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Quoted phrase not found in phrase index: "Hyperammonemia, type III"
Page 1
Hyperammonemia and neonatal cardiac failure.
Adamovic T, Jouvet P, Vobecky S, Garel L, Rougemont AL, Alvarez F. Adamovic T, et al. Minerva Anestesiol. 2011 May;77(5):554-7. Epub 2011 Mar 2. Minerva Anestesiol. 2011. PMID: 21540812 Free article. Review.
Severe hyperammonemia (hyperNH3) in neonatal cardiac failure after cardiac surgery is rare. We report a case of a 2470-g female infant born at the week 37 of gestation with complex congenital heart disease (truncus arteriosus type III, interrupted aortic arch and tr …
Severe hyperammonemia (hyperNH3) in neonatal cardiac failure after cardiac surgery is rare. We report a case of a 2470-g female infan …
Portal-systemic encephalopathy in non-cirrhotic patients: classification of clinical types, diagnosis and treatment.
Watanabe A. Watanabe A. J Gastroenterol Hepatol. 2000 Sep;15(9):969-79. doi: 10.1046/j.1440-1746.2000.02283.x. J Gastroenterol Hepatol. 2000. PMID: 11059925 Review.
Type II designates a type of intra/extrahepatic shunt that originates from the umbilical part of the portal vein and serpentines in the liver, then leaves the liver. Type III (extrahepatic type) occurs most frequently. Type IV (extrahepatic) is …
Type II designates a type of intra/extrahepatic shunt that originates from the umbilical part of the portal vein and serpentin …
Follow-up of fatty acid β-oxidation disorders in expanded newborn screening era.
Janeiro P, Jotta R, Ramos R, Florindo C, Ventura FV, Vilarinho L, Tavares de Almeida I, Gaspar A. Janeiro P, et al. Eur J Pediatr. 2019 Mar;178(3):387-394. doi: 10.1007/s00431-018-03315-2. Epub 2019 Jan 7. Eur J Pediatr. 2019. PMID: 30617651
In order to characterize acute decompensations observed in FAO-deficient cases identified by ENS, a retrospective analysis was performed, covering a period of 9 years. Demographic data, number/type of acute decompensations, treatment, and follow-up were considered. ...
In order to characterize acute decompensations observed in FAO-deficient cases identified by ENS, a retrospective analysis was performed, co …
Novel ETF dehydrogenase mutations in a patient with mild glutaric aciduria type II and complex II-III deficiency in liver and muscle.
Wolfe LA, He M, Vockley J, Payne N, Rhead W, Hoppel C, Spector E, Gernert K, Gibson KM. Wolfe LA, et al. J Inherit Metab Dis. 2010 Dec;33 Suppl 3(0 3):S481-7. doi: 10.1007/s10545-010-9246-8. Epub 2010 Nov 19. J Inherit Metab Dis. 2010. PMID: 21088898 Free PMC article.
At age 4 years he developed recurrent vomiting with mild hyperammonemia and dehydration requiring frequent hospitalizations. Glutaric aciduria Type II was suspected based upon biochemical findings and managed with cornstarch, carnitine and riboflavin supplements. He …
At age 4 years he developed recurrent vomiting with mild hyperammonemia and dehydration requiring frequent hospitalizations. Glutaric …