Literature DB >> 10980645

Erythroid membrane protein defects in hereditary spherocytosis. A study of 62 Spanish cases.

M P Ricard, F Gilsanz, I Millan.   

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Year:  2000        PMID： 10980645

Source DB:  PubMed          Journal:  Haematologica        ISSN： 0390-6078            Impact factor:   9.941


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  3 in total

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.

Authors:  Chao Wang; Yazhou Cui; Yan Li; Xiao Liu; Jinxiang Han
Journal:  Intractable Rare Dis Res       Date:  2015-05

2.  Proteomic identification of erythrocyte membrane protein deficiency in hereditary spherocytosis.

Authors:  Selen Peker; Nejat Akar; Duygu Ozel Demiralp
Journal:  Mol Biol Rep       Date:  2011-06-26       Impact factor: 2.316

3.  Concomitant Hereditary Spherocytosis and Pyruvate Kinase Deficiency in a Spanish Family with Chronic Hemolytic Anemia: Contribution of Laser Ektacytometry to Clinical Diagnosis.

Authors:  Joan-Lluis Vives Corrons; Elena Krishnevskaya; Laura Montllor; Valentina Leguizamon; Marta Garcia Bernal
Journal:  Cells       Date:  2022-03-28       Impact factor: 6.600
  3 in total

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