Malignant hyperphenylalaninaemia—Current status (June 1977)

@article{Danks1978MalignantHS,
  title={Malignant hyperphenylalaninaemia—Current status (June 1977)},
  author={David M. Danks and Klaus Bartholom{\'e} and Barbara Clayton and H Ch Curtius and Helfried Gr{\"o}be and Seymour Kaufman and Rhys Leeming and W. Pfleiderer and Heinz Rembold and Françoise Rey},
  journal={Journal of Inherited Metabolic Disease},
  year={1978},
  volume={1},
  pages={49-53}
}
D. M. DANKS (Royal Children's Hospital, Parkville, 3052, ifielbourne, Australia) K. BARTItOLOMg (Kinderklinik der Universitdt, 6900 Heidelberg 1, tt~meislerweg 1-9, West Germany) B. E. CLAYTON (Department of Chemical Pathology,, Hospital for Sick Children, Great Ormond Street, London) H. Cua'nus (Biochemistry Department, Kinderspital, Zurich, Swilzerland) H. GR/SBt,: (Children's Hospital , Universily of Miinster, Munster, West Germany) S. KAUFMAN (Laboratory of Neurochemistry, Nationa… CONTINUE READING

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Hyperphenylalaninemia due to impaired dihydrobiopterin biosynthesis

European Journal of Pediatrics • 1981
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Highly Influenced

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Metabolism and metabolic roles of 6-polyhydroxyalkylpterins

Journal of Inherited Metabolic Disease • 1978
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Les hyperphenylalanindmies avec activit~ normale de la phenylalanine-hydroxylase

F. Rey, J. P. Harpey, R. J. Leeming, J. Aicardi, J. Rey
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Atypical PKU, seizures and developmental delay with dihydropteridine reductase deficiency

T. G. Brewster, I. F. Abroms, +6 authors S R.
Pediatr. Res • 1976

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