Changing trends of splenectomy in hereditary spherocytosis: The experience of a reference Centre in the last 40 years-Reference-Cited by-同舟云学术

Changing trends of splenectomy in hereditary spherocytosis: The experience of a reference Centre in the last 40 years

Published:2022-03-11 Issue:5 Volume:198 Page:912-915
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Vercellati Cristina¹^ORCID,Zaninoni Anna¹^ORCID,Marcello Anna P.¹^ORCID,Fermo Elisa¹^ORCID,Fattizzo Bruno¹^ORCID,Giannotta Juri A.¹^ORCID,Bianchi Paola¹^ORCID,Zanella Alberto¹,Barcellini Wilma¹^ORCID

Affiliation:

1. Hematology Unit Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico Milan Italy

Funder

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.18106

Reference15 articles.

1. Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect

2. Variable clinical severity of hereditary spherocytosis: Relation to erythrocytic spectrin concentration, osmotic fragility, and autohemolysis

3. Hereditary spherocytosis—defects in proteins that connect the membrane skeleton to the lipid bilayer

4. The molecular basis of hereditary red cell membrane disorders

5. Recommendations regarding splenectomy in hereditary hemolytic anemias

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