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d-alpha tocopherol and Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type

d-alpha tocopherol has been researched along with Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Burnett, JR; Hooper, AJ1
Buonuomo, PS; Mariotti, P; Ruggiero, A; Valeriani, M1
Aguglia, U; Annesi, F; Annesi, G; Civitelli, D; De Marco, EV; Quattrone, A; Tarantino, P; Torroni, A1

Reviews

1 review(s) available for d-alpha tocopherol and Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type

ArticleYear
Update on primary hypobetalipoproteinemia.
    Current atherosclerosis reports, 2014, Volume: 16, Issue:7

    Topics: Abetalipoproteinemia; Avitaminosis; Diet, Fat-Restricted; Humans; Hypobetalipoproteinemia, Familial, Apolipoprotein B; Hypobetalipoproteinemias; Vitamin A; Vitamin E; Vitamins

2014

Other Studies

2 other study(ies) available for d-alpha tocopherol and Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type

ArticleYear
Familial hypobetalipoproteinemia: early neurological, hematological, and ocular manifestations in two affected twins responding to vitamin supplementation.
    Current opinion in pediatrics, 2009, Volume: 21, Issue:6

    Topics: Acanthocytes; Apolipoproteins B; Child; Cholesterol, LDL; Dietary Supplements; Female; Follow-Up Studies; Genetic Predisposition to Disease; Humans; Hypobetalipoproteinemia, Familial, Apolipoprotein B; Leg; Male; Nerve Fibers; Nervous System Diseases; Pain; Retinal Diseases; Treatment Outcome; Twins; Vitamin A; Vitamin E; Vitamins

2009
SIL1 and SARA2 mutations in Marinesco-Sjögren and chylomicron retention diseases.
    Clinical genetics, 2007, Volume: 71, Issue:3

    Topics: Base Sequence; Chylomicrons; Guanine Nucleotide Exchange Factors; Homozygote; Humans; Hypobetalipoproteinemia, Familial, Apolipoprotein B; Male; Molecular Sequence Data; Monomeric GTP-Binding Proteins; Mutation; Pedigree; Sequence Analysis, DNA; Spinocerebellar Degenerations; Vitamin E

2007