Zobrazeno 1 - 10
of 19
pro vyhledávání: '"A. N. Kotin"'
Publikováno v:
Учёные записки Санкт-Петербургского государственного медицинского университета им. Акад. И.П. Павлова, Vol 25, Iss 4, Pp 75-80 (2019)
Introduction. Hirschsprung’s disease is a congenital anomaly characterized by the absence of ganglion cells in submucosal and intramuscular layers of intestinal wall that leads to the intestinal obstruction. 70–80 % of cases are isolated malforma
Externí odkaz:
https://doaj.org/article/d9de6c4b8c8946b6a5d04ca8bd3bff2f
Publikováno v:
Вестник хирургии имени И.И. Грекова, Vol 175, Iss 3, Pp 44-46 (2016)
An analysis of treatment results was made in 216 patients with intussusception of bowels at the period from 2000 to 2015. The authors showed that it would be reasonable to carry out a conservative therapy in the cases of recurrent intussusception in
Externí odkaz:
https://doaj.org/article/d6c5b964b2bf41c19dffd1ab211cff7b
Autor:
S. A. Karavaeva, T. K. Nemilova, A. N. Kotin, T. V. Patrikeeva, S. V. Starevskaya, N. A. Il’Ina, N. A. Borisova
Publikováno v:
Вестник хирургии имени И.И. Грекова, Vol 174, Iss 1, Pp 40-42 (2015)
The article presents the experience of treatment of newborn children and infants with congenital malformations of the lung and mediastinum, which required a surgery. Children (138 cases) were treated during recent 18 years. There was a prevalence of
Externí odkaz:
https://doaj.org/article/fd8f6312dbea44239790b12ec0654fa8
Publikováno v:
Russian Journal of Pediatric Surgery. 26:5-9
Introduction. Minimally invasive procedures used in the treatment of children with Hirschsprung’s disease (HD) have reduced the rate of complications and allowed to perform these surgeries at any age. In literature, one can find much information on
Autor:
Tatiana V. Patrikeeva, Yuri V. Levadnev, Tatiana V. Simonova, Alexey N. Kotin, Svetlana A. Karavaeva, Maria V. Golubeva
Publikováno v:
Russian Journal of Pediatric Surgery, Anesthesia and Intensive Care. 11:387-394
BACKGROUND: Extrathoracic lung sequestration is a rare variant of a developmental malformation that can be diagnosed prenatally and should be included in the differential diagnosis of abdominal tumor-like formations. CASES REPORT: From 1996 to 2020,
Publikováno v:
Russian Journal of Pediatric Surgery, Anesthesia and Intensive Care. 10:17-24
Background. The cystic form of biliary atresia is a rare form of atresia of the biliary tract, which is a relatively favorable variant of the defect and can be diagnosed antenatally. In practice, it is important not only to suspect this diagnosis, bu
Publikováno v:
Russian Journal of Pediatric Surgery. 24:161-166
Introduction. Cysts of the common bile duct or choledoch cysts (CC) are congenital cystic dilatation of the extrahepatic and / or intrahepatic bile ducts. The etiology is not fully clear, but it has been proven that abnormal pancreatobiliary anastomo
Publikováno v:
Pediatrician (St. Petersburg). 11:83-90
Hirschsprungs disease usually manifests from the first days of life and is diagnosed in the newborn period. In some patients Hirschsprungs disease cant be diagnosed in the newborn period because of different forms of disease and clinical features. Fr
Publikováno v:
Russian Journal of Pediatric Surgery, Anesthesia and Intensive Care. 11:36
Publikováno v:
Russian Journal of Pediatric Surgery, Anesthesia and Intensive Care. 11:106