Search Results - "Ulas, V Iu"

Variations of heterochromatic chromosomal regions and chromosome abnormalities in children with autism: identification of genetic markers in autistic spectrum disorders by Vorsanova, S G, Iurov, I Iu, Demidova, I A, Voinova-Ulas, V Iu, Kravets, V S, Solov'ev, I V, Gorbachevskaia, N L, Iurov, Iu B

“…In the present study, the cytogenetic and molecular cytogenetic analysis of 90 children with autism and their mothers (18 subjects) was carried out. Chromosome…”
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Epigenetic study of Rett's syndrome as an adequate model for autistic disorders by Iurov, I Iu, Vorsanova, S G, Voinova-Ulas, V Iu, Villard, L, Demidova, I A, Giunti, L, Guivabyccu-Uzielli, M L, Budilov, A V, Beresheva, A K, Novikov, P V, Iurov, Iu V

“…Rett's syndrome (RTT) is a severe hereditary disorder of the nervous system. MECP2 gene mutations are considered as a primary cause of the disease. In the…”
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Genotype-phenotype correlations in Rett syndrome: the study of Russian cohort of patients by Vorsanova, S G, Ulas, V Iu, Iurov, Iu B, Giovanucci-Uzielli, M L, Demidova, I A, Gianti, L, Villard, L, Iurov, I Iu, Beresheva, A K, Novikov, P V

“…Rett syndrome (RTT) is a severe neurodevelopmental disorder caused by mutations in methyl-CpG-binding protein 2 gene (MECP2). We carried out a mutations…”
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The indices of the thrombocyte serotonin system and of the nerve growth factor system in children with hereditary disorders of neuropsychic development by Brusov, O S, Zlobina, G P, Nikolaeva, E A, Ulas, V Iu, Faktor, M I, Pavlova, O A, Danilovskaia, E V, Kliushnik, T P, Kazantseva, L Z

“…Indices of both platelet serotoninergic system and the system of nerve growth factor (NGF) were examined in children with neurofibromatosis (15 patients),…”
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Cytogenetic and molecular genetic diagnostics of Rett syndrome in children by Vorsanova, S G, Demidova, I A, Ulas, V Iu, Solov'ev, I V, Kravets, V S, Kazantseva, L Z, Iurov, Iu B

“…Rett syndrome in 32 children (31 girls and 1 boy) was diagnosed according to International association on Rett syndrome. The phenomenon of the presence of…”
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Contemporary views on Rett's syndrome: clinical, cytogenetic and molecular studies by Vorsanova, S G, Ulas, V Iu, Demidova, I A, Kravets, V S, Iurov, Iu B

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World congress on Rett syndrome by Gorbachevskaia, N L, Ulas, V Iu

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