heme has been researched along with Syndrome in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (55.56) | 18.7374 |
| 1990's | 1 (11.11) | 18.2507 |
| 2000's | 1 (11.11) | 29.6817 |
| 2010's | 2 (22.22) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Merli, GJ; Weitz, HH | 1 |
| Berger, LC; Duffy, SP; Eiden, MV; Saraon, P; Shing, J; Tailor, CS; Wilde, A | 1 |
| Kasap, B; Kavukcu, S; Soylu, A; Türkmen, M | 1 |
| Grenier, A; Meister, A; New, MI; Rifkind, AB; Sassa, S; Starkman, H; Steinherz, PG; Stoner, E; Wellner, D; Wellner, VP | 1 |
| Bottomley, SS | 1 |
| Fitzsimons, E; May, A | 1 |
| Bottomley, RH; Bottomley, SS; Hussein, KK; Shaw, MT | 1 |
| Eriksen, L; Hofstad, F; Seip, M | 1 |
2 review(s) available for heme and Syndrome
| Article | Year |
|---|---|
Sideroblastic anaemia.
Topics: 5-Aminolevulinate Synthetase; Adult; Anemia, Sideroblastic; Blood Transfusion; Bone Marrow; Chloramphenicol; Deferoxamine; Erythroblasts; Ethanol; Female; Ferrochelatase; Heme; Hemochromatosis; Humans; Iron Deficiencies; Isoniazid; Male; Melphalan; Myeloproliferative Disorders; Pyridoxine; Syndrome | 1982 |
Sideroblastic anaemia.
Topics: 5-Aminolevulinate Synthetase; Anemia, Sideroblastic; Biological Transport; Chloramphenicol; Copper; DNA, Mitochondrial; Erythrocytes; Ferrochelatase; Genetic Linkage; Globins; Heme; Humans; Hydroxymethylbilane Synthase; Iron; Mutation; Pyridoxal Phosphate; Syndrome; X Chromosome | 1994 |
7 other study(ies) available for heme and Syndrome
| Article | Year |
|---|---|
Web Exclusives. The consult guys--what does aortic stenosis have to do with heme positive stool?
Topics: Aged, 80 and over; Aortic Valve Stenosis; Arteriovenous Malformations; Colonoscopy; Feces; Gastrointestinal Tract; Heme; Humans; Male; Platelet Adhesiveness; Syndrome; von Willebrand Diseases | 2014 |
The Fowler syndrome-associated protein FLVCR2 is an importer of heme.
Topics: Animals; Biological Transport; Brain Diseases; Cats; Cell Line; Cricetinae; Cricetulus; Female; Heme; Humans; Membrane Transport Proteins; Oocytes; Pregnancy; Receptors, Virus; RNA, Small Interfering; Syndrome; Tissue Distribution; Xenopus laevis | 2010 |
An adolescent girl with Meyer-Betz syndrome.
Topics: Adolescent; Female; Follow-Up Studies; Heme; Humans; Leg; Muscle Weakness; Muscular Diseases; Myoglobinuria; Pain; Physical Exertion; Rhabdomyolysis; Syndrome | 2006 |
Biochemical studies of a patient with hereditary hepatorenal tyrosinemia: evidence of glutathione deficiency.
Topics: Erythrocytes; Fanconi Syndrome; Female; Glutathione; Heme; Humans; Infant; Liver; Liver Diseases; Mass Spectrometry; Mixed Function Oxygenases; Phosphates; Pyrroles; Rickets; Syndrome; Tyrosine | 1984 |
Haem synthesis in the Diamond-Blackfan syndrome.
Topics: Anemia, Aplastic; Bone Marrow; Child, Preschool; Dose-Response Relationship, Drug; Erythrocytes, Abnormal; Erythropoietin; Female; Heme; Humans; Male; Syndrome | 1975 |
The relationship of erythromonocytic leukemia to other myeloproliferative disorders.
Topics: Aged; Bone Marrow Cells; Bone Marrow Examination; Chromosomes; Clone Cells; Erythropoiesis; Female; Heme; Hemoglobinuria, Paroxysmal; Humans; Leukemia, Erythroblastic, Acute; Leukemia, Myeloid; Male; Middle Aged; Myeloproliferative Disorders; Periodic Acid; Polycythemia Vera; Primary Myelofibrosis; Syndrome | 1973 |
Congenital erythropoietic porphyria with a hitherto undescribed porphyrin pattern.
Topics: Anemia, Hemolytic; Bone Marrow Diseases; Chromatography, Paper; Erythrocytes; Erythropoiesis; Feces; Heme; Humans; Infant; Male; Photosensitivity Disorders; Porphyrias; Porphyrins; Syndrome | 1973 |