Literature DB >> 4103092

Kell phenotypes in chronic granulomatous disease: a potential trnsfusion hazard.

E R Giblett, S J Klebanoff, S H Pincus.   

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Year:  1971        PMID： 4103092     DOI： 10.1016/s0140-6736(71)91738-7

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


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  4 in total

Review 1.  Genetic model for the Rh blood-group system.

Authors:  R E Rosenfield; F H Allen; P Rubinstein
Journal:  Proc Natl Acad Sci U S A       Date:  1973-05       Impact factor: 11.205

2.  Staphylococci surviving intracellularly in phagocytes from patients suffering from chronic granulomatous disease are killed in vitro by antibiotics encapsulated in liposomes.

Authors:  J Roesler; S Hockertz; B Vogt; M L Lohmann-Matthes
Journal:  J Clin Invest       Date:  1991-10       Impact factor: 14.808

3.  Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.

Authors:  U Francke; H D Ochs; B de Martinville; J Giacalone; V Lindgren; C Distèche; R A Pagon; M H Hofker; G J van Ommen; P L Pearson
Journal:  Am J Hum Genet       Date:  1985-03       Impact factor: 11.025

Review 4.  NADPH Oxidase Deficiency: A Multisystem Approach.

Authors:  Giuliana Giardino; Maria Pia Cicalese; Ottavia Delmonte; Maddalena Migliavacca; Boaz Palterer; Lorenzo Loffredo; Emilia Cirillo; Vera Gallo; Francesco Violi; Claudio Pignata
Journal:  Oxid Med Cell Longev       Date:  2017-12-21       Impact factor: 6.543
  4 in total

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