Maruszak A - Search Results

1

Myofibrillar myopathy in the genomic context.

Fichna JP, Maruszak A, Żekanowski C. Fichna JP, et al. Among authors: maruszak a. J Appl Genet. 2018 Nov;59(4):431-439. doi: 10.1007/s13353-018-0463-4. Epub 2018 Sep 10. J Appl Genet. 2018. PMID: 30203143 Review.

2

Pathogenic Mutations and Putative Phenotype-Affecting Variants in Polish Myofibrillar Myopathy Patients.

Potulska-Chromik A, Jędrzejowska M, Gos M, Rosiak E, Kierdaszuk B, Maruszak A, Opuchlik A, Zekanowski C, Fichna JP. Potulska-Chromik A, et al. Among authors: maruszak a. J Clin Med. 2021 Feb 26;10(5):914. doi: 10.3390/jcm10050914. J Clin Med. 2021. PMID: 33652732 Free PMC article.

3

Mitochondrial DNA in pathogenesis of Alzheimer's and Parkinson's diseases.

Maruszak A, Gaweda-Walerych K, Sołtyszewski I, Zekanowski C. Maruszak A, et al. Acta Neurobiol Exp (Wars). 2006;66(2):153-76. doi: 10.55782/ane-2006-1602. Acta Neurobiol Exp (Wars). 2006. PMID: 16886726 Free article. Review.

4

PIN1 gene variants in Alzheimer's disease.

Maruszak A, Safranow K, Gustaw K, Kijanowska-Haładyna B, Jakubowska K, Olszewska M, Styczyńska M, Berdyński M, Tysarowski A, Chlubek D, Siedlecki J, Barcikowska M, Zekanowski C. Maruszak A, et al. BMC Med Genet. 2009 Nov 12;10:115. doi: 10.1186/1471-2350-10-115. BMC Med Genet. 2009. PMID: 19909517 Free PMC article.

5

Mitochondrial dysfunction and Alzheimer's disease.

Maruszak A, Żekanowski C. Maruszak A, et al. Prog Neuropsychopharmacol Biol Psychiatry. 2011 Mar 30;35(2):320-30. doi: 10.1016/j.pnpbp.2010.07.004. Epub 2010 Jul 16. Prog Neuropsychopharmacol Biol Psychiatry. 2011. PMID: 20624441 Review.

6

ANO5 mutations in the Polish limb girdle muscular dystrophy patients: Effects on the protein structure.

Jarmula A, Łusakowska A, Fichna JP, Topolewska M, Macias A, Johnson K, Töpf A, Straub V, Rosiak E, Szczepaniak K, Dunin-Horkawicz S, Maruszak A, Kaminska AM, Redowicz MJ. Jarmula A, et al. Among authors: maruszak a. Sci Rep. 2019 Aug 8;9(1):11533. doi: 10.1038/s41598-019-47849-3. Sci Rep. 2019. PMID: 31395899 Free PMC article.

7

Two novel presenilin 1 gene mutations connected with frontotemporal dementia-like clinical phenotype: genetic and bioinformatic assessment.

Zekanowski C, Golan MP, Krzyśko KA, Lipczyńska-Łojkowska W, Filipek S, Kowalska A, Rossa G, Pepłońska B, Styczyńska M, Maruszak A, Religa D, Wender M, Kulczycki J, Barcikowska M, Kuźnicki J. Zekanowski C, et al. Among authors: maruszak a. Exp Neurol. 2006 Jul;200(1):82-8. doi: 10.1016/j.expneurol.2006.01.022. Epub 2006 Mar 20. Exp Neurol. 2006. PMID: 16546171

8

TOMM40 rs10524523 polymorphism's role in late-onset Alzheimer's disease and in longevity.

Maruszak A, Pepłońska B, Safranow K, Chodakowska-Żebrowska M, Barcikowska M, Zekanowski C. Maruszak A, et al. J Alzheimers Dis. 2012;28(2):309-22. doi: 10.3233/JAD-2011-110743. J Alzheimers Dis. 2012. PMID: 22008263

9

Association between plasma biomarkers, CDK5 polymorphism and the risk of Alzheimer's disease.

Czapski GA, Maruszak A, Styczyńska M, Żekanowski C, Safranow K, Strosznajder JB. Czapski GA, et al. Among authors: maruszak a. Acta Neurobiol Exp (Wars). 2012;72(4):397-411. doi: 10.55782/ane-2012-1911. Acta Neurobiol Exp (Wars). 2012. PMID: 23377270 Free article.

10

Sigma receptor type 1 gene variation in a group of Polish patients with Alzheimer's disease and mild cognitive impairment.

Maruszak A, Safranow K, Gacia M, Gabryelewicz T, Słowik A, Styczyńska M, Pepłońska B, Golan MP, Zekanowski C, Barcikowska M. Maruszak A, et al. Dement Geriatr Cogn Disord. 2007;23(6):432-8. doi: 10.1159/000101990. Epub 2007 Apr 23. Dement Geriatr Cogn Disord. 2007. PMID: 17457031

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