125 related articles for article (PubMed ID: 3725428)
1. A case of congenital dyserythropoietic anemia in a male Chinese.
Szeto SC; Ng CS
Pathology; 1986 Jan; 18(1):165-8. PubMed ID: 3725428
[TBL] [Abstract][Full Text] [Related]
2. Congenital dyserythropoietic anemia type II associated with G6PD Seattle in a Sicilian child.
Gangarossa S; Romano V; Miraglia del Giudice E; Perrotta S; Iolascon A; Schiliro G
Acta Haematol; 1995; 93(1):36-9. PubMed ID: 7725848
[TBL] [Abstract][Full Text] [Related]
3. Congenital dyserythropoietic anaemia type II associated with a new type of G6PD deficiency (G6PD Gabrovizza).
Ventura A; Panizon F; Soranzo MR; Veneziano G; Sansone G; Testa U; Luzzatto L
Acta Haematol; 1984; 71(4):227-34. PubMed ID: 6426235
[TBL] [Abstract][Full Text] [Related]
4. [Congenital non spherocytic hemolytic anemia due to G-6PD deficiency: physiological and biochemical study of an unusual variant. Relationship to Benevento G-6PD].
Kahn A; Leger J; Boivin P; Hollard D; Hakim J
Biochimie; 1973; 55(9):1121-8. PubMed ID: 4150430
[No Abstract] [Full Text] [Related]
5. Glucose-6-phosphate dehydrogenase activity of erythrocytes in hemolytic anemia.
Maj S
Pol Med J; 1966; 5(5):975-80. PubMed ID: 5958807
[No Abstract] [Full Text] [Related]
6. Glucose 6 phosphate dehydrogenase deficiency: Description of a novel and de novo variant associated with chronic nonspherocytic hemolytic anemia.
Chaves A; Eandi Eberle S; Avalos Gomez V; Milanesio B; Fernandez D; Albero A; Aguirre F; Aizpurua L; Dieuzeide MP; Pepe C; Feliu-Torres A
Clin Biochem; 2020 Jul; 81():63-64. PubMed ID: 32387441
[No Abstract] [Full Text] [Related]
7. Nonimmune hydrops fetalis caused by G6PD deficiency hemolytic crisis and congenital dyserythropoietic anemia.
Molad M; Waisman D; Rotschild A; Auslander R; Kessel I; Soloviechick M; Goldberg Y; Shabad E
J Perinatol; 2013 Jun; 33(6):490-1. PubMed ID: 23719252
[TBL] [Abstract][Full Text] [Related]
8. Congenital dyserythropoietic anemia with ultrastructural features of type I and II.
Schuppler J; Cornu P; Krey G; Gudat F; Speck B
Blut; 1975 Nov; 31(5):271-82. PubMed ID: 1191780
[TBL] [Abstract][Full Text] [Related]
9. Congential dyserythropoietic anemia--type IV.
Benjamin JT; Rosse WF; Daldorf FG; McMillan CW
J Pediatr; 1975 Aug; 87(2):210-6. PubMed ID: 1097617
[TBL] [Abstract][Full Text] [Related]
10. Frequency of glucose 6 phosphate dehydrogenase deficiency and related hemolytic anemia in Riyadh, Saudi Arabia.
Gandapur AS; Qureshi F; Mustafa G; Baksh S; Ramzan M; Khan MA
J Ayub Med Coll Abbottabad; 2002; 14(3):24-6. PubMed ID: 12476860
[TBL] [Abstract][Full Text] [Related]
11. [Morphological studies of erythrocytes in congenital dyserythropoietic anemia type II].
Koehler M; Schmidt-Riese L; Brandeis WE
Acta Haematol Pol; 1990; 21(2):144-52. PubMed ID: 2131714
[TBL] [Abstract][Full Text] [Related]
12. [ON A CASE OF HEMOLYTIC ANEMIA DUE TO SULFAMETHOXYPYRIDAZINE IN A SUBJECT WITH ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY].
SALVIOLI GP
Clin Pediatr (Bologna); 1963 Dec; 45():963-71. PubMed ID: 14191932
[No Abstract] [Full Text] [Related]
13. [Congenital non-spherocytic hemolytic jaundice with glucose-6-phosphate dehydrogenase deficiency. 2 cases].
BOUSSER J; CHRISTOL D; BOIVIN P; MALLASSENET R; LODS JC
Nouv Rev Fr Hematol; 1963; 3():505-11. PubMed ID: 14014524
[No Abstract] [Full Text] [Related]
14. Identification of a Novel Mutation in the SEC23B Gene Associated With Congenital Dyserythropoietic Anemia Type II Through the Use of Next-generation Sequencing Panel in an Undiagnosed Case of Nonimmune Hereditary Hemolytic Anemia.
Aydin Koker S; Karapinar TH; Oymak Y; Bianchi P; Fermo E; Gozmen S; Vergin C
J Pediatr Hematol Oncol; 2018 Oct; 40(7):e421-e423. PubMed ID: 29846281
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. Studies of ineffective erythropoiesis and peripheral haemolysis in congenital dyserythropoietic anaemia type II.
Barosi G; Cazzola M; Stefanelli M; Ascari E
Br J Haematol; 1979 Oct; 43(2):243-50. PubMed ID: 508633
[TBL] [Abstract][Full Text] [Related]
17. Biosynthetic and structural studies of hemoglobin in a patient with congenital dyserythropoietic anemia type I.
Harkness DR; Villa L; Berman I; Wilson JB; Huisman TH
Hemoglobin; 1977; 1(7):663-77. PubMed ID: 914641
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Combined G-6PD and 6-PGD deficiency in a Hindu boy.
Dash S; Bhagwat AG
Acta Haematol; 1977; 57(6):351-3. PubMed ID: 407765
[TBL] [Abstract][Full Text] [Related]
20. [CHRONIC, NON-SPHEROCYTIC HEMOLYTIC JAUNDICE IN TOTAL ABSENCE OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE ACTIVITY OF THE ERYTHROCYTES].
HENNEMANN HH; ESSERS U; STECHER G
Klin Wochenschr; 1964 Dec; 42():1250. PubMed ID: 14332708
[No Abstract] [Full Text] [Related]
[Next] [New Search]