Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Tatiana V. Latysheva"'
Autor:
L Selimzianova, Aleksander V. Polyakov, N.B. Kuzmenko, Leyla Namazova-Baranova, N I Ilina, Eliso M. Dzhobava, Elena Vishneva, Tatiana V. Latysheva, Irina A. Manto, A.N. Pampura, Elena A. Latysheva, Anna Shcherbina, E. A. Bliznetz, Natalia M. Nenasheva, E. A. Viktorova
Publikováno v:
Russian Journal of Allergy. 18:77-114
Hereditary angioedema is a rare, potentially life-threatening genetic disease that manifests with skin and mucous/submucosal swelling that occurs under the influence of bradykinin. The clinical guidelines for hereditary angioedema (code for the Inter
Autor:
Daria O. Timoshenko, Aleksander V. Polyakov, Liubov V. Aleshina, Tatiana V. Latysheva, Elvira R. Gilvanova, Galina A. Kameneva, Elena A. Latysheva, Maria A. Platonova, Valentina A. Fedorova, E. A. Bliznetz, Yulia A. Bocherova, Irina A. Manto
Publikováno v:
Russian Journal of Allergy. 18:5-19
BACKGROUND: In 2018, a new form of hereditary angioedema without C1-inhibitor deficiency hereditary angioedema with a mutation in the plasminogen gene was identified. The world scientific literature describes a small number of patients with this form
Publikováno v:
Russian Journal of Allergy. 18:131-137
Angioedema is caused by a local increase in vascular permeability induced by bradykinin or mast cell mediators. The main challenge of the differential diagnosis of angioedema lies in the fact that different pathophysiological processes may lead to a