Related Experiment Videos

[Galactosemia, generally with a fulminating course. 10 cases found through an early detection program]

S Scheibenreiter, O Thalhammer

Wiener Klinische Wochenschrift

|February 11, 1972

Summary

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

Long-term outcome of patients with argininosuccinate lyase deficiency diagnosed by newborn screening in Austria.

Molecular genetics and metabolism·2010

Clinical and neuropsychological outcome in 33 patients with biotinidase deficiency ascertained by nationwide newborn screening and family studies in Austria.

European journal of pediatrics·2001

[Maternal phenylketonuria: dietary treatment of a 2 generation illness].

Zeitschrift fur Geburtshilfe und Neonatologie·2000

[An adult patient with phenylketonuria before and one year after reinstitution of diet therapy].

Wiener klinische Wochenschrift·1999

Hyperprolactinemia, a tool in treatment control of tetrahydrobiopterin deficiency: endocrine studies in an affected girl.

Pediatric research·1998

Molecular heterogeneity of classical and Duarte galactosemia: mutation analysis by denaturing gradient gel electrophoresis.

Human mutation·1997

See all related articles