Literature DB >> 22703120

Incidental detection of Chiari malformation in Fanconi anaemia.

S Deepak Amalnath1, Rama Subramanian1, R P Swaminathan1, N Indumathi2.   

Abstract

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Year:  2012        PMID： 22703120     DOI： 10.1111/j.1365-2141.2012.09195.x

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


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  3 in total

1.  Fanconi anemia: correlating central nervous system malformations and genetic complementation groups.

Authors:  Benjamin A Johnson-Tesch; Rakhee S Gawande; Lei Zhang; Margaret L MacMillan; David R Nascene
Journal:  Pediatr Radiol       Date:  2017-03-10

2.  Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation.

Authors:  Eric F Lock; Karen L Soldano; Melanie E Garrett; Heidi Cope; Christina A Markunas; Herbert Fuchs; Gerald Grant; David B Dunson; Simon G Gregory; Allison E Ashley-Koch
Journal:  BMC Genomics       Date:  2015-01-22       Impact factor: 3.969

3.  Central nervous system abnormalities in Fanconi anaemia: patterns and frequency on magnetic resonance imaging.

Authors:  Stavros M Stivaros; Robert Alston; Neville B Wright; Kate Chandler; Denise Bonney; Robert F Wynn; Andrew M Will; Maqsood Punekar; Sean Loughran; John-Paul Kilday; Detlev Schindler; Leena Patel; Stefan Meyer
Journal:  Br J Radiol       Date:  2015-09-15       Impact factor: 3.039
  3 in total

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