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Page 1
[Nijmegen breakage syndrome in Slovakia].
Seemanová E, Pohanka V, Seeman P, Misovicová N, Behunová J, Kvasnicová M, Dlholucký S, Valachová A, Cisarik F, Veghová E, Varon R, Sperling K. Seemanová E, et al. Among authors: cisarik f. Cas Lek Cesk. 2004;143(8):538-41; discussion 542. Cas Lek Cesk. 2004. PMID: 15446459 Czech.
Influence of different spectra of NOTCH3 variants on the clinical phenotype of CADASIL - experience from Slovakia.
Juhosová M, Chandoga J, Cisárik F, Dallemule S, Ďurina P, Jarásková D, Jungová P, Kantarská D, Kvasnicová M, Mistrík M, Pastoráková A, Petrovič R, Valachová A, Zelinková H, Barošová J, Böhmer D, Štofko J. Juhosová M, et al. Among authors: cisarik f. Neurogenetics. 2023 Jan;24(1):1-16. doi: 10.1007/s10048-022-00704-6. Epub 2022 Nov 19. Neurogenetics. 2023. PMID: 36401683
Genetics and genomic medicine in Slovakia.
Kádaši L, Cisárik F. Kádaši L, et al. Among authors: cisarik f. Mol Genet Genomic Med. 2015 Jan;3(1):8-13. doi: 10.1002/mgg3.122. Mol Genet Genomic Med. 2015. PMID: 25629075 Free PMC article. No abstract available.
Variability in kyphomelic dysplasia.
Cisarik F, Kozlowski K, Masel J, Sillence D. Cisarik F, et al. Pediatr Radiol. 1999 Jul;29(7):551-7. doi: 10.1007/s002470050644. Pediatr Radiol. 1999. PMID: 10398797
Lethal kyphomelic dysplasia.
Cisarik F, Baxova A, Kozlowski K. Cisarik F, et al. J Paediatr Child Health. 1996 Apr;32(2):188-90. doi: 10.1111/j.1440-1754.1996.tb00920.x. J Paediatr Child Health. 1996. PMID: 9156533
28 results