Hypercaloric enteral nutrition in patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled phase 2 trial

scientific article

Hypercaloric enteral nutrition in patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled phase 2 trial is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/S0140-6736(14)60222-1
P932PMC publication ID4176708
P698PubMed publication ID24582471

P50authorEric A MacklinQ45310572
Shafeeq S LadhaQ58144250
Terry Heiman-PattersonQ63214703
Jonathan D GlassQ88095339
Hiroshi MitsumotoQ90084178
Merit E CudkowiczQ95746107
P2093author name stringRobert Lawson
Hong Yu
Ericka P Simpson
Jonathan Katz
Tahseen Mozaffar
Anne-Marie Wills
Jane Hubbard
Rup Tandan
Benjamin Brooks
Jau-Shin Lou
Daniela Grasso
Deborah Gelinas
Gregory P Hanes
Katy Mahoney
MDA Clinical Research Network
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No benefit of dietary restriction on disease onset or progression in amyotrophic lateral sclerosis Cu/Zn-superoxide dismutase mutant miceQ33865534
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Body mass index, not dyslipidemia, is an independent predictor of survival in amyotrophic lateral sclerosisQ34187004
Nutritional status of patients with amyotrophic lateral sclerosis: relation to the proximity of deathQ34375696
Energy intake and amyotrophic lateral sclerosisQ34582888
Survival of patients with ALS following institution of enteral feeding is related to pre-procedure oximetry: a retrospective review of 98 patients in a single centreQ36425117
Prediagnostic body fat and risk of death from amyotrophic lateral sclerosis: the EPIC cohortQ36687156
Premorbid body mass index and risk of amyotrophic lateral sclerosisQ36737158
Evidence for defective energy homeostasis in amyotrophic lateral sclerosis: benefit of a high-energy diet in a transgenic mouse modelQ37285915
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 NeurologyQ37613342
Energy metabolism in amyotrophic lateral sclerosisQ37805077
Nutritional state, energy intakes and energy expenditure of amyotrophic lateral sclerosis (ALS) patientsQ37907556
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Effect of nutritional supplementation with milk whey proteins in amyotrophic lateral sclerosis patientsQ43065229
Body mass index (BMI) as predictor of ALSFRS-R score decline in ALS patientsQ44276835
Energy requirement assessed by doubly-labeled water method in patients with advanced amyotrophic lateral sclerosis managed by tracheotomy positive pressure ventilation.Q51333827
Amyotrophic lateral sclerosisQ55877676
El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases aQ55984319
High-caloric food supplements in the treatment of amyotrophic lateral sclerosis: A prospective interventional studyQ58125259
Management of ALS: nutritional careQ71657294
Individuals with amyotrophic lateral sclerosis are in caloric balance despite losses in massQ71832749
Nutritional status is a prognostic factor for survival in ALS patientsQ73016942
Effects of enteral feeding with eicosapentaenoic acid, gamma-linolenic acid, and antioxidants in mechanically ventilated patients with severe sepsis and septic shockQ79931066
Dyslipidemia is a protective factor in amyotrophic lateral sclerosisQ80503053
P433issue9934
P407language of work or nameEnglishQ1860
P921main subjectplaceboQ269829
amyotrophic lateral sclerosisQ206901
phase II clinical trialQ42824440
P304page(s)2065-2072
P577publication date2014-02-28
P1433published inThe LancetQ939416
P1476titleHypercaloric enteral nutrition in patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled phase 2 trial
P478volume383

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