Literature DB >> 7741575

Paroxysmal nocturnal haemoglobinuria and Budd-Chiari syndrome.

H A Wyatt1, A P Mowat, M Layton.   

Abstract

An 11 year old boy developed pancytopenia, haemolysis, and Budd-Chiari syndrome. The venous thrombosis extended to involve other intra-abdominal vessels before paroxysmal nocturnal haemoglobinuria was recognised as the underlying haematological abnormality. Earlier diagnosis would have made curative bone marrow transplantation a possibility.

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Year:  1995        PMID: 7741575      PMCID: PMC1511044          DOI: 10.1136/adc.72.3.241

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  3 in total

Review 1.  Phosphatidylinositol-linked proteins and paroxysmal nocturnal hemoglobinuria.

Authors:  W F Rosse
Journal:  Blood       Date:  1990-04-15       Impact factor: 22.113

2.  Marrow transplantation for paroxysmal nocturnal hemoglobinuria.

Authors:  K Kawahara; R P Witherspoon; R Storb
Journal:  Am J Hematol       Date:  1992-04       Impact factor: 10.047

3.  Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria.

Authors:  J Takeda; T Miyata; K Kawagoe; Y Iida; Y Endo; T Fujita; M Takahashi; T Kitani; T Kinoshita
Journal:  Cell       Date:  1993-05-21       Impact factor: 41.582

  3 in total
  2 in total

Review 1.  Paroxysmal nocturnal hemoglobinuria in children.

Authors:  Marry M van den Heuvel-Eibrink
Journal:  Paediatr Drugs       Date:  2007       Impact factor: 3.022

2.  Paroxysmal nocturnal hemoglobinuria in childhood and adolescence--a retrospective analysis of 18 cases.

Authors:  Rahul Naithani; Manoranjan Mahapatra; Pankhi Dutta; Rajat Kumar; Hara Prasad Pati; Ved Prakash Choudhry
Journal:  Indian J Pediatr       Date:  2008-08-31       Impact factor: 1.967

  2 in total

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