Hypertrophic cardiomyopathy in mitochondrial disorders: description of an uncommon clinical case.

about

Hypertrophic cardiomyopathy in mitochondrial disorders: description of an uncommon clinical case.

Item

http://www.wikidata.org/entity/Q54099566

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

Hypertrophic cardiomyopathy in ...... of an uncommon clinical case.

@en

Hypertrophic cardiomyopathy in ...... of an uncommon clinical case.

@nl

type

Item

label

Hypertrophic cardiomyopathy in ...... of an uncommon clinical case.

@en

Hypertrophic cardiomyopathy in ...... of an uncommon clinical case.

@nl

prefLabel

Hypertrophic cardiomyopathy in ...... of an uncommon clinical case.

@en

Hypertrophic cardiomyopathy in ...... of an uncommon clinical case.

@nl

P1476

Hypertrophic cardiomyopathy in ...... n of an uncommon clinical case

@en

P2093

Antonio Parente

http://www.w3.org/2001/XMLSchema#string

Bruno Trimarco

http://www.w3.org/2001/XMLSchema#string

Caterina Marciano

http://www.w3.org/2001/XMLSchema#string

Claudia D'Andrea

http://www.w3.org/2001/XMLSchema#string

Fabiana De Martino

http://www.w3.org/2001/XMLSchema#string

Fabio Marsico

http://www.w3.org/2001/XMLSchema#string

Francesco Raimondi

http://www.w3.org/2001/XMLSchema#string

Pasquale Perrone Filardi

http://www.w3.org/2001/XMLSchema#string

Santo Dellegrottaglie

http://www.w3.org/2001/XMLSchema#string

Stefania Paolillo

http://www.w3.org/2001/XMLSchema#string

P2860

Mitochondrial trifunctional protein deficiency: a severe fatty acid oxidation disorder with cardiac and neurologic involvement

Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing

Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management.

2013 ESC Guidelines on cardiac pacing and cardiac resynchronization therapy: the Task Force on cardiac pacing and resynchronization therapy of the European Society of Cardiology (ESC). Developed in collaboration with the European Heart Rhythm Associ

Cardiomyopathy in children with mitochondrial disease; clinical course and cardiological findings.

Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency.

The genetics and pathology of oxidative phosphorylation.

Increased mitochondrial mass in mitochondrial myopathy mice

Gene regulatory mechanisms governing energy metabolism during cardiac hypertrophic growth.

Heart transplantation in children with mitochondrial cardiomyopathy.

P304

1201-1204

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/EJHF.858

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

L Capasso

P577

2017-06-06T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

28585276

http://www.w3.org/2001/XMLSchema#string