Kuźma-Kozakiewicz M - Search Results

1

Dyslipidemia in patients with amyotrophic lateral sclerosis - a case control retrospective study.

Chełstowska B, Barańczyk-Kuźma A, Kuźma-Kozakiewicz M. Chełstowska B, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2021 May;22(3-4):195-205. doi: 10.1080/21678421.2020.1832119. Epub 2020 Oct 26. Amyotroph Lateral Scler Frontotemporal Degener. 2021. PMID: 33103950

2

Tau isoforms expression in transgenic mouse model of amyotrophic lateral sclerosis.

Usarek E, Kuźma-Kozakiewicz M, Schwalenstöcker B, Kaźmierczak B, Münch C, Ludolph AC, Barańczyk-Kuźma A. Usarek E, et al. Neurochem Res. 2006 May;31(5):597-602. doi: 10.1007/s11064-006-9057-3. Epub 2006 May 23. Neurochem Res. 2006. PMID: 16770730

3

New therapeutic targets for amyotrophic lateral sclerosis.

Kuzma-Kozakiewicz M, Kwiecinski H. Kuzma-Kozakiewicz M, et al. Expert Opin Ther Targets. 2011 Feb;15(2):127-43. doi: 10.1517/14728222.2011.542152. Epub 2010 Dec 7. Expert Opin Ther Targets. 2011. PMID: 21133819 Review.

4

Mice with mutation in dynein heavy chain 1 do not share the same tau expression pattern with mice with SOD1-related motor neuron disease.

Kuźma-Kozakiewicz M, Usarek E, Ludolph AC, Barańczyk-Kuźma A. Kuźma-Kozakiewicz M, et al. Neurochem Res. 2011 Jun;36(6):978-85. doi: 10.1007/s11064-011-0436-z. Epub 2011 Mar 6. Neurochem Res. 2011. PMID: 21380844 Free PMC article.

5

Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family.

Berdyński M, Kuźma-Kozakiewicz M, Ricci C, Kubiszewska J, Millecamps S, Salachas F, Łusakowska A, Carrera P, Meininger V, Battistini S, Kwieciński H, Zekanowski C. Berdyński M, et al. Amyotroph Lateral Scler. 2012 Jan;13(1):132-6. doi: 10.3109/17482968.2011.600316. Epub 2011 Aug 30. Amyotroph Lateral Scler. 2012. PMID: 21877919

6

Differences in glutathione S-transferase pi expression in transgenic mice with symptoms of neurodegeneration.

Kaźmierczak B, Kuźma-Kozakiewicz M, Usarek E, Barańczyk-Kuźma A. Kaźmierczak B, et al. Acta Biochim Pol. 2011;58(4):621-6. Epub 2011 Nov 30. Acta Biochim Pol. 2011. PMID: 22132373

7

Kinesin expression in the central nervous system of humans and transgenic hSOD1G93A mice with amyotrophic lateral sclerosis.

Kuźma-Kozakiewicz M, Chudy A, Gajewska B, Dziewulska D, Usarek E, Barańczyk-Kuźma A. Kuźma-Kozakiewicz M, et al. Neurodegener Dis. 2013;12(2):71-80. doi: 10.1159/000339529. Epub 2012 Sep 21. Neurodegener Dis. 2013. PMID: 23006449

8

Changes in kinesin expression in the CNS of mice with dynein heavy chain 1 mutation.

Kuźma-Kozakiewicz M, Kaźmierczak B, Usarek E, Barańczyk-Kuźma A. Kuźma-Kozakiewicz M, et al. Acta Biochim Pol. 2013;60(1):51-5. Epub 2013 Mar 5. Acta Biochim Pol. 2013. PMID: 23460941

9

SMN1 gene duplications are more frequent in patients with progressive muscular atrophy.

Kuźma-Kozakiewicz M, Jędrzejowska M, Kaźmierczak B. Kuźma-Kozakiewicz M, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2013 Sep;14(5-6):457-62. doi: 10.3109/21678421.2013.771367. Epub 2013 Mar 12. Amyotroph Lateral Scler Frontotemporal Degener. 2013. PMID: 23477310

10

Analysis of PITX3 gene in patients with multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration.

Jamrozik Z, Berdynski M, Zekanowski C, Baranczyk-Kuzma A, Sławek J, Kuzma-Kozakiewicz M, Maruszak A, Kwiecinski H. Jamrozik Z, et al. Ann Clin Lab Sci. 2013 Spring;43(2):151-3. Ann Clin Lab Sci. 2013. PMID: 23694789

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