Search

Your search keyword '"Hemoglobinopathies diagnosis"' showing total 117 results
Start Over Descriptor "Hemoglobinopathies diagnosis" Publication Year Range More than 50 years ago
117 results on '"Hemoglobinopathies diagnosis"'

1. Hemoglobin Duarte: (alpha2beta2 62(E6)Ala leads to Pro): a new unstable hemoglobin with increased oxygen affinity.

Author

Beutler E, Lang A, and Lehmann H

Subjects
Adult, Alanine analysis, Amino Acid Sequence, Amino Acids analysis, Anemia, Hemolytic diagnosis, Cell Survival, Chromium Radioisotopes, Electrophoresis, Paper, Electrophoresis, Starch Gel, Erythrocyte Count, Fetal Hemoglobin analysis, Globins analysis, Hematocrit, Hemoglobinometry, Humans, Inclusion Bodies, Male, Pedigree, Peptides analysis, Proline analysis, Reticulocytes, Splenomegaly diagnosis, Thalassemia genetics, Hemoglobinopathies diagnosis, Hemoglobins, Abnormal analysis
Published
1974

2. Hemoglobin S-G (S-D) syndrome.

Author

McCurdy PR, Lorkin PA, Casey R, Lehmann H, Uddin DE, and Dickson LG

Subjects
Adult, Anemia, Sickle Cell diagnosis, Blood Protein Electrophoresis, Chromium Radioisotopes, Diagnosis, Differential, Erythrocyte Count, Erythrocytes physiology, Female, Hematocrit, Hemoglobinopathies diagnosis, Humans, Male, Oxygen blood, Phosphorus Radioisotopes, Physical Exertion, Reticulocytes, Syndrome, Hemoglobin, Sickle analysis, Hemoglobinopathies blood, Hemoglobins, Abnormal analysis
Published
1974
Full Text
View/download PDF

3. Iris atrophy in hemoglobin SC disease.

Author

Chambers J, Puglisi J, Kernitsky R, and Wise GN

Subjects
Adult, Age Factors, Angiography, Black People, Female, Fluoresceins, Hemoglobin, Sickle, Humans, Retinal Pigments, Sex Factors, Vision Disorders diagnosis, Vision Disorders etiology, Vision Tests, Hemoglobin C, Hemoglobinopathies diagnosis, Hemoglobins, Abnormal, Iris, Optic Atrophy
Published
1974
Full Text
View/download PDF

5. Concentration of fetal red blood cells from a mixture of maternal and fetal blood by anti-i serum--an aid to prenatal diagnosis of hemoglobinopathies.

Author

Kan Y, Nathan DG, Cividalli G, and Crookston MC

Subjects
Anemia, Sickle Cell blood, Blood, Carbon Radioisotopes, Cell Separation, Fetus, Gestational Age, Hemagglutination Tests, Hemoglobinopathies diagnosis, Leucine metabolism, Methods, Prenatal Diagnosis, Tritium, Umbilical Cord, Erythrocytes metabolism, Fetal Hemoglobin metabolism, Immune Sera, Isoantibodies
Published
1974

7. Ocular manifestations in sickle cell disease.

Author

Armaly MF

Subjects
Anemia, Sickle Cell classification, Anemia, Sickle Cell diagnosis, Anemia, Sickle Cell pathology, Arterial Occlusive Diseases etiology, Conjunctiva pathology, Eye blood supply, Hemoglobin C, Hemoglobin, Sickle, Hemoglobinopathies diagnosis, Humans, Iris pathology, Regional Blood Flow, Retina pathology, Retinal Detachment etiology, Retinal Diseases etiology, Retinal Hemorrhage etiology, Vitreous Body pathology, Anemia, Sickle Cell complications, Eye Manifestations
Published
1974

8. [Biochemical diagnosis and therapy of molecular diseases].

Author

Perlès R

Subjects
Amino Acid Metabolism, Inborn Errors diagnosis, Carbohydrate Metabolism, Inborn Errors diagnosis, Hemoglobinopathies diagnosis, Humans, Metabolism, Inborn Errors therapy, Metabolism, Inborn Errors diagnosis
Published
1974

9. An approach to the diagnosis of haemolytic anaemia. II.

Author

Kimber RJ

Subjects
Anemia, Hemolytic, Congenital etiology, Blood Protein Electrophoresis, Cell Membrane, Erythrocytes, Abnormal metabolism, Female, Glucosephosphate Dehydrogenase Deficiency chemically induced, Glucosephosphate Dehydrogenase Deficiency diagnosis, Glucosephosphate Dehydrogenase Deficiency metabolism, Hemoglobinopathies diagnosis, Hemoglobins, Abnormal, Heterozygote, Homozygote, Humans, Thalassemia diagnosis, Thalassemia genetics, Anemia, Hemolytic diagnosis
Published
1974
Full Text
View/download PDF

10. Automated technique for the estimation of fetal haemoglobin.

Author

Brook SR, Huntsman RG, Marshall TD, McLellan DS, Semple MJ, and Crane RS

Subjects
Anemia, Sickle Cell diagnosis, Autoanalysis methods, Child, Hemoglobin C Disease diagnosis, Hemoglobinopathies diagnosis, Humans, Infant, Newborn, Protein Denaturation, Sodium Hydroxide, Thalassemia diagnosis, Fetal Hemoglobin analysis
Abstract

An automated alkali denaturation technique which measures fetal haemoglobin is described. This method offers greater speed and a lower standard deviation than comparable manual methods.

Published
1974
Full Text
View/download PDF

12. Microchromatography of hemoglobins. II. A rapid method for the determination of hemoglobin A2.

Author

Efremov CD, Huisman TH, Bowman K, Wrightstone RN, and Shroeder WA

Subjects
Anemia, Sickle Cell blood, Blood Proteins, Chromatography, Gel, Costs and Cost Analysis, Electrophoresis, Erythrocytes analysis, Hemoglobin, Sickle, Hemoglobinopathies diagnosis, Heterozygote, Humans, Hydrogen-Ion Concentration, Mass Screening, Mathematics, Methods, Specimen Handling, Temperature, Thalassemia blood, Time Factors, Chromatography, DEAE-Cellulose
Published
1974

15. In utero diagnosis of hemoglobinopathies. Hemoglobin synthesis in fetal red cells.

Author

Chang H, Hobbins JC, Cividalli G, Frigoletto FD, Mahoney MJ, Kan YW, and Nathan DG

Subjects
Amniotic Fluid cytology, Blood, Blood Specimen Collection, Carbon Radioisotopes, Chromatography, Erythrocytes metabolism, Extraembryonic Membranes blood supply, Female, Fetus cytology, Gestational Age, Globins biosynthesis, Hemoglobin, Sickle biosynthesis, Humans, Leucine metabolism, Methods, Needles, Placenta, Pregnancy, Tritium, Ultrasonography, Fetal Hemoglobin biosynthesis, Hemoglobinopathies diagnosis, Hemoglobins, Abnormal biosynthesis, Prenatal Diagnosis
Published
1974
Full Text
View/download PDF

16. Hemoglobinopathies in pregnancy.

Author

Horger EO 3rd

Subjects
Alleles, Anemia, Sickle Cell diagnosis, Black People, Chemical Phenomena, Chemistry, Erythrocytes metabolism, Erythrocytes, Abnormal analysis, Family Planning Services, Female, Fetal Hemoglobin analysis, Genetic Counseling, Hemoglobin C Disease blood, Hemoglobin H analysis, Hemoglobin, Sickle, Hemoglobinopathies classification, Hemoglobinopathies diagnosis, Hemoglobinopathies genetics, Homozygote, Humans, Oxygen Consumption, Pregnancy, Anemia, Sickle Cell blood, Hemoglobinopathies blood, Hemoglobins classification, Pregnancy Complications, Hematologic blood, Thalassemia blood
Published
1974
Full Text
View/download PDF

17. [Diseases caused by abnormal hemoglobins].

Author

Marti HR

Subjects
Africa, Anemia, Sickle Cell diagnosis, Anemia, Sickle Cell epidemiology, Black People, Diagnosis, Differential, Hemoglobin C Disease diagnosis, Hemoglobin C Disease epidemiology, Hemoglobinopathies diagnosis, Heterozygote, Homozygote, Humans, Methemoglobinemia congenital, Methemoglobinemia diagnosis, Hemoglobinopathies epidemiology, Hemoglobins, Abnormal
Published
1974

18. The role of a sickle cell center in comprehensive screening and counseling for sickle cell and related disorders.

Author

Lutcher CL, Huisman TH, Dorsey WM, Mayson S, Ludvigsen B, and Smith AT

Subjects
Adolescent, Adult, Aged, Anemia, Sickle Cell genetics, Blood Protein Electrophoresis, Child, Child, Preschool, Chromatography, Electrophoresis, Starch Gel, Female, Fetal Hemoglobin analysis, Georgia, Health Surveys, Hematocrit, Hemoglobin C Disease diagnosis, Hemoglobin C Disease epidemiology, Hemoglobin, Sickle analysis, Hemoglobinopathies epidemiology, Hemoglobins, Abnormal analysis, Humans, Infant, Infant, Newborn, Male, Middle Aged, Pilot Projects, Pregnancy, Solubility, Thalassemia diagnosis, Thalassemia epidemiology, Black or African American, Anemia, Sickle Cell diagnosis, Black People, Community Health Services, Genetic Counseling, Hemoglobinopathies diagnosis, Mass Screening
Published
1974
Full Text
View/download PDF

19. Screening of military recruits for hemoglobin variants.

Author

Uddin DE, Dickson LG, and Brodine CE

Subjects
Anemia, Sickle Cell diagnosis, Black People, Hemoglobin C Disease diagnosis, Hemoglobin, Sickle analysis, Hemoglobinopathies epidemiology, Heterozygote, Humans, Male, Methods, Multiphasic Screening, Phenotype, Sex Factors, Stress, Physiological complications, Thalassemia diagnosis, United States, Black or African American, Hemoglobinopathies diagnosis, Hemoglobins, Abnormal analysis, Military Medicine
Published
1974

20. The clinical features of unstable haemoglobin disease.

Author

White JM

Subjects
Glycated Hemoglobin analysis, Glycated Hemoglobin genetics, Hemoglobinopathies genetics, Hemoglobinopathies therapy, Hemoglobins, Abnormal analysis, Hemoglobins, Abnormal genetics, Heterozygote, Humans, Splenectomy, Hemoglobinopathies diagnosis
Published
1974

21. [Technic of rapid detection of hemoglobinopathies].

Author

Sarthou JL, Mark J, and Roux J

Subjects
Acetates, Blood Specimen Collection methods, Cellulose, Humans, Staining and Labeling, Time Factors, Blood Protein Electrophoresis methods, Hemoglobinopathies diagnosis, Hemoglobins, Abnormal analysis
Published
1974

22. The polycythemias and their relationship to erythropoietin.

Author

Jacob HS

Subjects
Alkylating Agents therapeutic use, Blood Cell Count, Blood Volume, Erythrocyte Count, Erythropoiesis, Hematocrit, Hemoglobinopathies diagnosis, Hemoglobins metabolism, Humans, Hypoxia complications, Oxygen Consumption, Polycythemia classification, Polycythemia genetics, Polycythemia Vera complications, Polycythemia Vera diagnosis, Polycythemia Vera etiology, Polycythemia Vera surgery, Polycythemia Vera therapy, Polycythemia Vera urine, Protein Binding, Erythropoietin analysis, Polycythemia Vera blood
Published
1974

24. Glycerol lysis time as a screening test for erythrocyte disorders.

Author

Gottfried EL and Robertson NA

Subjects
Anemia, Hypochromic diagnosis, Cell Membrane metabolism, Erythrocytes metabolism, Hemoglobinopathies diagnosis, Humans, Kidney Diseases blood, Lipid Metabolism, Mass Screening, Spherocytosis, Hereditary diagnosis, Thalassemia diagnosis, Erythrocytes, Abnormal, Glycerol, Hematologic Diseases diagnosis, Hemolysis
Published
1974

25. Automated dithionite test for rapid, inexpensive detection of hemoglobin S and non-S sickling hemoglobinopathies.

Author

Nalbandian RM, Nichols BM, Camp FR Jr, Lusher JM, Conte NF, Henry RL, and Wolf PL

Subjects
Adult, Autoanalysis instrumentation, Chemical Phenomena, Chemistry, Child, Colorimetry, Crystallization, Densitometry, Electrophoresis, Hemoglobin C analysis, Hemoglobin C Disease diagnosis, Hemoglobins analysis, Hemolysis, Heterozygote, Homozygote, Humans, Male, Mass Screening, Methods, Oxygen blood, Phosphates, Potassium, Saponins, Sodium, Time Factors, Anemia, Sickle Cell diagnosis, Hemoglobinopathies diagnosis, Hemoglobins, Abnormal analysis, Sulfites, Urea
Published
1971

26. Hemoglobinopathies.

Author

Perez AP

Subjects
Methods, Terminology as Topic, Hemoglobinopathies diagnosis
Published
1969

27. Fundus in sulfhemoglobinemia.

Author

Walsh TJ and Beehler C

Subjects
Aged, Hemoglobinopathies pathology, Humans, Male, Fundus Oculi, Hemoglobinopathies diagnosis, Sulfur blood
Published
1969

28. Recent progress in genetic hemolytic disorders: a practical approach.

Author

Van Eys J

Subjects
Anemia, Hemolytic diagnosis, Anemia, Hemolytic, Congenital etiology, Biological Transport, Cell Wall, Child, Preschool, Diagnosis, Differential, Erythrocytes metabolism, Erythrocytes, Abnormal, Hemoglobinopathies diagnosis, Humans, Anemia, Hemolytic, Congenital diagnosis, Metabolism, Inborn Errors diagnosis
Published
1970
Full Text
View/download PDF

29. Differentiation of anemias.

Author

Louis J

Subjects
Anemia chemically induced, Anemia etiology, Anemia, Hemolytic diagnosis, Anemia, Hypochromic diagnosis, Anemia, Macrocytic diagnosis, Bone Marrow Examination, Clinical Enzyme Tests, Diagnosis, Differential, Electrophoresis, Folic Acid blood, Hemoglobinopathies diagnosis, Hemoglobins biosynthesis, Hemorrhage diagnosis, Humans, Iron analysis, Metabolism, Inborn Errors, Schilling Test, Anemia diagnosis
Published
1969

33. Haemoglobinopathies in Burma. IV. Thalassaemia-haemoglobin E disease and thalassaemia major.

Author

Aung-Than-Batu, U-Hla-Pe, Khin-Kyi-Nyunt, and Tin-U

Subjects
Adolescent, Adult, Blood Protein Electrophoresis, Child, Child, Preschool, Female, Fetal Hemoglobin analysis, Hemoglobinometry, Hemoglobinopathies blood, Hemoglobinopathies diagnosis, Hemoglobins, Abnormal analysis, Hepatomegaly complications, Humans, Infant, Infant, Newborn, Jaundice complications, Male, Myanmar, Osmotic Fragility, Splenomegaly complications, Thalassemia blood, Thalassemia diagnosis, Hemoglobinopathies epidemiology, Thalassemia epidemiology
Published
1971

34. Sickle cell testing programs.

Author

Pearson HA and O'Brien RT

Subjects
Adolescent, Black or African American, Age Factors, Anemia, Sickle Cell complications, Anemia, Sickle Cell genetics, Blood, Diagnosis, Differential, Electrophoresis, Starch Gel, Ethnicity, Genetic Counseling, Hemoglobinopathies diagnosis, Humans, Hypoxia complications, Infant, Newborn, Puerto Rico, School Health Services, Umbilical Cord, United States, Anemia, Sickle Cell diagnosis, Infant, Newborn, Diseases diagnosis, Mass Screening
Published
1972
Full Text
View/download PDF

36. [Thin layer starch gel electrophoresis].

Author

Yamaoka K, Ota Y, and Seita M

Subjects
Hemoglobins, Abnormal analysis, Humans, Methods, Electrophoresis, Starch Gel, Hemoglobinopathies diagnosis
Published
1972

37. The laboratory investigation of haemoglobinopathies.

Author

Deedo SH

Subjects
Anemia, Sickle Cell diagnosis, Electrophoresis, Electrophoresis, Starch Gel, Hemoglobins analysis, Humans, Methods, Thalassemia diagnosis, Clinical Laboratory Techniques, Hemoglobinopathies diagnosis
Published
1973

38. Sickle-cell haemolglobin C disease and sickle-cell beta thalassaemia in white South Africans.

Author

Dunston T, Rowland R, Huntsman RG, and Yawson G

Subjects
Anemia, Sickle Cell genetics, Blood Protein Electrophoresis, Child, Child, Preschool, Electrophoresis, Polyacrylamide Gel, Hemoglobin C analysis, Hemoglobin C Disease genetics, Hemoglobinopathies diagnosis, Hemoglobins, Abnormal analysis, Humans, Male, Peptides analysis, South Africa, Thalassemia genetics, White People, Anemia, Sickle Cell epidemiology, Hemoglobin C Disease epidemiology, Thalassemia epidemiology
Published
1972

39. The identification of metabolic errors associated with hemolytic anemia.

Author

Fairbanks VF and Fernandez MN

Subjects
Clinical Enzyme Tests, Fluorescence, Hemoglobinopathies diagnosis, Hemolysis, Humans, Male, Anemia, Hemolytic, Congenital diagnosis, Glucosephosphate Dehydrogenase Deficiency diagnosis, Metabolism, Inborn Errors diagnosis
Published
1969

40. Differential diagnosis of anemia.

Author

Cameron DG

Subjects
Anemia etiology, Anemia, Aplastic diagnosis, Anemia, Hemolytic diagnosis, Anemia, Hypochromic diagnosis, Anemia, Macrocytic diagnosis, Anemia, Myelophthisic diagnosis, Anemia, Sideroblastic diagnosis, Diagnosis, Differential, Erythropoiesis, Folic Acid Deficiency complications, Hemoglobinopathies diagnosis, Hemolysis, Hemorrhage complications, Humans, Vitamin B 12 Deficiency complications, Anemia diagnosis
Published
1973
Full Text
View/download PDF

43. [Hemoglobin D Punjab in a German patient].

Author

Kohne E, König E, Roggenback HJ, Augener W, Brittinger G, and Kleihauer E

Subjects
Germany, West, Humans, Male, Middle Aged, Hemoglobinopathies diagnosis, Hemoglobins, Abnormal
Published
1972

44. [Hemoglobinopathies].

Author

Cabannes R and Bonhomme J

Subjects
Humans, Hemoglobinopathies diagnosis, Hemoglobinopathies pathology
Published
1972

45. [Hemoglobin S-C disease. 18 cases in Upper-Volta].

Author

Josserand C, Dujeu G, Sawadogo R, Pirame Y, Sagnet H, Thomas J, Revil H, and Mafart Y

Subjects
Adolescent, Adult, Aged, Black People, Burkina Faso, Child, Child, Preschool, Female, Hemoglobin C Disease complications, Hemoglobin C Disease diagnosis, Humans, Male, Middle Aged, Pregnancy, Pregnancy Complications, Hematologic, Hemoglobin C, Hemoglobinopathies diagnosis
Published
1970

46. [Hereditary hemolytic anemia].

Author

Dluholucký S

Subjects
Anemia, Hemolytic enzymology, Anemia, Hemolytic etiology, Diagnosis, Differential, Genetic Diseases, Inborn, Hemoglobinopathies diagnosis, Humans, Anemia, Hemolytic genetics
Published
1971

47. Treatment of haemoglobinopathies and allied disorders. Report of a WHO Scientific Group.

Subjects
Anemia, Sickle Cell classification, Anemia, Sickle Cell diagnosis, Anemia, Sickle Cell drug therapy, Anemia, Sickle Cell genetics, Blood Transfusion, Female, Genetic Counseling, Glucosephosphate Dehydrogenase blood, Glucosephosphate Dehydrogenase Deficiency classification, Glucosephosphate Dehydrogenase Deficiency diagnosis, Glucosephosphate Dehydrogenase Deficiency drug therapy, Glucosephosphate Dehydrogenase Deficiency genetics, Hemoglobinopathies classification, Hemoglobinopathies diagnosis, Hemoglobinopathies drug therapy, Hemoglobins, Abnormal analysis, Humans, Pregnancy, Prognosis, Thalassemia classification, Thalassemia diagnosis, Thalassemia drug therapy, Thalassemia genetics, Glucosephosphate Dehydrogenase Deficiency therapy, Hemoglobinopathies therapy
Published
1972

48. Sickledex test for hemoglobin S. A critique.

Author

Nalbandian RM, Henry NL, Lusher JM, Camp FR Jr, and Conte NF

Subjects
False Negative Reactions, False Positive Reactions, Humans, Mass Screening, Methods, Sodium, Anemia, Sickle Cell diagnosis, Hemoglobinopathies diagnosis, Hemoglobins, Abnormal analysis, Indicators and Reagents, Phosphates, Potassium, Saponins, Serologic Tests
Published
1971

49. The unstable haemoglobins.

Author

Huehns ER

Subjects
Amino Acids, Binding Sites, Erythrocytes, Hemoglobinopathies diagnosis, Hemoglobins, Abnormal biosynthesis, Humans, Oxygen, Partial Pressure, Anemia, Hemolytic, Congenital diagnosis, Hemoglobins, Abnormal analysis
Published
1970

50. Hb electrophoresis.

Subjects
Electrophoresis, Hemoglobins, Abnormal analysis, Humans, Hemoglobinopathies diagnosis
Published
1969

Catalog

Books, media, physical & digital resources
See catalog results