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3. [Hereditary spherocytosis. Report of 37 cases]. Sabrafen JS; Garcia San Miguel J; Rozman C Sangre (Barc); 1971; 16(1):7-31. PubMed ID: 5577374 [No Abstract] [Full Text] [Related]
4. [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]
5. 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]
6. [Current data on the pathogenesis of hereditary spherocytosis (Minkowski-Shauffard's anemia) (review of the literature and personal study)]. Kovalev IuR; Shabalov NP; Iuzhanina TA; Borisova TZ Probl Gematol Pereliv Krovi; 1970 Oct; 15(10):34-9. PubMed ID: 4255204 [No Abstract] [Full Text] [Related]
7. Incidence of hereditary spherocytosis in a population of jaundiced neonates. Saada V; Cynober T; Brossard Y; Schischmanoff PO; Sender A; Cohen H; Delaunay J; Tchernia G Pediatr Hematol Oncol; 2006; 23(5):387-97. PubMed ID: 16728359 [TBL] [Abstract][Full Text] [Related]
8. Rheologic studies of deoxygenated normal and hereditary spherocytosis blood and separated erythrocytes. Brereton W; Murphy JR J Lab Clin Med; 1974 Jan; 83(1):112-8. PubMed ID: 4808649 [No Abstract] [Full Text] [Related]
9. [Familial hereditary spherocytosis in the pediatric patient]. Güemez-Sandoval JC; Sierra-Cedillo JC; de León-Medina NM; Cardoza-Macías R; Cardoza-Macías F Bol Med Hosp Infant Mex; 1985 Jul; 42(7):440-4. PubMed ID: 2412570 [No Abstract] [Full Text] [Related]
10. Ankyrin deficiency is the most common defect in dominant and non dominant hereditary spherocytosis. Lanciotti M; Perutelli P; Valetto A; Di Martino D; Mori PG Haematologica; 1997; 82(4):460-2. PubMed ID: 9299863 [No Abstract] [Full Text] [Related]
11. Clinical profile of hereditary spherocytosis in North India. Panigrahi I; Phadke SR; Agarwal A; Gambhir S; Agarwal SS J Assoc Physicians India; 2002 Nov; 50():1360-7. PubMed ID: 12583462 [TBL] [Abstract][Full Text] [Related]
12. Correction of Fallot's tetralogy in a patient suffering from hereditary spherocytosis. Moyes DG; Holloway AM; Hutton WS S Afr Med J; 1974 Jul; 48(36):1535-6. PubMed ID: 4419248 [No Abstract] [Full Text] [Related]
13. [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]
14. [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]
15. Association of hereditary spherocytosis with familial adenomatous polyposis in a pedigree: a new syndrome or coincidence? Hirata K; Matsumoto K; Gondo K; Matsuzaki K; Akahane K; Higure A; Nakayama Y; Okamoto K; Konishi T; Nagata N; Itoh H J Gastroenterol; 2003; 38(1):79-81. PubMed ID: 12560926 [TBL] [Abstract][Full Text] [Related]
16. Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis. Eber SW; Gonzalez JM; Lux ML; Scarpa AL; Tse WT; Dornwell M; Herbers J; Kugler W; Ozcan R; Pekrun A; Gallagher PG; Schröter W; Forget BG; Lux SE Nat Genet; 1996 Jun; 13(2):214-8. PubMed ID: 8640229 [TBL] [Abstract][Full Text] [Related]
17. Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect. Mariani M; Barcellini W; Vercellati C; Marcello AP; Fermo E; Pedotti P; Boschetti C; Zanella A Haematologica; 2008 Sep; 93(9):1310-7. PubMed ID: 18641031 [TBL] [Abstract][Full Text] [Related]
18. Steroid therapy may be effective in augmenting hemoglobin levels during hemolytic crises in children with hereditary spherocytosis. Ballin A; Waisbourd-Zinman O; Saab H; Yacobovich J; Zoldan M; Barzilai-Birenbaum S; Yaniv I; Tamary H Pediatr Blood Cancer; 2011 Aug; 57(2):303-5. PubMed ID: 21480468 [TBL] [Abstract][Full Text] [Related]
19. One more red-cell abnormality. Lancet; 1969 Jul; 2(7611):94. PubMed ID: 4182772 [No Abstract] [Full Text] [Related]
20. 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] [Next] [New Search]