. E. Belaya |
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| Vol 27, No 4 (2024) |
A new heterozygous mutation in the CDKN1B gene in a patient affected by multiple endocrine neoplasia syndrome type 4 |
Abstract
PDF (Rus)
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A. S. Petrosyan, E. E. Bibik, R. H. Salimkhanov, E. V. Kovaleva, A. K. Eremkina, M. V. Utkina, E. A. Troshina, N. G. Mokrysheva |
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| Vol 26, No 2 (2023) |
Parathyroid carcinoma case-report in a patient with multinodular goiter and chronic kidney disease: difficulties in diagnosis and treatment (observation from practice) |
Abstract
PDF (Rus)
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A. A. Averkina, R. A. Zolotareva, I. V. Kim, E. V. Bondarenko, A. Yu. Abrosimov, M. V. Degtyarev, E. O. Mamedova, Zh. E. Belaya, L. Ya. Rozhinskaya |
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| Vol 26, No 2 (2023) |
The difficulties of diagnosing and determining the tactics of treating osteoporosis in severe spinal scoliosis case |
Abstract
PDF (Rus)
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T. T. Tsoriev, I. A. Skripnikova, O. V. Kosmatova, M. A. Kolchina |
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| Vol 26, No 2 (2023) |
Features of the clinical course of pachydermoperiostosis with a verified mutation in the European type gene |
Abstract
PDF (Rus)
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T. M. Frolova, O. O. Golounina, E. O. Mamedova, E. E. Litvinova, Zh. E. Belaya |
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