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Pediatric Pathology & Laboratory Medicine Volume 17, 1997 - Issue 2
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Original Article

Congenital Alveolar Proteinosis in the Netherlands: A Report of Five Cases with Immunohistochemical and Genetic Studies on Surfactant Apoproteins

Alfred A. de la Fuente Regional Pathology Laboratory, Enschede, The Netherlands
,
Wim F. Voorhout Laboratory of Veterinary Biochemistry, Department of Functional Morphology, School of Veterinary Medicine, Utrecht University, The Netherlands
&
Daphne E. deMello Department of Pathology, Cardinal Glennon Childrens Hospital, St. Louis University, St Louis, Missouri, USA
Pages 221-231 | Received 30 May 1995, Accepted 24 May 1996, Published online: 16 Apr 2010

Citations (7)

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Read on this site (2)

Sabina A Antoniu. (2010) GM-CSF pathway correction in pulmonary alveolar proteinosis. Expert Opinion on Biological Therapy 10:9, pages 1357-1365.
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Daphne E. deMello & Zhenwu Lin. (2001) Pulmonary Alveolar Proteinosis: A Review. Pediatric Pathology & Molecular Medicine 20:5, pages 413-432.
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Articles from other publishers (5)

Lawrence M. Nogee. 2011. Fetal and Neonatal Physiology. Fetal and Neonatal Physiology 1168 1180 .
Susan E. Wert, Jeffrey A. Whitsett & Lawrence M. Nogee. (2011) Genetic Disorders of Surfactant Dysfunction. Pediatric and Developmental Pathology 12:4, pages 253-274.
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Elisabeth Bruder, Jörg Hofmeister, Charalampos Aslanidis, Jürg Hammer, Lukas Bubendorf, Gerd Schmitz, Alex Rufle & Christoph Bührer. (2007) Ultrastructural and molecular analysis in fatal neonatal interstitial pneumonia caused by a novel ABCA3 mutation. Modern Pathology 20:10, pages 1009-1018.
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A. G. Kaspers, R. M. vanElburg & W. P. F. Fetter. (2000) Een voldragen pasgeborene met surfactansproteïne B-deficiëntie. Tijdschrift voor kindergeneeskunde 68:5, pages 71-74.
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Mohammed Tredano, Ruurd M. van Elburg, Ageeth G. Kaspers, Luc J. Zimmermann, Claude Houdayer, Pierre Aymard, William M. Hull, Jeffrey A. Whitsett, Jacques Elion, Matthias Griese & Michel Bahuau. (1999) CompoundSFTPB 1549C?GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency. Human Mutation 14:6, pages 502-509.
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