Pages that link to "Q39598557"

The following pages link to Morphological observations in skeletal muscle from patients with a mitochondrial myopathy (Q39598557):

Displaying 25 items.

• Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation). (Q32161682) ‎ (← links)
• Adult rat cardiomyocytes cultured in creatine-deficient medium display large mitochondria with paracrystalline inclusions, enriched for creatine kinase (Q33336132) ‎ (← links)
• Confocal scanning laser microscopy of mitochondria: a possible tool in the diagnosis of mitochondrial disorders (Q33350458) ‎ (← links)
• Mitochondrial creatine kinase: a major constituent of pathological inclusions seen in mitochondrial myopathies (Q35369919) ‎ (← links)
• Increased capillaries in mitochondrial myopathy: implications for the regulation of oxygen delivery (Q35706406) ‎ (← links)
• Mitochondrial encephalomyopathy with pilovacuolar inclusion or phenocopy with mitochondrial artefact? (Q36220580) ‎ (← links)
• Histomorphologic and ultrastructural recovery of myopathy in rats treated with low-level laser therapy (Q36303758) ‎ (← links)
• Rhabdomyolysis in Childhood: A Primer on Normal Muscle Function and Selected Metabolic Myopathies Characterized by Disordered Energy Production (Q36343648) ‎ (← links)
• Adult-onset mitochondrial myopathy (Q36682510) ‎ (← links)
• Presentation and diagnosis of mitochondrial disorders in children (Q37138129) ‎ (← links)
• Mitochondria-related encephalomyopathies (Q38635118) ‎ (← links)
• Secondary mitochondrial pathology (Q39156461) ‎ (← links)
• Mitochondrial genome: defects, disease, and evolution (Q41239978) ‎ (← links)
• The role of electron microscopy in the diagnosis of nonneoplastic muscle diseases (Q41497954) ‎ (← links)
• Mitochondrial encephalomyopathy with associated aminoacidopathy in a male sibship (Q42198273) ‎ (← links)
• Morphological methods in the diagnosis of mitochondrial encephalomyopathies: the role of electron microscopy (Q46612821) ‎ (← links)
• Co-expression Network Approach Reveals Functional Similarities among Diseases Affecting Human Skeletal Muscle (Q47135441) ‎ (← links)
• Absence of cytochrome c oxidase activity in a boy with dysfunction of renal tubules, brain and muscle (Q48142353) ‎ (← links)
• Demonstration of two isoforms of subunit VIIa of cytochrome c oxidase from human skeletal muscle. Implications for mitochondrial myopathies (Q49170886) ‎ (← links)
• Multiple mitochondrial alterations in a case of myopathy. (Q52648136) ‎ (← links)
• β-Turns as structural motifs for the proteolytic processing of seed proteins (Q57082676) ‎ (← links)
• Mitochondrial Diseases and Myopathies: A Series of Muscle Biopsy Specimens with Ultrastructural Changes in the Mitochondria (Q67488431) ‎ (← links)
• Defects in the cytochrome bc1 complex in mitochondrial diseases (Q69834284) ‎ (← links)
• Hereditary mitochondrial hypertrophic cardiomyopathy with mitochondrial myopathy of skeletal muscle, congenital cataract and lactic acidosis (Q70368445) ‎ (← links)
• Morphology of the mitochondria in heat shock protein 60 deficient fibroblasts from mitochondrial myopathy patients. Effects of stress conditions (Q71796194) ‎ (← links)