Literature DB >> 8789776

Phenotyping of phenylketonuric patients by oral phenylalanine loading.

A Ponzone, M Spada, L de Sanctis, I Dianzani.   

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Year:  1996        PMID: 8789776     DOI: 10.1007/bf01955198

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


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  4 in total

1.  Diurnal variations of serum phenylalanine in phenylketonuric children on low phenylalanine diet.

Authors:  F Güttler; E S Olesen; E Wamberg
Journal:  Am J Clin Nutr       Date:  1969-12       Impact factor: 7.045

2.  Differential diagnosis of hyperphenylalaninaemia by a combined phenylalanine-tetrahydrobiopterin loading test.

Authors:  A Ponzone; O Guardamagna; M Spada; S Ferraris; R Ponzone; L Kierat; N Blau
Journal:  Eur J Pediatr       Date:  1993-08       Impact factor: 3.183

3.  In vivo assessment of mutations in the phenylalanine hydroxylase gene by phenylalanine loading: characterization of seven common mutations.

Authors:  P Guldberg; I Mikkelsen; K F Henriksen; H C Lou; F Güttler
Journal:  Eur J Pediatr       Date:  1995-07       Impact factor: 3.183

Review 4.  Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood.

Authors:  F Güttler
Journal:  Acta Paediatr Scand Suppl       Date:  1980
  4 in total
  1 in total

1.  Beneficial Effects of Slow-Release Large Neutral Amino Acids after a Phenylalanine Oral Load in Patients with Phenylketonuria.

Authors:  Iris Scala; Daniela Concolino; Anna Nastasi; Giulia Esposito; Daniela Crisci; Simona Sestito; Stefania Ferraro; Lucia Albano; Margherita Ruoppolo; Giancarlo Parenti; Pietro Strisciuglio
Journal:  Nutrients       Date:  2021-11-10       Impact factor: 5.717

  1 in total

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