Serum haptoglobin and hemopexin levels are depleted in pediatric sickle cell disease patients

Rayra Pereira Santiago, Caroline Conceição Guarda, Camylla Vilas Boas Figueiredo, Luciana Magalhaes Fiuza, Milena Magalhães Aleluia, Corynne Stephanie Ahouefa Adanho, Magda Oliveira Seixas Carvalho, Thassila Nogueira Pitanga, Dalila Luciola Zanette, Isa Menezes Lyra, Valma Maria Lopes Nascimento, Gregory M. Vercellotti, John D. Belcher, Marilda Souza Goncalves

Research output: Contribution to journalLetterpeer-review

6 Scopus citations
Original languageEnglish (US)
Pages (from-to)34-36
Number of pages3
JournalBlood Cells, Molecules, and Diseases
Volume72
DOIs
StatePublished - Sep 2018

Bibliographical note

Funding Information:
This work was funded by FAPESB SUS0034/2013 and 8133/2014 and by NIH R01 HL114567 .

Funding Information:
JDB and GMV receive research funding from CSL Behring for work on haptoglobin and hemopexin supplementation in sickle cell disease.

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