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Literature DB >> 23632993

Disappearance of congenital noncompaction in hereditary cobalamin-C-deficiency 2.5 years after birth.

Josef Finsterer¹, Claudia Stöllberger.

Abstract

Entities: Disease

Year: 2013 PMID： 23632993 DOI： 10.1007/s10545-013-9612-4

Source DB: PubMed Journal: J Inherit Metab Dis ISSN： 0141-8955 Impact factor: 4.982

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3 in total

1. Noncompaction in mitochondrial myopathy: visible on microscopy but absent on macroscopic inspection.

Authors: Josef Finsterer; Claudia Stöllberger; Martin Grassberger; Daniel Gerger
Journal: Cardiology Date: 2013-05-31 Impact factor: 1.869

2. Noncompaction of the ventricular myocardium and hydrops fetalis in cobalamin C disease.

Authors: Pranoot Tanpaiboon; Jennifer L Sloan; Patrick F Callahan; Dorothea McAreavey; P Suzanne Hart; Uta Lichter-Konecki; Dina Zand; Charles P Venditti
Journal: JIMD Rep Date: 2012-12-29

Review 3. Cardiogenetics, neurogenetics, and pathogenetics of left ventricular hypertrabeculation/noncompaction.

Authors: Josef Finsterer
Journal: Pediatr Cardiol Date: 2009-01-29 Impact factor: 1.655

3 in total

1 in total

1. Right ventricular ablation as a therapeutic option for left ventricular hypertrabeculation / noncompaction.

Authors: Josef Finsterer; Claudia Stollberger
Journal: Indian Pacing Electrophysiol J Date: 2014-03-12

1 in total