Found: 9
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Increasing brain tyrosine in treated phenylketonuria.
- Published in:
- Journal of Inherited Metabolic Disease, 1998, v. 21, p. 5, doi. 10.1023/A:1005419914133
- By:
- Publication type:
- Article
Elevated galactose in newborn screening due to congenital absence of the portal vein.
- Published in:
- 1998
- By:
- Publication type:
- Case Study
Outcome at age 4 years in offspring of women with maternal phenylketonuria: the Maternal PKU Collaborative Study.
- Published in:
- 2000
- By:
- Publication type:
- journal article
A limited spectrum of phenylalanine hydroxylase mutations is observed in phenylketonuria patients in western Poland and implications for treatment with 6R tetrahydrobiopterin.
- Published in:
- Journal of Human Genetics, 2009, v. 54, n. 6, p. 335, doi. 10.1038/jhg.2009.37
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- Publication type:
- Article
Prenatal diagnosis of non-ketotic hyperglycinemia.
- Published in:
- Prenatal Diagnosis, 1986, v. 6, n. 4, p. 257, doi. 10.1002/pd.1970060405
- By:
- Publication type:
- Article
HEPATIC STEATOSIS DUE TO CONGENITAL ABSENCE OF THE PORTAL VEIN.
- Published in:
- Journal of Pediatric Gastroenterology & Nutrition, 1997, v. 25, n. 4, p. 474
- By:
- Publication type:
- Article
The connotative impact of color on the Rorschach and its relation to manifest anxiety.
- Published in:
- 1957
- By:
- Publication type:
- journal article
The effects of variance on personality impression formation.
- Published in:
- 1967
- By:
- Publication type:
- journal article
Bilateral lucency of the globus pallidus complicating methylmalonic acidemia.
- Published in:
- 1986
- By:
- Publication type:
- journal article