Literature DB >> 9266357

Complete reversal of moderate/severe brain MRI abnormalities in a patient with classical phenylketonuria.

J H Walter1, F White, J E Wraith, J P Jenkins, B P Wilson.   

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Year:  1997        PMID： 9266357     DOI： 10.1023/a:1005330012574

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


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  3 in total

1.  Magnetic resonance imaging of the brain in phenylketonuria.

Authors:  M A Cleary; J H Walter; J E Wraith; J P Jenkins; S M Alani; K Tyler; D Whittle
Journal:  Lancet       Date:  1994-07-09       Impact factor: 79.321

Review 2.  White matter abnormalities in patients with treated hyperphenylalaninaemia: magnetic resonance relaxometry and proton spectroscopy findings.

Authors:  U Bick; K Ullrich; U Stöber; H Möller; G Schuierer; A C Ludolph; C Oberwittler; J Weglage; U Wendel
Journal:  Eur J Pediatr       Date:  1993-12       Impact factor: 3.183

3.  Magnetic resonance imaging in phenylketonuria: reversal of cerebral white matter change.

Authors:  M A Cleary; J H Walter; J E Wraith; F White; K Tyler; J P Jenkins
Journal:  J Pediatr       Date:  1995-08       Impact factor: 4.406
  3 in total
  5 in total

1.  Generalized seizures aggravated by levetiracetam in an adult patient with phenylketonuria.

Authors:  Nese Dericioglu; Serap Saygi
Journal:  Metab Brain Dis       Date:  2010-04-28       Impact factor: 3.584

2.  Tract-based evaluation of white matter damage in individuals with early-treated phenylketonuria.

Authors:  Huiling Peng; Dawn Peck; Desirée A White; Shawn E Christ
Journal:  J Inherit Metab Dis       Date:  2013-09-17       Impact factor: 4.982

3.  Phenylketonuria: an inborn error of phenylalanine metabolism.

Authors:  Robin A Williams; Cyril D S Mamotte; John R Burnett
Journal:  Clin Biochem Rev       Date:  2008-02

4.  Meta-analysis of neuropsychological symptoms of adolescents and adults with PKU.

Authors:  J J Moyle; A M Fox; M Arthur; M Bynevelt; J R Burnett
Journal:  Neuropsychol Rev       Date:  2007-04-05       Impact factor: 7.444

5.  GTP-Cyclohydrolase I deficiency presenting as malignant hyperphenylalaninemia, recurrent hyperthermia and progressive neurological dysfunction in a South Asian child - a case report.

Authors:  Kavinda Chandimal Dayasiri; Nayani Suraweera; Deepal Nawarathne; U E Senanayake; B K T P Dayanath; Eresha Jasinge; Kumudu Weerasekara
Journal:  BMC Pediatr       Date:  2019-06-15       Impact factor: 2.125
  5 in total

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