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Volumn 51, Issue 3, 2009, Pages 409-410
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Early neonatal onset carbamoyl-phosphate synthase 1 deficiency treated with continuous hemodiafiltration and early living-related liver transplantation
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Author keywords
Carbamoyl phosphate synthase 1 deficiency; Continuous hemodiafiltration; Hyperammonemia; Liver transplantation
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Indexed keywords
ALANINE AMINOTRANSFERASE;
AMMONIA;
ARGININE;
ASPARTATE AMINOTRANSFERASE;
BENZOIC ACID;
CARNITINE;
CITRULLINE;
GLUCOSE;
GLUTAMIC ACID;
ORNITHINE;
PHENYLACETIC ACID;
PROTEIN;
ALANINE AMINOTRANSFERASE BLOOD LEVEL;
AMMONIA BLOOD LEVEL;
ARTICLE;
ASPARTATE AMINOTRANSFERASE BLOOD LEVEL;
BRAIN EDEMA;
CASE REPORT;
CATHETER;
CONTINUOUS HEMODIAFILTRATION;
DISEASE COURSE;
DISORDERS OF AMINO ACID AND PROTEIN METABOLISM;
DOUBLE LUMEN TUBE;
ECHOGRAPHY;
ENZYME ACTIVITY;
FEMALE;
HEART RIGHT ATRIUM;
HEPATOMEGALY;
HUMAN;
HYPERAMMONEMIA;
HYPERMETABOLISM;
LIVER BIOPSY;
LIVER TRANSPLANTATION;
LIVING DONOR;
MUSCLE HYPOTONIA;
NEWBORN;
PRIORITY JOURNAL;
PROTEIN INTAKE;
RESPIRATORY FAILURE;
SEIZURE;
TREATMENT OUTCOME;
AGE OF ONSET;
CARBAMOYL-PHOSPHATE SYNTHASE I DEFICIENCY DISEASE;
COMBINED MODALITY THERAPY;
FEMALE;
HEMODIAFILTRATION;
HUMANS;
HYPERAMMONEMIA;
INFANT, NEWBORN;
LIVER TRANSPLANTATION;
LIVING DONORS;
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EID: 66549096908
PISSN: 13288067
EISSN: 1442200X
Source Type: Journal
DOI: 10.1111/j.1442-200X.2009.02831.x Document Type: Article |
Times cited : (5)
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References (7)
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