Literature DB >> 25624984

Left ventricular noncompaction cardiomyopathy: adult association with 1p36 deletion syndrome.

James Lee1, Sarah Rinehart1, Venkateshewar Polsani1.   

Abstract

Entities:  

Keywords:  1p36 gene deletion; cardiomyopathy; left ventricular noncompaction cardiomyopathy; microdeletion syndrome

Mesh：

Year:  2014        PMID： 25624984      PMCID： PMC4300068          DOI： 10.14797/mdcj-10-4-258

Source DB:  PubMed          Journal:  Methodist Debakey Cardiovasc J        ISSN： 1947-6108


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  6 in total

Review 1.  Monosomy 1p36 deletion syndrome.

Authors:  Marzena Gajecka; Katherine L Mackay; Lisa G Shaffer
Journal:  Am J Med Genet C Semin Med Genet       Date:  2007-11-15       Impact factor: 3.908

2.  Left ventricular non-compaction: insights from cardiovascular magnetic resonance imaging.

Authors:  Steffen E Petersen; Joseph B Selvanayagam; Frank Wiesmann; Matthew D Robson; Jane M Francis; Robert H Anderson; Hugh Watkins; Stefan Neubauer
Journal:  J Am Coll Cardiol       Date:  2005-07-05       Impact factor: 24.094

3.  Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy.

Authors:  R Jenni; E Oechslin; J Schneider; C Attenhofer Jost; P A Kaufmann
Journal:  Heart       Date:  2001-12       Impact factor: 5.994

Review 4.  Noncompaction of the left ventricle: primary cardiomyopathy with an elusive genetic etiology.

Authors:  Michael V Zaragoza; Eloisa Arbustini; Jagat Narula
Journal:  Curr Opin Pediatr       Date:  2007-12       Impact factor: 2.856

5.  Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.

Authors:  Agatino Battaglia; H Eugene Hoyme; Bruno Dallapiccola; Elaine Zackai; Louanne Hudgins; Donna McDonald-McGinn; Nadia Bahi-Buisson; Corrado Romano; Charles A Williams; Lisa L Brailey; Lisa L Braley; Sameer M Zuberi; John C Carey
Journal:  Pediatrics       Date:  2008-02       Impact factor: 7.124

6.  Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.

Authors:  Anne-Karin Arndt; Sebastian Schafer; Jorg-Detlef Drenckhahn; M Khaled Sabeh; Eva R Plovie; Almuth Caliebe; Eva Klopocki; Gabriel Musso; Andreas A Werdich; Hermann Kalwa; Matthias Heinig; Robert F Padera; Katharina Wassilew; Julia Bluhm; Christine Harnack; Janine Martitz; Paul J Barton; Matthias Greutmann; Felix Berger; Norbert Hubner; Reiner Siebert; Hans-Heiner Kramer; Stuart A Cook; Calum A MacRae; Sabine Klaassen
Journal:  Am J Hum Genet       Date:  2013-06-13       Impact factor: 11.025
  6 in total
  1 in total

Review 1.  Left ventricular noncompaction cardiomyopathy: cardiac, neuromuscular, and genetic factors.

Authors:  Josef Finsterer; Claudia Stöllberger; Jeffrey A Towbin
Journal:  Nat Rev Cardiol       Date:  2017-01-12       Impact factor: 32.419
  1 in total

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