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 *

136 related articles for article (PubMed ID: 3663523)

  • 21. Glycoconjugate abnormalities in patients with congenital dyserythropoietic anaemia type I, II and III.
    Zdebska E; Gołaszewska E; Fabijańska-Mitek J; Schachter H; Shalev H; Tamary H; Sandström H; Wahlin A; Kościelak J
    Br J Haematol; 2001 Sep; 114(4):907-13. PubMed ID: 11564084
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Glycolipids and glycopeptides of red cell membranes in congenital dyserythropoietic anaemia type II (CDA II).
    Zdebska E; Anselstetter V; Pacuszka T; Krauze R; Chełstowska A; Heimpel H; Kościelak J
    Br J Haematol; 1987 Jul; 66(3):385-91. PubMed ID: 3620357
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A case of congenital dyserythropoietic anaemia with stomatocytosis, reduced bands 7 and 8 and normal cation content.
    Olivieri O; Girelli D; Vettore L; Balercia G; Corrocher R
    Br J Haematol; 1992 Feb; 80(2):258-60. PubMed ID: 1550788
    [No Abstract]   [Full Text] [Related]  

  • 24. 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]  

  • 25. 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]  

  • 26. HEMPAS disease: genetic defect of glycosylation.
    Fukuda MN
    Glycobiology; 1990 Sep; 1(1):9-15. PubMed ID: 2136385
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Congenital dyserythropoietic anemia type I: a freeze-fracture and thin section electron microscopic study.
    Hiraoka A; Kanayama Y; Yonezawa T; Kitani T; Tarui S; Hashimoto PH
    Blut; 1983 Jun; 46(6):329-38. PubMed ID: 6850102
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Defective organization of the erythroid cell membrane in a novel case of congenital anemia.
    Antonelou MH; Papassideri IS; Karababa FJ; Stravopodis DJ; Loutradi A; Margaritis LH
    Blood Cells Mol Dis; 2003; 30(1):43-54. PubMed ID: 12667986
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Congenital dyserythropoietic anemia type II (HEMPAS)].
    Fukuda MN
    Tanpakushitsu Kakusan Koso; 1992 Aug; 37(11 Suppl):1929-34. PubMed ID: 1410484
    [No Abstract]   [Full Text] [Related]  

  • 31. Reduced deformability of erythrocytes as feature of congenital dyserythropoietic anaemia type II (HEMPAS).
    Izzo P; Spagnuolo A; Manicone A; Nazzaro P; Lauta VM
    Clin Hemorheol Microcirc; 1999; 21(3-4):425-30. PubMed ID: 10711781
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Congenital dyserytropoietic anaemia, type II (HEMPAS) in three siblings.
    Chrobák L; Radochová D; Smetana K; Matĕja F; Kout M; Polák J; Dítĕ P; Pribroský J; Dvorácková I
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1980; 107(4):628-40. PubMed ID: 6162730
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. A case of congenital dyserythropoietic anemia type II (HEMPAS).
    Moriwaki Y; Matsui K; Fujioka H; Iwahashi N; Seno T; Tamura S; Yamamoto T; Amuro Y; Hada T; Higashino K
    Nihon Ketsueki Gakkai Zasshi; 1985 Feb; 48(1):29-36. PubMed ID: 4003011
    [No Abstract]   [Full Text] [Related]  

  • 35. A variant of the congenital dyserythropoietic anaemia type II with structural abnormalities in the granulocytic series.
    Vermylen C; Scheiff JM; Rodhain J; Ninane J; Cornu G
    Eur J Pediatr; 1986 Aug; 145(3):232-5. PubMed ID: 3769984
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Case report of congenital dyserythropoietic anemia (CDA) type I].
    Atono Y; Ogata H; Nohno R; Sakisaka S; Masiko N; Satoh K; Nakashima F; Tanikawa K; Ebata H; Murakami M
    Rinsho Ketsueki; 1987 Aug; 28(8):1414-8. PubMed ID: 3430753
    [No Abstract]   [Full Text] [Related]  

  • 37. Ultrastructural studies of an unusual variant of congenital dyserythropoietic anaemia type II.
    Dewar CL; Lowenthal RM
    Acta Haematol; 1980; 64(1):53-7. PubMed ID: 6774576
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Glycophorin A in two patients with congenital dyserythropoietic anemia type I and type II is partly unglycosylated.
    Zdebska E; Adamczyk-Popławska M; Kościelak J
    Acta Biochim Pol; 2000; 47(3):773-9. PubMed ID: 11310976
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Polylactosamines are not obligate receptors for invasion of Plasmodium falciparum malaria as shown in HEMPAS variant II-gal- erythrocytes.
    Dhume ST; Adams-Burton CR; Shumak KH; Laine RA
    Glycobiology; 1994 Dec; 4(6):903-8. PubMed ID: 7734852
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Transmission and scanning electron microscopy study on congenital dyserythropoietic anemia type I.
    Conde E; Mazo E; Baro J; Lafarga M; Cuadrado MA; Recio M; Zubizarreta A
    Acta Haematol; 1983; 70(4):243-9. PubMed ID: 6414210
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.