Literature DB >> 5101444

Urinary amino acid excretion in phenylketonuric, hyperphenylalaninemic, and normal patients.

D R Lines, H A Waisman.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1971        PMID： 5101444     DOI： 10.1016/s0022-3476(71)80230-5

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


× No keyword cloud information.
  4 in total

1.  Hypophosphatasia with phenylketonuria.

Authors:  M E Blaskovics; K N Shaw
Journal:  Z Kinderheilkd       Date:  1974

2.  In vivo disposal of phenylalanine in phenylketonuria: a study of two siblings.

Authors:  E Treacy; J J Pitt; K Seller; G N Thompson; S Ramus; R G Cotton
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

3.  Significant phenylalanine hydroxylation in vivo in patients with classical phenylketonuria.

Authors:  G N Thompson; D Halliday
Journal:  J Clin Invest       Date:  1990-07       Impact factor: 14.808

4.  Biochemical and neuropsychological effects of elevated plasma phenylalanine in patients with treated phenylketonuria. A model for the study of phenylalanine and brain function in man.

Authors:  W Krause; M Halminski; L McDonald; P Dembure; R Salvo; D Freides; L Elsas
Journal:  J Clin Invest       Date:  1985-01       Impact factor: 14.808
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.