BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

315 related articles for article (PubMed ID: 514807)

  • 21. Heterozygosity of CDAN II (HEMPAS) gene may be detected by the analysis of erythrocyte membrane glycoconjugates from healthy carriers.
    Zdebska E; Mendek-Czajkowska E; Ploski R; Woêniewicz B; Koscielak J
    Haematologica; 2002 Feb; 87(2):126-30. PubMed ID: 11836161
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A family with congenital dyserythropoietic anemia type II (HEMPAS).
    Omine M; Yamauchi H; Nogiwa E; Umegae S; Tsuchiya J; Maekawa T
    Nihon Ketsueki Gakkai Zasshi; 1981 Feb; 44(1):1-15. PubMed ID: 7315134
    [No Abstract]   [Full Text] [Related]  

  • 23. [Congenital dyserythropoietic anemia type II. Another case report].
    Hartwich G; Riemann J; Krönert E
    Med Klin; 1976 Nov; 71(48):2117-22. PubMed ID: 1004360
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Congenital dyserythropoietic anemia, type I. Clinico-hematological and ultrastructural study of a case diagnosed late].
    Sansone G; Intra E; Bandelloni R; Barban G; Zunin G
    Pathologica; 1987; 79(1064):705-14. PubMed ID: 3503229
    [No Abstract]   [Full Text] [Related]  

  • 25. Congenital dyserythropoietic anemia, type II with SEC23B exon 12 c.1385 A → G mutation, and pseudo-Gaucher cells in two siblings.
    Sharma P; Das R; Bansal D; Trehan A
    Hematology; 2015 Mar; 20(2):104-7. PubMed ID: 24801240
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Elderly dyserythropoietic anemia first diagnosed after presentation of hemorrhagic gastric ulcer].
    Okamura A; Matsui T; Yamaguchi A; Shimizu S; Kadowaki S; Chihara K; Fujimoto T; Kanki K; Fujio K
    Rinsho Ketsueki; 1999 Oct; 40(10):1074-80. PubMed ID: 10565224
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Long-term cinemicrography of erythroblasts from a patient with congenital dyserythropoietic anemia type III: direct observation of dysplastic erythroblast formation.
    Furukawa T; Inoue H; Sugita K; Eguchi M; Sakakibara H; Sugiyama S; Suda T
    Blood Cells; 1993; 19(2):493-506; discussion 507-8. PubMed ID: 8312576
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Congenital dyserythropoietic anaemia.
    Prasher N; Prasher BS
    J Assoc Physicians India; 1989 Jul; 37(7):467-8. PubMed ID: 2613664
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Favorable effect of splenectomy on anemia in 3 siblings with type II congenital dyserythropoietic anemia (HEMPAS). (Ultrastructural changes in erythrocytes after splenectomy)].
    Chrobák L; Spacek J
    Vnitr Lek; 1997 Oct; 43(10):635-8. PubMed ID: 9601875
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Congenital dyserythropoietic anemia type II: molecular basis and clinical aspects.
    Iolascon A; D'Agostaro G; Perrotta S; Izzo P; Tavano R; Miraglia del Giudice B
    Haematologica; 1996; 81(6):543-59. PubMed ID: 9009444
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Aberrant congenital dyserythropoietic anemia with negative acidified serum tests and features of thalassemia in a Kurdish family.
    Eldor A; Matzner Y; Kahane I; Levene C; Polliack A
    Isr J Med Sci; 1978 Nov; 14(11):1138-43. PubMed ID: 750540
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Evidence for the existence of two populations of erythroid cells in a case of congenital dyserythropoietic anaemia type II.
    Cazzola M; Barosi G; Lambertenghi-Deliliers G; Paolini F; Riccardi A
    Haematologica; 1982 Aug; 67(4):508-16. PubMed ID: 6815010
    [No Abstract]   [Full Text] [Related]  

  • 33. A case of congenital dyserythropoietic anemia type II associated with hemochromatosis.
    Tamura H; Matsumoto G; Itakura Y; Terai H; Ikebuchi K; Mitarai T; Isoda K
    Intern Med; 1992 Mar; 31(3):380-4. PubMed ID: 1611191
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Congenital dyserythropoietic anemia in a Chinese family with a mutation of the CDAN1-gene.
    Ru YX; Zhu XF; Yan WW; Gao JT; Schwarz K; Heimpel H
    Ann Hematol; 2008 Sep; 87(9):751-4. PubMed ID: 18575862
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A new case of congenital dyserythropoietic anaemia, type III: studies of the cell cycle distribution and ultrastructure of erythroblasts and of nucleic acid synthesis in marrow cells.
    Wickramasinghe SN; Parry TE; Williams C; Bond AN; Hughes M; Crook S
    J Clin Pathol; 1982 Oct; 35(10):1103-9. PubMed ID: 6182166
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Congenital dyserythropoietic anaemia type II (HEMPAS) and its molecular basis.
    Fukuda MN
    Baillieres Clin Haematol; 1993 Jun; 6(2):493-511. PubMed ID: 8043936
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Atypical congenital dyserythropoietic anemia].
    Schmidt U; Richter HJ; Samandari S
    Schweiz Med Wochenschr; 1987 Nov; 117(45):1776-80. PubMed ID: 3423766
    [TBL] [Abstract][Full Text] [Related]  

  • 38. An unusual type of congenital dyserythropoietic anemia with thalassemia features.
    Berrebi A; Nir E
    Isr J Med Sci; 1978 Nov; 14(11):1135-7. PubMed ID: 750539
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [A family of congenital dyserythropoietic anemia type II (HEMPAS)].
    Kuwabara T; Sakamoto F; Horikoshi H; Dan K; Kuriya S; Nomura T
    Rinsho Ketsueki; 1982 Dec; 23(12):1924-9. PubMed ID: 7166822
    [No Abstract]   [Full Text] [Related]  

  • 40. Congenital dyserythropoietic anaemia (CDA) type I--a case report with ultrastructural study.
    Ghosh K; Mohanty D; Bhagwat AG; Das KC
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1985; 112(5):716-22. PubMed ID: 2416648
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.