Compulsory hyperventilation and hypocapnia of patients with Leigh syndrome associated with SURF1 gene mutations as a cause of low serum bicarbonates

Journal of Inherited Metabolic Disease

Volumn 24, Issue 7, 2001, Pages 707-714

  Pronicka, E ^a   Piekutowska Abramczuk, D H ^a   Popowska, E ^a   Pronicki, M ^a   Karczmarewicz, E ^a   Sykut Cegielska Y ^a   Taybert, J ^a  

^a CHILDREN'S MEMORIAL HEALTH INSTITUTE   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

BICARBONATE; CYTOCHROME C OXIDASE; LACTIC ACID;

ARTICLE; BICARBONATE BLOOD LEVEL; BLOOD GAS; BLOOD SAMPLING; BRAIN INJURY; BRAIN PROTECTION; BREATHING; CARBON DIOXIDE TENSION; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; ENZYME DEFICIENCY; FEMALE; GENE MUTATION; HOSPITALIZATION; HUMAN; HYPERVENTILATION; HYPOCAPNIA; INFANT; LEIGH DISEASE; MALE; PH; RESPIRATORY ALKALOSIS; RETROSPECTIVE STUDY; SURVIVAL; URINALYSIS; VENOUS BLOOD; VENTILATOR;

ALKALOSIS, RESPIRATORY; BICARBONATES; CARBON DIOXIDE; CHILD; CHILD, PRESCHOOL; FEMALE; HUMANS; HYDROGEN-ION CONCENTRATION; HYPERVENTILATION; HYPOCAPNIA; INFANT; LEIGH DISEASE; MALE; MEMBRANE PROTEINS; MITOCHONDRIAL PROTEINS; MUTATION; PROTEINS; URINE;

EID: 0035668441     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1012937204315     Document Type: Article

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