Guidelines for the diagnosis and management of chylomicron retention disease based on a review of the literature and the experience of two centers.
about
Molecular characterization of Tunisian families with abetalipoproteinemia and identification of a novel mutation in MTTP geneMechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease riskMolecular analysis and intestinal expression of SAR1 genes and proteins in Anderson's disease (Chylomicron retention disease)Anderson's disease/chylomicron retention disease in a Japanese patient with uniparental disomy 7 and a normal SAR1B gene protein coding sequencePlasma and tissue concentrations of α-tocopherol and δ-tocopherol following high dose dietary supplementation in mice.Establishment of reference values of α-tocopherol in plasma, red blood cells and adipose tissue in healthy children to improve the management of chylomicron retention disease, a rare genetic hypocholesterolemiaThe endoplasmic reticulum coat protein II transport machinery coordinates cellular lipid secretion and cholesterol biosynthesis.Inherited hematological disorders due to defects in coat protein (COP)II complex.Low-density lipoprotein cholesterol: how low can we go?Diagnosis and management of familial dyslipoproteinemias.Abetalipoproteinemia and homozygous hypobetalipoproteinemia: a framework for diagnosis and management.Update on primary hypobetalipoproteinemia.Treatable causes of cerebellar ataxia.Mechanisms for exporting large-sized cargoes from the endoplasmic reticulum.Newcomers in paediatric GI pathology: childhood enteropathies including very early onset monogenic IBD.Low levels of very-long-chain n-3 PUFA in Atlantic salmon (Salmo salar) diet reduce fish robustness under challenging conditions in sea cages.Requirements of n-3 very long-chain PUFA in Atlantic salmon (Salmo salar L): effects of different dietary levels of EPA and DHA on fish performance and tissue composition and integrity.Nature of white opaque substance in gastric epithelial neoplasia as visualized by magnifying endoscopy with narrow-band imaging.Chylomicron Retention Disease: a Description of a New Mutation in a Very Rare Disease.
P2860
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P2860
Guidelines for the diagnosis and management of chylomicron retention disease based on a review of the literature and the experience of two centers.
description
2010 nî lūn-bûn
@nan
2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Guidelines for the diagnosis a ...... the experience of two centers.
@ast
Guidelines for the diagnosis a ...... the experience of two centers.
@en
Guidelines for the diagnosis a ...... the experience of two centers.
@nl
type
label
Guidelines for the diagnosis a ...... the experience of two centers.
@ast
Guidelines for the diagnosis a ...... the experience of two centers.
@en
Guidelines for the diagnosis a ...... the experience of two centers.
@nl
prefLabel
Guidelines for the diagnosis a ...... the experience of two centers.
@ast
Guidelines for the diagnosis a ...... the experience of two centers.
@en
Guidelines for the diagnosis a ...... the experience of two centers.
@nl
P2093
P2860
P356
P1476
Guidelines for the diagnosis a ...... the experience of two centers.
@en
P2093
Agnès Sassolas
Alain Lachaux
Claude C Roy
Colette Deslandres
Department of Nutrition-Hepato ...... nfant, Bron, Université Lyon 1
Department of Pediatrics, CHU Sainte-Justine Research Center, Université de Montréal
Emile Levy
Justine Castagnetti
Laurence Pugnet-Chardon
Lise Bouthillier
P2860
P2888
P356
10.1186/1750-1172-5-24
P5008
P577
2010-09-29T00:00:00Z
P5875
P6179
1043283254