Yordanova I - Search Results

1

KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.

Weckhuysen S, Mandelstam S, Suls A, Audenaert D, Deconinck T, Claes LR, Deprez L, Smets K, Hristova D, Yordanova I, Jordanova A, Ceulemans B, Jansen A, Hasaerts D, Roelens F, Lagae L, Yendle S, Stanley T, Heron SE, Mulley JC, Berkovic SF, Scheffer IE, de Jonghe P. Weckhuysen S, et al. Among authors: yordanova i. Ann Neurol. 2012 Jan;71(1):15-25. doi: 10.1002/ana.22644. Ann Neurol. 2012. PMID: 22275249

2

Four generations of epilepsy caused by an inherited microdeletion of the SCN1A gene.

Suls A, Velizarova R, Yordanova I, Deprez L, Van Dyck T, Wauters J, Guergueltcheva V, Claes LR, Kremensky I, Jordanova A, De Jonghe P. Suls A, et al. Among authors: yordanova i. Neurology. 2010 Jul 6;75(1):72-6. doi: 10.1212/WNL.0b013e3181e62088. Epub 2010 May 19. Neurology. 2010. PMID: 20484682

3

Generalized epilepsy with febrile seizures plus: novel SCN1A mutation.

Dimova PS, Yordanova I, Bojinova V, Jordanova A, Kremenski I. Dimova PS, et al. Among authors: yordanova i. Pediatr Neurol. 2010 Feb;42(2):137-40. doi: 10.1016/j.pediatrneurol.2009.09.007. Pediatr Neurol. 2010. PMID: 20117752

4

One novel Dravet syndrome causing mutation and one recurrent MAE causing mutation in SCN1A gene.

Yordanova I, Todorov T, Dimova P, Hristova D, Tincheva R, Litvinenko I, Yotovska O, Kremensky I, Todorova A. Yordanova I, et al. Neurosci Lett. 2011 Apr 25;494(2):180-3. doi: 10.1016/j.neulet.2011.03.008. Epub 2011 Mar 15. Neurosci Lett. 2011. PMID: 21396429

5

Molecular-genetic diagnostics of von Hippel-Lindau syndrome (VHL) in Bulgaria: first complex mutation event in the VHL gene.

Glushkova M, Dimova P, Yordanova I, Todorov T, Tourtourikov I, Mitev V, Todorova A. Glushkova M, et al. Among authors: yordanova i. Int J Neurosci. 2018 Feb;128(2):117-124. doi: 10.1080/00207454.2017.1372436. Epub 2017 Sep 13. Int J Neurosci. 2018. PMID: 28849724

6

BARTH SYNDROME IN MALE AND FEMALE SIBLINGS CAUSED BY A NOVEL MUTATION IN THE TAZ GENE.

Avdjieva-Tzavella DM, Todorova AP, Kathom H M, Ivanova MB, Yordanova IT, Todorov TP, Litvinenko IO, Dasheva-Dimitrova AT, Tincheva RS. Avdjieva-Tzavella DM, et al. Among authors: yordanova it. Genet Couns. 2016;27(4):495-501. Genet Couns. 2016. PMID: 30226969

7

Monoallelic expression of the TTR gene as a contributor to the age at onset and penetrance of TTR-related amyloidosis.

Yordanova I, Pavlova Z, Kirov A, Todorov T, Alexiev A, Sarafov S, Mateva L, Chamova T, Gospodinova M, Mitev V, Tournev I, Todorova A. Yordanova I, et al. Gene. 2019 Jul 15;705:16-21. doi: 10.1016/j.gene.2019.04.030. Epub 2019 Apr 11. Gene. 2019. PMID: 30981840

8

First cases of pyridoxine-dependent epilepsy in Bulgaria: novel mutation in the ALDH7A1 gene.

Tincheva S, Todorov T, Todorova A, Georgieva R, Stamatov D, Yordanova I, Kadiyska T, Georgieva B, Bojidarova M, Tacheva G, Litvinenko I, Mitev V. Tincheva S, et al. Among authors: yordanova i. Neurol Sci. 2015 Dec;36(12):2209-12. doi: 10.1007/s10072-015-2338-3. Epub 2015 Aug 1. Neurol Sci. 2015. PMID: 26232297

9

Schwerer Schub einer generalisierten pustulösen Psoriasis behandelt mit Spesolimab, einem monoklonalen Antikörper gegen IL‐36: Severe flare of generalized pustular psoriasis treated with spesolimab, an IL‐36‐directed monoclonal antibody.

Mateeva V, Vasilev P, Gospodinova K, Gincheva V, Shahid M, Kostova P, Lukanov T, Yordanova I. Mateeva V, et al. Among authors: yordanova i. J Dtsch Dermatol Ges. 2024 May;22(5):696-699. doi: 10.1111/ddg.15334_g. J Dtsch Dermatol Ges. 2024. PMID: 38730537 German. No abstract available.

10

Developing transmissible vaccines for animal infections.

Streicker DG, Griffiths ME, Antia R, Bergner L, Bowman P, de Moraes MVDS, Esvelt K, Famulare M, Gilbert A, He B, Jarvis MA, Kennedy DA, Kuzma J, Wanyonyi CN, Remien C, Rocke T, Rosenke K, Schreiner C, Sheen J, Simons D, Yordanova IA, Bull JJ, Nuismer SL. Streicker DG, et al. Among authors: yordanova ia. Science. 2024 Apr 19;384(6693):275-277. doi: 10.1126/science.adn3231. Epub 2024 Apr 18. Science. 2024. PMID: 38669579

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