Zobrazeno 1 - 10
of 20
pro vyhledávání: '"S. A. Dibirova"'
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 0, Iss 34, Pp 36-41 (2016)
The article presents a case of a very rare disorder – generalized eruptive keratoacanthoma of Grzybowski in a woman aged 82 years old. The disease is characterized by sudden emergence of hundreds or thousands of neoplasms (2–5 cm in diameters) ra
Externí odkaz:
https://doaj.org/article/1ef440c07ff84bca9f21398d3c3d5db3
Autor:
N. M. Kislitsyna, A. V. Shatskikh, S. M. Dibirova, D. M. Sultanova, M. P. Veselkova, S. V. Novikov
Publikováno v:
Oftalʹmologiâ, Vol 19, Iss 1, Pp 123-132 (2022)
Purpose: The vitreous body (CT), due to the complexity of its structure, remains one of the least studied anatomical structures to this day. In the literature there are attempts to describe the anatomy of the vitreous body, since the II century. The
Externí odkaz:
https://doaj.org/article/b981ba1e9596468cb4b08090a149a7af
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:
S. D. Dibirova
Publikováno v:
Biomedical Photonics, Vol 5, Iss 4, Pp 44-47 (2017)
The results of the follow-up of the patient with persistent forehead keratoacanthoma are represented. The patient underwent one course of PDT with intralesional administration of photosensitizer radachlorin at a dose of 0.75 ml/cm2 of tumor. The char
Externí odkaz:
https://doaj.org/article/0a16843ef9c6409685108fb4c25e280a
Publikováno v:
The EYE GLAZ. 24:7-12
Introduction. Vision plays a key role in the development of newborns and children. Early and severe visual impairment can affect motor skills, cognition, communication and social abilities. One of the main diagnostic indicators of the development of
Autor:
V. N. Galkin, Yu. S. Romanko, M. A. Kaplan, A. V. Molochkov, V. A. Molochkov, Zh. S. Kuntcevich, T. E. Sukhova, S. D. Dibirova
Publikováno v:
Biomedical Photonics, Vol 5, Iss 2, Pp 21-25 (2016)
The review is on treatment of keratoacanthomas using photodynamic therapy. The defining characteristic of keratoacanthoma among epithelial tumors is a rapid spontaneous regression in the case of typical keratoacanthoma and long-term persistence, recu
Externí odkaz:
https://doaj.org/article/188c16d6a5f6457ca334277514f667cf
Autor:
S. D. Dibirova
Publikováno v:
Biomedical Photonics, Vol 5, Iss 4, Pp 44-47 (2016)
The results of the follow-up of the patient with persistent forehead keratoacanthoma are represented. The patient underwent one course of PDT with intralesional administration of photosensitizer radachlorin at a dose of 0.75 ml/cm2 of tumor. The char
Externí odkaz:
https://doaj.org/article/ecb57cdaff6947fcbac4e43515bf098a
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
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
Autor:
N. M. Kislitsyna, A. V. Shatskikh, S. M. Dibirova, D. M. Sultanova, M. P. Veselkova, S. V. Kolesnik, S. V. Novikov
Publikováno v:
Офтальмохирургия, Vol 0, Iss 4, Pp 50-55 (2021)
Purpose. The key to understanding the development of any vitreoretinal pathology is a presence of a clear conception to possible variants of changes in the anatomical and topographic relationships of the posterior cortical layers of the vitreous body