Literature DB >> 24493316

Hypertrophic cardiomyopathy with familial chylomicronemia syndrome: is it an incidental finding or a new association?

Mehmet Gündüz1, Nevra Koç, Eda Özaydın, Filiz Ekici.   

Abstract

Entities:  

Mesh：

Year:  2014        PMID： 24493316     DOI： 10.1007/s12098-013-1331-1

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN： 0019-5456            Impact factor:   1.967


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  5 in total

1.  Familial chylomicronemia syndrome.

Authors:  M K Mohandas; J Jemila; A S Ajith Krishnan; T Thomas George
Journal:  Indian J Pediatr       Date:  2005-02       Impact factor: 1.967

Review 2.  Monogenic pediatric dyslipidemias: classification, genetics and clinical spectrum.

Authors:  Amit R Rahalkar; Robert A Hegele
Journal:  Mol Genet Metab       Date:  2007-11-26       Impact factor: 4.797

3.  Glycogen storage diseases presenting as hypertrophic cardiomyopathy.

Authors:  Michael Arad; Barry J Maron; Joshua M Gorham; Walter H Johnson; J Philip Saul; Antonio R Perez-Atayde; Paolo Spirito; Gregory B Wright; Ronald J Kanter; Christine E Seidman; J G Seidman
Journal:  N Engl J Med       Date:  2005-01-27       Impact factor: 91.245

Review 4.  Novel LPL mutations associated with lipoprotein lipase deficiency: two case reports and a literature review.

Authors:  Amit R Rahalkar; Fiona Giffen; Bryan Har; Josephine Ho; Katherine M Morrison; John Hill; Jian Wang; Robert A Hegele; Tisha Joy
Journal:  Can J Physiol Pharmacol       Date:  2009-03       Impact factor: 2.273

Review 5.  Molecular mechanisms of inherited cardiomyopathies.

Authors:  Diane Fatkin; Robert M Graham
Journal:  Physiol Rev       Date:  2002-10       Impact factor: 37.312
  5 in total

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