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Fatigue in chronic inflammatory demyelinating polyradiculoneuropathy

Muscle & nerve, 2020-12, Vol.62 (6), p.649-651

2020

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Molecular and Clinical Implications of Variant Repeats in Myotonic Dystrophy Type 1

International journal of molecular sciences, 2021-12, Vol.23 (1), p.354

2021

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Long-term outcome in patients with myasthenia gravis: one decade longitudinal study

Journal of neurology, 2022-04, Vol.269 (4), p.2039-2045

2022

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Cognitive impairment in myotonic dystrophy type 1 is associated with white matter damage

PloS one, 2014-08, Vol.9 (8), p.e104697-e104697

2014

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Guillain–Barré syndrome during pregnancy: A case series

The journal of obstetrics and gynaecology research, 2022-02, Vol.48 (2), p.477-482

2022

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Prospective analysis of disability and quality of life in patients with chronic inflammatory demyelinating polyradiculoneuropathy

Quality of life research, 2021-09, Vol.30 (9), p.2573-2579

2021

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Correction to: Prospective analysis of disability and quality of life in patients with chronic inflammatory demyelinating polyradiculoneuropathy

Quality of life research, 2021-09, Vol.30 (9), p.2581-2581

2021

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Hereditary myopathy with early respiratory failure: case report

The Egyptian journal of neurology, psychiatry and neurosurgery, 2023-03, Vol.59 (1), p.36

2023

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Bulbar-onset amyotrophic lateral sclerosis in a patient with genetically confirmed Huntington’s disease: a case study

The Egyptian journal of neurology, psychiatry and neurosurgery, 2024-12, Vol.60 (1), p.23

2024

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Transcranial brain parenchyma sonographic findings in patients with myotonic dystrophy type 1 and 2

Heliyon, 2024-03, Vol.10 (5), p.e26856-e26856, Article e26856

2024

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Autoimmune Diseases in Patients With Myotonic Dystrophy Type 2

Frontiers in neurology, 2022-07, Vol.13, p.932883-932883

2022

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Neuropathic pain in patients with Charcot-Marie-Tooth type 1A

Neurological sciences, 2020-03, Vol.41 (3), p.625-630

2020

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Cytokine Gene Polymorphisms in Patients with Chronic Inflammatory Demyelinating Polyneuropathy

Cells (Basel, Switzerland), 2023-08, Vol.12 (16), p.2033

2023

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Clusters of cognitive impairment among different phenotypes of myotonic dystrophy type 1 and type 2

Neurological sciences, 2017-03, Vol.38 (3), p.415-423

2017

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Long-term safety, tolerability, and efficacy of efgartigimod (ADAPT+): interim results from a phase 3 open-label extension study in participants with generalized myasthenia gravis

Frontiers in neurology, 2024-01, Vol.14, p.1284444-1284444

2024

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A longitudinal evaluation of fatigue in chronic inflammatory demyelinating polyneuropathy

Brain and behavior, 2022-08, Vol.12 (8), p.e2712-n/a

2022

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Non-routine cardiac tests still have no defined role in assessment of myotonic dystrophy type 2

Acta neurologica Belgica, 2020-08, Vol.120 (4), p.967-968

Peric, Stojan

2020

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Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease

Orphanet journal of rare diseases, 2018-09, Vol.13 (1), p.155-155, Article 155

2018

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Downregulation of LKB1/AMPK Signaling in Blood Mononuclear Cells Is Associated with the Severity of Guillain–Barre Syndrome

Cells (Basel, Switzerland), 2022-09, Vol.11 (18), p.2897

2022

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Clinical and epidemiological features of Guillain-Barré syndrome in the Western Balkans

Journal of the peripheral nervous system, 2014-12, Vol.19 (4), p.317-321

2014

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Guillain-Barré syndrome in the elderly

Journal of the peripheral nervous system, 2016-06, Vol.21 (2), p.105-110

2016

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Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease

Orphanet journal of rare diseases, 2019-08, Vol.14 (1), p.199-199, Article 199

2019

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Cerebral involvement and related aspects in myotonic dystrophy type 2

Neuromuscular disorders : NMD, 2021-08, Vol.31 (8), p.681-694

2021

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Repeat Interruptions Modify Age at Onset in Myotonic Dystrophy Type 1 by Stabilizing DMPK Expansions in Somatic Cells

Frontiers in genetics, 2018-11, Vol.9, p.601-601

2018

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Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weakness

Orphanet journal of rare diseases, 2017-11, Vol.12 (1), p.173-173, Article 173

2017

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Fatigue in chronic inflammatory demyelinating polyradiculoneuropathy

Molecular and Clinical Implications of Variant Repeats in Myotonic Dystrophy Type 1

Long-term outcome in patients with myasthenia gravis: one decade longitudinal study

Cognitive impairment in myotonic dystrophy type 1 is associated with white matter damage

Guillain–Barré syndrome during pregnancy: A case series

Prospective analysis of disability and quality of life in patients with chronic inflammatory demyelinating polyradiculoneuropathy

Correction to: Prospective analysis of disability and quality of life in patients with chronic inflammatory demyelinating polyradiculoneuropathy

Hereditary myopathy with early respiratory failure: case report

Bulbar-onset amyotrophic lateral sclerosis in a patient with genetically confirmed Huntington’s disease: a case study

Transcranial brain parenchyma sonographic findings in patients with myotonic dystrophy type 1 and 2

Autoimmune Diseases in Patients With Myotonic Dystrophy Type 2

Neuropathic pain in patients with Charcot-Marie-Tooth type 1A

Cytokine Gene Polymorphisms in Patients with Chronic Inflammatory Demyelinating Polyneuropathy

Clusters of cognitive impairment among different phenotypes of myotonic dystrophy type 1 and type 2

Long-term safety, tolerability, and efficacy of efgartigimod (ADAPT+): interim results from a phase 3 open-label extension study in participants with generalized myasthenia gravis

A longitudinal evaluation of fatigue in chronic inflammatory demyelinating polyneuropathy

Non-routine cardiac tests still have no defined role in assessment of myotonic dystrophy type 2

Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease

Downregulation of LKB1/AMPK Signaling in Blood Mononuclear Cells Is Associated with the Severity of Guillain–Barre Syndrome

Clinical and epidemiological features of Guillain-Barré syndrome in the Western Balkans

Guillain-Barré syndrome in the elderly

Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease

Cerebral involvement and related aspects in myotonic dystrophy type 2

Repeat Interruptions Modify Age at Onset in Myotonic Dystrophy Type 1 by Stabilizing DMPK Expansions in Somatic Cells

Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weakness

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