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JIMD Reports|February 23, 2013
Mutation spectrum of fumarylacetoacetase gene and clinical aspects of tyrosinemia type I diseaseA Dursun, R K Ozgül, S Sivri, et al.American Journal of Physiology. Gastrointestinal and Liver Physiology|August 29, 2000
Endothelin-1-induced PMN infiltration and mucosal dysfunction in the rat small intestineB K Oktar, T Coşkun, A Bozkurt, et al.Pediatric Research|February 1, 1997
A survey of the newborn populations in Belgium, Germany, Poland, Czech Republic, Hungary, Bulgaria, Spain, Turkey, and Japan for the G985 variant allele with haplotype analysis at the medium chain Acyl-CoA dehydrogenase gene locus: clinical and evolutionary considerationK Tanaka, N Gregersen, A Ribes, et al.Orphanet Journal of Rare Diseases|July 2, 2020
PKU dietary handbook to accompany PKU guidelinesA MacDonald, A M J van Wegberg, K Ahring, et al.Orphanet Journal of Rare Diseases|September 3, 2020
Correction to: PKU dietary handbook to accompany PKU guidelinesA MacDonald, A M J van Wegberg, K Ahring, et al.Molecular Genetics and Metabolism|May 16, 2025
European guidelines on diagnosis and treatment of phenylketonuria: First revisionA M J van Wegberg, A MacDonald, K Ahring, et al.Pageof 11