Literature DB >> 5110588

Disorders of amino acid metabolism--1971.

J H Menkes.   

Abstract

Mesh:

Substances:

Year:  1971        PMID: 5110588      PMCID: PMC1517982     

Source DB:  PubMed          Journal:  Calif Med        ISSN: 0008-1264


× No keyword cloud information.
  23 in total

1.  Phenylketonuria: mental development, behavior, and termination of low phenylalanine diet.

Authors:  I M Hackney; W B Hanley; W Davidson; L Lindsao
Journal:  J Pediatr       Date:  1968-05       Impact factor: 4.406

2.  Electroencephalographic abnormalities in phenylpyruvic oligophrenia.

Authors:  C W Watson; M P Nigam; R S Paine
Journal:  Neurology       Date:  1968-03       Impact factor: 9.910

3.  Phenylketonuria and intelligence: trimodal response to dietary treatment.

Authors:  R N Fuller; J B Shuman
Journal:  Nature       Date:  1969-02-15       Impact factor: 49.962

4.  Treatment of homocystinuria with pyridoxine. A preliminary study.

Authors:  N A Carson; I J Carré
Journal:  Arch Dis Child       Date:  1969-06       Impact factor: 3.791

5.  Neuropathology of phenylketonuria.

Authors:  N Malamud
Journal:  J Neuropathol Exp Neurol       Date:  1966-04       Impact factor: 3.685

6.  Phenylalanine deficiency syndrome.

Authors:  B M Rouse
Journal:  J Pediatr       Date:  1966-08       Impact factor: 4.406

7.  The therapy of maple syrup urine disease.

Authors:  S E Snyderman
Journal:  Am J Dis Child       Date:  1967-01

8.  Mental retardation in children of phenylketonuric mothers.

Authors:  C C Mabry; J C Denniston; J G Coldwell
Journal:  N Engl J Med       Date:  1966-12-15       Impact factor: 91.245

9.  Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation.

Authors:  V E Shih; M L Efron; H W Moser
Journal:  Am J Dis Child       Date:  1969-01

10.  Two years of PKU testing in California. The role of the laboratory.

Authors:  G C Cunningham
Journal:  Calif Med       Date:  1969-01
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.