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| Issue |
Title |
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| Vol 6, No 1 (2025) |
Primary immunodeficiency: selective IgA deficiency |
Abstract
PDF (Rus)
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Ahmed M. Abakarov, Nataliya A. Shipilova |
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| Vol 6, No 1 (2025) |
Hemorrhagic vasculitis with an atypical onset of the disease: case report |
Abstract
PDF (Rus)
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Denis A. Burlyay, Aleksandr Yu. Babko, Emma S. Grigoryan, Anna S. Nechaeva |
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| Vol 6, No 1 (2025) |
Duchenne muscle dystrophy detected in the neonatal period: case report |
Abstract
PDF (Rus)
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|
Anastasiya V. Grigor’eva |
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| Vol 6, No 1 (2025) |
X-linked dominant hypophosphatemic rickets: case report |
Abstract
PDF (Rus)
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Emma S. Grigoryan, Anna S. Nechaeva, Aleksandr Yu. Babko, Denis A. Burlyay |
| |
| Vol 6, No 1 (2025) |
A clinical case of Rett syndrome: the experience of observing an older preschool child |
Abstract
PDF (Rus)
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Sof’ya A. Kovalenkova, Ekaterina A. Kovalenkova, Dmitriy S. Krutikov |
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| Vol 6, No 1 (2025) |
A case report of generalized yersiniosis in a teenager: a difficult path to diagnosis |
Abstract
PDF (Rus)
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Aleksey V. Kuzin, Alina E. Sergeeva |
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| Vol 6, No 1 (2025) |
Chromosome 22 deletion syndrome (Di George’s syndrome), occurring against the background of cyclic vomiting syndrome |
Abstract
PDF (Rus)
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Mariya A. Lazareva, Veronika A. Mironova, Arina A. Gryaznova |
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| Vol 6, No 1 (2025) |
Rhinocerebral zygomycosis in a patient with systemic lupus erythematosus: case report |
Abstract
PDF (Rus)
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Alina A. Solov’eva, Daniil S. Labadin |
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| Vol 6, No 1 (2025) |
BCG-ostitis in a 3-year-old child: case report |
Abstract
PDF (Rus)
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Mariya A. Chaplina, Anna A. Chernova, Vladimir A. Chernov |
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| Vol 6, No 1 (2025) |
Type 1b glycogenosis in the compound heterozygous state: case report |
Abstract
PDF (Rus)
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Nikol P. Shimkova, Mariya A. Snegurenko, Eva Yukevich |
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