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81
CSF chitinase proteins in amyotrophic lateral sclerosis
Published 2019“…<p>Objective: To evaluate the classifier performance, clinical and biochemical correlations of cerebrospinal fluid (CSF) levels of the chitinase proteins Chitotriosidase-1 (CHIT1), Chitinase-3-like protein 1 (CHI3L1) and Chitinase-3-like protein 2 (CHI3L2) in amyotrophic lateral sclerosis (ALS).</p> <p>Methods: CSF levels of CHIT1, CHI3L1, CHI3L2, phosphorylated neurofilament heavy chain (pNFH) and C-reactive protein were measured by ELISA in a longitudinal cohort of patients with ALS (n=82), primary lateral sclerosis (PLS, n=10), ALS-mimic conditions (n=12), healthy controls (n=25) and asymptomatic carriers of ALS-causing genetic mutations (AGC; n=5).…”
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82
Defective cholesterol metabolism in amyotrophic lateral sclerosis.
Published 2016“…As neurons die cholesterol is released in the central nervous system (CNS), hence this sterol and its metabolites may represent a biomarker of neurodegeneration, including in amyotrophic lateral sclerosis (ALS) in which altered cholesterol levels have been linked to prognosis. …”
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83
Imaging cerebral activity in amyotrophic lateral sclerosis
Published 2019“…Advances in neuroimaging, complementing histopathological insights, have established a multi-system involvement of cerebral networks beyond the traditional neuromuscular pathological view of amyotrophic lateral sclerosis (ALS). The development of effective disease-modifying therapy remains a priority and this will be facilitated by improved biomarkers of motor system integrity against which to assess the efficacy of candidate drugs. …”
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Mechanisms, models and biomarkers in amyotrophic lateral sclerosis.
Published 2013“…The last 30 years have seen a major advance in the understanding of the clinical and pathological heterogeneity of amyotrophic lateral sclerosis (ALS), and its overlap with frontotemporal dementia. …”
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86
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Advances in the application of MRI to amyotrophic lateral sclerosis.
Published 2010“…IMPORTANCE OF THE FIELD: With the emergence of therapeutic candidates for the incurable and rapidly progressive neurodegenerative condition of amyotrophic lateral sclerosis (ALS), it will be essential to develop easily obtainable biomarkers for diagnosis, as well as monitoring, in a disease where clinical examination remains the predominant diagnostic tool. …”
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88
Murine experimental models of amyotrophic lateral sclerosis: an update
Published 2024-04-01“…Introduction: Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease whose aetiology is unknown. …”
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89
Motor neuron replacement therapy for amyotrophic lateral sclerosis
Published 2022-01-01Subjects: “…amyotrophic lateral sclerosis; motor neuron replacement; neural progenitor cells; neural stem cells; stem cells…”
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90
The complexity of multidisciplinary respiratory care in amyotrophic lateral sclerosis
Published 2023-09-01“…Motor neurone disease/amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder with no known cure, where death is usually secondary to progressive respiratory failure. …”
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91
Defective Oligodendroglial Lineage and Demyelination in Amyotrophic Lateral Sclerosis
Published 2021-03-01“…Motor neurons and their axons reaching the skeletal muscle have long been considered as the best characterized targets of the degenerative process observed in amyotrophic lateral sclerosis (ALS). However, the involvement of glial cells was also more recently reported. …”
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92
Oropharyngeal Dysphagia as the Main Expression of Amyotrophic Lateral Sclerosis
Published 2022-05-01Subjects: Get full text
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93
The Role of Nucleocytoplasmic Transport Defects in Amyotrophic Lateral Sclerosis
Published 2021-11-01“…There is ample evidence that nucleocytoplasmic-transport deficits could play an important role in the pathology of amyotrophic lateral sclerosis (ALS). However, the currently available data are often circumstantial and do not fully clarify the exact causal and temporal role of nucleocytoplasmic transport deficits in ALS patients. …”
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94
Comorbidity Pattern Analysis for Predicting Amyotrophic Lateral Sclerosis
Published 2021-01-01Subjects: Get full text
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95
Anti-ganglioside antibodies in amyotrophic lateral sclerosis revisited.
Published 2015-01-01“…BACKGROUND:Amyotrophic Lateral Sclerosis (ALS) is a devastating neurodegenerative disorder with typical onset in the 5th- 6th decade of life. …”
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96
Muscle ultrasound imaging in the diagnosis of amyotrophic lateral sclerosis
Published 2015-02-01“…Amyotrophic lateral sclerosis (ALS) is the most common form of motor neuron disease. …”
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97
Cortical markers of cognitive syndromes in amyotrophic lateral sclerosis
Published 2018-01-01“…Amyotrophic lateral sclerosis (ALS) can be associated with a spectrum of cognitive and behavioural symptoms, but the related patterns of focal cortical atrophy in non-demented ALS patients remain largely unknown. …”
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98
RNA Deregulation in Amyotrophic Lateral Sclerosis: The Noncoding Perspective
Published 2021-09-01“…This review aims to explore the link between ncRNA dysregulation and amyotrophic lateral sclerosis (ALS), the most frequent motoneuron (MN) disorder in adults. …”
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99
Alterations in Leptin Signaling in Amyotrophic Lateral Sclerosis (ALS)
Published 2021-09-01Subjects: Get full text
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100
Repetitive nerve stimulation on survival in amyotrophic lateral sclerosis
Published 2023-08-01Subjects: Get full text
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