Zobrazeno 1 - 10
of 37
pro vyhledávání: '"O. L. Nechvolodova"'
Autor:
O. L. Nechvolodova, L. K. Mikhailova
Publikováno v:
N.N. Priorov Journal of Traumatology and Orthopedics. 1:43-47
A clinical and radiological analysis of 107 cases of hereditary systemic diseases of the skeleton with a predominant lesion of the germ (fizar) and metaphyseal zones, which are combined into the group "spondylophysial-metaphyseal dysplasia", was carr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e60323c16717cc38bf9599553717e3d1
https://doi.org/10.17816/vto63951
https://doi.org/10.17816/vto63951
Publikováno v:
N.N. Priorov Journal of Traumatology and Orthopedics. 5:15-18
The aim of the study was to increase the accuracy of clinical diagnosis and detection of asymptomatic pelvic ring injuries. The method of multiprojection radiologic examination of pelvis was elaborated to avoid the necessity of traumatic rotation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de32f820d74a8112055597919cbb5386
https://doi.org/10.17816/vto104482
https://doi.org/10.17816/vto104482
Publikováno v:
N.N. Priorov Journal of Traumatology and Orthopedics. 5:31-34
The first description in Russian literature of osteofibrous dysplasy in children is presented. It is grounded on the analysis of diagnostic peculiarities and treatment of 24 patients in the period from 1966 to 1996 The main diagnostic criteria by cli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::886d595b66f3ec00892fccad7b4dcb71
https://doi.org/10.17816/vto104382
https://doi.org/10.17816/vto104382
Autor:
O. L. Nechvolodova, E. M. Meerson, L. K. Mikhailova, G. I. Nikitina, V. K. Il’ina, V. Ya. Bruskina, S. I. Mitin
Publikováno v:
N.N. Priorov Journal of Traumatology and Orthopedics. 3:40-44
The thesises detected do not allow to keep the pathogenesis of PD within the framework of the theory of primary vessels occlusion. In children with PD marked anomalies including the retardation of bone growth, increased rate of signs of general dyspl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67877f6505aa102904e2fda8241fd29d
https://doi.org/10.17816/vto102464
https://doi.org/10.17816/vto102464
Publikováno v:
N.N. Priorov Journal of Traumatology and Orthopedics. 3:34-37
With the purpose of the improvement of the x-ray diagnosis of the thoracic vertebral body compression fractures in children the roentgenometry of the thoracic vertebral bodies was performed in children in norm by age aspect. The main criteria, i.e. w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92cb4c40c282bbd275a27ae56c989928
https://doi.org/10.17816/vto64076
https://doi.org/10.17816/vto64076
Publikováno v:
Genetika. 21(1)
Data on the prevalence of hereditary diseases in five regions of the Kostroma province were obtained and analysed. It was shown that the ascertainment was close to the truncate selection for the rural population and to the single selection for the ur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::082bf8e67720607eef106584a7aa19cd
https://pubmed.ncbi.nlm.nih.gov/3156065
https://pubmed.ncbi.nlm.nih.gov/3156065
Autor:
O L, Nechvolodova, G P, Iukina
Publikováno v:
Revmatologiia (Moscow, Russia). (4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::47ac82a6cf5167734095a4bb73506b17
https://pubmed.ncbi.nlm.nih.gov/6422531
https://pubmed.ncbi.nlm.nih.gov/6422531
Autor:
V N, Burdygin, T N, Shishkina, O L, Nechvolodova, G G, Okropiridze, A A, Petrakov, S I, Lipkin, A I, Gladshteĭn
Publikováno v:
Khirurgiia. (8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::df65bb3e6ddee76696b259de3b74207b
https://pubmed.ncbi.nlm.nih.gov/2811118
https://pubmed.ncbi.nlm.nih.gov/2811118
Publikováno v:
Genetika. 21(8)
The diversity of hereditary pathology in 5 regions of Kostroma district was studied. 32 nosological forms of autosomal dominant, 30 autosomal recessive and 7 X-linked recessive disorders were found. The most frequent autosomal dominant disorders were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3a80234e3a900f474ea4ba57616c8dbc
https://pubmed.ncbi.nlm.nih.gov/2932368
https://pubmed.ncbi.nlm.nih.gov/2932368
Publikováno v:
Ortopediia travmatologiia i protezirovanie. (6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::56c5dc145f937e75145f24ab1abd5872
https://pubmed.ncbi.nlm.nih.gov/6773013
https://pubmed.ncbi.nlm.nih.gov/6773013