Anna Fidzianska

Pawinskiego St. 5
Warsaw, MZ 02106, Poland

Last Updated: 09/26/2026

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Found 13 publications

Limb-girdle muscular dystrophy with severe heart failure overlapping with lipodystrophy in a patient with LMNA mutation p.Ser334del.

Limb-girdle muscular dystrophy with severe heart failure overlapping with lipodystrophy in a patient with LMNA mutation p.Ser334del.

Journal: Journal of applied genetics

Published: July 19, 2016

The Frequency of c.550delA Mutation of the CANP3 Gene in the Polish LGMD2A Population.

The Frequency of c.550delA Mutation of the CANP3 Gene in the Polish LGMD2A Population.

Journal: Genetic testing and molecular biomarkers

Published: October 21, 2015

Does aberrant architecture of nuclear LINC complex stop muscle cell development?

Does aberrant architecture of nuclear LINC complex stop muscle cell development?

Journal: Clinical neuropathology

Published: April 02, 2015

Low symptomatic malignant cardiac arrhythmia in a patient with lamin-related congenital muscular dystrophy.

Low symptomatic malignant cardiac arrhythmia in a patient with lamin-related congenital muscular dystrophy.

Journal: Kardiologia polska

Published: March 27, 2015

Might prepatterned acetylcholine-receptor clusters on surface myotubes be a sign of neuromuscular-junction maturation failure?

Might prepatterned acetylcholine-receptor clusters on surface myotubes be a sign of neuromuscular-junction maturation failure?

Journal: Folia neuropathologica

Published: December 31, 2013

Is mutation p.Arg168Gly in TPM3 gene responsible for Type 1 fiber hypoplasia and cap structure formation?

Is mutation p.Arg168Gly in TPM3 gene responsible for Type 1 fiber hypoplasia and cap structure formation?

Journal: Clinical neuropathology

Published: August 09, 2013

Severe phenotypes of SMARD1 associated with novel mutations of the IGHMBP2 gene and nuclear degeneration of muscle and Schwann cells.

Severe phenotypes of SMARD1 associated with novel mutations of the IGHMBP2 gene and nuclear degeneration of muscle and Schwann cells.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: March 21, 2013

Morphologic and clinical aspects of Danon disease in a patient with a mutation c.137G > A in the LAMP-2 gene.

Morphologic and clinical aspects of Danon disease in a patient with a mutation c.137G > A in the LAMP-2 gene.

Journal: Neuropediatrics

Published: March 19, 2013

LMNA mutations in Polish patients with dilated cardiomyopathy: prevalence, clinical characteristics, and in vitro studies.

LMNA mutations in Polish patients with dilated cardiomyopathy: prevalence, clinical characteristics, and in vitro studies.

Journal: BMC medical genetics

Published: January 24, 2013

Myopathy in the course of carnitine palmitoyltransferase II deficiency

Myopathy in the course of carnitine palmitoyltransferase II deficiency

Journal: Neurologia i neurochirurgia polska

Published: January 16, 2013

Cardiac involvement in neuronal ceroid lipofuscinosis

Cardiac involvement in neuronal ceroid lipofuscinosis

Journal: Kardiologia polska

Published: December 31, 2012

Did giant mitochondria delay muscle maturation? An uncommon congenital myopathy.

Did giant mitochondria delay muscle maturation? An uncommon congenital myopathy.

Journal: Muscle & nerve

Published: June 14, 2012

Showing 1-12 of 13

Last Updated: 09/26/2026