retinol and Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type

retinol has been researched along with Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (66.67)	29.6817
2010's	1 (33.33)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Burnett, JR; Hooper, AJ	1
Averna, M; Barbagallo, CM; Cannizzaro, A; Cefalù, AB; Fayer, F; Licata, G; Minà, M; Noto, D; Pinto, A; Sciumè, C; Tuttolomondo, A; Valenti, V	1
Buonuomo, PS; Mariotti, P; Ruggiero, A; Valeriani, M	1

Reviews

1 review(s) available for retinol and Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type

Article	Year
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 retinol and Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type

Article	Year
Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia. Atherosclerosis, 2009, Volume: 206, Issue:1 Topics: Adolescent; Adult; Apolipoproteins B; Carrier Proteins; Child; Diterpenes; Female; Humans; Hyperlipidemias; Hypobetalipoproteinemia, Familial, Apolipoprotein B; Intestinal Mucosa; Intra-Abdominal Fat; Lipid Metabolism; Male; Middle Aged; Mutation, Missense; Postprandial Period; Retinyl Esters; Triglycerides; Vitamin A	2009
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

Article

Year

Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia.

Atherosclerosis, 2009, Volume: 206, Issue:1

Topics: Adolescent; Adult; Apolipoproteins B; Carrier Proteins; Child; Diterpenes; Female; Humans; Hyperlipidemias; Hypobetalipoproteinemia, Familial, Apolipoprotein B; Intestinal Mucosa; Intra-Abdominal Fat; Lipid Metabolism; Male; Middle Aged; Mutation, Missense; Postprandial Period; Retinyl Esters; Triglycerides; Vitamin A

2009

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