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| Issue |
Title |
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| No 2 (2026) |
Differential Diagnosis of Nonclassic CAH and PCOS Based on Urinary Steroid Profiling by Gas Chromatography–Mass Spectrometry |
Abstract
PDF (Rus)
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M. I. Yarmolinskaya, O. B. Glavnova, N. S. Osinovskaya, N. V. Vorokhobina, L. I. Velikanova, K. D. Musevich |
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| No 2 (2026) |
Savelyeva LV. Isolated hypogonadotropic hypogonadism caused by a mutation in the WDR11 gene: a clinical case report |
Abstract
PDF (Rus)
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D. V. Ivanova, A. N. Zvyagintseva, E. V. Morozova, S. I. Motkova, L. V. Savelyeva |
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| No 1 (2026) |
Gestational diabetes mellitus in the mother and congenital hyperinsulinism in the proband, caused by an ABCC8 gene mutation |
Abstract
PDF (Rus)
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M. A. Plehanova, F. F. Burumkulova |
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| No 1 (2026) |
Correction of male hypogonadism caused by anabolic steroid use |
Abstract
PDF (Rus)
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K. E. Gaidaichuk, R. V. Rozhivanov, E. R. Rozhivanova, E. N. Andreeva, G. A. Mel’nichenko, N. G. Mokrysheva |
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| No 3 (2025) |
Clinical case of disorder of sex development, 46 XY, SRY+ |
Abstract
PDF (Rus)
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V. D. Ankina, E. V. Morozova, A. F. Vesnina, L. V. Savel’eva |
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| No 3 (2025) |
A case of delayed diagnosis of Bardet-Biedl syndrome |
Abstract
PDF (Rus)
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R. M. Guseinova, M. G. Rafaelyan, A. A. Averkina, E. D. Flitman, D. A. Kopytina, O. V. Vasyukova, I. R. Minniakhmetov, R. I. Khusainova |
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