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 *

102 related articles for article (PubMed ID: 2068039)

  • 1. Primary shunt hyperbilirubinaemia: a variant of the congenital dyserythropoietic anaemias.
    Bird AR; Knottenbelt E; Jacobs P; Maigrot J
    Postgrad Med J; 1991 Apr; 67(786):396-8. PubMed ID: 2068039
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The diagnostic challenge of congenital dyserythropoietic anaemia: two cases of 'CDA type II'.
    Dukka S; King MJ; Hill QA
    J Clin Pathol; 2014 Apr; 67(4):367-9. PubMed ID: 24385490
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Analysis of a family pedigree with primary shunt hyperbilirubinaemia].
    Lu F; Jin P; You Y; Qi X; Liu X; Liang J
    Zhonghua Nei Ke Za Zhi; 2002 Sep; 41(9):586-8. PubMed ID: 12421487
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An unclassified case of congenital dyserythropoietic anaemia with a severe neonatal onset.
    Sansone G; Masera G; Cantù-Rajnoldi A; Terzoli S
    Acta Haematol; 1992; 88(1):41-5. PubMed ID: 1414161
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dyserythropoiesis and congenital dyserythropoietic anaemias.
    Wickramasinghe SN
    Br J Haematol; 1997 Sep; 98(4):785-97. PubMed ID: 9326170
    [No Abstract]   [Full Text] [Related]  

  • 6. Transfusion-dependent congenital dyserythropoietic anaemia with intraerythroblastic inclusions of a non-globin protein.
    Iolascon A; Martire B; Lee MJ; Wickramasinghe SN
    Eur J Haematol; 2000 Aug; 65(2):140-3. PubMed ID: 10966176
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Congenital dyserythropoietic anaemia type II: a rare entity.
    Alam K; Aziz M; Varshney M; Maheshwari V; Basha M; Gaur K
    BMJ Case Rep; 2011 Apr; 2011():. PubMed ID: 22696622
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Short report: erythrocyte membranes from a patient with congenital dyserythropoietic anaemia type I (CDA-I) show identical, although less pronounced, glycoconjugate abnormalities to those from patients with CDA-II (HEMPAS).
    Zdebska E; Woźniewicz B; Adamowicz-Salach A; Kościelak J
    Br J Haematol; 2000 Sep; 110(4):998-1001. PubMed ID: 11054095
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Variant congenital dyserythropoietic anaemia with ringed sideroblasts.
    Brien WF; Mant MJ; Etches WS
    Clin Lab Haematol; 1985; 7(3):231-7. PubMed ID: 4075738
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Variants of congenital dyserythropoietic anaemia: an update.
    Boogaerts MA; Verwilghen RL
    Haematologia (Budap); 1982; 15(2):211-9. PubMed ID: 6761240
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Primary shunt hyperbilirubinaemia in a large four-generation family confirming autosomal dominant genetic disorder.
    Wang CL; Liu XW; Lu FG; Wu XP; Ouyang CH; Yang DY
    World J Gastroenterol; 2006 May; 12(19):3123-5. PubMed ID: 16718801
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The congenital dyserythropoietic anaemias.
    Delaunay J; Iolascon A
    Baillieres Best Pract Res Clin Haematol; 1999 Dec; 12(4):691-705. PubMed ID: 10895259
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital dyserythropoietic anaemia with erythroblastic multinuclearity.
    Bright M; Cobb J; Evans B; Parry TE
    J Clin Pathol; 1972 Jul; 25(7):561-9. PubMed ID: 5070252
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Growth differentiation factor 15 in patients with congenital dyserythropoietic anaemia (CDA) type II.
    Casanovas G; Swinkels DW; Altamura S; Schwarz K; Laarakkers CM; Gross HJ; Wiesneth M; Heimpel H; Muckenthaler MU
    J Mol Med (Berl); 2011 Aug; 89(8):811-6. PubMed ID: 21475976
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Congenital dyserythropoietic anaemia (type II) presenting with haemosiderosis.
    Bird AR; Jacobs P; Moores P
    Acta Haematol; 1987; 78(1):33-6. PubMed ID: 3116805
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Advances in the understanding of the congenital dyserythropoietic anaemias.
    Wickramasinghe SN; Wood WG
    Br J Haematol; 2005 Nov; 131(4):431-46. PubMed ID: 16281933
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Extra medullary hematopoiesis associated to congenital dyserythropoietic anemia II in adult].
    Jedidi I; Medhaffar M; Ghorbel M; Hdiji S; Makni F; Elloumi M; Kallel C
    Ann Biol Clin (Paris); 2012; 70(2):217-20. PubMed ID: 22484535
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lethal hydrops fetalis due to congenital dyserythropoietic anemia in a newborn: association of a new skeletal abnormality.
    Tekinalp G; Sarici SU; Erdinç AS; Gögüş S; Balci S; Gürgey A
    Pediatr Hematol Oncol; 2001 Dec; 18(8):537-42. PubMed ID: 11764104
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Congenital dyserythropoietic anemia].
    Uchida T; Kawachi Y; Ozaki S; Igaki T
    Nihon Rinsho; 1991 Mar; 49(3):593-8. PubMed ID: 2041185
    [No Abstract]   [Full Text] [Related]  

  • 20. Congenital dyserythropoiesis characterized by marked macrocytosis, vitamin B12- and folate-independent megaloblastic change and absence of the defining features of congenital dyserythropoietic anaemia types I or III.
    Wickramasinghe SN; Andrews VE; O'Hea AM
    Br J Haematol; 1996 Oct; 95(1):73-6. PubMed ID: 8857941
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.