Zobrazeno 1 - 10
of 23
pro vyhledávání: '"V I ALBANOVA"'
Publikováno v:
Vestnik Dermatologii i Venerologii, Vol 95, Iss 4, Pp 24-30 (2019)
Congenital epidermolysis bullosa (EB) is a clinically and genetically heterogeneous group of hereditary skin diseases characterized by the formation of blisters and/or erosions in response to minimal trauma. Etiopathogenetic methods for treating the
Externí odkaz:
https://doaj.org/article/6fc3245f0f484274bf133690c9cf744d
Publikováno v:
Vestnik Dermatologii i Venerologii, Vol 95, Iss 1, Pp 30-40 (2019)
Aim. To evaluate the clinical efficacy of modern atraumatic non-adherent wound dressings in patients with congenital epidermolysis bullosa. Materials and methods. The study involved 9 patients diagnosed with congenital epidermolysis bullosa (EB), inc
Externí odkaz:
https://doaj.org/article/98363f71048f4224b76412ae3f0eee74
Publikováno v:
Vestnik Dermatologii i Venerologii, Vol 0, Iss 6, Pp 149-157 (2017)
The goal of the study. Evaluating of the effectiveness of treatment of men with a diagnosis «Seborrheic dermatitis of the scalp» by the system using of retinol palmitate. Material and methods. 36 patients every day for 2 months received overnight p
Externí odkaz:
https://doaj.org/article/3311af281abe4048981e5197451c52b6
Publikováno v:
Vestnik Dermatologii i Venerologii, Vol 0, Iss 4, Pp 95-104 (2017)
The Kindler syndrome is one of the types of hereditary epidermolysis bullosa with its onset related to mutations of the KIND1 gene. The authors describe a case of a family with three members suffering from this rare disease. All of these patients hav
Externí odkaz:
https://doaj.org/article/07ccccb8a1ca4cb4840820eb60f461a4
Autor:
A. A. Kubanov, V. I. Albanova, A. E. Karamova, V. V. Chikin, L. YE. Melekhina, YE. V. Bogdanova
Publikováno v:
Vestnik Dermatologii i Venerologii, Vol 0, Iss 3, Pp 21-30 (2017)
Goal. To study the prevalence of hereditary epidermolysis bullosa (HEB) in the Russian Federation. Materials and methods. The data on the number of HEB patients by subjects of the Russian Federation as well as their age and disease type were obtained
Externí odkaz:
https://doaj.org/article/7836236d7fc8436685b1e5e2c9825c62
Autor:
A. E. Karamova, V. V. Chikin, V. I. Albanova, V. A. Smolyannikova, M. A. Nefedova, E. S. Monchakovskaya
Publikováno v:
Vestnik Dermatologii i Venerologii, Vol 0, Iss 3, Pp 83-89 (2017)
The article describes a case of squamous-cell carcinoma in a female patient aged 30 suffering from a rare inherited disease -recessive dystrophic epidermolysis bullosa (RDEB). RDEB is characterized by a high risk of squamous cell carcinoma in young p
Externí odkaz:
https://doaj.org/article/fd2ef1efb0dd47a7a9d5ce891f244e6c
Publikováno v:
Vestnik Dermatologii i Venerologii, Vol 0, Iss 3, Pp 46-53 (2017)
Recessive dystrophic epidermolysis bullosa (RDEB) is a severe inherited disease developing due to genetic abnormalities in the synthesis of Type VII collagen by fibroblasts. A low production rate of Type VII collagen and abnormalities related to the
Externí odkaz:
https://doaj.org/article/461812b9674e40aa8d31ff95eaefaa30
Publikováno v:
Vestnik Dermatologii i Venerologii, Vol 0, Iss 3, Pp 53-59 (2017)
Hereditary epidermolysis bullosa is a big group of hereditary diseases with the main manifestations in the form of blisters on the skin and mucous coat after slight mechanical injuries. It is not always possible to diagnose this disease based on the
Externí odkaz:
https://doaj.org/article/24fb65c9e2fe46f7a2e7f65a10f83fe0
Publikováno v:
Vestnik Dermatologii i Venerologii, Vol 0, Iss 6, Pp 47-56 (2017)
Today there are no ethiopathogenetic treatment methods for treating hereditary epidermolysis bullosa. All available treatment methods are symptomatic and are mainly aimed at patient care. Since severe forms of hereditary epidermolysis bullosa affect
Externí odkaz:
https://doaj.org/article/6578938e16c14f0395f1204108f8ce9a
Publikováno v:
Vestnik Dermatologii i Venerologii, Vol 95, Iss 1, Pp 30-40 (2019)
Aim. To evaluate the clinical efficacy of modern atraumatic non-adherent wound dressings in patients with congenital epidermolysis bullosa. Materials and methods. The study involved 9 patients diagnosed with congenital epidermolysis bullosa (EB), inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f773265e9d9c12547b559c9cdeaf448
https://doi.org/10.25208/0042-4609-2019-95-1-30-40
https://doi.org/10.25208/0042-4609-2019-95-1-30-40