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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

67 related articles for article (PubMed ID: 5861188)

  • 1. [On a new type of microcythemia with high Hb A 2 and high Hb F. Description of a family].
    Silvestroni E; Bianco I; Muratore F
    Prog Med (Napoli); 1965 Aug; 21(15):491-5. PubMed ID: 5861188
    [No Abstract]   [Full Text] [Related]  

  • 2. [Microcythemia with abundant Hb F and normal Hb A2 in three families of Puglie].
    Silvestroni E; Bianco I
    Policlinico Prat; 1965 Oct; 72(41):1381-8. PubMed ID: 5856487
    [No Abstract]   [Full Text] [Related]  

  • 3. Hb E trait and Hb E-thalassaemia in Sri Lanka.
    Ellepola SB; Beaven GH; Gunasekara LS; Arulanandan P
    Ceylon Med J; 1980; 25(1-2):29-34. PubMed ID: 6965237
    [No Abstract]   [Full Text] [Related]  

  • 4. [Association of Hb Lepore Boston and beta-+ thalassemia in a Spanish family].
    Romero C; Fernández Fuertes I; Hernández Jodra M; Navarro JL
    Sangre (Barc); 1983; 28(3):348-52. PubMed ID: 6623295
    [No Abstract]   [Full Text] [Related]  

  • 5. Hemoglobin E in Indochinese refugees.
    Cunningham TM
    West J Med; 1982 Sep; 137(3):186-90. PubMed ID: 7147932
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Study of hemopathy to Hb Lepore in a family group from Apulia].
    Tannoia N; Ciavarella N; Putignano A
    Policlinico Prat; 1967 Sep; 74(39):1332-5. PubMed ID: 5615912
    [No Abstract]   [Full Text] [Related]  

  • 7. Changing patterns of thalassemia worldwide.
    Vichinsky EP
    Ann N Y Acad Sci; 2005; 1054():18-24. PubMed ID: 16339647
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Double heterozygote hemoglobin D/B0 thalassemia. Report of 3 cases in a Portuguese family].
    Sousa Uva L; Fernandes A; Pilar M
    Nouv Rev Fr Hematol (1978); 1983; 25(6):387-90. PubMed ID: 6664837
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Low output hemoglobins which produce the phenotype of thalassemia.
    Adams JG; Steinberg MH
    Prog Clin Biol Res; 1981; 55():81-98. PubMed ID: 6895257
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hb E-beta thalassaemia in the West Malaysian Orang Asli (aborigines).
    Bolton JM; Lie-Injo Luan Eng
    Med J Malaya; 1969 Sep; 24(1):36-40. PubMed ID: 4244260
    [No Abstract]   [Full Text] [Related]  

  • 11. Thalassemia and Hb E-thalassemia in Bandung.
    Oman H; Wiradisuria S
    Paediatr Indones; 1969; 9(6):269-75. PubMed ID: 5397492
    [No Abstract]   [Full Text] [Related]  

  • 12. Haemoglobin E-beta-thalassaemia; a study of eight cases in Northwest India.
    Ghosh K; Chakrabarty AK; Mohanty D; Das KC
    Trop Geogr Med; 1983 Sep; 35(3):267-71. PubMed ID: 6196886
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hb Bleuland [alpha108(G15)Thr-->Asn, ACC-->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alpha-thalassemia phenotype.
    Harteveld CL; Versteegh FG; Kok PJ; van Rooijen-Nijdam IH; van Delft P; Giordano PC
    Hemoglobin; 2006; 30(3):349-54. PubMed ID: 16840225
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Italian observation of the disease caused by Hb Lepore homozygosity].
    Quattrin N; Ventruto V; Dini E
    Haematologica; 1966; 51(3):189-96. PubMed ID: 4959354
    [No Abstract]   [Full Text] [Related]  

  • 15. Ggamma -37 (A-->T): a new nondeletional hereditary persistence of fetal hemoglobin determinant associated with the rare codon 91 (+T) delta0-thalassemia.
    Bouva MJ; Harteveld CL; Bakker-Verweij G; van Delft P; Giordano PC
    Hemoglobin; 2006; 30(3):371-7. PubMed ID: 16840228
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Double heterozygosity for Hb New York [beta 113 GTG-->GAG; VAL-->GLU] and beta degrees-thalassemia mutations manifests as a thalassemia trait.
    Lee AC; Ma ES; Chan AY; Szeto SC; Chan LC
    Pediatr Hematol Oncol; 2008; 25(3):227-31. PubMed ID: 18432506
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [The association of beta zero-thalassemia and Hb D Punjab in a family of Indian origin. The second case reported in Spain].
    Ropero P; González FA; Sánchez J; Armada B; Martí E; Valdés B; Mora A; Villegas A
    Med Clin (Barc); 1997 Mar; 108(10):385-8. PubMed ID: 9139146
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hb St. Jozef, A Val-->Leu N-terminal mutation leading to retention of the methionine, and partial acetylation found in the globin gene in Cis with a -alpha3.7 thalassemia deletion.
    Harteveld CL; Versteegh FG; van Leer EH; Starreveld JS; Kok PJ; van Rooijen-Nijdam I; van Delft P; Zanella-Cleon I; Becchi M; Wajcman H; Giordano PC
    Hemoglobin; 2007; 31(3):313-23. PubMed ID: 17654068
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A case of association of hemoglobin D-beta microcythemia].
    Oldrini R; Salmini G; Maioio AT
    Haematologica; 1972; 58(9):515-21. PubMed ID: 4206223
    [No Abstract]   [Full Text] [Related]  

  • 20. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.
    Panyasai S; Fucharoen S; Surapot S; Fucharoen G; Sanchaisuriya K
    Haematologica; 2004 Jul; 89(7):777-81. PubMed ID: 15257928
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.