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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
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№6 / 2020
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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
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№6 / 2020
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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
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№6 / 2020
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Semenova E.V., Nechaeva G.I., Loginova E.N., Semenkin A.A.
Hereditary connective tissue disorders: a thematic bibliographic review of foreign publications
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№6 / 2020
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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
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№6 / 2020
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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
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№6 / 2020
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Rudoy A.S., Uryvaev A.M.
Pathogenesis of pre-malignant gastric lesions in patients with Marfan syndrome
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№6 / 2020
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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
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№6 / 2020
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Druk I.V., Nechaeva G.I., Rezinovskaya T.L.
Deficiency of body mass in a group of young-age patients with connective tissue dysplasia
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№6 / 2020
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Yagoda A.V., Airapetian L.A.
Polymorphisms of thrombophilia genes with some visceral signs of connective tissue dysplasia
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№6 / 2020
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Vershinina M.V., Nechaeva G.I., Gudilin V.A.
Relative cardiovascular risk in young patients with connective tissue dysplasia
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№6 / 2020
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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
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№6 / 2020
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