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

94 related items for PubMed ID: 2902306

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24. Southeast Asian ovalocytosis and a sickle cell trait in a young patient with sudden retinal stroke: a fortuitous association?
    Favale F, Gardembas M, Pajot O, Saada V, Fénéant-Thibault M, Delaunay J, Garçon L.
    Hemoglobin; 2009; 33(6):475-9. PubMed ID: 19958192
    [Abstract] [Full Text] [Related]

  • 25. Concurrent β-thalassaemia trait and Southeast Asian ovalocytosis associated with clinically significant iron loading.
    Chen Y, Law HY, Tan GP, Ang AL.
    Blood Cells Mol Dis; 2017 Mar; 63():25-26. PubMed ID: 28024237
    [No Abstract] [Full Text] [Related]

  • 26. Coinheritance of Hereditary Elliptocytosis and Deletional Hemoglobin H Disease.
    Charoenkwan P, Natesirinilkul R, Choeyprasert W, Kulsumritpon N, Sangiamporn O.
    J Pediatr Hematol Oncol; 2017 Mar; 39(2):e69-e70. PubMed ID: 28060122
    [Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. Hereditary pyropoikilocytosis and elliptocytosis: clinical, laboratory, and ultrastructural features in infants and children.
    Prchal JT, Castleberry RP, Parmley RT, Crist WM, Malluh A.
    Pediatr Res; 1982 Jun; 16(6):484-9. PubMed ID: 7099765
    [Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Ovalocytosis in normal and mentally retarded subjects.
    Wolman IJ, Walker A, Kiossoglou KA, Garrison M.
    Am J Ment Defic; 1966 Jan; 70(4):515-9. PubMed ID: 4222360
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. Hereditary elliptocytosis: an unusual presentation of hemolysis in the newborn associated with transient morphologic abnormalities.
    Austin RF, Desforges JF.
    Pediatrics; 1969 Aug; 44(2):196-200. PubMed ID: 5806250
    [No Abstract] [Full Text] [Related]

  • 36. Pyknocytosis in a neonate: an unusual presentation of hereditary elliptocytosis.
    Carpentieri U, Gustavson LP, Haggard ME.
    Clin Pediatr (Phila); 1977 Jan; 16(1):76-8. PubMed ID: 830464
    [No Abstract] [Full Text] [Related]

  • 37. Prevention of cerebral malaria in children in Papua New Guinea by southeast Asian ovalocytosis band 3.
    Allen SJ, O'Donnell A, Alexander ND, Mgone CS, Peto TE, Clegg JB, Alpers MP, Weatherall DJ.
    Am J Trop Med Hyg; 1999 Jun; 60(6):1056-60. PubMed ID: 10403343
    [Abstract] [Full Text] [Related]

  • 38. Hereditary elliptocytosis associated with pernicious anaemia.
    Ghosh ML.
    Acta Haematol; 1974 Jun; 51(1):51-4. PubMed ID: 4217073
    [No Abstract] [Full Text] [Related]

  • 39. Malaria protection in hereditary ovalocytosis: relation to red cell deformability, red cell parameters and degree of ovalocytosis.
    Bunyaratvej A, Butthep P, Kaewkettong P, Yuthavong Y.
    Southeast Asian J Trop Med Public Health; 1997 Jun; 28 Suppl 3():38-42. PubMed ID: 9640598
    [Abstract] [Full Text] [Related]

  • 40. Occurrence of the erythrocyte band 3 (AE1) gene deletion in relation to malaria endemicity in Papua New Guinea.
    Mgone CS, Koki G, Paniu MM, Kono J, Bhatia KK, Genton B, Alexander ND, Alpers MP.
    Trans R Soc Trop Med Hyg; 1996 Jun; 90(3):228-31. PubMed ID: 8758056
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 5.