Page last updated: 2024-08-23

heme and Thalassemias

heme has been researched along with Thalassemias in 62 studies

Research

Studies (62)

Timeframe	Studies, this research(%)	All Research%
pre-1990	55 (88.71)	18.7374
1990's	2 (3.23)	18.2507
2000's	4 (6.45)	29.6817
2010's	1 (1.61)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Rivella, S	1
Luo, WH; Tian, PL; Wan, JH; Wei, XC; Wu, BY; Xiong, F; Xu, XM; Zhou, WJ	1
YAMAMOTO, T	2
CAINE, TH; CARTWRIGHT, GE; HAUT, A; LEE, GR; WINTROBE, MM	1
HEILMEYER, L	2
MAYER, VK; MOORE, CV; VAVRA, JD	1
BANNERMAN, RM	1
FELDMAN, F; LICHTMAN, HC	1
BALDINI, M; DAMESHEK, W; STEINER, M	1
Beaumont, C; Canonne-Hergaux, F	1
Fornace, AJ; Hollander, MC; Miller, GF; Patterson, AD	1
Brennan, SO; Chan, T; Sheen, C	1
Costa, S; Fanciulli, G; Schettini, F; Zimbalatti, F	1
Bannerman, RM; Kreimer-Birnbaum, M	1
Coburn, RF; Goldwein, MI; Rother, ML; Shafer, BC; White, P; Williams, WJ	1
Koenig, HM; Marsh, WL	1
Alter, BP; Goff, SC	1
Rachmilewitz, EA; Shinar, E	2
el-Hazmi, MA; Lehmann, H	1
Jacobs, A	1
Anderson, KE; Kappas, A; Peterson, CM; Sassa, S	1
Kolski, GB; Miller, DR	1
Martelo, OJ	1
Amione, C; Gabutti, V; Leone, L; Monteleone, M	1
Steinberg, MH	1
Kirschner-Zilber, I; Rabizadeh, E; Shaklai, N; Shviro, Y	1
Cajozzo, A; Citarrella, P; Malleo, C	1
Blumberg, WE; Bradley, TB; Peisach, J; Rachmilewitz, EA	1
Harari, E; Rachmilewitz, EA	1
Rachmilewitz, EA; Thorell, B	1
Rachmilewitz, EA	1
Lehmann, H	2
Bannerman, RM; Glass, U; Kreimer-Birnbaum, M; Rusnak, PA	1
Pimstone, NR	1
Sullivan, AL; Weintraub, LR	1
Clegg, JB; Weatherall, DJ	2
Neuwirt, J; Ponka, P	1
Aoki, Y; Nakao, K; Takaku, F; Wada, O; Yano, Y	1
Anderson, BB; Mollin, DL	1
Hunter, AR; Jackson, RJ	1
Weatherall, DJ	2
Munteanu, N	1
Clotten, R; Heilmeyer, L; Heimpel, H; Schmidt, W	1
Harloe, LG	1
Beck, EA; Petitpierre-Gabathuler, MP	1
Perkins, RP	1
Sebahoun, G	1
Goodman, JR; Hall, SG	1
Astaldi, G; Burgio, GR; Priolisi, A	1
Becker, D; Kramer, S; Metz, J; Viljoen, E; Zail, SS	1
Palma-Carlos, AG	1
Cumming, RL; Dagg, HJ; Goldberg, A	1
Bargellesi, A; Conconi, F; Pontremoli, S	1
Hanna, M; Hanstein, A; Javid, J; Liem, HH; Muller-Eberhard, U	1
Robinson, SH	1
Honig, GR; Mason, RG; Rowan, BQ	1

Reviews

17 review(s) available for heme and Thalassemias

Article	Year
Ineffective erythropoiesis and thalassemias. Current opinion in hematology, 2009, Volume: 16, Issue:3 Topics: Animals; Cell Differentiation; Erythroid Cells; Erythropoiesis; Globins; Hematopoiesis, Extramedullary; Heme; Humans; Iron; Janus Kinase 2; Liver; Mice; Reactive Oxygen Species; Spleen; Thalassemia	2009
[ON THE SHUNT HYPERBILIRUBINEMIA]. Naika hokan. Japanese archives of internal medicine, 1964, Volume: 11 Topics: Anemia; Anemia, Hypochromic; Anemia, Pernicious; Anemia, Sickle Cell; Bilirubin; Blood Chemical Analysis; Carbon Isotopes; Erythropoiesis; Glycine; Heme; Hyperbilirubinemia; Hyperbilirubinemia, Hereditary; Jaundice; Leukemia; Leukemia, Myeloid; Metabolism; Physiology; Thalassemia	1964
[Erythrophagocytosis and recycling of heme iron in normal and pathological conditions; regulation by hepcidin]. Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine, 2005, Volume: 12, Issue:2 Topics: Anemia; Antimicrobial Cationic Peptides; Cation Transport Proteins; Erythrocyte Aging; Erythrocytes; Erythropoiesis; Ferritins; Heme; Hemochromatosis; Hepatocytes; Hepcidins; Humans; Inflammation; Intestinal Absorption; Iron; Macrophages; Models, Biological; Phagocytosis; Thalassemia	2005
The laboratory evaluation of microcytic red blood cells. Critical reviews in clinical laboratory sciences, 1982, Volume: 16, Issue:3 Topics: Adolescent; Adult; Anemia; Child; Child, Preschool; Erythrocytes; Erythrocytes, Abnormal; Female; Ferritins; Fetal Hemoglobin; Globins; Hematologic Diseases; Heme; Hemoglobin A2; Hemoglobins; Humans; Infant; Iron; Iron Deficiencies; Lead Poisoning; Male; Models, Biological; Porphyrias; Pregnancy; Thalassemia	1982
Haemoglobinopathies and red cell membrane function. Bailliere's clinical haematology, 1993, Volume: 6, Issue:2 Topics: Erythrocyte Membrane; Heme; Hemoglobinopathies; Humans; Iron; Oxidation-Reduction; Oxyhemoglobins; Porphyrins; Protein Denaturation; Thalassemia	1993
Diseases of disordered hemoglobin degradation. Advances in internal medicine, 1975, Volume: 20 Topics: Amino Acids; Anemia, Hemolytic; Animals; Bile; Bile Pigments; Bilirubin; Chemical Phenomena; Chemistry; Heinz Bodies; Heme; Hemoglobinopathies; Hemoglobins; Hemolysis; Humans; Mixed Function Oxygenases; Mutation; Rats; Thalassemia	1975
Oxidative denaturation of red blood cells in thalassemia. Seminars in hematology, 1990, Volume: 27, Issue:1 Topics: Erythrocytes; Globins; Heme; Hemeproteins; Humans; Iron; Membrane Lipids; Membrane Proteins; Oxidation-Reduction; Thalassemia	1990
Denaturation of the normal and abnormal hemoglobin molecule. Seminars in hematology, 1974, Volume: 11, Issue:4 Topics: Cytochromes; Electron Spin Resonance Spectroscopy; Globins; Heinz Bodies; Heme; Hemoglobin, Sickle; Hemoglobins; Hemoglobins, Abnormal; Humans; Iron; Methemoglobin; Oxidation-Reduction; Protein Conformation; Protein Denaturation; Solubility; Spectrophotometry; Structure-Activity Relationship; Thalassemia	1974
Renal degradation of hemoglobin. Seminars in hematology, 1972, Volume: 9, Issue:1 Topics: Amino Acids; Anemia, Hemolytic; Anemia, Sickle Cell; Animals; Bilirubin; Carbon Isotopes; Carbon Monoxide; Glomerular Filtration Rate; Haptoglobins; Heart Valve Prosthesis; Heme; Hemoglobins; Hemoglobinuria, Paroxysmal; Humans; Iron; Iron Isotopes; Kidney; Malaria; Microsomes; Oxygenases; Protein Binding; Rats; Thalassemia	1972
Sideroblastic anemias. An approach to diagnosis and management. The Medical clinics of North America, 1973, Volume: 57, Issue:2 Topics: Alcoholism; Anemia, Sideroblastic; Erythrocytes, Abnormal; Female; Folic Acid Deficiency; Genes; Heme; Humans; Iron; Isoniazid; Lead Poisoning; Male; Pyridoxine; Sex Chromosomes; Thalassemia; Transferrin	1973
In vitro hemoglobin synthesis in the thalassemia syndromes. International review of experimental pathology, 1974, Volume: 13, Issue:0 Topics: Amino Acids; Animals; Bone Marrow; Cell-Free System; Chromatography; Chromatography, Gel; Female; Fetal Diseases; Genes; Globins; Heme; Hemoglobin H; Hemoglobins; Hemoglobins, Abnormal; Heterozygote; Homozygote; Humans; In Vitro Techniques; Models, Structural; Pedigree; Pregnancy; RNA, Messenger; Thalassemia; Urea	1974
Haem synthesis and iron uptake by reticulocytes. British journal of haematology, 1974, Volume: 28, Issue:1 Topics: 5-Aminolevulinate Synthetase; Anemia, Sideroblastic; Animals; Biological Transport; Electron Transport; Erythrocytes; Globins; Heme; Hemoglobins; Humans; Iron; Kinetics; Mitochondria; Oxygen Consumption; Reticulocytes; Thalassemia; Transferrin	1974
The control of haemoglobin synthesis. Proceedings of the Royal Society of Medicine, 1967, Volume: 60, Issue:10 Topics: Adult; Amino Acid Sequence; Black People; Cytoplasm; Genetic Code; Globins; Heme; Hemoglobinopathies; Hemoglobins; Hemoglobins, Abnormal; Humans; Molecular Biology; RNA, Messenger; RNA, Transfer; Thalassemia	1967
Control mechanisms in human haemolgobin synthesis. Annual review of medicine, 1968, Volume: 19 Topics: Alleles; Genes, Regulator; Genetics, Medical; Globins; Heme; Hemoglobins; Hemoglobins, Abnormal; Humans; In Vitro Techniques; Molecular Biology; Reticulocytes; Thalassemia	1968
[Current state of knowledge of the pathology of heme synthesis]. Studii si cercetari de medicina interna, 1968, Volume: 9, Issue:4 Topics: Anemia, Hypochromic; Anemia, Sideroblastic; Hematologic Diseases; Heme; Humans; Porphyrias; Thalassemia	1968
[Synthesis of bilirubin]. Naika hokan. Japanese archives of internal medicine, 1968, Volume: 15, Issue:11 Topics: Anemia, Aplastic; Animals; Bilirubin; Carbon Isotopes; Dogs; Feces; Glycine; Heme; Humans; Hyperbilirubinemia; Jaundice; Leukemia, Myeloid; Liver Neoplasms; Thalassemia; Time Factors	1968
The control of human hemoglobin synthesis and function in health and disease. Progress in hematology, 1969, Volume: 6 Topics: Binding Sites; Biological Transport; Chromosome Aberrations; Chromosome Disorders; Fetal Hemoglobin; Genes; Genes, Regulator; Globins; Heme; Hemoglobins; Hemoglobins, Abnormal; Humans; Models, Chemical; Molecular Biology; Oxygen; Thalassemia	1969

Other Studies

45 other study(ies) available for heme and Thalassemias

Article	Year
Rapid determination of human globin chains using reversed-phase high-performance liquid chromatography. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2012, Jul-15, Volume: 901 Topics: Adult; alpha-Thalassemia; Analysis of Variance; Case-Control Studies; Chromatography, High Pressure Liquid; Chromatography, Reverse-Phase; Heme; Hemoglobin Subunits; Hemoglobins, Abnormal; Humans; Hydrogen-Ion Concentration; Infant, Newborn; Reproducibility of Results; ROC Curve; Sensitivity and Specificity; Thalassemia	2012
THE CHROMATOGRAPHY OF HEMINS FROM NORMAL AND ABNORMAL HUMAN ERYTHROCYTES. Blood, 1964, Volume: 23 Topics: Acetone; Acid-Base Equilibrium; Anemia; Anemia, Hemolytic; Anemia, Hypochromic; Carbon Monoxide; Chromatography; Erythrocytes; Heme; Hemin; Hemoglobins; Hemoglobins, Abnormal; Humans; Myoglobin; Research; Silicon Dioxide; Spectrophotometry; Spherocytosis, Hereditary; Thalassemia	1964
[ANEMIAS CAUSED BY ENZYME DEFECTS]. Munchener medizinische Wochenschrift (1950), 1964, Feb-28, Volume: 106 Topics: Adolescent; Anemia; Anemia, Hemolytic; Anemia, Hemolytic, Congenital Nonspherocytic; Anemia, Hypochromic; Carbohydrate Metabolism; Elliptocytosis, Hereditary; Enzymes; Erythrocytes; Favism; Glucosephosphate Dehydrogenase Deficiency; Glucosephosphates; Heme; Humans; Metabolic Diseases; Methemoglobinemia; Pentosephosphates; Porphyrias; Spherocytosis, Hereditary; Thalassemia	1964
IN VITRO HEME SYNTHESIS BY HUMAN BLOOD: ABNORMAL HEME SYNTHESIS IN THALASSEMIA MAJOR. The Journal of laboratory and clinical medicine, 1964, Volume: 63 Topics: beta-Thalassemia; Blood; Carbon Isotopes; Erythrocytes; Glycine; Heme; Hemoglobins; Humans; In Vitro Techniques; Iron; Iron Isotopes; Levulinic Acids; Porphyrins; Proteins; Thalassemia	1964
ABNORMALITIES OF HEME AND PYRROLE METABOLISM IN THALASSEMIA. Annals of the New York Academy of Sciences, 1964, Oct-07, Volume: 119 Topics: Heme; Humans; Metabolism; Pyrroles; Thalassemia	1964
IN VITRO PORPHOBILINOGEN AND PORPHYRIN SYNTHESIS IN THALASSEMIA MAJOR AND SICKLE CELL ANEMIA. Annals of the New York Academy of Sciences, 1964, Oct-07, Volume: 119 Topics: Amino Acid Oxidoreductases; Anemia; Anemia, Sickle Cell; beta-Thalassemia; Heme; In Vitro Techniques; Levulinic Acids; Metabolism; Porphobilinogen; Porphyrins; Thalassemia	1964
ENZYMATIC DEFECTS OF HEME SYNTHESIS IN THALASSEMIA. Annals of the New York Academy of Sciences, 1964, Oct-07, Volume: 119 Topics: Amino Acid Oxidoreductases; Bone Marrow Examination; Deferoxamine; Drug Therapy; Erythropoiesis; Heme; Humans; Levulinic Acids; Ligases; Metabolism; Thalassemia	1964
Gadd34 requirement for normal hemoglobin synthesis. Molecular and cellular biology, 2006, Volume: 26, Issue:5 Topics: Animals; Antigens, Differentiation; Catalytic Domain; Cell Cycle Proteins; Cells, Cultured; Diet; eIF-2 Kinase; Erythrocytes; Half-Life; Heme; Hemoglobins; Iron Deficiencies; Mice; Mice, Mutant Strains; Peptide Chain Initiation, Translational; Phosphoprotein Phosphatases; Protein Phosphatase 1; Protein Subunits; Reticulocytes; Thalassemia	2006
Novel hemoglobin (Hb Grey Lynn) substitution (alpha91Leu --> Phe) affects heme interactions and alpha1beta2 contacts. Clinical chemistry, 2007, Volume: 53, Issue:5 Topics: Adult; Crystallography, X-Ray; Female; Heme; Hemoglobins, Abnormal; Humans; Models, Molecular; Mutation; Protein Subunits; Thalassemia	2007
Haemoglobin synthesis from thalassemic reticulocytes. In vitro studies with Fe59 and Glycine-2-C14. Annales paediatrici. International review of pediatrics, 1966, Volume: 207, Issue:6 Topics: Carbon Isotopes; Child; Globins; Glycine; Heme; Hemoglobins; Humans; Iron Isotopes; Radiometry; Reticulocytes; Thalassemia	1966
Heme and globin synthesis control: observations in vivo in beta thalassemia. Science (New York, N.Y.), 1967, Mar-03, Volume: 155, Issue:3766 Topics: Blood Proteins; Carbon Isotopes; Globins; Glycine; Heme; Hemoglobins; Humans; Mutation; Thalassemia	1967
Carbon monoxide production associated with ineffective erythropoiesis. The Journal of clinical investigation, 1967, Volume: 46, Issue:12 Topics: Adolescent; Adult; Aged; Anemia; Anemia, Sideroblastic; Bile Pigments; Bilirubin; Carbon Isotopes; Carbon Monoxide; Chromium Isotopes; Erythropoiesis; Feces; Female; Glycine; Heme; Hemoglobinometry; Humans; Iron; Iron Isotopes; Leukopenia; Male; Middle Aged; Porphyrias; Thalassemia	1967
Electrophoretic separation of human embryonic globin demonstrates "alpha-thalassemia" in human leukemia cell line K562. Biochemical and biophysical research communications, 1980, Jun-16, Volume: 94, Issue:3 Topics: Cell Line; Electrophoresis, Polyacrylamide Gel; Embryo, Mammalian; Fetus; Globins; Heme; Humans; Leukemia, Myeloid; Molecular Weight; Thalassemia	1980
Interaction between iron deficiency and alpha-thalassaemia: the in vitro effect of haemin on alpha-chain synthesis. Acta haematologica, 1978, Volume: 60, Issue:1 Topics: Adolescent; Adult; Anemia, Hypochromic; Child; Child, Preschool; Female; Globins; Heme; Hemin; Humans; In Vitro Techniques; Infant; Iron Deficiencies; Male; Middle Aged; Thalassemia	1978
Advances in red cell anomalies. Nouvelle revue francaise d'hematologie, 1979, Volume: 21, Issue:1 Topics: Animals; Erythrocytes, Abnormal; Erythropoiesis; Female; Ferritins; Guanosine Triphosphate; Heme; Hemoglobins; Humans; Iron; Mice; Pregnancy; RNA; Thalassemia; Transcription, Genetic	1979
Increased erythrocyte uroporphyrinogen-l-synthetase, delta-aminolevulinic acid dehydratase and protoporphyrin in hemolytic anemias. The American journal of medicine, 1977, Volume: 63, Issue:3 Topics: Ammonia-Lyases; Anemia, Hemolytic; Anemia, Sickle Cell; Erythrocyte Count; Erythrocytes; Heme; Hemoglobinopathies; Hemolysis; Humans; Hydro-Lyases; Hydroxymethylbilane Synthase; Porphobilinogen Synthase; Porphyrins; Protoporphyrins; Reticulocytes; Thalassemia	1977
Heme synthesis in hereditary hemolytic anemias: decreased delta-aminolevulinic acid synthetase in hemoglobin Köln disease. Pediatric research, 1976, Volume: 10, Issue:7 Topics: 5-Aminolevulinate Synthetase; Adult; Anemia, Hemolytic, Congenital; Anemia, Sickle Cell; Erythrocytes; Heme; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Infant; Infant, Newborn; Porphobilinogen Synthase; Pyruvate Kinase; Thalassemia	1976
Reversed-phase high-performance liquid chromatography of human haemoglobin chains. Journal of chromatography, 1985, Mar-15, Volume: 321, Issue:2 Topics: Chromatography, High Pressure Liquid; Female; Fetal Blood; Heme; Hemoglobins; Humans; Infant, Newborn; Solvents; Temperature; Thalassemia	1985
Role of hemoglobin instability in premature red cell destruction. Progress in clinical and biological research, 1985, Volume: 195 Topics: Anemia, Hemolytic; Erythrocyte Aging; Heme; Hemoglobins, Abnormal; Humans; Macromolecular Substances; Thalassemia	1985
Accumulation and drainage of hemin in the red cell membrane. Biochimica et biophysica acta, 1985, Dec-05, Volume: 821, Issue:2 Topics: Albumins; Anemia, Sickle Cell; Dioxanes; Erythrocyte Aging; Erythrocyte Membrane; Heme; Hemin; Hemolysis; Humans; Thalassemia; Water	1985
[Use of the determination of haptoglobin and hemopexin in evaluation of the course of hemolytic syndromes of various types]. Haematologica, 1971, Volume: 56, Issue:11 Topics: Anemia, Hemolytic; Anemia, Hemolytic, Autoimmune; Anemia, Sickle Cell; Beta-Globulins; Favism; Haptoglobins; Heme; Hemopexin; Humans; Spherocytosis, Hereditary; Thalassemia	1971
Role of haemichromes in the formation of inclusion bodies in haemoglobin H disease. Nature, 1969, Apr-19, Volume: 222, Issue:5190 Topics: Adult; Blood Protein Electrophoresis; Cytoplasmic Granules; Electron Spin Resonance Spectroscopy; Erythrocytes; Female; Heinz Bodies; Heme; Hemoglobins, Abnormal; Heterozygote; Humans; Microscopy, Phase-Contrast; Middle Aged; Molecular Biology; Peptide Biosynthesis; Splenectomy; Thalassemia	1969
Slow rate of haemichrome formation from oxidized haemoglobin Bart's (4 ): a possible explanation for the unequal quantities of haemoglobins H ( 4 ) and Bart's in alpha-thalassaemia. British journal of haematology, 1972, Volume: 22, Issue:3 Topics: Bone Marrow Cells; Chemical Precipitation; Child; Electrophoresis; Erythrocytes; Female; Fetus; Heme; Hemoglobins, Abnormal; Heterozygote; Humans; Inclusion Bodies; Oxidation-Reduction; Solubility; Spectrophotometry; Thalassemia	1972
Hemichromes in single inclusion bodies in red cells of beta thalassemia. Blood, 1972, Volume: 39, Issue:6 Topics: Adolescent; Blood Protein Electrophoresis; Erythrocytes; Female; Fetal Hemoglobin; Heme; Hemeproteins; Hemoglobinometry; Hemoglobins; Humans; Inclusion Bodies; Proteins; Spectrophotometry; Splenectomy; Thalassemia	1972
Some aspects of the haemoglobinopathies. Transactions of the Royal Society of Tropical Medicine and Hygiene, 1974, Volume: 68, Issue:2 Topics: Amino Acid Sequence; Anemia, Sickle Cell; Fetal Hemoglobin; Genetic Variation; Heme; Hemoglobinometry; Hemoglobinopathies; Hemoglobins, Abnormal; Heterozygote; Humans; Imino Acids; Molecular Conformation; Mutation; Structure-Activity Relationship; Thalassemia	1974
Urinary pyrrole pigments in thalassemia and unstable hemoglobin diseases. Annals of the New York Academy of Sciences, 1974, Volume: 232, Issue:0 Topics: Blood Transfusion; Chromatography; Esters; Heme; Hemoglobinopathies; Pyrroles; Splenectomy; Thalassemia	1974
-Aminolevulinic acid synthetase activity of human bone marrow erythroid cells in various hematological disorders. The Tohoku journal of experimental medicine, 1972, Volume: 107, Issue:3 Topics: 5-Aminolevulinate Synthetase; Anemia, Hypochromic; Anemia, Sideroblastic; Bone Marrow; Bone Marrow Cells; Carbon Isotopes; Coenzyme A; Edetic Acid; Erythrocytes; Glycine; Hematologic Diseases; Hematopoietic Stem Cells; Heme; Humans; Hydrogen-Ion Concentration; Ketoglutaric Acids; Levulinic Acids; Magnesium; Porphyrias; Pyridoxal Phosphate; Thalassemia	1972
Red-cell metabolism of pyridoxine in sideroblastic anaemias and related anaemias. British journal of haematology, 1972, Volume: 23 Topics: Adenosine Triphosphate; Adult; Aged; Anemia, Hypochromic; Anemia, Sideroblastic; Biological Assay; Erythrocytes, Abnormal; Heme; Humans; In Vitro Techniques; Iron; Lacticaseibacillus casei; Middle Aged; Mitochondria; Pyridoxal; Pyridoxal Phosphate; Pyridoxine; Thalassemia; Vitamin B 6 Deficiency	1972
Control of haemoglobin synthesis: coordination of alpha and beta chain synthesis. Hamatologie und Bluttransfusion, 1972, Volume: 10 Topics: Animals; Carbon Radioisotopes; Chromatography, Gel; Cycloheximide; Globins; Heme; Hemoglobins; Humans; Iron; Lysine; Peptide Chain Initiation, Translational; Peptide Fragments; Puromycin; Rabbits; Reticulocytes; Thalassemia; Tritium	1972
[Studies on hemoglobin synthesis in erythrocytes. II. Formation of Fe59-hemoglobin in peripheral human erythrocytes in vitro]. Acta haematologica, 1967, Volume: 38, Issue:2 Topics: Anemia; Anemia, Hypochromic; Erythrocytes; Heme; Hemoglobins; Humans; In Vitro Techniques; Iron; Thalassemia	1967
Immunological determination of hemopexin in human serum. The American journal of medical technology, 1971, Volume: 37, Issue:10 Topics: Animals; Blood Protein Electrophoresis; Chemical Precipitation; Electrophoresis; Electrophoresis, Disc; Glycoproteins; Goats; Haptoglobins; Heme; Hemoglobins; Hemolysis; Humans; Immunodiffusion; Rabbits; Thalassemia	1971
Heme synthetase in thalassemia. Experientia, 1972, Feb-15, Volume: 28, Issue:2 Topics: Heme; Humans; In Vitro Techniques; Iron Isotopes; Ligases; Reticulocytes; Thalassemia	1972
Inherited disorders of hemoglobin synthesis and pregnancy. American journal of obstetrics and gynecology, 1971, Volume: 111, Issue:1 Topics: Abortion, Induced; Abortion, Therapeutic; Adult; Anemia, Sickle Cell; Cesarean Section; Female; Fetal Death; Fetal Hemoglobin; Hematopoiesis; Hematuria; Heme; Hemoglobin C Disease; Hemoglobinopathies; Hemoglobins; Humans; Infant, Newborn; Infertility, Female; Kidney Diseases; Lung Diseases; Maternal-Fetal Exchange; Obstetric Labor, Premature; Pre-Eclampsia; Pregnancy; Pregnancy Complications, Cardiovascular; Pregnancy Complications, Hematologic; Splenomegaly; Thalassemia; Uterine Hemorrhage	1971
[Chemical and genetic aspects of hemoglobinosynthesis]. Marseille medical, 1971, Volume: 108, Issue:9 Topics: Chemical Phenomena; Chemistry; Genes; Genes, Regulator; Globins; Heme; Hemoglobinopathies; Hemoglobins; Humans; Thalassemia	1971
Accumulation of iron in mitochondria of erythroblasts. British journal of haematology, 1967, Volume: 13, Issue:3 Topics: Anemia, Hemolytic; Anemia, Sideroblastic; Bone Marrow Examination; Chloramphenicol; Erythrocytes; Globins; Heme; Humans; Iron; Lead Poisoning; Leukemia, Erythroblastic, Acute; Microscopy, Electron; Mitochondria; Porphyrias; Thalassemia	1967
Evaluation of plasma iron turnover in Cooley's anemia. Annals of the New York Academy of Sciences, 1969, Nov-20, Volume: 165, Issue:1 Topics: Bone Marrow Examination; Heme; Humans; Iron; Iron Isotopes; Liver; Radiography; Spleen; Thalassemia	1969
The relationship between haem and globin synthesis by erythroid precursors in refractory normoblastic anaemia. Scandinavian journal of haematology, 1969, Volume: 6, Issue:5 Topics: Anemia, Hypochromic; Anemia, Pernicious; Anemia, Sideroblastic; Blood Proteins; Carbon Isotopes; Erythrocytes; Female; Globins; Glycine; Heme; Hemoglobins; Humans; Iron; Male; Porphyrins; Pyridoxine; Thalassemia; Vitamin B 12	1969
Remarks on the hemoglobin molecule, thalassemia and unstable hemoglobins. Humangenetik, 1970, Volume: 9, Issue:3 Topics: Carbon Dioxide; Globins; Heinz Bodies; Heme; Hemoglobins, Abnormal; Humans; Thalassemia	1970
[Anemias due to changes in the biosynthesis of heme and prophyrins]. Sangre, 1970, Volume: 15, Issue:3 Topics: Anemia; Anemia, Hypochromic; Anemia, Sideroblastic; Heme; Humans; Porphyrins; Thalassemia	1970
Disorders of iron utilization. Proceedings of the Royal Society of Medicine, 1970, Volume: 63, Issue:12 Topics: Aged; Anemia; Anemia, Aplastic; Anemia, Hypochromic; Anemia, Sideroblastic; Female; Heme; Hemoglobinuria, Paroxysmal; Hemosiderosis; Humans; Infections; Iron; Mononuclear Phagocyte System; Thalassemia; Transferrin	1970
Excess of alpha-globin synthesis in homozygous beta-thalassemia. Its cytoplasmic molecular forms. European journal of biochemistry, 1968, Volume: 5, Issue:3 Topics: Adult; Blood Proteins; Centrifugation, Density Gradient; Child; Child, Preschool; Chromatography, Ion Exchange; Cytoplasm; Erythrocytes; Globins; Heme; Hemoglobins; Hemolysis; Homozygote; Humans; Infant, Newborn; Infant, Premature; Leucine; Lysine; Peptides; Thalassemia; Tritium; Valine	1968
Plasma concentrations of hemopexin, haptoglobin and heme in patients with various hemolytic diseases. Blood, 1968, Volume: 32, Issue:5 Topics: Adolescent; Adult; Aged; Anemia, Hemolytic, Autoimmune; Anemia, Sickle Cell; Blood Proteins; Child; Haptoglobins; Heme; Hemoglobinuria, Paroxysmal; Humans; Middle Aged; Myoglobinuria; Porphyrias; Spherocytosis, Hereditary; Thalassemia	1968
Heme synthesis and hypochromic anemia. The New England journal of medicine, 1969, Mar-13, Volume: 280, Issue:11 Topics: Anemia, Hypochromic; Anemia, Sideroblastic; Erythrocytes; Heme; Humans; Iron; Ligases; Porphyrins; Thalassemia	1969
Unequal synthesis of complementary globin chains of human fetal hemoglobin by the effect of L-O-methylthreonine. The Journal of biological chemistry, 1969, Apr-25, Volume: 244, Issue:8 Topics: Blood Proteins; Carbon Isotopes; Chromatography, Gel; Complement System Proteins; Depression, Chemical; Erythroblastosis, Fetal; Female; Fetal Hemoglobin; Globins; Heme; Hemolysis; Humans; In Vitro Techniques; Infant, Newborn; Isoleucine; Leucine; Lysine; Peptide Biosynthesis; Pregnancy; Solubility; Thalassemia; Threonine	1969
[The clinical picture of erythropathies]. Folia haematologica; internationales Magazin fur Blutforschung, 1964, Volume: 9, Issue:3 Topics: Anemia, Hemolytic, Congenital; Anemia, Macrocytic; Anemia, Sickle Cell; Erythrocytes; Glucosephosphate Dehydrogenase Deficiency; Hematologic Diseases; Heme; Humans; Methemoglobinemia; Porphyrias; Spherocytosis, Hereditary; Thalassemia	1964