Literature DB >> 4408320

Neonatal screening for phenylketonuria. I. Effectiveness.

N A Holtzman, A G Meek, E D Mellits.   

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Year:  1974        PMID： 4408320

Source DB:  PubMed          Journal:  JAMA        ISSN： 0098-7484            Impact factor:   56.272


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  6 in total

1.  Genetic screening and public health.

Authors:  N A Holtzman
Journal:  Am J Public Health       Date:  1997-08       Impact factor: 9.308

2.  Screening for phenylketonuria in New York City. Threshold values reconsidered.

Authors:  H Hansen; A Shahidi; Z A Stein
Journal:  Public Health Rep       Date:  1978 May-Jun       Impact factor: 2.792

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

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

Review 4.  Diseases of phenylalanine metabolism.

Authors:  C E Parker
Journal:  West J Med       Date:  1979-10

5.  Fifteen-year experience with screening for phenylketonuria with an automated fluorometric method.

Authors:  H N Kirkman; C L Carroll; E G Moore; M S Matheson
Journal:  Am J Hum Genet       Date:  1982-09       Impact factor: 11.025

6.  Neonatal screening in Italy for congenital hypothyroidism and metabolic disorders: hyperphenylalaninemia, maple syrup urine disease and homocystinuria.

Authors:  I Antonozzi; R Dominici; M Andreoli; F Monaco
Journal:  J Endocrinol Invest       Date:  1980 Oct-Dec       Impact factor: 4.256
  6 in total

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