Page last updated: 2024-08-23

heme and Syndrome

heme has been researched along with Syndrome in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19905 (55.56)18.7374
1990's1 (11.11)18.2507
2000's1 (11.11)29.6817
2010's2 (22.22)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Merli, GJ; Weitz, HH1
Berger, LC; Duffy, SP; Eiden, MV; Saraon, P; Shing, J; Tailor, CS; Wilde, A1
Kasap, B; Kavukcu, S; Soylu, A; Türkmen, M1
Grenier, A; Meister, A; New, MI; Rifkind, AB; Sassa, S; Starkman, H; Steinherz, PG; Stoner, E; Wellner, D; Wellner, VP1
Bottomley, SS1
Fitzsimons, E; May, A1
Bottomley, RH; Bottomley, SS; Hussein, KK; Shaw, MT1
Eriksen, L; Hofstad, F; Seip, M1

Reviews

2 review(s) available for heme and Syndrome

ArticleYear
Sideroblastic anaemia.
    Clinics in haematology, 1982, Volume: 11, Issue:2

    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.
    Bailliere's clinical haematology, 1994, Volume: 7, Issue:4

    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

Other Studies

7 other study(ies) available for heme and Syndrome

ArticleYear
Web Exclusives. The consult guys--what does aortic stenosis have to do with heme positive stool?
    Annals of internal medicine, 2014, 02-18, Volume: 160, Issue:4

    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.
    Molecular and cellular biology, 2010, Volume: 30, Issue:22

    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.
    Clinical rheumatology, 2006, Volume: 25, Issue:6

    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.
    Pediatric research, 1984, Volume: 18, Issue:12

    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.
    British journal of haematology, 1975, Volume: 31, Issue:4

    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.
    The American journal of medicine, 1973, Volume: 55, Issue:3

    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.
    Acta paediatrica Scandinavica, 1973, Volume: 62, Issue:4

    Topics: Anemia, Hemolytic; Bone Marrow Diseases; Chromatography, Paper; Erythrocytes; Erythropoiesis; Feces; Heme; Humans; Infant; Male; Photosensitivity Disorders; Porphyrias; Porphyrins; Syndrome

1973