Found: 19 articles

Article Edition
Smolnova T.Yu., Trofimov D.Yu., Chuprynin V.D.
The role of tenascin gene (TNXB) mutation in Ellers-like phenotype formation in patients with genital prolapse
№6 / 2020
Smolnova T.Yu., Trofimov D.Yu., Chuprynin V.D., Chursin V.V.
Mutation in the ADAMTSL4 gene in a patient with a Marfan-like phenotype (Marfanoid appearance) without Ectopia lentis with uterine scar failure after cesarean section
№6 / 2020
Ivanova D.S., Viktorova I.A., Kochimov R.S, Adyrbayev A.M.
Diagnostics and tactics of management of patients with signs of connective tissue dysplasia, headache and disorder of sensitivity. Literature review
№6 / 2020
Semenova E.V., Nechaeva G.I., Loginova E.N., Semenkin A.A.
Hereditary connective tissue disorders: a thematic bibliographic review of foreign publications
№6 / 2020
Smolnova T.Yu., Trofimov D.Yu., Chuprynin V.D., Nechaeva G.I.
To the point about etiopathogenetic causes of Marfan-like phenotype (marfanoid appearance) formation
№6 / 2020
Akhiyarova K.E., Sadretdinova L.D., Akhmetova А.М., Gantseva Kh.Kh., Khusainova R.I., Tyurin A.V.
Study of bone mineral density in young people with pain syndrome of different localization
№6 / 2020
Rudoy A.S., Uryvaev A.M.
Pathogenesis of pre-malignant gastric lesions in patients with Marfan syndrome
№6 / 2020
Dakuko A.N., Krivtsova L.A., Nalobina A.N., Ivaschenko O.N., Plekhanova M.A.
Influence of connective tissue dysplasia at the formation of adaptive and functional capabilities in children engaging precise technical sports activities
№6 / 2020
Druk I.V., Nechaeva G.I., Rezinovskaya T.L.
Deficiency of body mass in a group of young-age patients with connective tissue dysplasia
№6 / 2020
Yagoda A.V., Airapetian L.A.
Polymorphisms of thrombophilia genes with some visceral signs of connective tissue dysplasia
№6 / 2020
Vershinina M.V., Nechaeva G.I., Gudilin V.A.
Relative cardiovascular risk in young patients with connective tissue dysplasia
№6 / 2020
Chernova A.A., Nikulina S.Yu., Matyushin G.V., Lebedeva I.I.
Signs of connective tissue dysplasia and the gene for endothelial nitric synthase type 3 (NOS3) in case of Wolff–Parkinson–White syndrome
№6 / 2020


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