phosphatidylcholines has been researched along with Leukoma in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 8 (88.89) | 18.7374 |
| 1990's | 1 (11.11) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ekins, MB; Kanes, GJ; Sgoutas, DS; Waring, GO | 1 |
| Benlian, P; Chisholm, JW; de Gennes, JL; Dolphin, PJ; Pouliquen, Y; Savoldelli, M; Teh, EM | 1 |
| Gjone, E | 2 |
| Blomhoff, JP; Gjone, E; Skarbövik, AJ; Teisberg, P | 1 |
| Borven, I; Egge, K; Gjone, E | 1 |
| Norum, KR | 1 |
| Hörven, I | 1 |
| Gjone, E; Hamnström, B; Norum, KR | 1 |
9 other study(ies) available for phosphatidylcholines and Leukoma
| Article | Year |
|---|---|
Oval lipid corneal opacities in beagles: VI. Quantitation of excess stromal cholesterol and phospholipid.
Topics: Animals; Cholesterol; Cholesterol Esters; Cornea; Corneal Opacity; Dogs; Female; Male; Phosphatidylcholines; Phosphatidylethanolamines; Phospholipids; Sphingomyelins; Triglycerides | 1983 |
Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144.
Topics: Adolescent; Apolipoproteins; Base Sequence; Codon; Cornea; Corneal Opacity; DNA Mutational Analysis; Electrophoresis, Agar Gel; Exons; Female; Frameshift Mutation; Gene Deletion; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Molecular Sequence Data; Phenotype; Phosphatidylcholine-Sterol O-Acyltransferase; Phosphatidylcholines; Polymerase Chain Reaction | 1999 |
Familial lecithin:cholesterol acyltransferase deficiency--a clinical survey.
Topics: Acyltransferases; Adult; Anemia; Apoproteins; Arteriosclerosis; Bone Marrow Cells; Cholesterol; Chromosomes, Human, 16-18; Corneal Opacity; Esters; Female; Histiocytes; Humans; Kidney Diseases; Kidney Glomerulus; Lipid Metabolism, Inborn Errors; Lipoproteins, LDL; Male; Metabolism, Inborn Errors; Middle Aged; Norway; Phosphatidylcholines; Proteinuria | 1974 |
Familial lecithin:cholesterol acyltransferase deficiency. Report of a third Norwegian family with two afflicted members.
Topics: Acyltransferases; Aged; Cholesterol; Chromatography, Gas; Chromatography, Gel; Chromatography, Thin Layer; Chromosomes, Human, 16-18; Corneal Opacity; Esters; Female; Humans; Immunoelectrophoresis; Lipoproteins, LDL; Lysophosphatidylcholines; Male; Metabolism, Inborn Errors; Middle Aged; Norway; Pedigree; Phosphatidylcholines; Phosphatidylethanolamines; Phospholipids; Proteinuria; Sphingomyelins; Triglycerides | 1974 |
Corneal and fundus changes in familial LCAT-deficiency.
Topics: Acyltransferases; Angioid Streaks; Cholesterol; Corneal Opacity; Female; Fluorescein Angiography; Follow-Up Studies; Fundus Oculi; Humans; Male; Metabolism, Inborn Errors; Phosphatidylcholines; Proteinuria; Retinal Hemorrhage; Syndrome; Visual Acuity; Visual Fields | 1974 |
Editorial: Familial LCAT deficiency.
Topics: Acyltransferases; Adult; Anemia; Arteriosclerosis; Cholesterol; Corneal Opacity; Erythrocyte Aging; Female; Histiocytes; Humans; Kidney; Kidney Failure, Chronic; Lipids; Lipoproteins; Male; Metabolism, Inborn Errors; Middle Aged; Phosphatidylcholines; Proteinuria; Retina; Visual Acuity; Visual Fields | 1973 |
[Familial lecithin-cholesterol-acyltransferase-deficiency].
Topics: Acyltransferases; Anemia; Cholesterol; Corneal Opacity; Humans; Metabolism, Inborn Errors; Phosphatidylcholines; Proteinuria | 1974 |
Ocular manifestations in familial lecithin: cholesterol acyltransferase deficiency.
Topics: Acyltransferases; Cholesterol; Corneal Opacity; Eye Diseases; Female; Fundus Oculi; Humans; Lipid Metabolism, Inborn Errors; Metabolism, Inborn Errors; Optic Atrophy; Papilledema; Phosphatidylcholines; Retinal Hemorrhage | 1974 |
Familial plasma lecithin: cholesterol acyltransferase deficiency.
Topics: Acyltransferases; Adolescent; Adult; Anemia, Hemolytic; Child; Child, Preschool; Cholesterol; Corneal Opacity; Erythrocytes; Female; Heparin; Humans; Lipid Metabolism, Inborn Errors; Lipids; Male; Middle Aged; Phosphatidylcholines; Proteinuria; Triglycerides | 1969 |