Search Results - "Basargina, EN"

175 Very rare case of Noonan syndrome, type 2 by Gandaeva, LA, Zhurkova, NV, Basargina, EN, Pushkov, AA, Degtayreva, TD, Miroshnichenko, VP, Kondakova, OB, Savostyanov, KV

“…BackgroundNoonan syndrome, type 2 (NS2) is rare autosomal recessive disorder of RASopathies group, caused by mutations in the LZTR1 gene. NS2 characterized by…”
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P771P36 deletion syndrome in children with cardiomyopathy: two clinical cases by Zhurkova, N V, Pushkov, A A, Savostyanov, K V, Basargina, EN, Pakhomov, A V, Ermolenko, V S, Derevianina, Y V

“…Background and aimsSyndrome deletion of chromosome region 1 p36 is a chromosome syndrome with multiple anomalies, congenital heart disease and mental…”
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GP33 High prevalence noonan syndrome in russian children with hypertrophic cardiomyopathy, diagnosed by next generation sequencing by Zhurkova, N, Savostyanov, K, Pushkov, AA, Vashakmadze, ND, Fedorova, N, Zharova, OP, Gandaeva, LA, Sdvigova, NA, Kondakova, OB, Basargina, EN

“…BackgraundNoonan syndrome - is rare autosomal dominant disorder from RASopathies group, characterized by facial dysmorphism, short stature, hypertrophic…”
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P77 1P36 deletion syndrome in children with cardiomyopathy: two clinical cases by Zhurkova, NV, Pushkov, AA, Savostyanov, KV, Basargina, EN, Pakhomov, AV, Ermolenko, VS, Derevianina, YV

“…Background and aimsSyndrome deletion of chromosome region 1 p36 is a chromosome syndrome with multiple anomalies, congenital heart disease and mental…”
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Biochemical and immunological markers of insufficiency of blood circulation in children with cardiomyopathies by Bershova, T. V., Shmatkova, Yu. V., Ivanov, A. P., Bakanov, M. I., Basargina, E. N., Zurabova, R. B., Monaenkova, S. V., Gerasimova, Yu. V.

“…Complex clinical-laboratory investigation of children with congestive heart failure developed on the basis of dilated cardiomyopathy and hypertrophic…”
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