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

Year Number of Results
2002 1
2004 8
2005 1
2006 2
2007 2
2008 1
2009 2
2010 3
2011 5
2012 2
2013 1
2014 6
2015 6
2016 2
2017 2
2018 1
2020 2
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42 results
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Page 1
[Therapeutic perspective in hereditary polyneuropathies].
Kochański A, Kabzińska D, Rzepnikowska W, Binięda K, Kiepura A. Kochański A, et al. Among authors: kabzinska d. 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 pathogenesis, experimental therapy and genetic counseling in hereditary sensory neuropathies.
Mroczek M, Kabzińska D, Kochański A. Mroczek M, et al. Among authors: kabzinska d. Acta Neurobiol Exp (Wars). 2015;75(2):126-43. Acta Neurobiol Exp (Wars). 2015. PMID: 26232991 Free article. Review.
Are electrophysiological criteria useful in distinguishing childhood demyelinating neuropathies?
Potulska-Chromik A, Ryniewicz B, Aragon-Gawinska K, Kabzinska D, Seroka A, Lipowska M, Kaminska AM, Kostera-Pruszczyk A. Potulska-Chromik A, et al. Among authors: kabzinska d. J Peripher Nerv Syst. 2016 Mar;21(1):22-6. doi: 10.1111/jns.12152. J Peripher Nerv Syst. 2016. PMID: 26663344
Pathogenic Effect of GDAP1 Gene Mutations in a Yeast Model.
Rzepnikowska W, Kaminska J, Kabzińska D, Kochański A. Rzepnikowska W, et al. Among authors: kabzinska d. Genes (Basel). 2020 Mar 14;11(3):310. doi: 10.3390/genes11030310. Genes (Basel). 2020. PMID: 32183277 Free PMC article.
[Molecular pathogenesis of hereditary motor and sensory neuropathy].
Kotruchow K, Kabzińska D, Karpińska K, Kochański A. Kotruchow K, et al. Among authors: kabzinska d. Postepy Biochem. 2011;57(3):283-93. Postepy Biochem. 2011. PMID: 22235654 Review. Polish.
Early-onset facioscapulohumeral muscular dystrophy type 1 with some atypical features.
Dorobek M, van der Maarel SM, Lemmers RJ, Ryniewicz B, Kabzińska D, Frants RR, Gawel M, Walecki J, Hausmanowa-Petrusewicz I. Dorobek M, et al. Among authors: kabzinska d. J Child Neurol. 2015 Apr;30(5):580-7. doi: 10.1177/0883073814528281. Epub 2014 Apr 9. J Child Neurol. 2015. PMID: 24717985
A novel TPM2 gene splice-site mutation causes severe congenital myopathy with arthrogryposis and dysmorphic features.
Mroczek M, Kabzińska D, Chrzanowska KH, Pronicki M, Kochański A. Mroczek M, et al. Among authors: kabzinska d. J Appl Genet. 2017 May;58(2):199-203. doi: 10.1007/s13353-016-0368-z. Epub 2016 Oct 10. J Appl Genet. 2017. PMID: 27726070 Free PMC article.
A Yeast-Based Model for Hereditary Motor and Sensory Neuropathies: A Simple System for Complex, Heterogeneous Diseases.
Rzepnikowska W, Kaminska J, Kabzińska D, Binięda K, Kochański A. Rzepnikowska W, et al. Among authors: kabzinska d. Int J Mol Sci. 2020 Jun 16;21(12):4277. doi: 10.3390/ijms21124277. Int J Mol Sci. 2020. PMID: 32560077 Free PMC article. Review.
The LITAF/SIMPLE I92V sequence variant results in an earlier age of onset of CMT1A/HNPP diseases.
Sinkiewicz-Darol E, Lacerda AF, Kostera-Pruszczyk A, Potulska-Chromik A, Sokołowska B, Kabzińska D, Brunetti CR, Hausmanowa-Petrusewicz I, Kochański A. Sinkiewicz-Darol E, et al. Among authors: kabzinska d. Neurogenetics. 2015 Jan;16(1):27-32. doi: 10.1007/s10048-014-0426-9. Epub 2014 Oct 24. Neurogenetics. 2015. PMID: 25342198 Free PMC article.
The Frequency of c.550delA Mutation of the CANP3 Gene in the Polish LGMD2A Population.
Dorobek M, Ryniewicz B, Kabzińska D, Fidziańska A, Styczyńska M, Hausmanowa-Petrusewicz I. Dorobek M, et al. Among authors: kabzinska d. Genet Test Mol Biomarkers. 2015 Nov;19(11):637-40. doi: 10.1089/gtmb.2015.0131. Epub 2015 Oct 20. Genet Test Mol Biomarkers. 2015. PMID: 26484845
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