Literature DB >> 5504066

Intelligence quotients and intelligence loss in patients with phenylketonuria and some variant states.

J L Berman, R Ford.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1970        PMID： 5504066     DOI： 10.1016/s0022-3476(70)80233-5

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


× No keyword cloud information.
  5 in total

Review 1.  Inborn errors of metabolism: clues to understanding human behavioral disorders.

Authors:  G S Omenn
Journal:  Behav Genet       Date:  1976-07       Impact factor: 2.805

2.  Effect of stopping low-phenylalanine diet on intellectual progress of children with phenylketonuria.

Authors:  I Smith; M E Lobascher; J E Stevenson; O H Wolff; H Schmidt; S Grubel-Kaiser; H Bickel
Journal:  Br Med J       Date:  1978-09-09

3.  [Urinary phenylalanine metabolites in hyperphenylalaninemia (author's transl)].

Authors:  P Koepp
Journal:  Klin Wochenschr       Date:  1976-11-01

4.  Behavioural deviance in children with early treated phenylketonuria.

Authors:  J E Stevenson; J Hawcroft; M Lobascher; I Smith; O H Wolff; P J Graham
Journal:  Arch Dis Child       Date:  1979-01       Impact factor: 3.791

5.  Cord-blood tyrosine levels in the full-term phenylketonuric fetus and the "justification hypothesis".

Authors:  C R Scriver; D E Cole; S A Houghton; H L Levy; A Grenier; C Laberge
Journal:  Proc Natl Acad Sci U S A       Date:  1980-10       Impact factor: 11.205
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.