Zobrazeno 1 - 2
of 2
pro vyhledávání: '"А. Yu. Shcherbina"'
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:
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