scholarly journals Assessment of GeneticsMutations in Genes CDAN1, SEC23B and Dell-15q22 in Inducate Congenital Dyserythropoietic Anemia Syndrome

2019 ◽  
Vol 4 (1) ◽  
pp. 1-3
Haematologica ◽  
2017 ◽  
Vol 102 (9) ◽  
pp. e371-e374 ◽  
Author(s):  
Roberta Russo ◽  
Immacolata Andolfo ◽  
Antonella Gambale ◽  
Gianluca De Rosa ◽  
Francesco Manna ◽  
...  

2002 ◽  
Vol 70 (1) ◽  
pp. 72-76 ◽  
Author(s):  
Erica Sigler ◽  
Dina Shaft ◽  
Mordechai Shtalrid ◽  
Lev Shvidel ◽  
Alain Berrebi ◽  
...  

PEDIATRICS ◽  
1973 ◽  
Vol 51 (5) ◽  
pp. 957-958
Author(s):  
G. Bennett Humphrey ◽  
Bahaod-Din Mojab ◽  
Ingomar Mutz

Reading the excellent article by Drs. Murphy and Oski, "Congenital Dyserythropoietic Anemia (CDA)",1 which further defines type II, produced a sense of deja vu. In the 1950s, nonspherocytic, hemolytic anemias (HNHA) were categorized as type I and II based on the in vitro autohemolysis test.2 This group of anemias has subsequently been demonstrated to be due to a series of enzymatic abnormalities in carbohydrate metabolism.3 In CDA, the morphological characteristics which define types I, II, and III probably reflect nuclear rather than cytoplasmic abnormalities.


2014 ◽  
Vol 53 (4) ◽  
pp. 272-273 ◽  
Author(s):  
Joo Y. Song ◽  
Anjali Pawar ◽  
Christin Collins

Blood ◽  
1997 ◽  
Vol 89 (8) ◽  
pp. 3068-3068 ◽  
Author(s):  
W.K. Hofmann ◽  
J.P. Kaltwasser ◽  
D. Hoelzer ◽  
P. Nielsen ◽  
E.E. Gabbe

Sign in / Sign up

Export Citation Format

Share Document