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18 in total

1. An evaluation of the treatment of phenylketonuria with diets low in phenylalanine.

Authors: W E KNOX
Journal: Pediatrics Date: 1960-07 Impact factor: 7.124

2. Variations in intelligence in phenylktonuria.

Authors: M W PARTINGTON
Journal: Can Med Assoc J Date: 1962-04-21 Impact factor: 8.262

3. Screening, counselling and treatment of hereditary metabolic disease; a survey of resources in Canada.

Authors: J C Haworth; J R Miller; C R Scriver
Journal: Can Med Assoc J Date: 1974-11-16 Impact factor: 8.262

4. Causes for high phenylalanine with normal tyrosine in newborn screening programs.

Authors: J L Berman; G C Cunningham; R W Day; R Ford; D Y Hsia
Journal: Am J Dis Child Date: 1969-01

5. Maternal phenylketonuria: dietary treatment during pregnancy.

Authors: L A Zaleski; R E Casey; W Zaleski
Journal: Can Med Assoc J Date: 1979-12-22 Impact factor: 8.262

6. Legislation and advances in medical knowledge--acceleration or inhibition?

Authors: S P Bessman
Journal: J Pediatr Date: 1966-08 Impact factor: 4.406

7. Proposed guidelines for screening of metabolic and endocrine diseases of dependent neonates of the U.S. Armed Forces. Derived from a survey of state guidelines for neonatal screening of metabolic diseases.

Authors: C M Tiwary
Journal: Clin Pediatr (Phila) Date: 1987-07 Impact factor: 1.168

Review 8. Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood.

Authors: F Güttler
Journal: Acta Paediatr Scand Suppl Date: 1980

9. Maternal phenylketonuria and hyperphenylalaninemia. An international survey of the outcome of untreated and treated pregnancies.

Authors: R R Lenke; H L Levy
Journal: N Engl J Med Date: 1980-11-20 Impact factor: 91.245

10. Maternal phenylketonuria and hyperphenylalaninemia: implications for medical practice in the United States.

Authors: A S Luder; C L Greene
Journal: Am J Obstet Gynecol Date: 1989-11 Impact factor: 8.661

1 in total

1. Phenylketonuria: variable phenotypic outcomes of the R261Q mutation and maternal PKU in the offspring of a healthy homozygote.

Authors: S Kleiman; L Vanagaite; J Bernstein; G Schwartz; N Brand; A Elitzur; S L Woo; Y Shiloh
Journal: J Med Genet Date: 1993-04 Impact factor: 6.318

1 in total