Response to: Comment on the "NASPGHAN Position Paper on the Diagnosis and Management of Pediatric Acute Liver Failure"
- PMID: 35149646
- DOI: 10.1097/MPG.0000000000003409
Response to: Comment on the "NASPGHAN Position Paper on the Diagnosis and Management of Pediatric Acute Liver Failure"
Comment on
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North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition Position Paper on the Diagnosis and Management of Pediatric Acute Liver Failure.J Pediatr Gastroenterol Nutr. 2022 Jan 1;74(1):138-158. doi: 10.1097/MPG.0000000000003268. J Pediatr Gastroenterol Nutr. 2022. PMID: 34347674
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Comment on the "NASPGHAN Position Paper on the Diagnosis and Management of Pediatric Acute Liver Failure".J Pediatr Gastroenterol Nutr. 2022 May 1;74(5):e130. doi: 10.1097/MPG.0000000000003408. J Pediatr Gastroenterol Nutr. 2022. PMID: 35149645 No abstract available.
References
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- Yildiz Y, Tokatli A.. Comment on the “NASPGHAN position paper on the diagnosis and management of pediatric acute liver failure”. J Pediatr Gastroenterol Nutr 2022; 74:e130.
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- Squires JE, Alonso EM, Ibrahim SH, et al. North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition position paper on the diagnosis and management of pediatric acute liver failure. J Pediatr Gastroenterol Nutr 2022; 74:138–158.
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- Spiekerkoetter U, Lindner M, Santer R, et al. Treatment recommendations in long-chain fatty acid oxidation defects: consensus from a workshop. J Inherit Metab Dis 2009; 32:498–505.
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- Leslie ND, Valencia CA, Strauss AW. Adam MP, Ardinger HH, Pagon RA, et al, et al. Very long-chain acyl-coenzyme A dehydrogenase deficiency. GeneReviews((R)) . Seattle (WA):1993.
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- Van Calcar SC, Sowa M, Rohr F, et al. Nutrition management guideline for very-long chain acyl-CoA dehydrogenase deficiency (VLCAD): an evidence- and consensus-based approach. Mol Genet Metab 2020; 131:23–37.
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