Nutritional status of patients with amyotrophic lateral sclerosis: relation to the proximity of death.
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Severe loss of appetite in amyotrophic lateral sclerosis patients: online self-assessment studyRecent advances in amyotrophic lateral sclerosisComplementary and Alternative Therapies in Amyotrophic Lateral SclerosisAmyotrophic Lateral Sclerosis: New Perpectives and UpdateAmyotrophic Lateral Sclerosis: An update for 2013 Clinical Features, Pathophysiology, Management and Therapeutic TrialsEffects of diabetes mellitus on amyotrophic lateral sclerosis: a systematic reviewThe creatine kinase/creatine connection to Alzheimer's disease: CK-inactivation, APP-CK complexes and focal creatine deposits1H-NMR-based metabolomic profiling of CSF in early amyotrophic lateral sclerosisAssociation Between Change in Body Mass Index, Unified Parkinson's Disease Rating Scale Scores, and Survival Among Persons With Parkinson Disease: Secondary Analysis of Longitudinal Data From NINDS Exploratory Trials in Parkinson Disease Long-term SCaloric restriction shortens lifespan through an increase in lipid peroxidation, inflammation and apoptosis in the G93A mouse, an animal model of ALS.Measures of bulbar and spinal motor function, muscle innervation, and mitochondrial function in ALS rats.Diagnosis and management of motor neurone disease.Genetically altering organismal metabolism by leptin-deficiency benefits a mouse model of amyotrophic lateral sclerosisPredictive equations over-estimate the resting energy expenditure in amyotrophic lateral sclerosis patients who are dependent on invasive ventilation support.Body mass index, not dyslipidemia, is an independent predictor of survival in amyotrophic lateral sclerosisHypercaloric enteral nutrition in patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled phase 2 trialManagement of motor neurone diseaseAdipose Tissue Distribution Predicts Survival in Amyotrophic Lateral SclerosisWeight loss, dysphagia and supplement intake in patients with amyotrophic lateral sclerosis (ALS): impact on quality of life and therapeutic options.Survey of current enteral nutrition practices in treatment of amyotrophic lateral sclerosisA review of creatine supplementation in age-related diseases: more than a supplement for athletes.Noninvasive ventilation reduces energy expenditure in amyotrophic lateral sclerosis.The management of motor neurone disease.Increased peripheral lipid clearance in an animal model of amyotrophic lateral sclerosis.Time-course and characterization of orolingual motor deficits in B6SJL-Tg(SOD1-G93A)1Gur/J miceThe longitudinal cerebrospinal fluid metabolomic profile of amyotrophic lateral sclerosisNutritional Status and Body Composition in Korean Myopathy Patients.Prediagnostic body fat and risk of death from amyotrophic lateral sclerosis: the EPIC cohort.Premorbid body mass index and risk of amyotrophic lateral sclerosisHypolipidemia in patients with amyotrophic lateral sclerosis: a possible gender difference?Nutrition and dietary supplements in motor neuron disease.TDP-43, an ALS linked protein, regulates fat deposition and glucose homeostasis.Reduced activity of AMP-activated protein kinase protects against genetic models of motor neuron disease.Evidence for defective energy homeostasis in amyotrophic lateral sclerosis: benefit of a high-energy diet in a transgenic mouse model.A high-fat jelly diet restores bioenergetic balance and extends lifespan in the presence of motor dysfunction and lumbar spinal cord motor neuron loss in TDP-43A315T mutant C57BL6/J mice.Estimating daily energy expenditure in individuals with amyotrophic lateral sclerosis.High-fat and ketogenic diets in amyotrophic lateral sclerosis.Amyotrophic Lateral Sclerosis and Metabolomics: Clinical Implication and Therapeutic Approach.The interplay between metabolic homeostasis and neurodegeneration: insights into the neurometabolic nature of amyotrophic lateral sclerosis.Metabolic Dysfunctions in Amyotrophic Lateral Sclerosis Pathogenesis and Potential Metabolic Treatments
P2860
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P2860
Nutritional status of patients with amyotrophic lateral sclerosis: relation to the proximity of death.
description
1996 nî lūn-bûn
@nan
1996 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年学术文章
@wuu
1996年学术文章
@zh-cn
1996年学术文章
@zh-hans
1996年学术文章
@zh-my
1996年学术文章
@zh-sg
1996年學術文章
@yue
name
Nutritional status of patients ...... ion to the proximity of death.
@ast
Nutritional status of patients ...... ion to the proximity of death.
@en
Nutritional status of patients ...... ion to the proximity of death.
@nl
type
label
Nutritional status of patients ...... ion to the proximity of death.
@ast
Nutritional status of patients ...... ion to the proximity of death.
@en
Nutritional status of patients ...... ion to the proximity of death.
@nl
altLabel
Nutritional status of patients ...... tion to the proximity of death
@en
Nutritional status of patients ...... tion to the proximity of death
@nl
prefLabel
Nutritional status of patients ...... ion to the proximity of death.
@ast
Nutritional status of patients ...... ion to the proximity of death.
@en
Nutritional status of patients ...... ion to the proximity of death.
@nl
P2093
P356
P1476
Nutritional status of patients ...... tion to the proximity of death
@en
Nutritional status of patients ...... ion to the proximity of death.
@en
P2093
A R Schneider
Berryman S
C J McClain
E J Kasarskis
J G Vanderleest
Kasarskis EJ
McClain CJ
S Berryman
Schneider AR
Vanderleest JG
P304
P356
10.1093/AJCN/63.1.130
P407
P577
1996-01-01T00:00:00Z