Literature DB >> 5689917

A prospective community survey for aminoacidaemias.

G M Komrower, M J Griffiths, B Fowler, A M Lambert.   

Abstract

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Year:  1968        PMID: 5689917      PMCID: PMC1902320     

Source DB:  PubMed          Journal:  Proc R Soc Med        ISSN: 0035-9157


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  4 in total

1.  A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS.

Authors:  R GUTHRIE; A SUSI
Journal:  Pediatrics       Date:  1963-09       Impact factor: 7.124

2.  Simple method for detection of phenylketonuria.

Authors:  H K BERRY; B SUTHERLAND; G M GUEST; J WARKANY
Journal:  J Am Med Assoc       Date:  1958-08-30

3.  Tyrosinaemia and tyrosyluria in infancy.

Authors:  P W Wong; A M Lambert; G M Komrower
Journal:  Dev Med Child Neurol       Date:  1967-10       Impact factor: 5.449

4.  Transient tyrosinemia of the newborn: dietary and clinical aspects.

Authors:  M E Avery; C L Clow; J H Menkes; A Ramos; C R Scriver; L Stern; B P Wasserman
Journal:  Pediatrics       Date:  1967-03       Impact factor: 7.124

  4 in total
  4 in total

Review 1.  Management of inherited metabolic disease.

Authors:  D N Raine
Journal:  Br Med J       Date:  1972-05-06

2.  Screening for inherited metabolic disease by plasma chromatography (Scriver) in a large city.

Authors:  D N Raine; J R Cooke; W A Andrews; D F Mahon
Journal:  Br Med J       Date:  1972-07-01

3.  Testing for phenylketonuria.

Authors:  J A Macleod
Journal:  Br Med J       Date:  1969-10-11

4.  Newborn screening for hereditary metabolic disorders in Manitoba, 1965-1970.

Authors:  J G Fox; D L Hall; J C Haworth; A Maniar; L Sekla
Journal:  Can Med Assoc J       Date:  1971-06-19       Impact factor: 8.262

  4 in total

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