Plasma Neurofilament Light Chain Is Elevated in Adaptor Protein Complex 4‐Related Hereditary Spastic Paraplegia

Blood GFAP as an emerging biomarker in brain and spinal cord disorders

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Characteristics of serum neurofilament light chain as a biomarker in hereditary spastic paraplegia type 4

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Cerebrospinal fluid neurofilament light chain predicts short-term prognosis in pediatric Guillain-Barré syndrome

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Serum GFAP and NfL Levels Differentiate Subsequent Progression and Disease Activity in Patients With Progressive Multiple Sclerosis

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Neurofilament light chain is a cerebrospinal fluid biomarker in hereditary spastic paraplegia

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Reference values for plasma neurofilament light chain in healthy Chinese children

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Systematic Analysis of Brain MRI Findings in Adaptor Protein Complex 4–Associated Hereditary Spastic Paraplegia

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Seven day pre-analytical stability of serum and plasma neurofilament light chain

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Serum neurofilament light chain in pediatric spinal muscular atrophy patients and healthy children

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Serum neurofilament light chain in adult and pediatric patients with myelin oligodendrocyte glycoprotein antibody‐associated disease: Correlation with relapses and seizures

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Serum neurofilament light chain is a useful biomarker in pediatric multiple sclerosis

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Blood NfL

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Adaptor protein complex 4 deficiency: a paradigm of childhood-onset hereditary spastic paraplegia caused by defective protein trafficking

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Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia

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Serum neurofilament light chain is increased in hereditary spastic paraplegias

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Neurofilaments as biomarkers in neurological disorders

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Comparison of three analytical platforms for quantification of the neurofilament light chain in blood samples: ELISA, electrochemiluminescence immunoassay and Simoa

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PNPLA6 mutations cause Boucher-Neuhäuser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum

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Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP)

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