74 related articles for article (PubMed ID: 6672868)
1. [Familial congenital spherocytosis].
Figueroa R; Rivera M; Tamburrino E; Moroso M
Rev Chil Pediatr; 1983; 54(5):340-4. PubMed ID: 6672868
[No Abstract] [Full Text] [Related]
2. The combination of hereditary spherocytosis and heterozygous beta-thalassaemia. A family study.
Aksoy M; Erdem S
Acta Haematol; 1968; 39(3):183-91. PubMed ID: 4970089
[No Abstract] [Full Text] [Related]
3. [A case of hereditary spherocytosis with decrease of osmotic fragility of the erythrocytes after incubation at 37 degrees C for 24 hours].
Cassi E; Vsica U; Bombara R
Policlinico Med; 1966 Oct; 73(5):281-98. PubMed ID: 5995755
[No Abstract] [Full Text] [Related]
4. [Effect of splenoctomy on 3 cases of congenital spherocyt- osis].
Hadnagy C; Dóczy P
Med Klin; 1966 Mar; 61(10):371-4. PubMed ID: 5991678
[No Abstract] [Full Text] [Related]
5. [Flow-assisted differential diagnosis of hemolytic anemia with spherocytosis: a case report].
Won DI
Korean J Lab Med; 2010 Aug; 30(4):339-44. PubMed ID: 20805704
[TBL] [Abstract][Full Text] [Related]
6. [Silent forms of hereditary spherocytosis].
Brabec V; Cermák J; Jarolím P
Vnitr Lek; 1999 Oct; 45(10):594-7. PubMed ID: 10951867
[TBL] [Abstract][Full Text] [Related]
7. Hypoplastic crisis in hereditary spherocytosis: simultaneous occurrence in separated family members.
Pierce LE
South Med J; 1971 Apr; 64(4):431-4. PubMed ID: 5552014
[No Abstract] [Full Text] [Related]
8. Haemolysis in athletes due to hereditary spherocytosis.
Godal HC; Refsum HE
Scand J Haematol; 1979 Jan; 22(1):83-6. PubMed ID: 424701
[TBL] [Abstract][Full Text] [Related]
9. Comparison and evaluation of three screening tests of hereditary spherocytosis in Chinese patients.
Tao YF; Deng ZF; Liao L; Qiu YL; Chen WQ; Lin FQ
Ann Hematol; 2015 May; 94(5):747-51. PubMed ID: 25501660
[TBL] [Abstract][Full Text] [Related]
10. Experience with measurement of erythrocyte osmotic fragility by a dialysis technique in congenital hereditary spherocytosis.
Hendley JO; Porter FS
J Lab Clin Med; 1969 Feb; 73(2):219-28. PubMed ID: 5764018
[No Abstract] [Full Text] [Related]
11. [Familial hereditary spherocytosis. Study in a rural zone of Baja California Sur].
Güémes Sandoval JC; Cañedo Colado JA
Salud Publica Mex; 1983; 25(3):279-84. PubMed ID: 6612494
[No Abstract] [Full Text] [Related]
12. Comparison study of the eosin-5'-maleimide binding test, flow cytometric osmotic fragility test, and cryohemolysis test in the diagnosis of hereditary spherocytosis.
Park SH; Park CJ; Lee BR; Cho YU; Jang S; Kim N; Koh KN; Im HJ; Seo JJ; Park ES; Lee JW; Yoo KH; Jung HL
Am J Clin Pathol; 2014 Oct; 142(4):474-84. PubMed ID: 25239414
[TBL] [Abstract][Full Text] [Related]
13. Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis.
Agre P; Asimos A; Casella JF; McMillan C
N Engl J Med; 1986 Dec; 315(25):1579-83. PubMed ID: 3785322
[TBL] [Abstract][Full Text] [Related]
14. [Hereditary spherocytosis: a case of high familial incidence].
Rolando P; de Campora E; Langella G; Esposito R
Pediatria (Napoli); 1983; 91(2-3):303-10. PubMed ID: 6664737
[No Abstract] [Full Text] [Related]
15. Prenatal diagnosis of hereditary spherocytosis with osmotic fragility test.
Celkan T; Alhaj S
Indian Pediatr; 2008 Jan; 45(1):63-4. PubMed ID: 18250512
[No Abstract] [Full Text] [Related]
16. [Microspherocytosis. Erythroid profile and its relation with different laboratory tests].
Aixála MT; Sarandría CN
Medicina (B Aires); 2001; 61(4):417-23. PubMed ID: 11563170
[TBL] [Abstract][Full Text] [Related]
17. Partial pyruvate kinase deficiency aggravates the phenotypic expression of band 3 deficiency in a family with hereditary spherocytosis.
van Zwieten R; van Oirschot BA; Veldthuis M; Dobbe JG; Streekstra GJ; van Solinge WW; Schutgens RE; van Wijk R
Am J Hematol; 2015 Mar; 90(3):E35-9. PubMed ID: 25388786
[TBL] [Abstract][Full Text] [Related]
18. A novel L1340P mutation in the ANK1 gene is associated with hereditary spherocytosis?
Bogusławska DM; Heger E; Listowski M; Wasiński D; Kuliczkowski K; Machnicka B; Sikorski AF
Br J Haematol; 2014 Oct; 167(2):269-71. PubMed ID: 24903897
[No Abstract] [Full Text] [Related]
19. [Experience with the glycerol lysis test in acid medium in diagnosis of hereditary spherocytosis].
Mittler U; Radig K; Kluba U; Aumann V; Röppnack R
Kinderarztl Prax; 1993 Aug; 61(6):219-22. PubMed ID: 8411849
[TBL] [Abstract][Full Text] [Related]
20. [Clinical course of congenital spherocytosis in both affected parents and all of their children].
Krasowska I; Urban M; Pawłowska A
Pediatr Pol; 1978 Mar; 53(3):381-3. PubMed ID: 652426
[No Abstract] [Full Text] [Related]
[Next] [New Search]