A. Kamińska

发表

Abnormal spontaneous activity in primary myopathic disorders

M. Gaweł, E. Szmidt-Sałkowska, M. Nojszewska, 2017, Muscle & nerve.

Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes

C. Żekanowski, I. Domitrz, A. Kamińska, 2016, Human Genomics.

Hsp27‐2D‐gel electrophoresis is a diagnostic tool to differentiate primary desminopathies from myofibrillar myopathies

S. Simon, K. Zerres, N. Romero, 2005, FEBS letters.

Quantitative Methods to Monitor RNA Biomarkers in Myotonic Dystrophy

R. Markus, K. Sobczak, A. Kaminska, 2018, Scientific Reports.

Familial inclusion body myopathy with desmin storage

A. Kaminska, A. Fidziańska, H. Drac, 1999, Acta Neuropathologica.

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

P. Golik, A. Łusakowska, E. Pronicka, 2015, Human Genetics.

Myosin VI Localization and Expression in Striated Muscle Pathology

E. Ehler, A. Kaminska, C. Żekanowski, 2014, Anatomical record.

Genome search for susceptibility loci of common idiopathic generalised epilepsies.

T. Wienker, A. Sundquist, J. Prud'homme, 2000, Human molecular genetics.

Muscle pathology in myotonic dystrophy: light and electron microscopic investigation in eighteen patients.

A. Kaminska, A. Nadaj-Pakleza, H. Kwiecinski, 2011, Folia morphologica.

Changing phenotypic expression in a patient with a mitochondrial encephalopathy due to 13042G>A de novo mutation—a 5 year follow up

H. Kwiecinski, E. Bartnik, E. Sitek, 2014, Metabolic Brain Disease.