Page last updated: 2024-08-21

d-alpha tocopherol and Autosomal Chromosome Disorders

d-alpha tocopherol has been researched along with Autosomal Chromosome Disorders in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19902 (50.00)18.7374
1990's1 (25.00)18.2507
2000's1 (25.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Andrus, PK; Cutting, FB; Gurney, ME; Hall, ED; Zhai, P1
De Zwart, FA; Elsendoorn, TJ; Mithoe, S; Osanto, S; Tates, AD; Van Dam, F; Weijl, NI; Zwinderman, AH1
Garg, BP; Lockman, LA; Swaiman, KF1
Butkus, A; Lewis, LA; Mars, H; Robertson, AL; Williams, GH1

Reviews

1 review(s) available for d-alpha tocopherol and Autosomal Chromosome Disorders

ArticleYear
Pathogenic mechanisms in familial amyotrophic lateral sclerosis due to mutation of Cu, Zn superoxide dismutase.
    Pathologie-biologie, 1996, Volume: 44, Issue:1

    Topics: Amyotrophic Lateral Sclerosis; Animals; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 21; Excitatory Amino Acid Antagonists; Humans; Mice; Mice, Transgenic; Mutation; Riluzole; Superoxide Dismutase; Thiazoles; Vitamin E

1996

Trials

1 trial(s) available for d-alpha tocopherol and Autosomal Chromosome Disorders

ArticleYear
Chemotherapy-induced chromosomal damage in peripheral blood lymphocytes of cancer patients supplemented with antioxidants or placebo.
    Mutation research, 2001, Nov-15, Volume: 498, Issue:1-2

    Topics: Adolescent; Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Antioxidants; Ascorbic Acid; Chromosome Aberrations; Chromosome Disorders; Chromosomes; Cisplatin; Dietary Supplements; DNA Mutational Analysis; Female; Hearing; Humans; Hypoxanthine Phosphoribosyltransferase; Kidney; Lymphocytes; Male; Micronucleus Tests; Middle Aged; Mutagenicity Tests; Neoplasms; Selenium; Vitamin E

2001

Other Studies

2 other study(ies) available for d-alpha tocopherol and Autosomal Chromosome Disorders

ArticleYear
Sea-blue histiocyte and posterior column dysfunction: a familial disorder.
    Neurology, 1975, Volume: 25, Issue:11

    Topics: Adolescent; Adult; Ceroid; Chromosome Aberrations; Chromosome Disorders; Female; Genes, Dominant; Histiocytes; Histocytochemistry; Humans; Lipidoses; Lipofuscin; Male; Pedigree; Syndrome; Vitamin E

1975
Familial hypo-beta-lipoproteinemia: a genetic disorder of lipid metabolism with nervous system involvement.
    The American journal of medicine, 1969, Volume: 46, Issue:6

    Topics: Abetalipoproteinemia; Adult; Anesthesia, Local; Cholesterol; Chromosome Aberrations; Chromosome Disorders; Demyelinating Diseases; Diet; Erythrocytes, Abnormal; Fatty Acids; Female; Humans; Immunodiffusion; Immunoelectrophoresis; Intestinal Mucosa; Jejunum; Lipoproteins; Male; Phospholipids; Triglycerides; Vitamin E

1969