phosphatidylcholines has been researched along with Anemia, Congenital Nonspherocytic Hemolytic in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (85.71) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chiba, K; Hattori, A; Imashuku, S; Kanno, H; Kato, A; Kato, K; Kita, S; Kojima, S; Miyano, S; Muramatsu, H; Oe, K; Ogawa, S; Okuno, Y; Shiraishi, Y; Sueyoshi, A; Sugihara, T; Tanaka, H; Tatsumi, Y; Usui, T; Wang, X; Yoshida, K | 1 |
| Igarashi, T; Kariyone, S; Kimura, H; Maezawa, M; Matsuda, S; Sakai, K; Takaku, F; Uchida, T | 1 |
| Alving, CR; Gockerman, JP; Joseph, KC | 1 |
| Jaffé, ER; Livermore, BM; Nathan, DG; Shohet, SB | 1 |
| Feig, SA; Jaffé, ER; Livermore, BM; Nathan, DG; Shohet, SB | 1 |
| Gottfried, EL; Jaffé, ER | 1 |
| Arakawa, T; Fujiwara, T; Katsushima, N | 1 |
7 other study(ies) available for phosphatidylcholines and Anemia, Congenital Nonspherocytic Hemolytic
| Article | Year |
|---|---|
PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus.
Topics: Anemia, Hemolytic, Congenital; Anemia, Hemolytic, Congenital Nonspherocytic; Asian People; Diabetes Mellitus; Family Health; Female; Hemochromatosis; Humans; Hydrops Fetalis; Ion Channels; Male; Mutation; Pedigree; Phosphatidylcholines | 2016 |
[A case of high phosphatidylcholine hemolytic anemia (author's transl)].
Topics: Adult; Anemia, Hemolytic, Congenital; Anemia, Hemolytic, Congenital Nonspherocytic; Erythrocyte Membrane; Humans; Male; Phosphatidylcholines | 1982 |
Abnormal lipid composition of the red cell membrane in congenital dyserythropoietic anemia type II (HEMPAS).
Topics: Anemia, Hemolytic, Congenital Nonspherocytic; Blood Cell Count; Cell Membrane; Cholesterol; Chromatography, Thin Layer; Erythrocytes; Erythropoiesis; Humans; Lipids; Phosphatidylcholines; Phospholipids; Sphingolipids | 1975 |
Hereditary hemolytic anemia associated with abnormal membrane lipids: mechanism of accumulation of phosphatidyl choline.
Topics: Acyltransferases; Adenosine Triphosphate; Anemia, Hemolytic, Congenital Nonspherocytic; Carbon Isotopes; Chromatography; Coenzyme A; Erythrocytes; Fatty Acids; Glucose; Humans; Linoleic Acids; Lysophosphatidylcholines; Phosphatidylcholines; Phosphatidylethanolamines; Phospholipids; Reticulocytes; Silicon Dioxide | 1971 |
Hereditary hemolytic anemia associated with abnormal membrane lipid. II. Ion permeability and transport abnormalities.
Topics: Anemia, Hemolytic, Congenital Nonspherocytic; Biological Transport, Active; Cell Membrane; Cell Membrane Permeability; Erythrocytes; Glycolysis; Humans; In Vitro Techniques; Ouabain; Phosphatidylcholines; Potassium; Sodium; Water | 1973 |
Hereditary nonspherocytic hemolytic disease associated with an altered phospholipid composition of the erythrocytes.
Topics: Adenosine Triphosphate; Adolescent; Adult; Anemia, Hemolytic, Congenital Nonspherocytic; Blood Glucose; Child; Cholesterol; Erythrocytes; Female; Glucosephosphate Dehydrogenase; Glutathione Reductase; Humans; Hyperbilirubinemia; Jaundice; Lipids; Male; Middle Aged; Osmotic Fragility; Phosphatidylcholines; Phospholipids; Pyruvate Kinase; Reticulocytes; Splenomegaly | 1968 |
A hemolytic anemia with abnormality of erythrocyte lipids and dwarfism--probably a new syndrome.
Topics: Amino Acids; Anemia, Hemolytic, Congenital Nonspherocytic; Child; Chromatography; Dwarfism; Erythrocytes; Fatty Acids; Fatty Acids, Essential; Female; Humans; Intellectual Disability; Lipids; Liver Function Tests; Phosphatidylcholines | 1966 |