Todorov T - Search Results

1

Fragile X mosaic male full mutation/normal allele detected by PCR/MS-MLPA.

Todorov T, Todorova A, Kirov A, Dimitrov B, Carvalho R, Nygren AO, Boneva I, Mitev V. Todorov T, et al. BMJ Case Rep. 2009;2009:bcr06.2008.0139. doi: 10.1136/bcr.06.2008.0139. Epub 2009 May 18. BMJ Case Rep. 2009. PMID: 21686918 Free PMC article.

2

A large deletion and novel point mutations in the calpain 3 gene (CAPN3) in Bulgarian LGMD2A patients.

Todorova A, Georgieva B, Tournev I, Todorov T, Bogdanova N, Mitev V, Mueller CR, Kremensky I, Horst J. Todorova A, et al. Among authors: todorov t. Neurogenetics. 2007 Aug;8(3):225-9. doi: 10.1007/s10048-007-0083-3. Epub 2007 Feb 23. Neurogenetics. 2007. PMID: 17318636

3

MLPA analysis/complete sequencing of the DMD gene in a group of Bulgarian Duchenne/Becker muscular dystrophy patients.

Todorova A, Todorov T, Georgieva B, Lukova M, Guergueltcheva V, Kremensky I, Mitev V. Todorova A, et al. Among authors: todorov t. Neuromuscul Disord. 2008 Aug;18(8):667-70. doi: 10.1016/j.nmd.2008.06.369. Epub 2008 Jul 23. Neuromuscul Disord. 2008. PMID: 18653336

4

A unified rapid PCR method for detection of normal and expanded trinucleotide alleles of CAG repeats in huntington chorea and CGG repeats in fragile X syndrome.

Todorov T, Todorova A, Georgieva B, Mitev V. Todorov T, et al. Mol Biotechnol. 2010 Jun;45(2):150-4. doi: 10.1007/s12033-010-9260-y. Mol Biotechnol. 2010. PMID: 20217280

5

Molecular basis of mental retardation in a sample from Bulgaria.

Todorov T, Todorova A, Avdjieva D, Dimova P, Angelova L, Tincheva R, Mitev V. Todorov T, et al. Genet Couns. 2010;21(2):257-62. Genet Couns. 2010. PMID: 20681229 No abstract available.

6

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. Among authors: todorov t. 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

7

Spontaneous recurrent mutations and a complex rearrangement in the MECP2 gene in the light of current models of mutagenesis.

Todorov T, Todorova A, Motoescu C, Dimova P, Iancu D, Craiu D, Stoian D, Barbarii L, Bojinova V, Mitev V. Todorov T, et al. Mutat Res. 2012 Jun 1;734(1-2):69-72. doi: 10.1016/j.mrfmmm.2012.04.001. Epub 2012 Apr 16. Mutat Res. 2012. PMID: 22525432

8

A novel PCDH19 mutation inherited from an unaffected mother.

Dimova PS, Kirov A, Todorova A, Todorov T, Mitev V. Dimova PS, et al. Among authors: todorov t. Pediatr Neurol. 2012 Jun;46(6):397-400. doi: 10.1016/j.pediatrneurol.2012.03.004. Pediatr Neurol. 2012. PMID: 22633638

9

Different methylation patterns in BWS/SRS cases clarified by MS-MLPA.

Lukova M, Todorova A, Todorov T, Mitev V. Lukova M, et al. Among authors: todorov t. Mol Biol Rep. 2013 Jan;40(1):263-8. doi: 10.1007/s11033-012-2057-2. Epub 2012 Oct 20. Mol Biol Rep. 2013. PMID: 23086270

10

15q13.3 microdeletions in a prospectively recruited cohort of patients with idiopathic generalized epilepsy in Bulgaria.

Kirov A, Dimova P, Todorova A, Mefford H, Todorov T, Saraylieva G, Bojinova V, Mitev V, Helbig I. Kirov A, et al. Among authors: todorov t. Epilepsy Res. 2013 May;104(3):241-5. doi: 10.1016/j.eplepsyres.2012.10.013. Epub 2013 Jan 23. Epilepsy Res. 2013. PMID: 23352738

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

500 results

Search Page

Filters