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Literature DB >> 4712783

Chronic lactic acidosis in association with myopathy.

M J Terlow, B D Lake, J K Lloyd.

Abstract

Entities: Disease

Mesh：

Substances：
Lactates
Pyruvates
Alanine

Year: 1973 PMID： 4712783 PMCID： PMC1648441 DOI： 10.1136/adc.48.6.489

Source DB: PubMed Journal: Arch Dis Child ISSN： 0003-9888 Impact factor: 3.791

× No keyword cloud information.

7 in total

1. Abnormal resting blood lactate. I. The significance of hyperlactatemia in hospitalized patients.

Authors: W E HUCKABEE
Journal: Am J Med Date: 1961-06 Impact factor: 4.965

2. Acidosis and lacticacidemia in extracorporeal circulation: the significance of perfusion flow rate and the relation to preperfusion respiratory alkalosis.

Authors: M S LITWIN; F G PANICO; C RUBINI; D E HARKEN; F D MOORE
Journal: Ann Surg Date: 1959-02 Impact factor: 12.969

3. A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study.

Authors: R LUFT; D IKKOS; G PALMIERI; L ERNSTER; B AFZELIUS
Journal: J Clin Invest Date: 1962-09 Impact factor: 14.808

4. Leigh's subacute necrotizing encephalopathy: clinical and biochemical study, with special reference to therapy with lipoate.

Authors: B E Clayton; R H Dobbs; A D Patrick
Journal: Arch Dis Child Date: 1967-10 Impact factor: 3.791

5. Amino acid metabolism in lactic acidosis.

Authors: E B Marliss; T T Aoki; C J Toews; P Felig; J J Connon; J Kyner; W E Huckabee; G F Cahill
Journal: Am J Med Date: 1972-04 Impact factor: 4.965

6. Intermittent cerebellar ataxia associated with hyperpyruvic acidemia, hyperalaninemia, and hyperalaninuria.

Authors: D Lonsdale; W R Faulkner; J W Price; R R Smeby
Journal: Pediatrics Date: 1969-06 Impact factor: 7.124

7. Skeletal muscle disease with abnormal mitochondria.

Authors: G K van Wijngaarden; J Bethlem; A E Meijer; W C Hülsmann; C A Feltkamp
Journal: Brain Date: 1967-09 Impact factor: 13.501

7 in total

8 in total

Chronic lactic acidosis in association with myopathy.

1. Abnormal resting blood lactate. I. The significance of hyperlactatemia in hospitalized patients.

2. Acidosis and lacticacidemia in extracorporeal circulation: the significance of perfusion flow rate and the relation to preperfusion respiratory alkalosis.

3. A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study.

4. Leigh's subacute necrotizing encephalopathy: clinical and biochemical study, with special reference to therapy with lipoate.

5. Amino acid metabolism in lactic acidosis.

6. Intermittent cerebellar ataxia associated with hyperpyruvic acidemia, hyperalaninemia, and hyperalaninuria.

7. Skeletal muscle disease with abnormal mitochondria.

1. On the pathogenesis of mitochondrial myopathies. An experimental study.

2. Recurrent exertional rhabdomyolysis and stunted growth.

Review 3. Mitochondrial myopathies. Clinical, morphological and biochemical aspects.

4. Familial megaconial myopathy: a real nosologic entity. Clinical and histopathologic studies in two siblings.

5. The histochemical characterization of the coupling state of skeletal muscle mitochondria.

6. Mitochondrial cytopathy. A multisystem disorder with ragged red fibres on muscle biopsy.

7. Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosis.

8. Chronic mild diarrhoea, stunted growth and neuromuscular abnormalities.