Výsledky vyhledávání - "G. I Sukolin"

[Variety of hereditary diseases in the Adygei Autonomous Region]

Autor: M Iu, Kadoshnikova, E K, Ginter, A N, Petrin, V I, Golubtsov, O V, Khlebnikova, V A, Galkina, L K, Mikhaĭlova, V V, Poleshchuk, G I, Sukolin

Publikováno v: Genetika. 27(7)

This report is one of the series of communications dedicated to medico-genetical description of the Adyg population in the autonomous national district. The peculiarities have been considered of the forms of hereditary diseases both in the Adyg and R

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5ebc916672f56c98d6616a51a17ab474
https://pubmed.ncbi.nlm.nih.gov/1836772

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[Load of hereditary diseases in the populations of the Adyg autonomic district]

Autor: A N, Petrin, E K, Ginter, V I, Golubtsov, M Iu, Kadoshnikova, V A, Galkina, O V, Khlebnikova, L K, Mikhaĭlova, V V, Poleshchuk, G I, Sukolin

Publikováno v: Genetika. 27(5)

Comparative analysis of the loads of hereditary diseases in two ethnically different populations coexisting in the Adyg national district was performed. The modes of inheritance of diseases studied were tested by segregational analysis. The results o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e863ca8254ccfdc309d56674921caf8d
https://pubmed.ncbi.nlm.nih.gov/1916257

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[Spectrum and territorial distribution of hereditary diseases in the population of the Krasnodar Krai]

Autor: A N, Petrin, E K, Ginter, V A, Galkina, V I, Golubtsov, M V, Khisamova, L K, Mikhaĭlova, O V, Khlevnikova, V V, Polishchuk, G I, Sukolin

Publikováno v: Genetika. 27(4)

The analysis of the spectrum of hereditary diseases in the population of the Krasnodar province is performed and the influence of the population dynamics factors on the spectrum is discussed. More than 130 nosological forms were discovered in the pop

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::16ea1de7421c9ccb347fa4719561d4a7
https://pubmed.ncbi.nlm.nih.gov/1831779

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[Genetic load of hereditary diseases in populations of the Krasnodar Krai]

Autor: A N, Petrin, V I, Golubtsov, V A, Galkina, E K, Ginter, A A, Revazov, M V, Khisamova, L K, Mikhaĭlova, O V, Khlevnikova, G I, Sukolin, V V, Poleshchuk

Publikováno v: Genetika. 27(2)

Medico-genetical study of populations living in Krasnodar district was carried out. The mean value of genetic load contributed by autosomal dominant diseases composed 0.92 +/- 0.06, this value being 0.56 +/- 0.04 for autosomal recessive and 0.36 +/-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1005390d3b5847b9f44ead40cb274270
https://pubmed.ncbi.nlm.nih.gov/1831430

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[Hallopeau-Siemens' congenital epidermolysis bullosa dystrophica]

Autor: A A, Aĭvazian, Iu A, Shekotikhina, G I, Sukolin

Publikováno v: Vestnik dermatologii i venerologii. (2)

Examination of apparently intact skin of patients with generalized Hallopeau-Siemens' dystrophic epidermolysis bullosa has shown that this condition may be diagnosed histologically only in case of manifest changes. If there are no apparent changes, e

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a95394505c8ea3de0c9780da6799da93
https://pubmed.ncbi.nlm.nih.gov/2343665

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[Early congenital lymphedema of the lower extremities combined with pachyonychia]

Autor: G I, Sukolin, O A, Pasportnikova

Publikováno v: Vestnik dermatologii i venerologii. (6)

A four-year-old girl with early congenital lymphedema of the lower limbs in combination with the nail plate involvement (pachyonychia) is described. Such a combination is not characteristic of early lymphedema, it is usually described in late edema o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::172e575678c3bb9066d022279fad991d
https://pubmed.ncbi.nlm.nih.gov/2220066

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[Acro-osteolysis simulating mycetoma of the foot (pseudomycetoma)]

Autor: G I, Sukolin, A G, Mkhitar'ian, D D, Agakishnev

Publikováno v: Vestnik dermatologii i venerologii. (11)

Idiopathic multicentric acro-osteolysis is a complex heterogenic disease that may simulate mycetoma. A ten-year-old child has developed the condition, diagnosed as mycetoma for 7 years. Medical genetic examination of the patient helped correctly diag

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6ea86f42011ebda6e536206a07b8ea46
https://pubmed.ncbi.nlm.nih.gov/2288160

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Indicators of activity of enzymes and whey protein in patients with Devergie's disease

Autor: Z. V. Kuklina, G I. Sukolin, A. M. Nikiforov, V. T. Kuklin

Publikováno v: Kazan medical journal. 76:235-235

The etiology and pathogenesis of pityriasis versicolor pilaris Devergie remain poorly understood to date. Among 46 patients with Devergie's disease, examined for the detection of protein and protein fractions, there were male (24) and female (22) per

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::db5c6b30ecb00db83b18512ae2fc77b8
https://doi.org/10.17816/kazmj100897

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