Dadali EL - Search Results

1

Clinical Manifestations of Various Molecular Cytogenetic Variants of Eight Cases of "8p Inverted Duplication/Deletion Syndrome".

Yurchenko DA, Minzhenkova ME, Dadali EL, Markova ZG, Rudenskaya GE, Matyushchenko GN, Kanivets IV, Shilova NV. Yurchenko DA, et al. Among authors: dadali el. Biomedicines. 2022 Feb 28;10(3):567. doi: 10.3390/biomedicines10030567. Biomedicines. 2022. PMID: 35327368 Free PMC article.

2

Complex Diagnostics of Non-Specific Intellectual Developmental Disorder.

Levchenko O, Dadali E, Bessonova L, Demina N, Rudenskaya G, Matyushchenko G, Markova T, Anisimova I, Semenova N, Shchagina O, Ryzhkova O, Zinchenko R, Galkina V, Voinova V, Nagieva S, Lavrov A. Levchenko O, et al. Int J Mol Sci. 2022 Jul 14;23(14):7764. doi: 10.3390/ijms23147764. Int J Mol Sci. 2022. PMID: 35887114 Free PMC article.

3

[Clinical and genetic characteristics of facioscapulohumeral muscular dystrophy Landuzi-Dezherina type 1].

Dadali EL, Sharkova IV, Zernov NV, Rudenskaya GE, Skoblov MY. Dadali EL, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2017;117(11):122-128. doi: 10.17116/jnevro2017117111122-128. Zh Nevrol Psikhiatr Im S S Korsakova. 2017. PMID: 29265097 Russian.

4

[Clinical and genetic characteristics of epilepsy caused by mutations in the PCDH19 gene (OMIM: 300088)].

Dadali EL, Mishina IA, Borovikov AO, Sharkov AA, Kanivets IV. Dadali EL, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2020;120(1):55-61. doi: 10.17116/jnevro202012001155. Zh Nevrol Psikhiatr Im S S Korsakova. 2020. PMID: 32105270 Russian.

5

Ataxia with Oculomotor Apraxia Type 4 with PNKP Common "Portuguese" and Novel Mutations in Two Belarusian Families.

Rudenskaya GE, Marakhonov AV, Shchagina OA, Lozier ER, Dadali EL, Akimova IA, Petrova NV, Konovalov FA. Rudenskaya GE, et al. Among authors: dadali el. J Pediatr Genet. 2019 Jun;8(2):58-62. doi: 10.1055/s-0039-1684008. Epub 2019 Mar 27. J Pediatr Genet. 2019. PMID: 31061747 Free PMC article.

6

KIF1A-related autosomal dominant spastic paraplegias (SPG30) in Russian families.

Rudenskaya GE, Kadnikova VA, Ryzhkova OP, Bessonova LA, Dadali EL, Guseva DS, Markova TV, Khmelkova DN, Polyakov AV. Rudenskaya GE, et al. Among authors: dadali el. BMC Neurol. 2020 Aug 3;20(1):290. doi: 10.1186/s12883-020-01872-4. BMC Neurol. 2020. PMID: 32746806 Free PMC article.

7

[AP4-assocated hereditary spastic paraplegias].

Rudenskaya GE, Guseva DM, Mironovich OL, Kadnikova VA, Dadali EL, Komar'kov IF, Novoselova OG, Ryzhkova OP. Rudenskaya GE, et al. Among authors: dadali el. Zh Nevrol Psikhiatr Im S S Korsakova. 2021;121(2):71-78. doi: 10.17116/jnevro202112102171. Zh Nevrol Psikhiatr Im S S Korsakova. 2021. PMID: 33728854 Russian.

8

[Diversity of CACNA1A-related disorders].

Rudenskaya GE, Sermyagina IG, Chukhrova AL, Dadali EL, Lozier ER, Shchagina OA. Rudenskaya GE, et al. Among authors: dadali el. Zh Nevrol Psikhiatr Im S S Korsakova. 2021;121(12):106-111. doi: 10.17116/jnevro2021121121106. Zh Nevrol Psikhiatr Im S S Korsakova. 2021. PMID: 35041321 Russian.

9

HINT1 gene pathogenic variants: the most common cause of recessive hereditary motor and sensory neuropathies in Russian patients.

Shchagina OA, Milovidova TB, Murtazina AF, Rudenskaya GE, Nikitin SS, Dadali EL, Polyakov AV. Shchagina OA, et al. Among authors: dadali el. Mol Biol Rep. 2020 Feb;47(2):1331-1337. doi: 10.1007/s11033-019-05238-z. Epub 2019 Dec 17. Mol Biol Rep. 2020. PMID: 31848916

10

Mitochondrial DNA maintenance disorders in 102 patients from different parts of Russia: Mutational spectrum and phenotypes.

Bychkov IO, Itkis YS, Tsygankova PG, Krylova TD, Mikhaylova SV, Klyushnikov SA, Pechatnikova NL, Degtyareva AV, Nikolaeva EA, Seliverstov YA, Kurbatov SA, Dadali EL, Rudenskaya GE, Illarioshkin SN, Zakharova EY. Bychkov IO, et al. Among authors: dadali el. Mitochondrion. 2021 Mar;57:205-212. doi: 10.1016/j.mito.2021.01.004. Epub 2021 Jan 21. Mitochondrion. 2021. PMID: 33486010

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