Evaluation of branched-chain amino acid intake in children with maple syrup urine disease and methylmalonic aciduria.

Journal of inherited metabolic disease1990Parsons HG, Carter RJ, Unrath M, et al.

Study designOther primary literature

SubjectHuman

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Study design: Other primary literature
Subject: Human
Publication year: 1990
Source: doi.org
Abstract display: Not reproduced here
Publication status: Active
Status checked: 17 Aug 2026
Collected: 3 Aug 2026
Freshness: Current
Review stage: Automated
Record status: Published

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Abstract

cc by 以外（cc by-nc / cc by-nc-nd / NONE 等）は抄録を再掲しない。DOI/PMID へのリンクのみ表示する。

MeSH

Amino Acid Metabolism, Inborn ErrorsAmino Acids, Branched-ChainAmmoniaBody WeightChild, PreschoolCreatinineDietary ProteinsFemaleFood, FormulatedGrowthHumansInfantInfant, NewbornIsoleucineLeucineMaleMalonatesMaple Syrup Urine DiseaseMethylmalonic AcidNutritional RequirementsValine

DOI 10.1007/bf01799675

PMID 2116544

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