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Genetic basis of autosomal dominant nocturnal frontal lobe epilepsy.
Rózycka A, Trzeciak WH. Rózycka A, et al. J Appl Genet. 2003;44(2):197-207. J Appl Genet. 2003. PMID: 12773798
A transcript coding for a partially duplicated form of α7 nicotinic acetylcholine receptor is absent from the CD4+ T-lymphocytes of patients with autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE).
Rozycka A, Dorszewska J, Steinborn B, Kempisty B, Lianeri M, Wisniewska K, Jagodzinski PP. Rozycka A, et al. Folia Neuropathol. 2013;51(1):65-75. doi: 10.5114/fn.2013.34198. Folia Neuropathol. 2013. PMID: 23553139
[Ion channel dysfunction in pathogenesis of idiopathic epilepsies].
Różycka A, Dorszewska J, Jagodziński PP. Różycka A, et al. Neurol Neurochir Pol. 2011 Jan-Feb;45(1):42-56. doi: 10.1016/s0028-3843(14)60059-1. Neurol Neurochir Pol. 2011. PMID: 21384293 Review. Polish.
The 1674+11C>T polymorphism of CHRNA4 is associated with juvenile myoclonic epilepsy.
Rozycka A, Steinborn B, Trzeciak WH. Rozycka A, et al. Seizure. 2009 Oct;18(8):601-3. doi: 10.1016/j.seizure.2009.06.007. Epub 2009 Jul 3. Seizure. 2009. PMID: 19577488
Evidence for S284L mutation of the CHRNA4 in a white family with autosomal dominant nocturnal frontal lobe epilepsy.
Rozycka A, Skorupska E, Kostyrko A, Trzeciak WH. Rozycka A, et al. Epilepsia. 2003 Aug;44(8):1113-7. doi: 10.1046/j.1528-1157.2003.07603.x. Epilepsia. 2003. PMID: 12887446
[Molecular and genetic basis of idiopathic nocturnal frontal lobe epilepsy].
Skorupska E, Rózycka A, Trzeciak WH. Skorupska E, et al. Among authors: rozycka a. Neurol Neurochir Pol. 2002 May-Jun;36(3):513-25. Neurol Neurochir Pol. 2002. PMID: 12185808 Review. Polish.
Association study of the 2-bp deletion polymorphism in exon 6 of the CHRFAM7A gene with idiopathic generalized epilepsy.
Rozycka A, Dorszewska J, Steinborn B, Lianeri M, Winczewska-Wiktor A, Sniezawska A, Wisniewska K, Jagodzinski PP. Rozycka A, et al. DNA Cell Biol. 2013 Nov;32(11):640-7. doi: 10.1089/dna.2012.1880. Epub 2013 Sep 11. DNA Cell Biol. 2013. PMID: 24024466 Free PMC article.
Coexistence of ACE (I/D) and PAI-1 (4G/5G) gene variants in recurrent miscarriage in Polish population.
Kurzawińska G, Barlik M, Drews K, Różycka A, Seremak-Mrozikiewicz A, Ożarowski M, Klejewski A, Czerny B, Wolski H. Kurzawińska G, et al. Among authors: rozycka a. Ginekol Pol. 2016;87(4):271-6. doi: 10.17772/gp/62203. Ginekol Pol. 2016. PMID: 27321098
The MAOA, COMT, MTHFR and ESR1 gene polymorphisms are associated with the risk of depression in menopausal women.
Różycka A, Słopień R, Słopień A, Dorszewska J, Seremak-Mrozikiewicz A, Lianeri M, Maciukiewicz M, Warenik-Szymankiewicz A, Grzelak T, Kurzawińska G, Drews K, Klejewski A, Jagodziński PP. Różycka A, et al. Maturitas. 2016 Feb;84:42-54. doi: 10.1016/j.maturitas.2015.10.011. Epub 2015 Oct 30. Maturitas. 2016. PMID: 26620113
Mutations in the exon 7 of Trp53 gene and the level of p53 protein in double transgenic mouse model of Alzheimer's disease.
Dorszewska J, Oczkowska A, Suwalska M, Rozycka A, Florczak-Wyspianska J, Dezor M, Lianeri M, Jagodzinski PP, Kowalczyk MJ, Prendecki M, Kozubski W. Dorszewska J, et al. Among authors: rozycka a. Folia Neuropathol. 2014;52(1):30-40. doi: 10.5114/fn.2014.41742. Folia Neuropathol. 2014. PMID: 24729341
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