Search Results - "Wiedau‐Pazos, Martina"
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Assessment of feasibility and utility of universal referral to specialty palliative care in a multidisciplinary amyotrophic lateral sclerosis clinic: A cohort study
Published in Muscle & nerve (01-06-2021)“…Introduction Although the value of palliative care integration in multidisciplinary amyotrophic lateral sclerosis (ALS) clinics has been increasingly…”
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Long‐term edaravone efficacy in amyotrophic lateral sclerosis: Post‐hoc analyses of Study 19 (MCI186‐19)
Published in Muscle & nerve (01-02-2020)“…Background In a Phase 3 study, amyotrophic lateral sclerosis (ALS) patients experienced significantly less physical functional decline with 24‐week edaravone…”
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Longitudinal specialty palliative care for people with amyotrophic lateral sclerosis using a universal referral method
Published in Muscle & nerve (01-08-2022)Get full text
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Mexiletine for muscle cramps in amyotrophic lateral sclerosis: A randomized, double‐blind crossover trial
Published in Muscle & nerve (01-07-2018)“…ABSTRACT Introduction: More than 90% of amyotrophic lateral sclerosis (ALS) patients have muscle cramps, but evidence‐based treatments have not been available…”
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Directed Differentiation of Human‐Induced Pluripotent Stem Cells Generates Active Motor Neurons
Published in Stem cells (Dayton, Ohio) (01-04-2009)“…The potential for directed differentiation of human‐induced pluripotent stem (iPS) cells to functional postmitotic neuronal phenotypes is unknown. Following…”
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Induction of Nrf2 and xCT are involved in the action of the neuroprotective antibiotic ceftriaxone in vitro
Published in Journal of neurochemistry (01-10-2009)“…In amyotrophic lateral sclerosis, down-regulation of the astrocyte-specific glutamate excitatory amino acid transporter 2 is hypothesized to increase…”
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IL-17A is increased in the serum and in spinal cord CD8 and mast cells of ALS patients
Published in Journal of neuroinflammation (09-11-2010)“…The contribution of inflammation to neurodegenerative diseases is increasingly recognized, but the role of inflammation in sporadic amyotrophic lateral…”
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Edaravone efficacy in amyotrophic lateral sclerosis with reduced forced vital capacity: Post-hoc analysis of Study 19 (MCI186-19) [clinical trial NCT01492686]
Published in PloS one (14-06-2022)“…Edaravone slowed the rate of functional decline in subjects with amyotrophic lateral sclerosis (ALS) in phase 3 study MCI186-19 (Study 19). One of the Study 19…”
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Transcriptome analysis in whole blood reveals increased microbial diversity in schizophrenia
Published in Translational psychiatry (10-05-2018)“…The role of the human microbiome in health and disease is increasingly appreciated. We studied the composition of microbial communities present in blood across…”
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Resurgent Na+ Current Offers Noise Modulation in Bursting Neurons
Published in PLoS computational biology (01-06-2019)“…Neurons utilize bursts of action potentials as an efficient and reliable way to encode information. It is likely that the intrinsic membrane properties of…”
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Charcot-Marie-Tooth disease CMT4A: GDAP1 increases cellular glutathione and the mitochondrial membrane potential
Published in Human molecular genetics (01-01-2012)“…Mutations in GDAP1 lead to recessively or dominantly inherited peripheral neuropathies (Charcot-Marie-Tooth disease, CMT), indicating that GDAP1 is essential…”
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Integrative gene–tissue microarray-based approach for identification of human disease biomarkers: application to amyotrophic lateral sclerosis
Published in Human molecular genetics (15-08-2010)“…Advances in genomics and proteomics permit rapid identification of disease-relevant genes and proteins. Challenges include biological differences between…”
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A Genomic Screen for Modifiers of Tauopathy Identifies Puromycin-Sensitive Aminopeptidase as an Inhibitor of Tau-Induced Neurodegeneration
Published in Neuron (Cambridge, Mass.) (07-09-2006)“…Neurofibrillary tangles (NFT) containing tau are a hallmark of neurodegenerative diseases, including Alzheimer's disease (AD). NFT burden correlates with…”
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Wnt-pathway activation during the early stage of neurodegeneration in FTDP-17 mice
Published in Neurobiology of aging (01-01-2009)“…Abstract Glycogen synthase kinase-3beta (GSK-3β), a key component of the Wnt signaling pathway, has been recognized as an important tau kinase with a potential…”
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Altered Reactivity of Superoxide Dismutase in Familial Amyotrophic Lateral Sclerosis
Published in Science (American Association for the Advancement of Science) (26-01-1996)“…A subset of individuals with familial amyotrophic lateral sclerosis (FALS) possesses dominantly inherited mutations in the gene that encodes copper-zinc…”
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Human embryonic stem cell-derived motor neurons expressing SOD1 mutants exhibit typical signs of motor neuron degeneration linked to ALS
Published in Disease models & mechanisms (01-03-2009)“…Human embryonic stem cell (hESC)-derived neurons have the potential to model neurodegenerative disorders. Here, we demonstrate the expression of a mutant gene,…”
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Puromycin-sensitive aminopeptidase (PSA/NPEPPS) impedes development of neuropathology in hPSA/TAUP301L double-transgenic mice
Published in Human molecular genetics (01-05-2011)Get full text
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Circuit-Specific Early Impairment of Proprioceptive Sensory Neurons in the SOD1(G93A) Mouse Model for ALS
Published in The Journal of neuroscience (30-10-2019)“…Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease in which motor neurons degenerate, resulting in muscle atrophy, paralysis, and fatality…”
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Circuit-Specific Early Impairment of Proprioceptive Sensory Neurons in the SOD1G93A Mouse Model for ALS
Published in The Journal of neuroscience (30-10-2019)“…Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease in which motor neurons degenerate, resulting in muscle atrophy, paralysis, and fatality…”
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Palliative Care Consults in an Inpatient Setting for Patients With Amyotrophic Lateral Sclerosis
Published in American journal of hospice & palliative medicine (01-09-2021)“…Background: Limited data about the frequency and outcomes of palliative care (PC) specialty consultations for patients with amyotrophic lateral sclerosis (ALS)…”
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