Mihaylova V - Search Results

1

Spectrum of mutations in the Wilson disease gene (ATP7B) in the Bulgarian population.

Todorov T, Savov A, Jelev H, Panteleeva E, Konstantinova D, Krustev Z, Mihaylova V, Tournev I, Tankova L, Tzolova N, Kremensky I. Todorov T, et al. Among authors: mihaylova v. Clin Genet. 2005 Nov;68(5):474-6. doi: 10.1111/j.1399-0004.2005.00516.x. Clin Genet. 2005. PMID: 16207219 No abstract available.

2

A novel mutation in ATP7B gene associated with severe neurological and psychiatric symptoms.

Mihaylova V, Todorov T, Tournev I, Cherninkova S, Nikoevski N, Raicheva M, Iankova P, Petrova I, Savov A, Kremesky I. Mihaylova V, et al. Eur Neurol. 2006;55(2):99-100. doi: 10.1159/000092783. Epub 2006 Apr 21. Eur Neurol. 2006. PMID: 16636554 Free article. No abstract available.

3

Wilson's disease in two consecutive generations in a Bulgarian Roma family.

Mihaylova V, Todorov T, Jelev H, Cherninkova S, Raycheva M, Savov A, Kremensky I, Tournev I. Mihaylova V, et al. J Neurol. 2007 Oct;254(10):1462-3. doi: 10.1007/s00415-007-0564-1. Epub 2007 Aug 14. J Neurol. 2007. PMID: 17694349 No abstract available.

4

Unique PABPN1 gene mutation in a large Bulgarian family with OPMD.

Mihaylova V, Müller T, Petrova I, Tournev I, Cherninkova S, Walter MC, Deschauer M. Mihaylova V, et al. J Neurol. 2008 Apr;255(4):609-11. doi: 10.1007/s00415-008-0769-y. Epub 2008 Feb 19. J Neurol. 2008. PMID: 18274805 No abstract available.

5

Ethnic specific background of mutations in Bulgarian patients with Wilson disease.

Todorov T, Savov A, Mihaylova V, Buettner J, Koseva O, Krustev Z, Jelev H, Tournev I, Penkov V, Konstantinova D, Tankova L, Tzolova N, Kremensky I, Schmidt H. Todorov T, et al. Among authors: mihaylova v. Genet Couns. 2007;18(4):445-50. Genet Couns. 2007. PMID: 18286826 No abstract available.

6

Genetic heterogeneity and minor CYP1B1 involvement in the molecular basis of primary congenital glaucoma in Gypsies.

Sivadorai P, Cherninkova S, Bouwer S, Kamenarova K, Angelicheva D, Seeman P, Hollingsworth K, Mihaylova V, Oscar A, Dimitrova G, Kaneva R, Tournev I, Kalaydjieva L. Sivadorai P, et al. Among authors: mihaylova v. Clin Genet. 2008 Jul;74(1):82-7. doi: 10.1111/j.1399-0004.2008.01024.x. Epub 2008 Jun 5. Clin Genet. 2008. PMID: 18537981

7

Neurological symptoms, genotype-phenotype correlations and ethnic-specific differences in Bulgarian patients with Wilson disease.

Mihaylova V, Todorov T, Jelev H, Kotsev I, Angelova L, Kosseva O, Georgiev G, Ganeva R, Cherninkova S, Tankova L, Savov A, Tournev I. Mihaylova V, et al. Neurologist. 2012 Jul;18(4):184-9. doi: 10.1097/NRL.0b013e31825cf3b7. Neurologist. 2012. PMID: 22735241

8

Evoked Potentials in Patients With Wilson Disease.

Mihaylova VM, Kosseva OR, Kotzev IA, Georgiev G, Kremensky IM, Todorov TN, Tournev IL. Mihaylova VM, et al. J Clin Neurophysiol. 2022 Sep 1;39(6):510-512. doi: 10.1097/WNP.0000000000000797. Epub 2020 Nov 10. J Clin Neurophysiol. 2022. PMID: 33181595

9

Highly variable neural involvement in sphingomyelinase-deficient Niemann-Pick disease caused by an ancestral Gypsy mutation.

Mihaylova V, Hantke J, Sinigerska I, Cherninkova S, Raicheva M, Bouwer S, Tincheva R, Khuyomdziev D, Bertranpetit J, Chandler D, Angelicheva D, Kremensky I, Seeman P, Tournev I, Kalaydjieva L. Mihaylova V, et al. Brain. 2007 Apr;130(Pt 4):1050-61. doi: 10.1093/brain/awm026. Epub 2007 Mar 14. Brain. 2007. PMID: 17360762

10

Severe neuropsychiatric symptoms in two siblings with intermediate type of Niemann-Pick disease.

Mihaylova V, Hantke J, Cherninkova S, Krastev S, Radionova M, Raicheva M, Sinigerska I, Jelev H, Jablensky A, Kalaydjieva L, Tournev I. Mihaylova V, et al. J Neurol. 2008 Sep;255(9):1434-5. doi: 10.1007/s00415-008-0953-0. Epub 2008 Jul 14. J Neurol. 2008. PMID: 18677631 No abstract available.

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