Literature DB >> 2880182

Ultrastructure of liver in inherited disorders of fat oxidation.

B D Lake, P T Clayton, J V Leonard, A K Bhuiyan, K Bartlett, A A Green.   

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Year:  1987        PMID： 2880182     DOI： 10.1016/s0140-6736(87)91752-1

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


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  5 in total

1.  Clinical and biological features at diagnosis in mitochondrial fatty acid beta-oxidation defects: a French pediatric study of 187 patients.

Authors:  Julien Baruteau; Philippe Sachs; Pierre Broué; Michèle Brivet; Hendy Abdoul; Christine Vianey-Saban; Hélène Ogier de Baulny
Journal:  J Inherit Metab Dis       Date:  2012-10-03       Impact factor: 4.982

Review 2.  Secondary alterations of human hepatocellular peroxisomes.

Authors:  D De Craemer
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

3.  Post-mortem visualization of peroxisomes in rat and in human liver.

Authors:  D De Craemer; M Espeel; M Langendries; R B Schutgens; T Hashimoto; F Roels
Journal:  Histochem J       Date:  1990-01

4.  Medium-chain acyl CoA dehydrogenase deficiency: electron microscopic differentiation from Reye syndrome.

Authors:  R Santer; E Schmidt-Sommerfeld; Y K Leung; J E Fischer; E Lebenthal
Journal:  Eur J Pediatr       Date:  1990-12       Impact factor: 3.183

Review 5.  Liver pathology and immunocytochemistry in congenital peroxisomal diseases: a review.

Authors:  F Roels; M Espeel; D De Craemer
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982
  5 in total

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