Literature DB >> 7552601

Fatal familial surfactant protein B deficiency.

R Ball, P A Chetcuti, D Beverley.   

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Year:  1995        PMID： 7552601      PMCID： PMC2528373          DOI： 10.1136/fn.73.1.f53

Source DB:  PubMed          Journal:  Arch Dis Child Fetal Neonatal Ed        ISSN： 1359-2998            Impact factor:   5.747


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  3 in total

1.  Brief report: deficiency of pulmonary surfactant protein B in congenital alveolar proteinosis.

Authors:  L M Nogee; D E de Mello; L P Dehner; H R Colten
Journal:  N Engl J Med       Date:  1993-02-11       Impact factor: 91.245

2.  A mutation in the surfactant protein B gene responsible for fatal neonatal respiratory disease in multiple kindreds.

Authors:  L M Nogee; G Garnier; H C Dietz; L Singer; A M Murphy; D E deMello; H R Colten
Journal:  J Clin Invest       Date:  1994-04       Impact factor: 14.808

3.  Molecular and phenotypic variability in the congenital alveolar proteinosis syndrome associated with inherited surfactant protein B deficiency.

Authors:  D E deMello; L M Nogee; S Heyman; H F Krous; M Hussain; T A Merritt; W Hsueh; J E Haas; K Heidelberger; R Schumacher
Journal:  J Pediatr       Date:  1994-07       Impact factor: 4.406
  3 in total
  2 in total

Review 1.  Surfactant apoprotein B deficiency.

Authors:  P A Chetcuti; R J Ball
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  1995-11       Impact factor: 5.747

2.  Surfactant Protein B Deficiency Caused by Homozygous C248X Mutation-A Case Report and Review of the Literature.

Authors:  Stefan Kurath-Koller; Bernhard Resch; Raimund Kraschl; Christian Windpassinger; Ernst Eber
Journal:  AJP Rep       Date:  2015-03-02
  2 in total

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