Zobrazeno 1 - 10
of 201
pro vyhledávání: '"S. S. Nikitin"'
Generalized form of tularemia in pediatric surgeon practice: Difficulties of diagnosis and treatment
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 67, Iss 6, Pp 98-103 (2023)
Tularemia in the practice of a pediatric surgeon is a rare disease, and abdominal and generalized forms of it are not detected without specific laboratory diagnostics. The long-term serious condition of patients, intoxication, abdominal pain with exc
Externí odkaz:
https://doaj.org/article/cc5dc505c01f45068909ceab6b80f357
Autor:
P. V. Glybochko, Yu. G. Alyaev, T. G. Markosyan, S. S. Nikitin, V. A. Grigoiyan, E. E. Babalov
Publikováno v:
Сеченовский вестник, Vol 0, Iss 2, Pp 43-50 (2022)
Aim. Assessment of functional status of muscles of pelvic floor and conductive ability of corticospinal tract in healthy men and patients with erectile dysfunction (ED) with compiling the database of electromyography parameters.Methods. 52 patients w
Externí odkaz:
https://doaj.org/article/4a089c022b41476791d4ffc37940fbde
Autor:
S. N. Bardakov, A. М. Emelin, S. S. Nikitin, A. N. Khelkovskaya-Sergeeva, I. S. Limaev, A. F. Murtazina, V. A. Tsargush, M. V. Gusev, Ya. V. Safronova, V. S. Kaimonov, A. A. Isaev, R. V. Deev
Publikováno v:
Нервно-мышечные болезни, Vol 12, Iss 4, Pp 73-87 (2022)
Differential diagnosis of inflammatory myopathies with hereditary muscular dystrophies accompanied by a secondary inflammatory process is a time‑consuming clinical and pathomorphological task. In particular, false diagnosis of polymyositis in patie
Externí odkaz:
https://doaj.org/article/b2e69f02488b40eaa34fb3cd3cd8b162
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 67, Iss 5, Pp 89-95 (2022)
Около 15% всех нарушений мочеиспускания приходится на довольно опасное нарушение уродинамики — дисфункциональное мочеиспускание, или д
Externí odkaz:
https://doaj.org/article/f7ef166b50224111b99b615d4b731a26
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 67, Iss 4, Pp 108-114 (2022)
Neurogenic detrusor overactivity is a dangerin terms of the formation of vesicoureteralreflux, pyelonephritis, and chronic kidney disease. The standard treatment for neurogenic detrusor overactivity is intermittent catheterization of the bladder in c
Externí odkaz:
https://doaj.org/article/619de4c3c207431784b8307eac6818ce
Publikováno v:
Нервно-мышечные болезни, Vol 12, Iss 3, Pp 52-58 (2022)
Juvenile amyotrophic lateral sclerosis (ALS) presents a group of few rare monogenic disorders with onset from early childhood up to 25 years and much more benign course than “classic” ALS. Autosomal dominant ALS type 4 (ALS4) related to SETX gene
Externí odkaz:
https://doaj.org/article/fe625f08ae5247868f55108e5507e172
Publikováno v:
Медицинский совет, Vol 0, Iss 12, Pp 205-211 (2022)
The article is dedicated to the 40th anniversary of the pediatric endoscopic service of the Republic of Karelia. In the introductory part of the article, the authors briefly describe the history of the appearance of endoscopy in the world, which date
Externí odkaz:
https://doaj.org/article/be21a6e3cce9487f8c707870a7c62ca2
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 67, Iss 2, Pp 83-93 (2022)
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://doaj.org/article/8e2e82a7d69d4843bc5440ac9572435e
Autor:
T. A. Gremyakova, S. V. Artemyeva, N. D. Vashakmadze, I. P. Vitkovskaya, V. I. Guzeva, O. V. Guzeva, L. M. Kuzenkova, S. V. Mikhailova, L. P. Nazarenko, T. M. Pervunina, N. L. Pechatnikova, T. V. Podkletnova, G. E. Sakbaeva, A. A. Stepanov, V. M. Suslov, O. I. Gremyakova, N. I. Shakhovskaya, S. S. Nikitin
Publikováno v:
Нервно-мышечные болезни, Vol 12, Iss 2, Pp 10-18 (2022)
Duchenne muscular dystrophy (DMD) is a fatal neuromuscular disease due to a mutation in the gene encoding dystrophin synthesis. In patients, muscle damage and atrophy progresses, the ability to move independently decreases as well as respiratory and
Externí odkaz:
https://doaj.org/article/2d5cb1f3844a45cb95295db2a3337785
Autor:
T. V. Markova, V. M. Kenis, S. S. Nikitin, E. V. Melchenko, T. S. Nagornova, D. V. Osipova, A. E. Alieva, Ya. S. Yugeno, E. Yu. Zakharova, E. L. Dadali
Publikováno v:
Нервно-мышечные болезни, Vol 12, Iss 2, Pp 37-46 (2022)
Background. Multiple epiphysal dysplasia (MED) type 1 (OMIM: 132400) is one of 7 genetic variants of this group of skeletal dysplasias described to date. The disease is caused by mutations in the COMP gene located on chromosome 19p13.1. The presence
Externí odkaz:
https://doaj.org/article/3e21228b2bc24db9bb3aecb71518e8be