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卷 21, 编号 2 (2024)
Experience of lanadelumab usage for long-term prophylaxis of attacks in hereditary angioedema in patients of the Moscow region
Proskurina E., Morozova N., Kokushkin K.
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(Rus)
卷 17, 编号 3 (2020)
A case of hereditary angioedema with late adulthood onset
Pokalyukhina J., Abramova N.
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(Rus)
卷 20, 编号 2 (2023)
Myoferline gene mutation сan be associated with recurrent angioedema
Fomina D., Serdotetskova S., Bobrikova E., Alekseeva J., Roppelt A., Lysenko M.
PDF
(Rus)
卷 19, 编号 1 (2022)
Hereditary angioedema with C1-inhibitor deficiency: a retrospective study of 194 patients
Manto I., Latysheva E., Timoshenko D., Gornostaeva Y., Kostinova A., Medunitsyna E., Myasnikova T., Romanova T., Setdikova N., Frolov E., Shubina O., Latysheva T.
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(Rus) PDF
(Eng)
卷 20, 编号 2 (2023)
Preliminary results of a non-interventional single-center study evaluating the efficacy of long-term use of lanadelumab in routine clinical practice in the Russian Federation
Latysheva E., Manto I., Aleshina L., Bobrikova E., Viktorova E., Gracheva E., Demina D., Fomina D., Shcherbina A., Latysheva T.
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(Rus) PDF
(Eng)
卷 8, 编号 3 (2011)
THE GENETIC AND CLINICAL ASPECTS OF HAE, NEWPOSSIBILITIES OF THE DISEASE EXACERBATIONS TREATMENT
Latysheva T., Polyakov A., Dmitrieva A., Medunitsyna E., Latysheva T., Polyakov A., Dmitrieva A., Medunitsyna E.
PDF
(Rus)
卷 20, 编号 3 (2023)
Case of newly diagnosed primary immunodeficiency at age 65
Demko I., Sobko E., Shestakova N., Kraposhina A.
PDF
(Rus)
卷 20, 编号 1 (2023)
Familial case of hereditary angioneurotic angioedema, caused by deficiency in the C1 inhibitor complement system
Kovzel E., Nurpeisov T., Gani B., Volodchenko S., Zhamanbaeva Z., Syzdykova A., Batyrbaeva A.
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(Rus)
卷 16, 编号 3 (2019)
Long-term prophylaxis in HAE patients
Latysheva T., Latysheva E., Manto I.
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(Rus)
卷 18, 编号 2 (2021)
Hereditary angioedema. Clinical guidelines. (D84.1)
Bliznetz E., Viktorova E., Vishneva E., Dzhobava E., Il'ina N., Kuzmenko N., Latysheva E., Latysheva T., Manto I., Namazova-Baranova L., Nenasheva N., Pampura A., Polyakov A., Selimzianova L., Shcherbina A.
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(Rus)
卷 18, 编号 2 (2021)
Hereditary Angioedema (HAE) with a mutation in the plasminogen gene: a retrospective study of a cohort of 14 patients from Russia
Manto I., Latysheva E., Bliznetz E., Timoshenko D., Aleshina L., Bocherova Y., Gilvanova E., Kameneva G., Platonova M., Fedorova V., Polyakov A., Latysheva T.
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(Rus) PDF
(Eng)
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