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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2004 6
2005 3
2006 6
2007 4
2008 2
2009 2
2010 3
2011 7
2012 3
2013 1
2014 5
2015 4
2016 1
2017 3
2018 4
2020 2
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52 results
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Page 1
A role for the GDAP1 gene in the molecular pathogenesis of Charcot‑Marie‑Tooth disease.
Rzepnikowska W, Kochański A. Rzepnikowska W, et al. Among authors: kochanski a. Acta Neurobiol Exp (Wars). 2018;78(1):1-13. Acta Neurobiol Exp (Wars). 2018. PMID: 29694336 Free article. Review.
Charcot‑Marie‑Tooth type 1A drug therapies: role of adenylyl cyclase activity and G‑protein coupled receptors in disease pathomechanism.
Kiepura AJ, Kochański A. Kiepura AJ, et al. Among authors: kochanski a. Acta Neurobiol Exp (Wars). 2018;78(3):198-209. Acta Neurobiol Exp (Wars). 2018. PMID: 30295677 Free article. Review.
[Therapeutic perspective in hereditary polyneuropathies].
Kochański A, Kabzińska D, Rzepnikowska W, Binięda K, Kiepura A. Kochański A, et al. Postepy Biochem. 2018 Dec 29;64(4):288-299. doi: 10.18388/pb.2018_142. Postepy Biochem. 2018. PMID: 30656913 Free article. Review. Polish.
Molecular modelling of mitofusin 2 for a prediction for Charcot-Marie-Tooth 2A clinical severity.
Beręsewicz M, Charzewski Ł, Krzyśko KA, Kochański A, Zabłocka B. Beręsewicz M, et al. Among authors: kochanski a. Sci Rep. 2018 Nov 15;8(1):16900. doi: 10.1038/s41598-018-35133-9. Sci Rep. 2018. PMID: 30442897 Free PMC article.
Molecular pathogenesis, experimental therapy and genetic counseling in hereditary sensory neuropathies.
Mroczek M, Kabzińska D, Kochański A. Mroczek M, et al. Among authors: kochanski a. Acta Neurobiol Exp (Wars). 2015;75(2):126-43. Acta Neurobiol Exp (Wars). 2015. PMID: 26232991 Free article. Review.
Molecular genetics studies in Polish Charcot-Marie-Tooth families.
Kochański A. Kochański A. Folia Neuropathol. 2005;43(2):65-73. Folia Neuropathol. 2005. PMID: 16012907 Free article. Review.
[Pathogenic mutation or polymorphism? (How to find criteria)].
Kochański A. Kochański A. Med Wieku Rozwoj. 2006 Jan-Mar;10(1 Pt 2):335-41. Med Wieku Rozwoj. 2006. PMID: 17028397 Review. Polish.
Mutations in the neurofilament light chain gene (NEFL)--a study of a possible pathogenous effect.
Kochański A. Kochański A. Folia Neuropathol. 2004;42(3):187-90. Folia Neuropathol. 2004. PMID: 15535039 Review.
[Charcot-Marie-Tooth disorders: past, today and tomorrow].
Kochański A. Kochański A. Neurol Neurochir Pol. 2006 Jul-Aug;40(4):327-35. Neurol Neurochir Pol. 2006. PMID: 16967355 Review. Polish.
A novel de novo COL6A1 mutation emphasizes the role of intron 14 donor splice site defects as a cause of moderate-progressive form of ColVI myopathy - a case report and review of the genotype-phenotype correlation.
Koppolu AA, Madej-Pilarczyk A, Rydzanicz M, Kosińska J, Gasperowicz P, Dorszewska J, Kozubski W, Steinborn B, Kochański AM, Płoski R. Koppolu AA, et al. Among authors: kochanski am. Folia Neuropathol. 2017;55(3):214-220. doi: 10.5114/fn.2017.70486. Folia Neuropathol. 2017. PMID: 28984114 Free article. Review.
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