List of works - Marta Lipowska

A novel homozygous mutation in the WNK1/HSN2 gene causing hereditary sensory neuropathy type 2.

scientific article

Abnormal spontaneous activity in primary myopathic disorders

scientific article published on 21 December 2016

Are electrophysiological criteria useful in distinguishing childhood demyelinating neuropathies?

scientific article published on 01 March 2016

Carpal tunnel syndrome in children

scientific article published on 01 October 2013

Clinical, electrophysiological, and molecular findings in early onset hereditary neuropathy with liability to pressure palsy

scientific article published on 30 October 2014

Determinants of Quality of Life in Myasthenia Gravis Patients

scientific article published on 23 September 2020

Does quantitative EMG differ myotonic dystrophy type 2 and type 1?

scientific article published on 25 June 2014

Motor Unit Number Index (MUNIX) as a biomarker of motor unit loss in post-polio syndrome versus needle EMG

scientific article published on 09 March 2019

Motor unit loss estimation by the multipoint incremental MUNE method in children with spinal muscular atrophy--a preliminary study

scientific article published on 25 November 2014

Motor unit number estimation as a complementary test to routine electromyography in the diagnosis of amyotrophic lateral sclerosis

scientific article

Motor unit reorganization in progressive muscular dystrophies and congenital myopathies

scientific article published on 06 June 2015

Peripheral nerve involvement in myotonic dystrophy type 2 - similar or different than in myotonic dystrophy type 1?

scientific article published on 06 May 2015

Screening for late-onset Pompe disease in Poland

scientific article published on 18 June 2019

Serum interleukin 15 levels in patients with seropositive myasthenia gravis do not correlate with disease severity

scientific article published on 06 January 2018

Spectrum of transthyretin gene mutations and clinical characteristics of Polish patients with cardiac transthyretin amyloidosis

scientific article published on 13 August 2020

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

scientific article published on 10 November 2018

Transthyretin-related Familial Amyloid Polyneuropathy (TTR-FAP) caused by a very rare, de novo mutation in a Polish patient

scientific article published on 2 November 2015

Transthyretin-related familial amyloid polyneuropathy (ATTR-FAP) in Poland - genetic and clinical presentation

scientific article published on 29 December 2020

List of works by Marta Lipowska