Literature DB >> 6132037

Successful bone-marrow transplantation for reticular dysgenesis.

R J Levinsky, K Tiedeman.   

Abstract

A male infant with reticular dysgenesis received a bone-marrow transplant from his HLA-identical brother. Severe graft-versus-host disease developed but he responded to high-dose methylprednisolone. 3 years after grafting, the child is thriving with full haematological reconstitution and normal cell-mediated and humoral immunity. This is the first report of the survival beyond 17 weeks of a child with reticular dysgenesis.

Entities:  

Mesh：

Year:  1983        PMID： 6132037     DOI： 10.1016/s0140-6736(83)91968-2

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


  7 in total

Review 1.  Severe combined immunodeficiencies (SCID).

Authors:  A Fischer
Journal:  Clin Exp Immunol       Date:  2000-11       Impact factor: 4.330

Review 2.  Neutrophil disorders and their management.

Authors:  R Lakshman; A Finn
Journal:  J Clin Pathol       Date:  2001-01       Impact factor: 3.411

3.  Reticular dysgenesis: international survey on clinical presentation, transplantation, and outcome.

Authors:  Manfred Hoenig; Chantal Lagresle-Peyrou; Ulrich Pannicke; Luigi D Notarangelo; Fulvio Porta; Andrew R Gennery; Mary Slatter; Morton J Cowan; Polina Stepensky; Hamoud Al-Mousa; Daifulah Al-Zahrani; Sung-Yun Pai; Waleed Al Herz; Hubert B Gaspar; Paul Veys; Koichi Oshima; Kohsuke Imai; Hiromasa Yabe; Lenora M Noroski; Nico M Wulffraat; Karl-Walter Sykora; Pere Soler-Palacin; Hideki Muramatsu; Mariam Al Hilali; Despina Moshous; Klaus-Michael Debatin; Catharina Schuetz; Eva-Maria Jacobsen; Ansgar S Schulz; Klaus Schwarz; Alain Fischer; Wilhelm Friedrich; Marina Cavazzana
Journal:  Blood       Date:  2017-03-22       Impact factor: 22.113

Review 4.  Displacement bone marrow transplantation for some inborn errors.

Authors:  J R Hobbs
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

5.  Severe combined immunodeficiency (SCID) associated neutropenia: a lesson from monozygotic twins.

Authors:  T Niehues; K Schwarz; M Schneider; H Schroten; E Schröder; V Stephan; V Wahn
Journal:  Arch Dis Child       Date:  1996-04       Impact factor: 3.791

6.  Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness.

Authors:  Chantal Lagresle-Peyrou; Emmanuelle M Six; Capucine Picard; Frédéric Rieux-Laucat; Vincent Michel; Andrea Ditadi; Corinne Demerens-de Chappedelaine; Estelle Morillon; Françoise Valensi; Karen L Simon-Stoos; James C Mullikin; Lenora M Noroski; Céline Besse; Nicolas M Wulffraat; Alina Ferster; Manuel M Abecasis; Fabien Calvo; Christine Petit; Fabio Candotti; Laurent Abel; Alain Fischer; Marina Cavazzana-Calvo
Journal:  Nat Genet       Date:  2008-11-30       Impact factor: 38.330

Review 7.  The inherited bone marrow failure syndromes.

Authors:  S Deborah Chirnomas; Gary M Kupfer
Journal:  Pediatr Clin North Am       Date:  2013-12       Impact factor: 3.278
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.