Serum vitamin B12 concentrations within reference values do not exclude functional vitamin B12 deficiency in PKU patients of various ages
Authors:
- Marieke HoeksmaMHMarieke Hoeksma
- Anne-Lise Bjorke MonsenAMAnne-Lise Bjorke Monsen
- M. Rebecca FokkemaMFM. Rebecca Fokkema
- Dirk-Jan ReijngoudDRDirk-Jan Reijngoud
- Margreet van RijnMRMargreet van Rijn
- Francjan J. van SpronsenFSFrancjan J. van Spronsen
- 1 January 2011
- journal article
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 102 (1) , 13-17
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- Total homocysteine, B-vitamins and genetic polymorphisms in patients with classical phenylketonuriaMolecular Genetics and Metabolism, 2008
- Vitamin B12 Sources and BioavailabilityExperimental Biology and Medicine, 2007
- Vitamin B12 and vitamin B6 supplementation is needed among adults with phenylketonuria (PKU)Journal of Inherited Metabolic Disease, 2006
- Homocysteine, folic acid and vitamin B12 in relation to pre- and postnatal health aspectsClinical Chemistry and Laboratory Medicine (CCLM), 2005
- Behavioural factors related to metabolic control in patients with phenylketonuriaJournal of Inherited Metabolic Disease, 2004
- Cobalamin Status and Its Biochemical Markers Methylmalonic Acid and Homocysteine in Different Age Groups from 4 Days to 19 YearsClinical Chemistry, 2003
- Optimal use of markers for cobalamin and folate status in a psychogeriatric populationInternational Journal of Geriatric Psychiatry, 2002
- Factors affecting the variation in plasma phenylalanine in patients with phenylketonuria on diet.Archives of Disease in Childhood, 1996
- Plasma Amino Acid Response to Ingestion of L-Amino Acids and Whole ProteinJournal of Pediatric Gastroenterology and Nutrition, 1993
- Controlled diet in phenylketonuria may cause serum carnitine deficiencyJournal of Inherited Metabolic Disease, 1993