Zobrazeno 1 - 7
of 7
pro vyhledávání: '"L. P. Melikyan"'
Autor:
B. A. Kobrinskii, N. A. Blagosklonov, N. S. Demikova, E. A. Nikolaeva, Y. Y. Kotalevskaya, L. P. Melikyan, Y. M. Zinovieva
Publikováno v:
Бюллетень сибирской медицины, Vol 21, Iss 2, Pp 67-73 (2022)
Aim. To improve the efficiency of diagnosis of hereditary lysosomal storage diseases using an intelligent computerbased decision support system.Materials and methods. Descriptions of 35 clinical cases from the literature and depersonalized data of 52
Externí odkaz:
https://doaj.org/article/ec32c9b1a68040e2a8eca19a9eed480e
Autor:
L. P. Melikyan, E. A. Bliznetz, M. I. Shtaut, A. O. Sedova, T. M. Sorokina, L. F. Kurilo, A. V. Polyakov, V. B. Chernykh
Publikováno v:
Андрология и генитальная хирургия, Vol 22, Iss 2, Pp 66-77 (2021)
Introduction. The effect of polymorphic variants of the androgen receptor gene (AR) on spermatogenesis and semen parameters in men with different genotypes for other loci has not been sufficiently studied.The aim of this work was to study the effect
Externí odkaz:
https://doaj.org/article/13c20e72995745cbb1d303cd207bb975
Autor:
L. P. Melikyan, V. B. Chernykh
Publikováno v:
Андрология и генитальная хирургия, Vol 20, Iss 2, Pp 35-39 (2019)
Genetic factors are a common cause of severe pathozoospermia and male infertility. An increase in the length of trinucleotide repeats causes a number of progressive neurodegenerative diseases, including spinal bulbar muscular atrophy — Kennedy synd
Externí odkaz:
https://doaj.org/article/5675aa7b5a884313ab0bab57eea98104
Autor:
Yu. L. Mizernitskiy, A. A. Novak, I. E. Zorina, S. E. Ryabova, I. A. Kovalev, E. G. Verchenko, V. S. Bereznitskiy, L. P. Melikyan, L. V. Egorov
Publikováno v:
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 67:88-92
Heterotaxy syndrome is a congenital malformation in which the internal organs of the chest and abdominal cavity have an abnormal location. People suffering from this syndrome have multiple complex defects in the heart, blood vessels, spleen, liver, l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17a7ab4d5aeb47d00fcbf25d25939573
https://doi.org/10.21508/1027-4065-2022-67-6-88-92
https://doi.org/10.21508/1027-4065-2022-67-6-88-92
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 65, Iss 6, Pp 84-90 (2021)
The Ehlers-Danlos syndrome is a rare (orphan) disease characterized by the connective tissue dysplasia, fragility of the blood vessels and tissues, and variable clinical pattern. The vascular type of Ehlers-Danlos syndrome, which belongs to Group A a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2199c7a5ac1ee9cb636881bcc26d1e1
https://doi.org/10.21508/1027-4065-2020-65-6-84-90
https://doi.org/10.21508/1027-4065-2020-65-6-84-90
Autor:
L. P. Melikyan, O. L. Mironovich, I. A. Kuznetsova, A. O. Sedova, L. F. Kurilo, Alexander V. Polyakov, T. M. Sorokina, O. A. Solovova, M. I. Shtaut, E. A. Bliznetz, V. B. Chernykh
Publikováno v:
Russian Journal of Genetics. 56:1000-1005
CAGn polymorphism in exon 1 of the androgen receptor (AR/HUMARA) gene is associated with pathozoospermia and male infertility, but its effect on spermatogenesis and male fertility is not well understood. The article presents the results of a study of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52e7f8debf8da9ee144d65c869ba9034
https://doi.org/10.1134/s1022795420080104
https://doi.org/10.1134/s1022795420080104
