Familial infantile lactic acidosis
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference37 articles.
1. Lactate metabolism, studies of a child with a serious congenital deviation;Hartmann;J. Pediat.,1962
2. Chronic acidosis due to an error in lactate and pyruvate metabolism. Report of two cases;Israels;Pediatrics,1964
3. Abnormal resting blood lactate. II. Lactic acidosis;Huckabee;Am. J. Med.,1961
4. Abnormal resting blood lactate. I. The significance of hyperlactatemia in hospitalized patients;Huckabee;Am. J. Med.,1961
5. Spontaneous lactic acidosis, the nature of the acid-base disturbance and considerations in diagnosis and management;Waters;Am. J. Med.,1963
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1. Inherited Lactic Acidosis: Correction of the Defect in Cultured Fibroblasts;Pediatric Research;1984-11
2. Pyruvate dehydrogenase deficiencies;Inherited Disorders of Carbohydrate Metabolism;1980
3. Coma diabeticum;Diabetes mellitus • B;1977
4. Urinary lactate excretion in normal children and in children with enzyme defects of carbohydrate metabolism;Clinica Chimica Acta;1976-02
5. Fatal Lactic Acidosis in a Newborn Attributable to a Congenital Defect of Pyruvate Dehydrogenase;Pediatric Research;1976-01
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