Zobrazeno 1 - 3
of 3
pro vyhledávání: '"S. А. Dibirova"'
Autor:
A. L. Kozlova, V. O. Bludova, V. I. Burlakov, E. V. Raykina, T. V. Varlamova, М. А. Kurnikova, А. N. Remizov, G. V. Tereshchenko, А. А. Moiseeva, S. А. Dibirova, А. L. Khoreva, А. А. Roppelt, Yu. А. Rodina, N. B. Kuzmenko, А. А. Mukhina, Е. I. Каlashnikova, L. N. Igisheva, N. V. Martynova, О. V. Zhogova, S. B. Zimin, О. V. Barabanova, Yu. V. Kotova, G. А. Novichkova, А. Yu. Shcherbina
Publikováno v:
Научно-практическая ревматология, Vol 59, Iss 3, Pp 326-334 (2021)
The aim of this study was to analyze the clinical, laboratory and molecular genetic data of 26 patients (15 boys, 11 girls) diagnosed with mevalonate kinase deficiency syndrome (MKD).Subjects and methods. The age of MKD manifestation ranged from 0 to
Externí odkaz:
https://doaj.org/article/f66c1aefc43645eeae9a70d9f988db5e
Autor:
A. L. Kozlova, V. I. Burlakov, Z. A. Nesterenko, V. O. Bludova, E. V. Raykina, T. V. Varlamova, М. А. Kurnikova, A. А. Moiseeva, S. А. Dibirova, N. Yu. Kan, А. L. Horeva, А. А. Roppelt, D. V. Yukhacheva, E. V. Deripapa, Yu. А. Rodina, O. A. Shvets, E. A. Deordieva, N. B. Kuzmenko, А. А. Mukhina, G. А. Novichkova, A. Yu. Shcherbina
Publikováno v:
Pediatric Hematology/Oncology and Immunopathology. 21:88-92
The aim of this study was to analyze the clinical, laboratory and molecular genetic data of 20 patients (9 boys, 11 girls) diagnosed with cryopyrin-associated periodic syndrome (CAPS) with an assessment of the efficacy and safety of therapy in 6 pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::548d8bcc97cdb18347fe3838b114cf06
https://doi.org/10.24287/1726-1708-2022-21-1-88-92
https://doi.org/10.24287/1726-1708-2022-21-1-88-92
Autor:
А. N. Remizov, Yu. V. Kotova, А. А. Mukhina, E. V. Raykina, Е. I. Каlashnikova, Yu. А. Rodina, L. N. Igisheva, N. V. Martynova, О. V. Barabanova, A. L. Kozlova, S. А. Dibirova, М. А. Kurnikova, N. B. Kuzmenko, G. А. Novichkova, А. L. Khoreva, T. V. Varlamova, V. O. Bludova, А. Yu. Shcherbina, О. V. Zhogova, G. V. Tereshchenko, V. I. Burlakov, А. А. Roppelt, А. А. Moiseeva, S. B. Zimin
Publikováno v:
Научно-практическая ревматология, Vol 59, Iss 3, Pp 326-334 (2021)
The aimof this study was to analyze the clinical, laboratory and molecular genetic data of 26 patients (15 boys, 11 girls) diagnosed with mevalonate kinase deficiency syndrome (MKD).Subjects and methods. The age of MKD manifestation ranged from 0 to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::024cdf22b9aa3020940f712fe63f59a0
https://doi.org/10.47360/1995-4484-2021-326-334
https://doi.org/10.47360/1995-4484-2021-326-334