Bichev S - Search Results

1

Limb girdle muscular dystrophy 2G in a religious minority of Bulgarian Muslims homozygous for the c.75G>A, p.Trp25X mutation.

Chamova T, Bichev S, Todorov T, Gospodinova M, Taneva A, Kastreva K, Zlatareva D, Krupev M, Hadjiivanov R, Guergueltcheva V, Grozdanova L, Tzoneva D, Huebner A, V der Hagen M, Schoser B, Lochmüller H, Todorova A, Tournev I. Chamova T, et al. Among authors: bichev s. Neuromuscul Disord. 2018 Aug;28(8):625-632. doi: 10.1016/j.nmd.2018.05.005. Epub 2018 May 17. Neuromuscul Disord. 2018. PMID: 29935994

2

GNE myopathy in Roma patients homozygous for the p.I618T founder mutation.

Chamova T, Guergueltcheva V, Gospodinova M, Krause S, Cirak S, Kaprelyan A, Angelova L, Mihaylova V, Bichev S, Chandler D, Naydenov E, Grudkova M, Djukmedzhiev P, Voit T, Pogoryelova O, Lochmüller H, Goebel HH, Bahlo M, Kalaydjieva L, Tournev I. Chamova T, et al. Among authors: bichev s. Neuromuscul Disord. 2015 Sep;25(9):713-8. doi: 10.1016/j.nmd.2015.07.004. Epub 2015 Jul 13. Neuromuscul Disord. 2015. PMID: 26231298

3

Cognitive Impairment and Brain Imaging Characteristics of Patients with Congenital Cataracts, Facial Dysmorphism, Neuropathy Syndrome.

Chamova T, Zlatareva D, Raycheva M, Bichev S, Kalaydjieva L, Tournev I. Chamova T, et al. Among authors: bichev s. Behav Neurol. 2015;2015:639539. doi: 10.1155/2015/639539. Epub 2015 Apr 28. Behav Neurol. 2015. PMID: 26060356 Free PMC article.

4

Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency.

Guergueltcheva V, Peeters K, Baets J, Ceuterick-de Groote C, Martin JJ, Suls A, De Vriendt E, Mihaylova V, Chamova T, Almeida-Souza L, Ydens E, Tzekov C, Hadjidekov G, Gospodinova M, Storm K, Reyniers E, Bichev S, van der Ven PF, Fürst DO, Mitev V, Lochmüller H, Timmerman V, Tournev I, De Jonghe P, Jordanova A. Guergueltcheva V, et al. Among authors: bichev s. Neurology. 2011 Dec 13;77(24):2105-14. doi: 10.1212/WNL.0b013e31823dc51e. Epub 2011 Nov 30. Neurology. 2011. PMID: 22131542

5

Association between loss of dp140 and cognitive impairment in duchenne and becker dystrophies.

Chamova T, Guergueltcheva V, Raycheva M, Todorov T, Genova J, Bichev S, Bojinova V, Mitev V, Tournev I, Todorova A. Chamova T, et al. Among authors: bichev s. Balkan J Med Genet. 2013 Jun;16(1):21-30. doi: 10.2478/bjmg-2013-0014. Balkan J Med Genet. 2013. PMID: 24265581 Free PMC article.

6

APC promoter 1B deletion in familial polyposis--implications for mutation-negative families.

Kadiyska TK, Todorov TP, Bichev SN, Vazharova RV, Nossikoff AV, Savov AS, Mitev VI. Kadiyska TK, et al. Among authors: bichev sn. Clin Genet. 2014 May;85(5):452-7. doi: 10.1111/cge.12210. Epub 2013 Jun 24. Clin Genet. 2014. PMID: 23725351

7

Novel mutations in the DYNC1H1 tail domain refine the genetic and clinical spectrum of dyneinopathies.

Peeters K, Bervoets S, Chamova T, Litvinenko I, De Vriendt E, Bichev S, Kancheva D, Mitev V, Kennerson M, Timmerman V, De Jonghe P, Tournev I, MacMillan J, Jordanova A. Peeters K, et al. Among authors: bichev s. Hum Mutat. 2015 Mar;36(3):287-91. doi: 10.1002/humu.22744. Hum Mutat. 2015. PMID: 25512093

8

EGFR mutations in patients with non small-cell lung cancer in Bulgaria and treatment with gefitinib.

Damyanov D, Koynov K, Naseva E, Bichev S. Damyanov D, et al. Among authors: bichev s. J BUON. 2015 Jan-Feb;20(1):136-41. J BUON. 2015. PMID: 25778308 Free article.

9

Molecular screening for fragile X syndrome in children with unexplained intellectual disability and/or autistic behaviour.

Stoyanova M, Hachmeriyan M, Levkova M, Bichev S, Georgieva M, Mladenov V, Angelova L. Stoyanova M, et al. Among authors: bichev s. Folia Med (Plovdiv). 2022 Feb 28;64(1):27-32. doi: 10.3897/folmed.64.e60518. Folia Med (Plovdiv). 2022. PMID: 35851904

10

Epidermal growth factor receptor mutations in East European non-small cell lung cancer patients.

Bichev SN, Marinova DM, Slavova YG, Savov AS. Bichev SN, et al. Cell Oncol (Dordr). 2015 Apr;38(2):145-53. doi: 10.1007/s13402-014-0211-7. Epub 2014 Dec 23. Cell Oncol (Dordr). 2015. PMID: 25534657

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