These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
116 related items for PubMed ID: 5154971
1. The chemistry of the thalassemic syndromes. Rebuck JW. Ann Clin Lab Sci (1971); 1971; 1(3):227-30. PubMed ID: 5154971 [No Abstract] [Full Text] [Related]
2. The present status of the heterogeneity of fetal hemoglobin in beta-thalassemia: an attempt to unify some observations in thalassemia and related conditions. Huisman TH, Schroeder WA, Efremov GD, Duma H, Mladenovski B, Hyman CB, Rachmilewitz EA, Bouver N, Miller A, Brodie A, Shelton JR, Shelton JB, Apell G. Ann N Y Acad Sci; 1974; 232(0):107-24. PubMed ID: 4528800 [No Abstract] [Full Text] [Related]
3. Heterogeneity of fetal hemoglobin among Israel families with beta-thalassemia. Rachmilewitz EA, Huisman TH, Schroeder WA. Isr J Med Sci; 1973; 9(9):1464-8. PubMed ID: 4775133 [No Abstract] [Full Text] [Related]
4. Hemoglobin Duarte: (alpha2beta2 62(E6)Ala leads to Pro): a new unstable hemoglobin with increased oxygen affinity. Beutler E, Lang A, Lehmann H. Blood; 1974 Apr; 43(4):527-35. PubMed ID: 4361395 [No Abstract] [Full Text] [Related]
5. [Rattus norvegicus rat hemoglobin and its characteristics (review)]. Grigor'eva GI. Zh Evol Biokhim Fiziol; 1980 Apr; 16(5):499-505. PubMed ID: 6158817 [No Abstract] [Full Text] [Related]
6. Decrease in the concentrations of hemoglobins A2 and F in a beta-thalassemic heterozygote in the course of lymphosarcoma with bone marrow involvement. Aksoy M, Erdem S, Dinçol G, Dinçol K. New Istanbul Contrib Clin Sci; 1974 Jun; 11(1):3-7. PubMed ID: 4479979 [No Abstract] [Full Text] [Related]
7. The starch gel quantitative electrophoresis of haemoglobin as screening in the thalassaemia syndromes. Ricco G, Gallo E, Mazza U, Bianco G, Prato V. Acta Haematol; 1969 Jun; 42(2):99-105. PubMed ID: 4982583 [No Abstract] [Full Text] [Related]
8. In vitro regulation of Hb synthesis: studies in normal subjects and thalassemic patients. Peschle C, Migliaccio AR, Migliaccio G, Mastroberardino G, Gianni AM, Comi P, Ottolenghi S, Giglioni B. Birth Defects Orig Artic Ser; 1982 Jun; 18(7):131-8. PubMed ID: 6186307 [No Abstract] [Full Text] [Related]
17. [Polymorphism of human fetal hemoglobin. II. Incidence of the A-gamma(75) Ileu-replaced-by-thr globin chain in the Spanish population and in various thalassemic syndromes]. Baiget M, Colls M, De Pablos JM, Aventin A, Del Río E, Gimferrer E. Sangre (Barc); 1983 Jun; 28(5):551-6. PubMed ID: 6198735 [No Abstract] [Full Text] [Related]
19. Genetic implications of the interaction of two types of beta-thalassemia genes in a patient with thalassemia major. Russo G, Mollica F, Pavone L, Musumeci S, Baglioni C. Blood; 1973 Nov; 42(5):763-9. PubMed ID: 4746100 [No Abstract] [Full Text] [Related]