Literature DB >> 6422143

Differential diagnosis of variant forms of hyperphenylalaninaemia by urinary pterins.

H Hayakawa, K Narisawa, N Arai, K Tada, N Matsuo, T Tanaka, K Naritomi.   

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Year:  1983        PMID： 6422143     DOI： 10.1007/bf01800743

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  4 in total

1.  Analysis of reduced forms of biopterin in biological tissues and fluids.

Authors:  T Fukushima; J C Nixon
Journal:  Anal Biochem       Date:  1980-02       Impact factor: 3.365

2.  Neopterin and biopterin levels in patients with atypical forms of phenylketonuria.

Authors:  J C Nixon; C L Lee; S Milstien; S Kaufman; K Bartholomé
Journal:  J Neurochem       Date:  1980-10       Impact factor: 5.372

3.  Hyperphenylalaninemia due to dihydropteridine reductase deficiency: diagnosis by enzyme assays on dried blood spots.

Authors:  N Arai; K Narisawa; H Hayakawa; K Tada
Journal:  Pediatrics       Date:  1982-09       Impact factor: 7.124

4.  Diagnosis of variants of hyperphenylalaninemia by determination of pterins in urine.

Authors:  J L Dhondt; C Largilliere; P Ardouin; J P Farriaux; M Dautrevaux
Journal:  Clin Chim Acta       Date:  1981-03-05       Impact factor: 3.786
  4 in total
  1 in total

1.  Improved identification of heterozygotes for phenylketonuria using blood neopterin and biopterin.

Authors:  T Alós; Y Bel; M L Cabello; J L Catalá; J Dalmau; J Ferré; A M García; P Ruiz-Vázquez
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982
  1 in total

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