Literature DB >> 6352885

Diagnosis of variant forms of hyperphenylalaninemia using filter paper spots of urine.

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

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Year:  1983        PMID： 6352885     DOI： 10.1016/s0022-3476(83)80589-7

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  5 in total

1.  Screening for tetrahydrobiopterin deficiency in newborns using dried urine on filter paper.

Authors:  N Blau; L Kierat; C W Heizmann; W Endres; T Giudici; M Wang
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

2.  Phenylketonuria due to dihydropteridine reductase deficiency: presentation of two cases.

Authors:  R Longhi; E Riva; R Valsasina; S Paccanelli; M Giovannini
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982

3.  The Comparison of Iodine-Type and MnO2-Type Oxidation for Measuring the Levels of Urine Neopterin and Biopterin in Patients with Hyperphenylalaninemia: A Descriptive-Analytic Study in Iran.

Authors:  Atena Askarizadeh; Shohreh Khatami; Soghra Rouhi Dehnabeh
Journal:  Indian J Clin Biochem       Date:  2018-08-23

4.  Follow-up study of a nation-wide neonatal metabolic screening program in Japan. A collaborative study group of neonatal screening for inborn errors of metabolism in Japan.

Authors:  K Tada; H Tateda; S Arashima; K Sakai; T Kitagawa; K Aoki; S Suwa; M Kawamura; T Oura; M Takesada
Journal:  Eur J Pediatr       Date:  1984-08       Impact factor: 3.183

5.  Strategy for the screening of tetrahydrobiopterin deficiency among hyperphenylalaninaemic patients: 15-years experience.

Authors:  J L Dhondt
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982
  5 in total

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