Literature DB >> 12858209

Homozygous alpha-thalassemia treated with intrauterine transfusions and postnatal hematopoietic stem cell transplantation.

I Thornley, L Lehmann, W S Ferguson, I Davis, E N Forman, E C Guinan.   

Abstract

Entities:  

Mesh：

Year:  2003        PMID： 12858209     DOI： 10.1038/sj.bmt.1704129

Source DB:  PubMed          Journal:  Bone Marrow Transplant        ISSN： 0268-3369            Impact factor:   5.483


× No keyword cloud information.
  5 in total

Review 1.  An international registry of survivors with Hb Bart's hydrops fetalis syndrome.

Authors:  Duantida Songdej; Christian Babbs; Douglas R Higgs
Journal:  Blood       Date:  2017-01-05       Impact factor: 22.113

Review 2.  Hydrops fetalis caused by homozygous alpha-thalassemia and Rh antigen alloimmunization: report of a survivor and literature review.

Authors:  Divya-Devi Joshi; H James Nickerson; Michael J McManus
Journal:  Clin Med Res       Date:  2004-11

Review 3.  Advances in the management of α-thalassemia major: reasons to be optimistic.

Authors:  Paulina Horvei; Tippi MacKenzie; Sandhya Kharbanda
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2021-12-10

4.  Fetal gene therapy of alpha-thalassemia in a mouse model.

Authors:  Xiao-Dong Han; Chin Lin; Judy Chang; Michel Sadelain; Y W Kan
Journal:  Proc Natl Acad Sci U S A       Date:  2007-05-11       Impact factor: 11.205

5.  Successful matched unrelated donor stem cell transplant in Hemoglobin Bart's disease.

Authors:  M Y Elsaid; C M Capitini; C A Diamond; M Porte; M Otto; K B DeSantes
Journal:  Bone Marrow Transplant       Date:  2016-06-13       Impact factor: 5.483
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.