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 *

180 related articles for article (PubMed ID: 197608)

  • 1. [Clinical and biological aspects of beta-thalassemia. Apropos of 176 cases].
    Belhani M; Dahmane M; Richard F; Trabuchet G; Benabadji M; Colonna P; Labie D
    Sem Hop; 1977 Apr; 53(16):891-7. PubMed ID: 197608
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia.
    Honig GR; Gunay U; Mason RG; Vida LN; Ferenc C
    Pediatr Res; 1976 Jun; 10(6):613-20. PubMed ID: 1272638
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Alpha-thalassemia in a pool of individuals of Eti-Turk origin with hemoglobin S (Hb S).
    Jama H; Gürgey A; Altay C
    Turk J Pediatr; 1987; 29(1):1-14. PubMed ID: 3433374
    [No Abstract]   [Full Text] [Related]  

  • 4. [Hemoglobinosis SC ("African rheumatism") and the hemoglobin C heterozygous carrier state].
    Kononiachenko VA; Troitskaia OV; Iushkova NM; Iudina LI
    Probl Gematol Pereliv Krovi; 1979 Nov; 24(11):20-4. PubMed ID: 504093
    [No Abstract]   [Full Text] [Related]  

  • 5. Sickle cell syndromes. III. Silent-carrier alpha-thalassemia in combination with hemoglobin S and hemoglobin C.
    Honig GR; Mason RG; Tremaine LM; Vida LN
    Pediatr Res; 1979 Oct; 13(10):1109-11. PubMed ID: 503635
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Double heterozygous Hb O Arab/beta-thalassemia in a Tunisian child].
    Haji F; Chadli A; Fattoum S; Souilem J; Hassine L
    Arch Inst Pasteur Tunis; 1985 Dec; 62(4):341-53. PubMed ID: 2423045
    [TBL] [Abstract][Full Text] [Related]  

  • 7. What determines severity in sickle-cell disease?
    Schechter AN; Bunn HF
    N Engl J Med; 1982 Feb; 306(5):295-7. PubMed ID: 6172711
    [No Abstract]   [Full Text] [Related]  

  • 8. [Biological profile of sickle cell anemia in Morocco. A propos of 85 cases].
    Omari M; Naji M; Agoumi N
    Maghrib Tibbi; 1982; 4(2-3):175-82. PubMed ID: 7182694
    [No Abstract]   [Full Text] [Related]  

  • 9. Hemoglobin C-beta (0) thalassemia.
    Ozsoylu S; Sipahioglu H; Altay F
    Isr J Med Sci; 1989 Jul; 25(7):410-2. PubMed ID: 2759839
    [No Abstract]   [Full Text] [Related]  

  • 10. [Intermediate thalassemia. Study of 5 cases in their clinical, ferrokinetic and erythrokinetic aspects].
    Muñoz JA; Martín MV; Risueño CE; Freire J; Pajares M; Campos J
    Sangre (Barc); 1989 Oct; 34(5):346-9. PubMed ID: 2482545
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Clinical considerations on 7 cases of Hb C-thalassemia].
    Polosa P; Motta L; Calcagno G
    Haematologica; 1970; 55(5):333-57. PubMed ID: 4995788
    [No Abstract]   [Full Text] [Related]  

  • 12. [Influence of alpha-thalassemia on the hematologic expression of homozygote drepanocytosis].
    de Montalembert M; Dode C; Maier-Redelsperger M; Labie D; Girot R
    Arch Fr Pediatr; 1987; 44(7):517-9. PubMed ID: 3426374
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Double heterozygote HbC-beta(O) thalassemia. A new case of this combination in a Caucasian subject].
    Vives Corrons JL; Vallespí MT; Jou JM; Aguilar i Basocompte JL
    Sangre (Barc); 1983; 28(5):656-62. PubMed ID: 6665699
    [No Abstract]   [Full Text] [Related]  

  • 14. The association of sickle cell anemia with heterozygous and homozygous alpha-thalassemia-2: in vitro HB chain synthesis.
    Felice AE; Webber B; Miller A; Mayson SM; Harris HF; Henson JB; Gravely ME; Huisman TH
    Am J Hematol; 1979; 6(2):91-106. PubMed ID: 474574
    [No Abstract]   [Full Text] [Related]  

  • 15. Interaction of the alpha alpha alpha globin gene haplotype and sickle haemoglobin.
    Higgs DR; Clegg JB; Weatherall DJ; Serjeant BE; Serjeant GR
    Br J Haematol; 1984 Aug; 57(4):671-8. PubMed ID: 6331494
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and laboratory study of sickle cell/beta-thalassemia.
    Maeda K; Van Slyck EJ; Hawley RC
    Henry Ford Hosp Med J; 1986; 34(4):282-4. PubMed ID: 3583796
    [No Abstract]   [Full Text] [Related]  

  • 17. [Sickle cell disease: laboratory and hemoglobin study].
    Wajcman H; Galacteros F
    Bull Soc Pathol Exot; 2001 May; 94(2):80-4. PubMed ID: 11475032
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Modification of hemoglobin H disease by sickle trait.
    Matthay KK; Mentzer WC; Dozy AM; Kan YW; Bainton DF
    J Clin Invest; 1979 Oct; 64(4):1024-32. PubMed ID: 479366
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Haemoglobin S/beta thalassaemia in a Greek family: a case study (author's transl)].
    Fischer M; Hopmeier P; Lurf M; Neuwald C; Lachmann D
    Wien Klin Wochenschr; 1979 Jan; 91(2):45-8. PubMed ID: 433279
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [HbC/beta-thalassemia association. Eleven cases observed in Tunisia].
    Fattoum S; Guemira F; Abdennebi M; Ben Abdeladhim A
    Ann Pediatr (Paris); 1993 Jan; 40(1):45-8. PubMed ID: 8442646
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.