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SCN1A mutation spectrum in a cohort of Bulgarian patients with GEFS+ phenotype.
Turk J Pediatr. 2020;62(5):711-725. doi: 10.24953/turkjped.2020.05.002.
Turk J Pediatr. 2020.
PMID: 33108073
Free article.
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: bojidarova m.
Neurol Sci. 2015 Dec;36(12):2209-12. doi: 10.1007/s10072-015-2338-3. Epub 2015 Aug 1.
Neurol Sci. 2015.
PMID: 26232297
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Molecular genetic diagnostics of tuberous sclerosis complex in Bulgaria: six novel mutations in the TSC1 and TSC2 genes.
Glushkova M, Bojinova V, Koleva M, Dimova P, Bojidarova M, Litvinenko I, Todorov T, Iluca E, Calusaru C, Neagu E, Craiu D, Mitev V, Todorova A.
Glushkova M, et al. Among authors: bojidarova m.
J Genet. 2018 Jun;97(2):419-427.
J Genet. 2018.
PMID: 29932062
Free article.
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The Bulgarian version of the Childhood Health Assessment Questionnaire (CHAQ) and the Child Health Questionnaire (CHQ).
Mihaylova D, Ruperto N, Kibarova V, Teltcharova-Mihaylovska A, Kalaikov D, Stefanov S, Lisichki K, Bojidarova M; Paediatric Rheumatology International Trials Organisation.
Mihaylova D, et al. Among authors: bojidarova m.
Clin Exp Rheumatol. 2001 Jul-Aug;19(4 Suppl 23):S30-4.
Clin Exp Rheumatol. 2001.
PMID: 11510327
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The Bulgarian version of the Juvenile Arthritis Multidimensional Assessment Report (JAMAR).
Mihaylova D, Varbanova B, Stefanov S, Teltcharova-Mihaylovska A, Lisichki K, Bojidarova M, Consolaro A, Bovis F, Ruperto N; Paediatric Rheumatology International Trials Organisation (PRINTO).
Mihaylova D, et al. Among authors: bojidarova m.
Rheumatol Int. 2018 Apr;38(Suppl 1):75-82. doi: 10.1007/s00296-018-3940-5. Epub 2018 Apr 7.
Rheumatol Int. 2018.
PMID: 29637337
Free PMC article.
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