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Myasthenia gravis—treatment and severity in nationwide cohort

Acta neurologica Scandinavica, 2022-04, Vol.145 (4), p.471-478

2022

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Treatment outcome in juvenile‐onset myasthenia gravis

Muscle & nerve, 2019-05, Vol.59 (5), p.549-554

2019

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Role of autoantibody levels as biomarkers in the management of patients with myasthenia gravis: A systematic review and expert appraisal

European journal of neurology, 2023-01, Vol.30 (1), p.266-282

2023

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Reply to the Letter to the Editor in response to “Role of autoantibody levels as biomarkers in the management of patients with myasthenia gravis: A systematic review and expert appraisal”

European journal of neurology, 2023-04, Vol.30 (4), p.1162-1164

2023

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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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The remarkable phenotypic variability of the p.Arg269HiS variant in the TRPV4 gene

Muscle & nerve, 2019-01, Vol.59 (1), p.129-133

2019

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Prevalence and impact of autoimmune thyroid disease on myasthenia gravis course

Brain and behavior, 2016-10, Vol.6 (10), p.e00537-n/a

2016

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Transient global amnesia - hippocampal lesions in magnetic resonance imaging

Journal of stroke and cerebrovascular diseases, 2023-03, Vol.32 (3), p.106951-106951, Article 106951

2023

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Effect of age and gender on the number of motor units in healthy subjects estimated by the multipoint incremental MUNE method

Journal of clinical neurophysiology, 2014-06, Vol.31 (3), p.272-278

2014

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Observation of the natural course of type 3 spinal muscular atrophy: data from the polish registry of spinal muscular atrophy

Orphanet journal of rare diseases, 2021-03, Vol.16 (1), p.150-150, Article 150

2021

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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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Long-term nusinersen treatment across a wide spectrum of spinal muscular atrophy severity: a real-world experience

Orphanet journal of rare diseases, 2023-08, Vol.18 (1), p.230-230, Article 230

2023

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Ultra-low radiation dose protocol for CT-guided intrathecal nusinersen injections for patients with spinal muscular atrophy and severe scoliosis

Neuroradiology, 2021-04, Vol.63 (4), p.539-545

2021

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Randomized phase 2 trial and open-label extension of domagrozumab in Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2020-06, Vol.30 (6), p.492-502

2020

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Application of imaging techniques to objectify the Finger Tapping test used in the diagnosis of Parkinson's disease

Bulletin of the Polish Academy of Sciences. Technical sciences, 2023, Vol.71 (2), p.144886-144886

2023

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Targeted Next-Generation Sequencing Reveals Mutations in Non-coding Regions and Potential Regulatory Sequences of Calpain-3 Gene in Polish Limb–Girdle Muscular Dystrophy Patients

Frontiers in neuroscience, 2021-10, Vol.15, p.692482-692482

2021

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Deep learning vs feature engineering in the assessment of voice signals for diagnosis in Parkinson’s disease

Bulletin of the Polish Academy of Sciences. Technical sciences, 2021, Vol.69 (3)

2021

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Novel Col12A1 variant expands the clinical picture of congenital myopathies with extracellular matrix defects

Muscle & nerve, 2017-02, Vol.55 (2), p.277-281

2017

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Amifampridine phosphate (Firdapse®) is effective and safe in a phase 3 clinical trial in LEMS

Muscle & nerve, 2016-05, Vol.53 (5), p.717-725

2016

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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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Real World Evidence on the Effectiveness of Nusinersen within the National Program to Treat Spinal Muscular Atrophy in Poland

Healthcare (Basel), 2023-05, Vol.11 (10), p.1515

2023

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Generation of DMBi002-A human induced pluripotent stem cell line from patient with Spinal muscular atrophy type 3

Stem cell research, 2021-12, Vol.57, p.102563-102563, Article 102563

2021

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VAV1 and BAFF, via NFκB pathway, are genetic risk factors for myasthenia gravis

Annals of clinical and translational neurology, 2014-05, Vol.1 (5), p.329-339

2014

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

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

2021

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Myasthenia gravis—treatment and severity in nationwide cohort

Treatment outcome in juvenile‐onset myasthenia gravis

Role of autoantibody levels as biomarkers in the management of patients with myasthenia gravis: A systematic review and expert appraisal

Reply to the Letter to the Editor in response to “Role of autoantibody levels as biomarkers in the management of patients with myasthenia gravis: A systematic review and expert appraisal”

Screening for late‐onset Pompe disease in Poland

The remarkable phenotypic variability of the p.Arg269HiS variant in the TRPV4 gene

Prevalence and impact of autoimmune thyroid disease on myasthenia gravis course

Transient global amnesia - hippocampal lesions in magnetic resonance imaging

Effect of age and gender on the number of motor units in healthy subjects estimated by the multipoint incremental MUNE method

Observation of the natural course of type 3 spinal muscular atrophy: data from the polish registry of spinal muscular atrophy

Determinants of Quality of Life in Myasthenia Gravis Patients

Long-term nusinersen treatment across a wide spectrum of spinal muscular atrophy severity: a real-world experience

Ultra-low radiation dose protocol for CT-guided intrathecal nusinersen injections for patients with spinal muscular atrophy and severe scoliosis

Randomized phase 2 trial and open-label extension of domagrozumab in Duchenne muscular dystrophy

Application of imaging techniques to objectify the Finger Tapping test used in the diagnosis of Parkinson's disease

Targeted Next-Generation Sequencing Reveals Mutations in Non-coding Regions and Potential Regulatory Sequences of Calpain-3 Gene in Polish Limb–Girdle Muscular Dystrophy Patients

Deep learning vs feature engineering in the assessment of voice signals for diagnosis in Parkinson’s disease

Novel Col12A1 variant expands the clinical picture of congenital myopathies with extracellular matrix defects

Amifampridine phosphate (Firdapse®) is effective and safe in a phase 3 clinical trial in LEMS

Lower BAFF Levels in Myasthenic Patients Treated with Glucocorticoids

Real World Evidence on the Effectiveness of Nusinersen within the National Program to Treat Spinal Muscular Atrophy in Poland

Generation of DMBi002-A human induced pluripotent stem cell line from patient with Spinal muscular atrophy type 3

VAV1 and BAFF, via NFκB pathway, are genetic risk factors for myasthenia gravis

Abnormal spontaneous activity in primary myopathic disorders

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

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