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| Online First |
TARGETED THERAPY IN THE TREATMENT OF NODULAR PRURIGO |
Abstract
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Natalia Shestakova, Daria Demina, Marina Leonova |
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| Vol 26, No 3 (2024) |
Applications of EMbedding and backscattered scanning electron microscopy for morphological and functional assessment of the thymus forcedly removed in children with congenital heart defects during the first weeks of life |
Abstract
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A. V. Shabaldin, R. A. Mukhamadiyarov, V. A. Koshelev, A. V. Vedernikova, Yu. I. Rovda, E. O. Grishacheva, I. K. Khalivopulo, N. N. Minyailova, A. A. Lyapin |
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| Vol 26, No 2 (2024) |
Experience of cytokine therapy in the treatment of recurrent cervical cancer |
Abstract
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E. A. Bykova, N. A. Falaleeva, S. A. Myalina, P. V. Shegai, L. Yu. Grivtsova |
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| Vol 24, No 6 (2022) |
A case of long-term tolerance after kidney transplantation |
Abstract
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A. A. Korzhenevsky, N. P. Korzhenevskaya |
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| Vol 23, No 1 (2021) |
Common variable immunodeficiency disorder: a clinical case |
Abstract
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E. A. Sobko, I. V. Demko, I. A. Soloveva, A. Yu. Kraposhina, N. V. Gordeeva, D. A. Anikin, N. S. Pronkina, O. P. Ischenko |
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| Vol 23, No 1 (2021) |
Сlinical case of focal alopecia in a child with atopy |
Abstract
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A. A. Barilo, S. V. Smirnova, I. M. Olyanina |
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| Vol 22, No 6 (2020) |
Successful long-term prophylaxis of hereditary pregnancy-associated angioedema with plasma-derived C1-inhibitor concentrate: a case report |
Abstract
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D. V. Demina, A. O. Makeeva, L. M. Kudelya, E. V. Novikova, V. A. Kozlov |
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| Vol 22, No 3 (2020) |
Significance of individual management plan for the patients with hereditary lymphangioedema during pregnancy and lactation, and in newborns |
Abstract
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E. N. Bobrikova, A. R. Denisova, T. S. Kotomina, S. A. Serdotetskova, D. S. Fomina |
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| Vol 22, No 3 (2020) |
Phenotypic manifestation of homozygous partial deletion of the chromosome 1 segment spanning CFHR3 region |
Abstract
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I. A. Tuzankina, M. A. Bolkov, N. S. Zhuravleva, Yu. O. Vaseneva, Kh. Shinvari, O. V. Schipacheva |
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| Vol 22, No 2 (2020) |
Eosinophilic granulomatosis with polyangiitis in comorbidpatient: is the immunological diagnostics always unambiguous |
Abstract
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V. N. Marchenko, E. A. Bruchkus, A. A. Lebedeva, D. A. Davydov, N. L. Shaporova, O. V. Dudina, O. A. Smul’skaya, M. K. Zinakova |
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| Vol 22, No 2 (2020) |
Clinical case of primary immunodeficiency: X-linked agammaglobulinemia |
Abstract
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E. V. Kuvschinova, L. M. Kurtasova, A. G. Borisov, A. R. Schmidt, T. A. Gerasimova |
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| Vol 19, No 1 (2017) |
FAMILIAL CASE OF CHROMOSOME 22q11.2 DELETION SYNDROME |
Abstract
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I. A. Tuzankina, S. S. Deryabina, E. V. Vlasova, M. A. Bolkov |
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| Vol 16, No 1 (2014) |
DIAGNOSTIC VALUE OF IMMUNOLOGICAL EXAMINATION IN SPECIFYING A ROLE OF HERPESVIRUS INFECTION IN DEVELOPMENT OF HEMORRHAGIC VASCULITIS WITH RENAL IMPAIRMENT |
Abstract
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R. A. Belovolova, L. V. Mavrina, G. M. Letifov, L. F. Ovsyannikova, N. V. Selutin, M. Yu. Ovsyannikova |
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