Zobrazeno 1 - 10
of 39
pro vyhledávání: '"буллезный эпидермолиз"'
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 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
Publikováno v:
Vestnik Dermatologii i Venerologii, Vol 0, Iss 3, Pp 109-118 (2017)
The article describes present-day information on the pathogenesis, clinical picture, treatment and differential diagnostics of epidermolysis bullosa acquisita, an autoimmune skin disease caused by the production of anti-Type VII collagen autoantibodi
Externí odkaz:
https://doaj.org/article/8a5b342525fd4d428fd7343b71b671e2
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
Autor:
V. I. Al'banova, M. A. Nefedova
Publikováno v:
Vestnik Dermatologii i Venerologii, Vol 0, Iss 2, Pp 64-72 (2017)
The article describes the case of acquired bullous epidermolysis in a woman of 45 years old, suffering from a disease from 2.5 years. As a child, she was diagnosed with herpetiform dermatitis on the base of a clinical picture and histological data. A
Externí odkaz:
https://doaj.org/article/486ae42ec2c248e5b3457ed65a671e1d
Publikováno v:
Сучасна педіатрія. Україна; № 3(131) (2023): Сучасна педіатрія. Україна; 126-133
Modern Pediatrics. Ukraine; No. 3(131) (2023): Modern pediatrics. Ukraine; 126-133
Modern Pediatrics. Ukraine; № 3(131) (2023): Modern pediatrics. Ukraine; 126-133
Modern Pediatrics. Ukraine; No. 3(131) (2023): Modern pediatrics. Ukraine; 126-133
Modern Pediatrics. Ukraine; № 3(131) (2023): Modern pediatrics. Ukraine; 126-133
Today, more than 300 million people worldwide suffer from one or more rare diseases. Epidermolysis bullosa (EB) is a heterogeneous group of hereditary diseases characterized by a genetic predisposition to a hypersensitive body reaction to minor skin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=scientific_p::61cfb97f5b403aa9377cd2a4f9675c2b
http://mpu.med-expert.com.ua/article/view/282512
http://mpu.med-expert.com.ua/article/view/282512
Publikováno v:
Ukrainian Journal of Dermatology, Venerology, Cosmetology; № 4 (2019); 102-106
Украинский журнал дерматологии, венерологии, косметологии; № 4 (2019); 102-106
Український журнал дерматології, венерології, косметології; № 4 (2019); 102-106
Украинский журнал дерматологии, венерологии, косметологии; № 4 (2019); 102-106
Український журнал дерматології, венерології, косметології; № 4 (2019); 102-106
Objective — to provide a brief professional information review regarding the latest international developments in the treatment of patients with epidermolysis bullosa (EB).Materials and methods. At the scientific and practical conferences that took
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20ce599fca7254e9f6c5f6b7599511b9
https://doi.org/10.30978/ujdvk2019-4-102
https://doi.org/10.30978/ujdvk2019-4-102