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Diagnostic Challenges and Clinical Characteristics of Hepatitis E Virus-Associated Guillain-Barré Syndrome

JAMA neurology, 2017-01, Vol.74 (1), p.26

2017

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Biochemical and clinical biomarkers in adult SMA 3–4 patients treated with nusinersen for 22 months

Annals of clinical and translational neurology, 2022-08, Vol.9 (8), p.1241-1251

2022

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Expanded phenotypic spectrum of the m.8344A>G “MERRF” mutation: data from the German mitoNET registry

Journal of neurology, 2016-05, Vol.263 (5), p.961-972

2016

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Patient-reported impact of myasthenia gravis in the real world: findings from a digital observational survey-based study (MyRealWorld MG)

BMJ open, 2023-05, Vol.13 (5), p.e068104-e068104

2023

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Screening for lipoprotein receptor-related protein 4-, agrin-, and titin-antibodies and exploring the autoimmune spectrum in myasthenia gravis

Journal of neurology, 2017-06, Vol.264 (6), p.1193-1203

2017

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Histopathological correlations and fat replacement imaging patterns in recessive limb‐girdle muscular dystrophy type 12

Journal of cachexia, sarcopenia and muscle, 2023-06, Vol.14 (3), p.1468-1481

2023

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The Latin American experience with a next generation sequencing genetic panel for recessive limb-girdle muscular weakness and Pompe disease

Orphanet journal of rare diseases, 2020-01, Vol.15 (1), p.11-11, Article 11

2020

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Patient-reported burden of myasthenia gravis: baseline results of the international prospective, observational, longitudinal real-world digital study MyRealWorld-MG

BMJ open, 2023-01, Vol.13 (1), p.e066445-e066445

2023

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Author Response: Prospective Natural History Study in 24 Adult Patients With LGMDR12 Over 2 Years of Follow-up: Quantitative MRI and Clinical Outcome Measures

Neurology, 2023-02, Vol.100 (7), p.354-354

2023

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Clinical and biometrical 12-month follow-up in patients after reconstruction of the sural nerve biopsy defect by the collagen-based nerve guide Neuromaix

European journal of medical research, 2017-09, Vol.22 (1), p.34-34, Article 34

2017

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Six-Minute Walk Distance Is a Useful Outcome Measure to Detect Motor Decline in Treated Late-Onset Pompe Disease Patients

Cells (Basel, Switzerland), 2022-01, Vol.11 (3), p.334

2022

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Clinical spectrum of the anti-GQ1b antibody syndrome: a case series of eight patients

Acta neurologica Belgica, 2019-03, Vol.119 (1), p.29-36

2019

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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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Comparison of elevated phosphorylated neurofilament heavy chains in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 2018-04, Vol.89 (4), p.367-373

2018

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Diagnostic challenge and therapeutic dilemma in necrotizing myopathy

Neurology, 2013-09, Vol.81 (10), p.932-935

2013

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Neurofilament markers for ALS correlate with extent of upper and lower motor neuron disease

Neurology, 2017-06, Vol.88 (24), p.2302-2309

2017

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Prospective Natural History Study in 24 Adult Patients With LGMDR12 Over 2 Years of Follow-up: Quantitative MRI and Clinical Outcome Measures

Neurology, 2022-08, Vol.99 (6), p.e638

2022

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Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study

Acta neuropathologica, 2009-03, Vol.117 (3), p.293-307

2009

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Attention to 3-D Shape, 3-D Motion, and Texture in 3-D Structure from Motion Displays

Journal of cognitive neuroscience, 2004-05, Vol.16 (4), p.665-682

2004

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DNAJB2 Expression in Normal and Diseased Human and Mouse Skeletal Muscle

The American journal of pathology, 2010-06, Vol.176 (6), p.2901-2910

2010

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Anti-Ku + myositis: an acquired inflammatory protein-aggregate myopathy

Acta neuropathologica, 2024-07, Vol.148 (1), p.6, Article 6

2024

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Lessons for future clinical trials in adults with Becker muscular dystrophy: Disease progression detected by muscle magnetic resonance imaging, clinical and patient‐reported outcome measures

European journal of neurology, 2024-07, Vol.31 (7), p.e16282-n/a

2024

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Maternal copy-number variations in the DMD gene as secondary findings in noninvasive prenatal screening

Genetics in medicine, 2019-12, Vol.21 (12), p.2774-2780

2019

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Diagnostic Challenges and Clinical Characteristics of Hepatitis E Virus-Associated Guillain-Barré Syndrome

Biochemical and clinical biomarkers in adult SMA 3–4 patients treated with nusinersen for 22 months

Expanded phenotypic spectrum of the m.8344A>G “MERRF” mutation: data from the German mitoNET registry

Patient-reported impact of myasthenia gravis in the real world: findings from a digital observational survey-based study (MyRealWorld MG)

Screening for lipoprotein receptor-related protein 4-, agrin-, and titin-antibodies and exploring the autoimmune spectrum in myasthenia gravis

Histopathological correlations and fat replacement imaging patterns in recessive limb‐girdle muscular dystrophy type 12

The Latin American experience with a next generation sequencing genetic panel for recessive limb-girdle muscular weakness and Pompe disease

Patient-reported burden of myasthenia gravis: baseline results of the international prospective, observational, longitudinal real-world digital study MyRealWorld-MG

Author Response: Prospective Natural History Study in 24 Adult Patients With LGMDR12 Over 2 Years of Follow-up: Quantitative MRI and Clinical Outcome Measures

Clinical and biometrical 12-month follow-up in patients after reconstruction of the sural nerve biopsy defect by the collagen-based nerve guide Neuromaix

Six-Minute Walk Distance Is a Useful Outcome Measure to Detect Motor Decline in Treated Late-Onset Pompe Disease Patients

Clinical spectrum of the anti-GQ1b antibody syndrome: a case series of eight patients

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

Comparison of elevated phosphorylated neurofilament heavy chains in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis

PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease

Diagnostic challenge and therapeutic dilemma in necrotizing myopathy

Neurofilament markers for ALS correlate with extent of upper and lower motor neuron disease

Prospective Natural History Study in 24 Adult Patients With LGMDR12 Over 2 Years of Follow-up: Quantitative MRI and Clinical Outcome Measures

Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study

Attention to 3-D Shape, 3-D Motion, and Texture in 3-D Structure from Motion Displays

DNAJB2 Expression in Normal and Diseased Human and Mouse Skeletal Muscle

Anti-Ku + myositis: an acquired inflammatory protein-aggregate myopathy

Lessons for future clinical trials in adults with Becker muscular dystrophy: Disease progression detected by muscle magnetic resonance imaging, clinical and patient‐reported outcome measures

Congenital Myasthenic Syndromes in Belgium: Genetic and Clinical Characterization of Pediatric and Adult Patients

Maternal copy-number variations in the DMD gene as secondary findings in noninvasive prenatal screening

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