183 related articles for article (PubMed ID: 25984425)
1. A systematic review of hereditary spherocytosis reported in Chinese biomedical journals from 1978 to 2013 and estimation of the prevalence of the disease using a disease model.
Wang C; Cui Y; Li Y; Liu X; Han J
Intractable Rare Dis Res; 2015 May; 4(2):76-81. PubMed ID: 25984425
[TBL] [Abstract][Full Text] [Related]
2. Using inpatient data to estimate the prevalence of Wegener's granulomatosis in China.
Liu X; Cui Y; Li Y; Wang C; Zhao H; Han J
Intractable Rare Dis Res; 2016 Feb; 5(1):31-5. PubMed ID: 26989646
[TBL] [Abstract][Full Text] [Related]
3. Misdiagnosis of two cases of hereditary spherocytosis in a family and review of published reports.
Deng Z; Liao L; Yang W; Lin F
Clin Chim Acta; 2015 Feb; 441():6-9. PubMed ID: 25485852
[TBL] [Abstract][Full Text] [Related]
4. Hypophosphatemic Rickets in Colombia: A Prevalence-Estimation Model in Rare Diseases. 2018.
Huertas-Quintero JA; Losada-Trujillo N; Cuellar-Ortiz DA; Velasco-Parra HM
Lancet Reg Health Am; 2022 Mar; 7():100131. PubMed ID: 36777652
[TBL] [Abstract][Full Text] [Related]
5. Estimating epidemiological data of Multiple sclerosis using hospitalized data in Shandong Province, China.
Liu X; Cui Y; Han J
Orphanet J Rare Dis; 2016 Jun; 11(1):73. PubMed ID: 27259479
[TBL] [Abstract][Full Text] [Related]
6. Osmotic gradient ektacytometry: A valuable screening test for hereditary spherocytosis and other red blood cell membrane disorders.
Llaudet-Planas E; Vives-Corrons JL; Rizzuto V; Gómez-Ramírez P; Sevilla Navarro J; Coll Sibina MT; García-Bernal M; Ruiz Llobet A; Badell I; Velasco-Puyó P; Dapena JL; Mañú-Pereira MM
Int J Lab Hematol; 2018 Feb; 40(1):94-102. PubMed ID: 29024480
[TBL] [Abstract][Full Text] [Related]
7. Prevalence of scleroderma in Spain: an approach for estimating rare disease prevalence using a disease model.
Villaverde-Hueso A; de la Paz MP; Martín-Arribas MC; Sánchez-Valle E; Ramírez-González A; Biairdi P
Pharmacoepidemiol Drug Saf; 2008 Nov; 17(11):1100-7. PubMed ID: 18816486
[TBL] [Abstract][Full Text] [Related]
8. Cryohemolysis test as a diagnostic tool for hereditary spherocytosis.
Iglauer A; Reinhardt D; Schröter W; Pekrun A
Ann Hematol; 1999 Dec; 78(12):555-7. PubMed ID: 10647879
[TBL] [Abstract][Full Text] [Related]
9. Interaction of hereditary spherocytosis and alpha thalassaemia: a family study.
Li CK; Ng MH; Cheung KL; Lam TK; Shing MM
Acta Haematol; 1994; 91(4):201-5. PubMed ID: 7976119
[TBL] [Abstract][Full Text] [Related]
10. Aplastic crisis associated with parvovirus B19 in an adult with hereditary spherocytosis.
Beland SS; Daniel GK; Menard JC; Miller NM
J Ark Med Soc; 1997 Sep; 94(4):163-4. PubMed ID: 9308316
[TBL] [Abstract][Full Text] [Related]
11. Italian cancer figures--Report 2015: The burden of rare cancers in Italy.
; Busco S; Buzzoni C; Mallone S; Trama A; Castaing M; Bella F; Amodio R; Bizzoco S; Cassetti T; Cirilli C; Cusimano R; De Angelis R; Fusco M; Gatta G; Gennaro V; Giacomin A; Giorgi Rossi P; Mangone L; Mannino S; Rossi S; Pierannunzio D; Tavilla A; Tognazzo S; Tumino R; Vicentini M; Vitale MF; Crocetti E; Dal Maso L
Epidemiol Prev; 2016; 40(1 Suppl 2):1-120. PubMed ID: 26951748
[TBL] [Abstract][Full Text] [Related]
12. Iron overload in hereditary spherocytosis: association with HLA-linked hemochromatosis.
Edwards CQ; Skolnick MH; Dadone MM; Kushner JP
Am J Hematol; 1982 Sep; 13(2):101-9. PubMed ID: 7137169
[TBL] [Abstract][Full Text] [Related]
13. A tetranucleotide deletion in the ANK1 gene causes hereditary spherocytosis; a case of misdiagnosis.
Zhu F; Liang M; Xu L; Peng Z; Cai D; Wei X; Lin L; Shang X
Gene; 2020 Feb; 726():144226. PubMed ID: 31669644
[TBL] [Abstract][Full Text] [Related]
14. Previously undiagnosed hereditary spherocytosis in a patient with jaundice and pyelonephritis: a case report.
Tateno Y; Suzuki R; Kitamura Y
J Med Case Rep; 2016 Dec; 10(1):337. PubMed ID: 27906107
[TBL] [Abstract][Full Text] [Related]
15. [Hemochromatosis associated with hereditary spherocytosis].
López DE; Kohan M; Ferreño D; Raffa MP; Prytyka A
Acta Gastroenterol Latinoam; 1997; 27(4):267-70. PubMed ID: 9580054
[TBL] [Abstract][Full Text] [Related]
16. Absence of phosphorylation-induced gelation of erythrocyte membrane skeletons: a diagnostic tool for hereditary spherocytosis.
Armbrust R; Eber SW; Schröter W
Ann Hematol; 1992 Feb; 64(2):93-6. PubMed ID: 1554801
[TBL] [Abstract][Full Text] [Related]
17. Hereditary Spherocytosis in a Middle-aged Man Complicated with Common Bile Duct Stones.
Sawahara H; Iwamuro M; Harada R; Yoshioka M; Niguma T; Mimura T; Yamamoto K
Intern Med; 2015; 54(12):1509-12. PubMed ID: 26073240
[TBL] [Abstract][Full Text] [Related]
18. Protein C deficiency leading to pulmonary thromboembolism in a patient with hereditary spherocytosis.
Bhargava K; Chandra N; Omar AK; Mathur A
Indian Heart J; 2006; 58(6):444-6. PubMed ID: 19057057
[TBL] [Abstract][Full Text] [Related]
19. Tokyo-1 Mutation: Hereditary Spherocytosis in a Hispanic Newborn Presenting as Early Onset Severe Hyperbilirubinemia.
Tan AW; Leung P; Patil UP
Fetal Pediatr Pathol; 2018 Aug; 37(4):296-300. PubMed ID: 30207817
[TBL] [Abstract][Full Text] [Related]
20. Topological Structures and Membrane Nanostructures of Erythrocytes after Splenectomy in Hereditary Spherocytosis Patients via Atomic Force Microscopy.
Li Y; Lu L; Li J
Cell Biochem Biophys; 2016 Sep; 74(3):365-71. PubMed ID: 27557951
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
