Literature DB >> 13815022

An enzymic disorder in the erythrocytes of paroxysmal nocturnal haemoglobinuria: a deficiency in acetylcholinesterase activity.

G DE SANDRE, G GHIOTTO.   

Abstract

Entities:  

Keywords:  CHOLINESTERASE/blood; HEMOGLOBINURIA, PAROXYSMAL/blood

Mesh：

Substances：

Year:  1960        PMID： 13815022     DOI： 10.1111/j.1365-2141.1960.tb06215.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN： 0007-1048            Impact factor:   6.998


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  3 in total

1.  [Enzyme pathology of the blood cells].

Authors:  K U BLUM
Journal:  Blut       Date:  1962-06

Review 2.  Complement-mediated haemolysis and the role of blood transfusion in paroxysmal nocturnal haemoglobinuria.

Authors:  Tolulase Olutogun; Ilaria Cutini; Rosario Notaro; Lucio Luzzatto
Journal:  Blood Transfus       Date:  2015-02-02       Impact factor: 3.443

3.  Identification of three novel mutations in the PIG-A gene in paroxysmal nocturnal haemoglobinuria (PNH) patients.

Authors:  A Savoia; L Ianzano; C Lunardi; G De Sandre; M Carotenuto; P Musto; L Zelante
Journal:  Hum Genet       Date:  1996-01       Impact factor: 4.132
  3 in total

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