Page last updated: 2024-08-24

lathosterol and Lipid Metabolism, Inborn Error

lathosterol has been researched along with Lipid Metabolism, Inborn Error in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's1 (25.00)29.6817
2010's1 (25.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Bujo, H; Ikewaki, K; Inagaki, K; Ito, K; Kishimoto, Y; Kuzuya, M; Miida, T; Okamura, T; Shoji, T; Tada, H; Yamashita, S; Yanai, H; Yoshida, H; Yoshida, M1
DeBarber, AE; Jones, PJH; Mymin, D; Myrie, SB; Othman, RA; Roullet, JB; Steiner, RD1
Andria, G; Balli, F; Cervasio, M; Corso, G; D'Armiento, M; Ferrari, P; Hall, CM; Parenti, G; Parisi, I; Rivasi, F; Rossi, M; Vecchione, R1
Hofman, KJ; Kelley, RI; Rossiter, JP1

Trials

1 trial(s) available for lathosterol and Lipid Metabolism, Inborn Error

ArticleYear
Thyroid Hormone Status in Sitosterolemia Is Modified by Ezetimibe.
    The Journal of pediatrics, 2017, Volume: 188

    Topics: Adolescent; Adult; Anticholesteremic Agents; Cholestanol; Cholestenones; Cholesterol; Ezetimibe; Female; Humans; Hypercholesterolemia; Intestinal Diseases; Lipid Metabolism, Inborn Errors; Male; Middle Aged; Phytosterols; Sitosterols; Thyrotropin; Thyroxine; Triiodothyronine; Young Adult

2017

Other Studies

3 other study(ies) available for lathosterol and Lipid Metabolism, Inborn Error

ArticleYear
Reference Intervals of Serum Non-Cholesterol Sterols by Gender in Healthy Japanese Individuals.
    Journal of atherosclerosis and thrombosis, 2020, May-01, Volume: 27, Issue:5

    Topics: ATP Binding Cassette Transporter, Subfamily G, Member 5; ATP Binding Cassette Transporter, Subfamily G, Member 8; Cholesterol; Cholesterol, Dietary; Chromatography, Gas; Female; Humans; Hypercholesterolemia; Intestinal Diseases; Japan; Lipid Metabolism, Inborn Errors; Lipoproteins; Male; Middle Aged; Phytosterols; Reference Values; Reproducibility of Results; Sex Factors; Sitosterols

2020
Clinical phenotype of lathosterolosis.
    American journal of medical genetics. Part A, 2007, Oct-15, Volume: 143A, Issue:20

    Topics: Child; Child, Preschool; Cholesterol; Congenital Abnormalities; Female; Humans; Lipid Metabolism, Inborn Errors; Male; Oxidoreductases Acting on CH-CH Group Donors; Phenotype; Smith-Lemli-Opitz Syndrome

2007
Smith-Lemli-Opitz syndrome: prenatal diagnosis by quantification of cholesterol precursors in amniotic fluid.
    American journal of medical genetics, 1995, Apr-10, Volume: 56, Issue:3

    Topics: Amniotic Fluid; Cholesterol; Dehydrocholesterols; Female; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Syndrome

1995