Zobrazeno 1 - 10
of 86
pro vyhledávání: '"гемофилия"'
Publikováno v:
Качественная клиническая практика, Vol 0, Iss 4, Pp 58-67 (2024)
It is important for public health to monitor and improve the health indicators of the population using the system of patient's quality of life (HRQoL) assessment regardless of the nosology of the disease. The use of HRQoL assessment provides health a
Externí odkaz:
https://doaj.org/article/4eab541c721c40fbb77cf1917b9ac946
Publikováno v:
Качественная клиническая практика, Vol 0, Iss 4, Pp 15-24 (2024)
Relevance. Therapy of hemophilia A, B and Willebrand's disease is carried out under the program of 14 VZN due to the use of federal budget funds. The use of funding is increasing in line with the growth of the total number of patients. In 2022,85.99
Externí odkaz:
https://doaj.org/article/75eb2c3bd737400e898b921bb092d91c
Publikováno v:
Medicina v Kuzbasse, Vol 22, Iss 4, Pp 24-27 (2023)
This article considers the peculiarities of preparing and management of patients with haemophilia before dental interventions. It's imperative to provide dental care to patients suffering from haemophilia after consultation with haematologist and oth
Externí odkaz:
https://doaj.org/article/3dbf8e616fd94c3594fc583ab91735de
Autor:
Юлия Олеговна Рождественская, Анастасия Владимировна Миронова, Ирина Владимировна Болгова, Яна Вячеславовна Юнкина, Светлана Ивановна Елгина, Вадим Гельевич Мозес, Елена Владимировна Рудаева, Наталья Степановна Черных, Кира Борисовна Мозес, Яэль Центер
Publikováno v:
Мать и дитя в Кузбассе, Vol 24, Iss 1, Pp 85-88 (2023)
Hemophilia is a disease caused by hereditary deficiency of plasma coagulation factors VIII (FVIII) (hemophilia A) or IX (FIX) (hemophilia B) and characterized by hematomic bleeding. The main therapeutic measures in patients with hemophilia are aimed
Externí odkaz:
https://doaj.org/article/fc911132bc204f9fb403af0330a82118
Publikováno v:
Качественная клиническая практика, Vol 0, Iss 2, Pp 22-29 (2021)
Objective: to review the data on the efficacy and consumption of octocog alfa and rurioctoctog alfa pegol in standard prophylaxis and individualized prophylaxis in hemophilia A patients based on published international data. Material and methods: a s
Externí odkaz:
https://doaj.org/article/d36975204b65479fb7c110928a23e0a0
Publikováno v:
Эндодонтия Today, Vol 14, Iss 1, Pp 63-68 (2020)
The authors tested a palatal cystotomy option in the treatment of extensive cystic formation of the maxilla in a patient with hemophilia. The use of this technique in a patient with a factor VIII deficiency were reasonable and based on existing exper
Externí odkaz:
https://doaj.org/article/86e62fd8854249f59490cf3a1603c951
Гемофилия – заболевание, обусловленное наследственным дефицитом плазменных факторов свертывания VIII (FVIII) (гемофилия А) или IX (FIX) (гемофи
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::759e211dc9d282dac26345700210bc58
Publikováno v:
Сучасна педіатрія. Україна; № 8(128) (2022): Сучасна педіатрія. Україна; 68-79
Modern Pediatrics. Ukraine; No. 8(128) (2022): Modern pediatrics. Ukraine; 68-79
Modern Pediatrics. Ukraine; № 8(128) (2022): Modern pediatrics. Ukraine; 68-79
Modern Pediatrics. Ukraine; No. 8(128) (2022): Modern pediatrics. Ukraine; 68-79
Modern Pediatrics. Ukraine; № 8(128) (2022): Modern pediatrics. Ukraine; 68-79
Hemophilia A is an X-linked recessive disorder caused by a deficiency of plasma coagulation FVIII, which may be inherited or arise from a spontaneous mutation. FVIII deficiency leads to a decrease in normal hemostasis and is manifested by spontaneous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=scientific_p::4e1fdf6130b32f6f57ee4ee996d9df80
http://mpu.med-expert.com.ua/article/view/273153
http://mpu.med-expert.com.ua/article/view/273153
Autor:
T. A. Fedorova, E. V. Strelnikova
Publikováno v:
Медицинский совет, Vol 0, Iss 9, Pp 68-75 (2014)
Back in 1630, Shah Jahan built the famous Taj Mahal Palace in the memory of his wife Mumtaz who died as a result of postpartum massive bleeding giving birth to her fourteenth child. [1] To this day, bleeding continues to be one of the most common obs
Externí odkaz:
https://doaj.org/article/ef0fc6ec2f0f479ea4be086b7a9f6614
Publikováno v:
Clinical anatomy and operative surgery; Vol. 4 No. 3 (2005); 29-31
Клиническая анатомия и оперативная хирургия; Том 4 № 3 (2005); 29-31
Клінічна анатомія та оперативна хірургія; Том 4 № 3 (2005); 29-31
Клиническая анатомия и оперативная хирургия; Том 4 № 3 (2005); 29-31
Клінічна анатомія та оперативна хірургія; Том 4 № 3 (2005); 29-31
The authors have presented а characteristic of results oftreating acute hemarthroses of the knee joints in patients with hemophilia Ьу means of arthrocentesis Ьу washing out the synovial cavity and employing the traditional technique. А higher
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=scientific_p::794f4e064a5da1f19c20423513b167a1
http://kaos.bsmu.edu.ua/article/view/258903
http://kaos.bsmu.edu.ua/article/view/258903