S. Bichev

发表

Comparative Characteristics of Napsin A, TTF 1 and EGFR Mutation Expression in Mucinous Lung Cell Carcinomas

Sylvia N Genova, Veselin T. Belovezhdov, S. Bichev, 2017, Folia medica.

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

Hanns Lochmüller, B. Schoser, A. Huebner, 2017, Neuromuscular Disorders.

EGFR mutation status yield from bronchoalveolar lavage in patients with primary pulmonary adenocarcinoma compared to a venous blood sample and tissue biopsy

S. Bichev, E. Mekov, N. Yanev, 2021, PeerJ.

Comprehensive Genetic Evaluation of Children With Syndromic Craniosynostosis by a Combination of Cytogenetics, Multiplex Ligation-dependent Probe Amplification and Array-based Comparative Genomic Hybridisation

S. Bichev, S. Hadjidekova, D. Avdjieva-Tzavella, 2021 .

Novel Mutations in the DYNC1H1 Tail Domain Refine the Genetic and Clinical Spectrum of Dyneinopathies

V. Timmerman, A. Jordanova, I. Litvinenko, 2015, Human mutation.

Association Between Loss of Dp140 and Cognitive Impairment in Duchenne and Becker Dystrophies

T. Todorov, M. Raycheva, V. Mitev, 2013, Balkan journal of medical genetics : BJMG.

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

M. Georgieva, Mari Hachmeriyan, L. Angelova, 2022, Folia medica.

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

M. Bahlo, H. Goebel, L. Kalaydjieva, 2015, Neuromuscular Disorders.

Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency

Hanns Lochmüller, V. Timmerman, A. Suls, 2011, Neurology.

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

Y. Slavova, A. Savov, S. Bichev, 2015, Cellular Oncology.

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

E. Naseva, K. Koynov, D. Damyanov, 2015, Journal of B.U.ON. : official journal of the Balkan Union of Oncology.

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

Y. Slavova, A. Savov, S. Bichev, 2014, Cellular Oncology.

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

L. Kalaydjieva, M. Raycheva, I. Tournev, 2015, Behavioural neurology.

APC promoter 1B deletion in familial polyposis—implications for mutation‐negative families

T. Todorov, T. Kadiyska, S. Bichev, 2014, Clinical genetics.

Comprehensive Genetic Evaluation of Bulgarian Children with Syndromic Craniosynostosis

S. Bichev, S. Hadjidekova, D. Avdjieva-Tzavella, 2022, Balkan journal of medical genetics : BJMG.