Pages that link to "Q48735604"
Jump to navigation
Jump to search
The following pages link to Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin. (Q48735604):
Displaying 45 items.
- Mitochondrial myopathy: a genetic study of 71 cases (Q24522304) (← links)
- Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorder (Q28280475) (← links)
- Defects in mitochondrial respiratory complexes III and IV, and human pathologies. (Q30331712) (← links)
- A mitochondrial encephalomyopathy with a partial cytochrome c oxidase deficiency of muscle (Q33631123) (← links)
- Neonatal metabolic myopathies (Q33637042) (← links)
- Mitochondrial respiratory chain disorders and the liver (Q33759088) (← links)
- Mitochondrial myopathy diagnosis (Q33829449) (← links)
- Oxidative phosphorylation disease diagnosis (Q33836199) (← links)
- Inherited mitochondrial DNA depletion (Q34195471) (← links)
- Congenital deficiency of two polypeptide subunits of the iron-protein fragment of mitochondrial complex I. (Q34559294) (← links)
- Cytochrome c oxidase deficiency (Q35038648) (← links)
- Deficiency of complex III of the mitochondrial respiratory chain in a patient with facioscapulohumeral disease (Q35196436) (← links)
- mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases (Q35196481) (← links)
- Defects of the mitochondrial respiratory chain complexes in three pediatric cases with hypotonia and cardiac involvement (Q35229968) (← links)
- Disorders associated with depletion of mitochondrial DNA (Q35243839) (← links)
- Treatment of congenital lactic acidosis with dichloroacetate (Q35257790) (← links)
- Organic acidurias: a review. Part 1. (Q37254022) (← links)
- Potential Non-Hypoxic/Ischemic Causes of Increased Cerebral Interstitial Fluid Lactate/Pyruvate Ratio: A Review of Available Literature (Q37845209) (← links)
- Defects of the respiratory chain. (Q37901947) (← links)
- Molecular defects in cytochrome oxidase in mitochondrial diseases (Q39245103) (← links)
- Myopathies due to enzyme deficiencies (Q39477219) (← links)
- Cytochrome oxidase deficiency: clinical and biochemical heterogeneity (Q39509017) (← links)
- The biochemical basis of mitochondrial diseases (Q39642608) (← links)
- Mitochondrial encephalomyopathies: what next? (Q41180845) (← links)
- Regional mitochondrial respiratory activity in Huntington's disease brain (Q41360902) (← links)
- Fatal infantile liver failure associated with mitochondrial DNA depletion (Q41905348) (← links)
- Valproate-induced hepatic failure in a case of cytochrome c oxidase deficiency (Q42285317) (← links)
- Hypertrophic cardiomyopathy and mtDNA depletion. Successful treatment with heart transplantation (Q43814302) (← links)
- Clinical characteristics and muscle pathology in myopathic mitochondrial DNA depletion (Q44147990) (← links)
- Defects in muscle fiber growth in fatal infantile cytochrome c oxidase deficiency (Q48163470) (← links)
- Depletion of mitochondrial DNA in the liver of a patient with lactic acidemia and hypoketotic hypoglycemia (Q48985903) (← links)
- Adult Onset Lipid Storage in Gastric Mucosa and Skeletal Muscle Fibers Associated with Gastric Pain, Progressive Muscle Weakness and Partial Deficiency of Cytochrome C Oxidase (Q54306727) (← links)
- Hepatic failure in disorders of oxidative phosphorylation with neonatal onset (Q56241335) (← links)
- Fatal neonatal liver failure and mitochondrial cytopathy (oxidative phosphorylation deficiency): A light and electron microscopic study of the liver (Q63681442) (← links)
- Variation in retinal changes and muscle pathology in mitochondriopathies (Q69447758) (← links)
- Mitochondrial diseases (Q69487919) (← links)
- Mitochondrial myopathies (Q69812514) (← links)
- de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiency (Q69824858) (← links)
- Depletion of mitochondrial deoxyribonucleic acid in a family with fatal neonatal liver disease (Q71072135) (← links)
- Metabolic myopathies (Q71509055) (← links)
- Renal amino acid transport in adults with oxidative phosphorylation diseases (Q72318333) (← links)
- Liver cytochrome c oxidase deficiency in a case of neonatal-onset hepatic failure (Q72416019) (← links)
- Microvesicular steatosis, hemosiderosis and rapid development of liver cirrhosis in a patient with Pearson's syndrome (Q72995595) (← links)
- The kidney in mitochondrial cytopathies (Q73182916) (← links)
- Cirrhosis in a Child With Deficiency ofMitochondrial Respiratory-Chain Succinate–Cytochromec–Oxidoreductase (Q73583027) (← links)