Knowledge insufficient: the management of haemoglobin SC disease-Reference-Cited by-同舟云学术

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Knowledge insufficient: the management of haemoglobin SC disease

Published:2016-12-16 Issue:4 Volume:176 Page:515-526
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Pecker Lydia H.¹²,Schaefer Beverly A.³,Luchtman-Jones Lori³

Affiliation:

1. Center for Cancer and Blood Disorders; Children's National Medical Center; Washington DC USA

2. Department of Pediatrics; The George Washington University School of Medicine and Health Sciences; Washington DC USA

3. Cancer and Blood Diseases Institute; Division of Hematology; Cincinnati Children's Hospital Medical Center; Cincinnati OH USA

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.14444/fullpdf

Reference122 articles.

1. Priapism in sickle-cell disease; incidence, risk factors and complications - an international multicentre study;Adeyoju;BJU International,2002

2. Plasma levels of some coagulation parameters in steady state HBSC disease patients;Ajuwon;The Pan African Medical Journal,2014

3. Bone involvement in sickle cell disease;Almeida;British Journal of Haematology,2005

4. How I treat priapism;Anele;Blood,2015

5. Acute splenic complications in children with sickle cell-hemoglobin C disease;Aquino;The Journal of Pediatrics,1997

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2. Automated red blood cell exchange with a post‐procedure haematocrit targeted at 34% in the chronic management of sickle cell disease;British Journal of Haematology;2024-07-30

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4. Seeing haemoglobin SC: Challenging the misperceptions;British Journal of Haematology;2024-06-23

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