Zobrazeno 1 - 10
of 13
pro vyhledávání: '"M. V. Mashkova"'
Publikováno v:
Issledovaniâ i Praktika v Medicine, Vol 5, Iss 4, Pp 91-97 (2018)
Purpose. To improve the technology of cancer patients' rehabilitation in the multidisciplinary hospital using an interdisciplinary approach at the stages of combined treatment of malignant tumors.Patients and methods. The analysis of 845 cases of adm
Externí odkaz:
https://doaj.org/article/0f8cf5aec4fc43c8be7f0758643d141b
Autor:
M F Ballyuzek, M V Mashkova
Publikováno v:
Терапевтический архив, Vol 87, Iss 8, Pp 111-118 (2015)
Available updates have changed our idea about cachexia as a terminal condition, which could consider it as a combined metabolic syndrome that gives rise to the worse course of the underlying disease, the lower efficiency of specific therapy, and high
Externí odkaz:
https://doaj.org/article/2fd29b7e3ebe4d518be5c13b767b2f4d
Publikováno v:
Advances in Gerontology. 7:228-235
We investigated 103 newly diagnosed stage II–IV cancer patients aged 28–78 years before the beginning of their anticancer therapy. The signs of cachexia syndrome were diagnosed and staged (precachexia or fully-fledged cachexia), including the age
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36f29697f37eb86d82da83fb26c13ec3
https://doi.org/10.1134/s2079057017030043
https://doi.org/10.1134/s2079057017030043
Publikováno v:
Advances in gerontology = Uspekhi gerontologii. 30(1)
We have examined 103 patients at the age from 28 to 78 with the newly diagnosed oncological disease at stages II-IV before the beginning of anticancer treatment. The identification of the signs of the cachexia syndrome and its stage (pre-cachexia, ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cfbe813913d58b666885173fe9814df9
https://pubmed.ncbi.nlm.nih.gov/28557393
https://pubmed.ncbi.nlm.nih.gov/28557393
Publikováno v:
Advances in gerontology = Uspekhi gerontologii. 28(2)
With a growing number of the elderly population, it is important to remember about the potential pathologic conditions, one of the main features of which is the weight loss (cachexia, anorexia, sarcopenia, hypermetabolism/hypercatabolism syndrome and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::12b0c3f0a90d9f4b7e38d33686055291
https://pubmed.ncbi.nlm.nih.gov/26856099
https://pubmed.ncbi.nlm.nih.gov/26856099
Publikováno v:
Tsitologiia. 18(2)
The applications of the fluorescent staining of chromosomes with quinacrine mustard allowed to identify a dicentric Y-chromosome in two patients with defected external gynaetalies: a boy of 15 years old and a girl of 2 years old. Both the patients ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c54f5c20fa78876a787be7813f80f5f6
https://pubmed.ncbi.nlm.nih.gov/59989
https://pubmed.ncbi.nlm.nih.gov/59989
Autor:
D K, Verlinskaia, M V, Mashkova
Publikováno v:
Tsitologiia. 19(11)
The large submetacentric abnormal late replicating X-chromosomes were found in three patients under karyological studies of 168 patients with Turner's syndrome. G- and C-banding revealed that abnormal chromosomes are three variants of isodicentric ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b7acb7a3e43c63e4c3825795db6e95f
https://pubmed.ncbi.nlm.nih.gov/601863
https://pubmed.ncbi.nlm.nih.gov/601863
Autor:
M V, Mashkova, D K, Verlinskaia
Publikováno v:
Tsitologiia. 18(7)
A loss of part of the short arm of the X-chromosome and a partial trisomy of chromosome 2 were detected in a girl with the Shereshevsky--Turner syndrome; her karyotype was 46, Xt (X,2) (Xqter leads to Xp11 : : 2q36 leads to 2q ter). The patient's mot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cdccf8c1d6da10b7b2a858f34a4569c4
https://pubmed.ncbi.nlm.nih.gov/982591
https://pubmed.ncbi.nlm.nih.gov/982591
Autor:
I V, Butomo, M V, Mashkova
Publikováno v:
Tsitologiia. 19(11)
A child with the Down syndrome revealed besides a regular trisomy 21, an enlargment of the short arm of chromosome 10, and the deletion of the long arm of chromosome 12. The proband's mother, who was phenothypically normal woman, appeared to be a car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4e610f0e8a64fc505478359080d76c23
https://pubmed.ncbi.nlm.nih.gov/146289
https://pubmed.ncbi.nlm.nih.gov/146289
Publikováno v:
Ortopediia travmatologiia i protezirovanie. (10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a2774908faf773422183c2ad3337ef6c
https://pubmed.ncbi.nlm.nih.gov/530608
https://pubmed.ncbi.nlm.nih.gov/530608