[Total carnitine level in infants with cystic fibrosis and deficit supplementation by means of pharmacologic preparations and diet. Introductory remarks]

Autor:	H, Woś, M, Krauze, E, Bujniewicz, U, Chlebowczyk, Z, Mastalerz, M, Szymańska, I, Maliszewska
Rok vydání:	1995
Předmět:	Enteral Nutrition Treatment Outcome Cystic Fibrosis Liver Function Tests Carnitine Food Fortified Humans Infant Cardiomegaly Infant Food Hepatomegaly Ultrasonography
Zdroj:	Pediatria polska. 70(8)
ISSN:	0031-3939
Popis:	Carnitine deficiency in the serum was found in 5 infants with cystic fibrosis, impaired liver function and neurological symptoms. Clinical improvement and progressive normalization of the carnitine level in the serum, as well of the biochemical parameters of liver function were obtained after enteral pharmacotherapy and a carnitine-rich diet.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::351a35cc57bbfd85c08cc88fa0bd750b https://pubmed.ncbi.nlm.nih.gov/8668368 Zobrazit plný text záznamu