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Determinants of Quality of Life in Myasthenia Gravis Patients

Frontiers in neurology, 2020-09, Vol.11, p.553626-553626

2020

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Lower BAFF Levels in Myasthenic Patients Treated with Glucocorticoids

Archivum Immunologiae et Therapiae Experimentalis, 2021-12, Vol.69 (1), p.22-22, Article 22

2021

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Pediatric CIDP: Diagnosis and Management. A Single-Center Experience

Frontiers in neurology, 2021-07, Vol.12, p.667378-667378

2021

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Corrigendum: Pediatric CIDP: Diagnosis and Management. A Single-Center Experience

Frontiers in neurology, 2022-01, Vol.12, p.784144-784144

2022

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Postępowanie z pacjentem z polineuropatią zapalną w okresie pandemii COVID-19

Polski przegląd neurologiczny, 2020-06, Vol.16 (2), p.84-87

Lipowska, Marta

2020

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Urological complications after stroke

Aktualności neurologiczne, 2019-01, Vol.19 (3), p.125-131

2019

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

Acta biochimica Polonica, 2012-01, Vol.59 (3), p.413

2012

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P19-S Can nerve conduction studies help to distinguish motor CIDP and MMN?

Clinical neurophysiology, 2019-07, Vol.130 (7), p.e100-e100

2019

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Efficacy, Safety, and Tolerability of Efgartigimod in Patients with Chronic Inflammatory Demyelinating Polyneuropathy: Results from the ADHERE Trial (PL5.002)

Neurology, 2024-04, Vol.102 (17_supplement_1)

2024

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Przewlekła zapalna polineuropatia demielinizacyjna — rozpoznanie i leczenie na podstawie kryteriów EAN/PNS z 2021 roku

Polski przegląd neurologiczny, 2023-10, Vol.19 (3), p.190-201

2023

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P342 Diagnostic utility of MUNIX method in estimation of motor units loss in post-polio syndrome

Clinical neurophysiology, 2017-09, Vol.128 (9), p.e289-e289

2017

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P340 The MUNE method as a complementary test to routine EMG in amyotrophic lateral sclerosis

Clinical neurophysiology, 2017-09, Vol.128 (9), p.e288-e288

2017

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Facial onset sensory and motor neuronopathy syndrome - a rare variant of motor neurone disease

Neurologia i neurochirurgia polska, 2021-01, Vol.55 (3), p.325-327

2021

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

Journal of electromyography and kinesiology, 2019-06, Vol.46, p.35-40

2019

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P84-F Subacute polyneuropathy partially responsive to immunomodulatory treatment coexisting with POLG mutation

Clinical neurophysiology, 2019-07, Vol.130 (7), p.e91-e92

2019

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P48-T Short exercise and short exercise with cooling tests in recessive myotonia congenita (Becker disease)

Clinical neurophysiology, 2019-07, Vol.130 (7), p.e53-e53

2019

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

Cardiology journal, 2022-12, Vol.29 (6), p.985-993

2022

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Co-occurrence of CAPN3 homozygous mutation and CCTG expansion in the CNBP gene in a patient with muscular dystrophy

Postępy psychiatrii neurologii, 2024-06, Vol.33 (2), p.109-114

2024

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Screening for late‐onset Pompe disease in Poland

Acta neurologica Scandinavica, 2019-10, Vol.140 (4), p.239-243

2019

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

Journal of electromyography and kinesiology, 2016-02, Vol.26, p.60-65

2016

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

Neuromuscular disorders : NMD, 2015-03, Vol.25 (3), p.216-221

2015

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Diagnosis and treatment of transthyretin amyloidosis cardiomyopathy: A position statement of the Polish Cardiac Society

Kardiologia polska (1957), 2023, Vol.81 (11), p.1167-1185

2023

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Diagnosis and treatment of transthyretin amyloidosis cardiomyopathy: A position statement of the Polish Cardiac Society

Kardiologia polska, 2023, Vol.81 (11), p.1167

2023

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Abnormal spontaneous activity in primary myopathic disorders

Muscle & nerve, 2017-09, Vol.56 (3), p.427-432

2017

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Determinants of Quality of Life in Myasthenia Gravis Patients

Lower BAFF Levels in Myasthenic Patients Treated with Glucocorticoids

Pediatric CIDP: Diagnosis and Management. A Single-Center Experience

Corrigendum: Pediatric CIDP: Diagnosis and Management. A Single-Center Experience

Postępowanie z pacjentem z polineuropatią zapalną w okresie pandemii COVID-19

Urological complications after stroke

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

P19-S Can nerve conduction studies help to distinguish motor CIDP and MMN?

Efficacy, Safety, and Tolerability of Efgartigimod in Patients with Chronic Inflammatory Demyelinating Polyneuropathy: Results from the ADHERE Trial (PL5.002)

Safety, tolerability, and efficacy of subcutaneous efgartigimod in patients with chronic inflammatory demyelinating polyradiculoneuropathy (ADHERE): a multicentre, randomised-withdrawal, double-blind, placebo-controlled, phase 2 trial

Przewlekła zapalna polineuropatia demielinizacyjna — rozpoznanie i leczenie na podstawie kryteriów EAN/PNS z 2021 roku

P342 Diagnostic utility of MUNIX method in estimation of motor units loss in post-polio syndrome

P340 The MUNE method as a complementary test to routine EMG in amyotrophic lateral sclerosis

Facial onset sensory and motor neuronopathy syndrome - a rare variant of motor neurone disease

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

P84-F Subacute polyneuropathy partially responsive to immunomodulatory treatment coexisting with POLG mutation

P48-T Short exercise and short exercise with cooling tests in recessive myotonia congenita (Becker disease)

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

Co-occurrence of CAPN3 homozygous mutation and CCTG expansion in the CNBP gene in a patient with muscular dystrophy

Screening for late‐onset Pompe disease in Poland

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

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

Diagnosis and treatment of transthyretin amyloidosis cardiomyopathy: A position statement of the Polish Cardiac Society

Diagnosis and treatment of transthyretin amyloidosis cardiomyopathy: A position statement of the Polish Cardiac Society

Abnormal spontaneous activity in primary myopathic disorders

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