Search Results - "SHOESMITH, C"
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Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology
Published in Neurology (13-10-2009)“…To systematically review evidence bearing on the management of patients with amyotrophic lateral sclerosis (ALS). The authors analyzed studies from 1998 to…”
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Practice Parameter update: The care of the patient with amyotrophic lateral sclerosis: Multidisciplinary care, symptom management, and cognitive/behavioral impairment (an evidence-based review): Report of the Quality Standards Subcommittee of the American Academy of Neurology
Published in Neurology (13-10-2009)“…To systematically review evidence bearing on the management of patients with amyotrophic lateral sclerosis (ALS). The authors analyzed studies from 1998 to…”
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Neurodevelopmental effects of genetic frontotemporal dementia in young adult mutation carriers
Published in Brain (London, England : 1878) (02-05-2023)“…Abstract While frontotemporal dementia has been considered a neurodegenerative disease that starts in mid-life or later, it is now clearly established that…”
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High-dose corticosteroids for acute cytomegalovirus-associated transverse myelitis in the immunocompetent patient: a case report and systematic review
Published in Journal of neurovirology (01-06-2019)“…We present an immunocompetent patient with transverse myelitis (TM) during acute cytomegalovirus (CMV) infection, as evidenced by a reactive serum CMV IgM and…”
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Regional spread pattern predicts survival in patients with sporadic amyotrophic lateral sclerosis
Published in European journal of neurology (01-06-2012)“…Background and purpose: Sporadic amyotrophic lateral sclerosis (sALS) is a disease with a focal clinical onset and contiguous spread. We examined patterns of…”
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Establishing a Canadian registry of patients with amyotrophic lateral sclerosis
Published in Canadian journal of neurological sciences (01-01-2013)“…Amyotrophic lateral sclerosis (ALS) is a devastating cause of progressive weakness, respiratory failure and death. To date there is no effective therapy to…”
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Safety and efficacy of ceftriaxone for amyotrophic lateral sclerosis: a multi-stage, randomised, double-blind, placebo-controlled trial
Published in Lancet neurology (01-11-2014)“…Summary Background Glutamate excitotoxicity might contribute to the pathophysiology of amyotrophic lateral sclerosis. In animal models, decreased excitatory…”
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TDP43 is a human low molecular weight neurofilament ( hNFL) mRNA-binding protein
Published in Molecular and cellular neuroscience (01-06-2007)“…The human TAR DNA-binding protein (TDP43) colocalizes with ubiquitinated inclusions in motor neurons in amyotrophic lateral sclerosis (ALS). TDP43 is both a…”
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MOTOR NEURON DISORDERS AND NEUROPATHIES
Published in Neuromuscular disorders : NMD (01-10-2021)Get full text
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Ventricular volume expansion in presymptomatic genetic frontotemporal dementia
Published in Neurology (29-10-2019)“…OBJECTIVETo characterize the time course of ventricular volume expansion in genetic frontotemporal dementia (FTD) and identify the onset time and rates of…”
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Prognosis of amyotrophic lateral sclerosis with respiratory onset
Published in Journal of neurology, neurosurgery and psychiatry (01-06-2007)“…Respiratory muscle involvement is a recognised, but often late, complication of amyotrophic lateral sclerosis (ALS). The clinical features and prognosis of 21…”
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A modified Camel and Cactus Test detects presymptomatic semantic impairment in genetic frontotemporal dementia within the GENFI cohort
Published in Applied neuropsychology. Adult (2022)“…Impaired semantic knowledge is a characteristic feature of some forms of frontotemporal dementia (FTD), particularly the sporadic disorder semantic dementia…”
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Magnetic resonance imaging study of extracellular fluid tracer movement in brains of immature rats with hydrocephalus
Published in Neurological research (New York) (01-01-2000)“…Hydrocephalus is associated with brain compression and accumulation of neurotransmitter waste products in the brain and cerebrospinal fluid. We postulated that…”
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White matter hyperintensities in progranulin-associated frontotemporal dementia: A longitudinal GENFI study
Published in NeuroImage clinical (01-01-2019)“…Frontotemporal dementia (FTD) is a heterogeneous group of neurodegenerative disorders with both sporadic and genetic forms. Mutations in the progranulin gene…”
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Practice Parameter update: The care of the patient with amyotrophic lateral sclerosis: Drug, nutritional, and respiratory therapies (an evidence-based review): Report of the Quality Standards Subcommittee of the American Academy of Neurology I
Published in Neurology (2009)Get full text
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Early symptoms in symptomatic and preclinical genetic frontotemporal lobar degeneration
Published in Journal of neurology, neurosurgery and psychiatry (01-09-2020)“…ObjectivesThe clinical heterogeneity of frontotemporal dementia (FTD) complicates identification of biomarkers for clinical trials that may be sensitive during…”
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Soy protein modification of rat polycystic kidney disease
Published in The American journal of physiology (01-03-1998)“…We undertook a study to determine whether soy protein feeding would ameliorate renal injury in the Han:SPRD-cy rat model of polycystic kidney disease (PKD)…”
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