Mitochondrial myopathy enzyme panel:CCnt:Pt:Tiss:Qn

Known as: panel de enzimas de las miopatías mitocondriales:contenido catalítico:punto en el tiempo:tejido, no especificado:cuantitativo:, Митохондриальная миопатия энзим панель:КаталСод:ТчкВрм:Тк:Колич, Mitochondriale myopathie enzympanel:Catalytisch gehalte:Moment:Weefsel en uitstrijkjes:Kwantitatief 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1968-2015
02419682015

Papers overview

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2012
2012
Familial dilated cardiomyopathy (F-DCM) describes a clinically and genetically heterogeneous group of diseases, mostly inherited… (More)
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2012
2012
Parmi les auto-anticorps spécifiques des myosites, les anticorps dirigés contre la « signal recognition particle » (SRP) [1] sont… (More)
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2004
2004
A case of acid maltase deficiency with myopathy in a 19 year old male, which appeared clinically as atypical muscular dystrophy… (More)
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2004
2004
Eight cases of so-called congenital muscular dystrophy are reported. The so-called congenital muscular dystrophy is a primary… (More)
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2001
2001
Myotonien sind Muskelerkrankungen, die mit einer verzögerten Entspannung nach willkürlicher Innervation oder mit myotonen… (More)
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2000
2000
Hintergrund: Die Immigrantenosteomalazie stellt eine zunehmend häufige Form eines Vitamin-D-Mangelzustands dar, der… (More)
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1997
1997
The aim of this prospective study was to classify cardiac involvement in myopathies by means of a comprehensive cardiac… (More)
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1981
1981
Two brothers are described with a distal myopathy different from the known hereditary distal myopathies. Early adult onset… (More)
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1976
1976
The mild, generalized myopathy (glycogenosis type II) of a 23-year-old male, previously thought to have progressive muscular… (More)
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1968
1968
Type I fibers in m. gastrocnemius can be divided into a large group (67.5%) of medium sized fibers, a small group (7%) of reduced… (More)
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