Zobrazeno 1 - 10
of 36
pro vyhledávání: '"S L, Morozov"'
Autor:
A. K. Mironova, I. M. Osmanov, I. N. Zakharova, M. I. Pykov, E. L. Tumanova, S. L. Morozov, T. I. Vokuyeva
Publikováno v:
Медицинский совет, Vol 0, Iss 17, Pp 182-190 (2021)
Introduction. One of the urgent issues in the first stage of nursing premature infants is acute kidney injury. The incidence of neonatal acute kidney injury in developing countries is 3.9/1000 live births, with 34.5/1000 among neonatal intensive care
Externí odkaz:
https://doaj.org/article/a26f6b7e87aa4659bf6e659b80b2fb9a
Publikováno v:
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 68:86-92
Barakat Syndrome (MIM#146255) is a rare autosomal dominant disease caused by GATA3 gene mutation and manifested by hypoparathyroidism (H), sensorineural deafness (D), and renal disease (R). HDR syndrome characterized by high clinical variability and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2da316f441c774cec6b6d171688c73ce
https://doi.org/10.21508/1027-4065-2023-68-2-86-92
https://doi.org/10.21508/1027-4065-2023-68-2-86-92
Publikováno v:
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 68:22-28
Idiopathic nephrotic syndrome is the most common glomerular disease in children, with a prevalence of 1.15–16.9 cases per 100,000 children per year worldwide. In some cases, nephrotic syndrome has a frequently relapsing course or dependence on ster
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b560b4f1e04a079a5e1fbaee27fa3f2e
https://doi.org/10.21508/1027-4065-2023-68-2-22-28
https://doi.org/10.21508/1027-4065-2023-68-2-22-28
Publikováno v:
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 68:128-132
The survival rate among children with cancer was significantly improved in recent years. About 40% of these patients, however, suffer from late complications of anticancer treatment. Risk factors of late kidney impairment include beginning of specifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1a953de3ff207faeaaa2774418f6f4f
https://doi.org/10.21508/1027-4065-2023-68-1-128-132
https://doi.org/10.21508/1027-4065-2023-68-1-128-132
Publikováno v:
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 67:83-93
The most severe consequence of a spinal hernia, affecting the entire life of a person, is a spinal neurogenic bladder. Its symptoms limit the child’s socialization, and the problem of urination needs constant use of various aids. At the same time,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6823964b2605c4215ac82a9f89657a6f
https://doi.org/10.21508/1027-4065-2022-67-2-83-93
https://doi.org/10.21508/1027-4065-2022-67-2-83-93
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 66, Iss 6, Pp 33-38 (2022)
The concept of the steroid resistance in children with nephrotic syndrome, who were initially sensitive to steroids, has been known for a long time. Despite several foreign studies, this problem remains largely unexplored. The results of the presente
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc44c62ec9a1152f618e4ac797fec8f5
https://doi.org/10.21508/1027-4065-2021-66-6-33-38
https://doi.org/10.21508/1027-4065-2021-66-6-33-38
Autor:
S. L. Morozov, V. V. Dlin
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 66, Iss 5, Pp 67-74 (2021)
Idiopathic nephrotic syndrome is the most common glomerulopathy in children, with a prevalence of approximately 16 per 100,000 of child population worldwide. Any chronic glomerular disease has the same type of development mechanism. Regardless of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12f6aa1a99259e8285b9b4e4a3016c78
https://doi.org/10.21508/1027-4065-2021-66-5-67-74
https://doi.org/10.21508/1027-4065-2021-66-5-67-74
Publikováno v:
Nephrology (Saint-Petersburg). 25:90-94
Tuberous sclerosis is a polysystemic, genetically determined, autosomal dominant orphan disease that affects approximately 1 in 10,000 people worldwide. Kidney damage in tuberous sclerosis is the leading cause of death due to serious complications, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e77a9e6ca6ae98a1eddf053e11047e0e
https://doi.org/10.36485/1561-6274-2021-25-4-90-94
https://doi.org/10.36485/1561-6274-2021-25-4-90-94
Autor:
V. V. Dlin, S. L. Morozov
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 66, Iss 2, Pp 6-12 (2021)
The term “personalized medicine” appeared only 20 years ago, but individual approaches to the therapy were known for more than a hundred years. The genome decoding and development of pharmacogenetics in recent decades have opened up new ways for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a59950c6216e11f1f659c38eaeef160
https://www.ped-perinatology.ru/jour/article/view/1367
https://www.ped-perinatology.ru/jour/article/view/1367
Publikováno v:
Nephrology (Saint-Petersburg). 25:83-89
Idiopathic nephrotic syndrome is the most common childhood glomerulopathy. Despite modern advances in medicine, idiopathic NS is still a big problem, this is due to the fact that the mechanisms of pathogenesis are not fully understood, and the lack o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0fd927c15fe6257ca9ba6b7e161f9bd
https://doi.org/10.36485/1561-6274-2021-25-1-83-89
https://doi.org/10.36485/1561-6274-2021-25-1-83-89