<p>(<b>A</b>) Representative phosphorous MR spectra of VL muscle of FSHD patients, upper with a normal fat fraction, lower with a high fat fraction. (<b>B</b>) PCr/ATP decreases with fat fraction (mean±SD). In intermediately fat infiltrated muscles the PCr/ATP is already decreased significantly from 4.15±1.00 to 3.57±0.88. Completely fat infiltrated muscles do not show a further decrease of this ratio. (<b>C</b>) Significant correlation between PCr/ATP and muscle strength (p<0.001, R<sup>2</sup> = 0.29). Pi = inorganic phosphate; PCr = phosphocreatine; ATP = adenosine triphosphate.</p
To assess the changes in phosphodiester (PDE)-levels, detected by 31P magnetic resonance spectroscop...
Changes in high-energy phosphate levels in single human skeletal muscle fibres after 10 s of maximal...
1991-1994, 1985.-In muscle phosphorylase deficiency (Mc-Ardle’s disease) there is an abnormally rapi...
Facioscapulohumeral muscular dystrophy (FSHD) is characterized by asymmetric dysfunctioning of indiv...
Facioscapulohumeral muscular dystrophy (FSHD) is an untreatable disease, characterized by asymmetric...
<div><p>Facioscapulohumeral muscular dystrophy (FSHD) is an untreatable disease, characterized by as...
Facioscapulohumeral muscular dystrophy (FSHD) is an untreatable disease, characterized by asymmetric...
Contains fulltext : 89916.pdf (publisher's version ) (Closed access)Facioscapulohu...
Contains fulltext : 137803.pdf (publisher's version ) (Open Access)Facioscapulohum...
Defects in skeletal muscle energy metabolism are indicative of systemic disorders such as obesity or...
<p>Resting state ADP/ATP ratio showed moderate correlation with the percentage frequency of COX defi...
Background: The aim of this study was to determine 31PMRS reference spectrum and intracellular pH of...
Defects in skeletal muscle energy metabolism are indicative of systemic disorders such as obesity or...
Background: The aim of this study was to determine 31PMRS reference spectrum and intracellular pH of...
<div><p>Objectives</p><p>To assess the changes in phosphodiester (PDE)-levels, detected by <sup>31</...
To assess the changes in phosphodiester (PDE)-levels, detected by 31P magnetic resonance spectroscop...
Changes in high-energy phosphate levels in single human skeletal muscle fibres after 10 s of maximal...
1991-1994, 1985.-In muscle phosphorylase deficiency (Mc-Ardle’s disease) there is an abnormally rapi...
Facioscapulohumeral muscular dystrophy (FSHD) is characterized by asymmetric dysfunctioning of indiv...
Facioscapulohumeral muscular dystrophy (FSHD) is an untreatable disease, characterized by asymmetric...
<div><p>Facioscapulohumeral muscular dystrophy (FSHD) is an untreatable disease, characterized by as...
Facioscapulohumeral muscular dystrophy (FSHD) is an untreatable disease, characterized by asymmetric...
Contains fulltext : 89916.pdf (publisher's version ) (Closed access)Facioscapulohu...
Contains fulltext : 137803.pdf (publisher's version ) (Open Access)Facioscapulohum...
Defects in skeletal muscle energy metabolism are indicative of systemic disorders such as obesity or...
<p>Resting state ADP/ATP ratio showed moderate correlation with the percentage frequency of COX defi...
Background: The aim of this study was to determine 31PMRS reference spectrum and intracellular pH of...
Defects in skeletal muscle energy metabolism are indicative of systemic disorders such as obesity or...
Background: The aim of this study was to determine 31PMRS reference spectrum and intracellular pH of...
<div><p>Objectives</p><p>To assess the changes in phosphodiester (PDE)-levels, detected by <sup>31</...
To assess the changes in phosphodiester (PDE)-levels, detected by 31P magnetic resonance spectroscop...
Changes in high-energy phosphate levels in single human skeletal muscle fibres after 10 s of maximal...
1991-1994, 1985.-In muscle phosphorylase deficiency (Mc-Ardle’s disease) there is an abnormally rapi...