Dadali E - Search Results

1

Identification of a Novel de Novo Variant in the SYT2 Gene Causing a Rare Type of Distal Hereditary Motor Neuropathy.

Mironovich O, Dadali E, Malmberg S, Markova T, Ryzhkova O, Poliakov A. Mironovich O, et al. Among authors: dadali e. Genes (Basel). 2020 Oct 22;11(11):1238. doi: 10.3390/genes11111238. Genes (Basel). 2020. PMID: 33105646 Free PMC article.

2

A Two-Year Clinical Description of a Patient with a Rare Type of Low-GGT Cholestasis Caused by a Novel Variant of USP53.

Shatokhina O, Semenova N, Demina N, Dadali E, Polyakov A, Ryzhkova O. Shatokhina O, et al. Among authors: dadali e. Genes (Basel). 2021 Oct 14;12(10):1618. doi: 10.3390/genes12101618. Genes (Basel). 2021. PMID: 34681012 Free PMC article.

3

Clinical and Genetic Characteristics of COL2A1-Associated Skeletal Dysplasias in 60 Russian Patients: Part I.

Markova T, Kenis V, Melchenko E, Osipova D, Nagornova T, Orlova A, Zakharova E, Dadali E, Kutsev S. Markova T, et al. Among authors: dadali e. Genes (Basel). 2022 Jan 13;13(1):137. doi: 10.3390/genes13010137. Genes (Basel). 2022. PMID: 35052477 Free PMC article.

4

[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.

5

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. Among authors: dadali e. Int J Mol Sci. 2022 Jul 14;23(14):7764. doi: 10.3390/ijms23147764. Int J Mol Sci. 2022. PMID: 35887114 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

[Clinical-genetic characteristics of hereditary motor-sensory neuropathy type 1 X].

Sharkova IV, Milovidova TB, Dadali EL, Poliakov AV. Sharkova IV, et al. Among authors: dadali el. Zh Nevrol Psikhiatr Im S S Korsakova. 2012;112(7):42-7. Zh Nevrol Psikhiatr Im S S Korsakova. 2012. PMID: 23011429 Russian.

8

[Clinical-genetic correlations in the hereditary motor-sensor neuropathy caused by mutations in the MPZ (P0) gene].

Milovidova TB, Dadali EL, Fedotov VP, Shchagina OA, Poliakov AV. Milovidova TB, et al. Among authors: dadali el. Zh Nevrol Psikhiatr Im S S Korsakova. 2011;111(12):48-55. Zh Nevrol Psikhiatr Im S S Korsakova. 2011. PMID: 22433810 Russian.

9

[Clinical-genetic analysis of limb-girdle muscular dystrophy 2 type I].

Ryzhkova OP, Sharkova IV, Dadali EL, Petrunina EL, Poliakov AV. Ryzhkova OP, et al. Among authors: dadali el. Zh Nevrol Psikhiatr Im S S Korsakova. 2012;112(6):55-9. Zh Nevrol Psikhiatr Im S S Korsakova. 2012. PMID: 22983245 Russian.

10

[Hereditary motor and sensory neuropathy type 4A].

Shagina OA, Dadali EL, Fedotov VP, Tiburkova TB, Poliakov AV. Shagina OA, et al. Among authors: dadali el. Zh Nevrol Psikhiatr Im S S Korsakova. 2010;110(5 Pt 1):13-6. Zh Nevrol Psikhiatr Im S S Korsakova. 2010. PMID: 21322820 Russian.

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