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List of works by Biruta Kierdaszuk

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

scientific article published on 30 January 2013

Abnormal spontaneous activity in primary myopathic disorders

scientific article published on 21 December 2016

Comprehensive evaluation of EMG and biopsy findings supported by computer simulations - A preliminary study

scientific article published on 02 June 2018

Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)

scientific article published on 24 November 2020

Electromyographic findings in sporadic inclusion body myositis

scientific article published on 11 February 2018

Identification of the first in Poland CACNA1A gene mutation in familial hemiplegic migraine. Case report

scientific article published on 21 January 2017

Inclusion body myositis: therapeutic approaches. A case report ⬇️

scientific article published on 01 January 2011

Intraosseous lipoma of the sphenoid: a case study

scientific article published on 28 May 2013

Meningitis and Ramsay-Hunt syndrome in a 17-year old girl

scientific article published on 01 November 2019

Mitochondrial cytopathies: clinical, morphological and genetic characteristics.

scientific article

Mitochondrial encephalomyopathy: towards diagnosis. A case report

scientific article published on 23 January 2014

Mitochondrial encephalopathy in a patient with a 13042G>A de novo mutation

scientific article published on 10 August 2012

Multiple metastatic intracranial lesions associated with left atrial myxoma

scientific article

Myosin VI localization and expression in striated muscle pathology.

scientific article

Progressive External Ophthalmoplegia in Polish Patients-From Clinical Evaluation to Genetic Confirmation

scientific article published on 31 December 2020

Screening for late-onset Pompe disease in Poland

scientific article published on 18 June 2019

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

scientific article published in January 2015

The frequency of mitochondrial polymerase gamma related disorders in a large Polish population cohort

scientific article published on 10 November 2018

Ultrastructural changes in microvessels in familial hemiplegic migraine with CACNA1A mutation

scientific article published on 01 November 2018

Yeast model analysis of novel polymerase gamma variants found in patients with autosomal recessive mitochondrial disease.

scientific article published on 16 June 2015

[Elevated plasma creatine kinase activity - does it always indicate muscle disease?]

scientific article published on 01 May 2012

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

scientific article published on 01 July 2012

[The role of skeletal muscle biopsy in the diagnosis of neuromuscular disorders]

scientific article published on 01 September 2010

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