Mariusz Berdynski

Mariusz Berdynski

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Mariusz Berdynski

Mariusz Berdynski

Publications by authors named "Mariusz Berdynski"

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19Publications

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TREM2 variants in neurodegenerative disorders in the Polish population. Homozygosity and compound heterozygosity in FTD patients.

Amyotroph Lateral Scler Frontotemporal Degener 2018 08 20;19(5-6):407-412. Epub 2018 Mar 20.

a Department of Neurodegenerative Disorders , Mossakowski Medical Research Centre Polish Academy of Sciences , Warsaw , Poland.

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http://dx.doi.org/10.1080/21678421.2018.1451894DOI Listing
August 2018

Comprehensive analysis to explain reduced or increased SOD1 enzymatic activity in ALS patients and their relatives.

Amyotroph Lateral Scler Frontotemporal Degener 2017 08 21;18(5-6):457-463. Epub 2017 Mar 21.

a Department of Pharmacology and Clinical Neurosciences , Umeå University , Umeå , Sweden.

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http://dx.doi.org/10.1080/21678421.2017.1301481DOI Listing
August 2017

Sporadic inclusion body myositis: clinical, pathological, and genetic analysis of eight Polish patients.

Folia Neuropathol 2015 ;53(4):355-66

Prof. Anna M. Kaminska, Department of Neurology, Medical University of Warsaw, 1A Banacha St., 02-097 Warsaw, Poland, phone: +48 22 599 28 58, fax: +48 22 599 18 57, e-mail:

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http://dx.doi.org/10.5114/fn.2015.56550DOI Listing
December 2016

Association of ADORA1 rs2228079 and ADORA2A rs5751876 Polymorphisms with Gilles de la Tourette Syndrome in the Polish Population.

PLoS One 2015 28;10(8):e0136754. Epub 2015 Aug 28.

Department of Neurodegenerative Disorders, Mossakowski Medical Research Centre, Polish Academy of Sciences, Warsaw, Poland.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0136754PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4552818PMC
May 2016

Frontotemporal lobar degeneration with MAPT mutation in an Italian-Polish family. A case report.

Folia Neuropathol 2014 ;52(4):457-66

Prof. Teresa Wierzba-Bobrowicz, Department of Neuropathology, Institute of Psychiatry and Neurology, 9 Sobieskiego St., 02-957 Warsaw, Poland, e-mail:

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http://dx.doi.org/10.5114/fn.2014.47848DOI Listing
December 2015

The BTBD9 gene polymorphisms in Polish patients with Gilles de la Tourette syndrome.

Acta Neurobiol Exp (Wars) 2014 ;74(2):218-26

Department of Neurology, Medical University of Warsaw, Warsaw, Poland,

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April 2015

Myosin VI localization and expression in striated muscle pathology.

Anat Rec (Hoboken) 2014 Sep;297(9):1706-13

Department of Biochemistry, Laboratory of Molecular Basis of Cell Motility, Nencki Institute of Experimental Biology, Warsaw, Poland.

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http://dx.doi.org/10.1002/ar.22967DOI Listing
September 2014

A novel MAPT mutation, G55R, in a frontotemporal dementia patient leads to altered Tau function.

PLoS One 2013 27;8(9):e76409. Epub 2013 Sep 27.

Neuroscience Research Institute and Department of Molecular, Cellular and Developmental Biology, University of California Santa Barbara, Santa Barbara, California, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0076409PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3785453PMC
July 2014

A novel mutation in the DNM2 gene impairs dynamin 2 localization in skeletal muscle of a patient with late onset centronuclear myopathy.

Neuromuscul Disord 2013 Mar 30;23(3):219-28. Epub 2013 Jan 30.

Department of Neurology, Medical University of Warsaw, 1a Banacha St., 02-097 Warsaw, Poland.

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http://dx.doi.org/10.1016/j.nmd.2012.12.007DOI Listing
March 2013

[TDP-43 proteinopathies - from frontotemporal lobar degeneration to inclusion body myositis].

Neurol Neurochir Pol 2012 Jul-Aug;46(4):384-91

Katedra i Klinika Neurologii, Warszawski Uniwersytet Medyczny, Warszawa.

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http://dx.doi.org/10.5114/ninp.2012.30271DOI Listing
January 2013

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

Amyotroph Lateral Scler 2012 Jan 30;13(1):132-6. Epub 2011 Aug 30.

Laboratory of Neurogenetics, Department of Neurodegenerative Disorders, Mossakowski Medical Research Centre, Polish Academy of Sciences, Pawińskiego 5, Warsaw, Poland.

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http://dx.doi.org/10.3109/17482968.2011.600316DOI Listing
January 2012

PIN1 gene variants in Alzheimer's disease.

BMC Med Genet 2009 Nov 12;10:115. Epub 2009 Nov 12.

Department of Neurodegenerative Disorders, Mossakowski Medical Research Centre, Polish Academy of Sciences, Pawińskiego 5, 02-106 Warszawa, Poland.

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http://dx.doi.org/10.1186/1471-2350-10-115DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2781804PMC
November 2009