Publications by authors named "Pia Hougaard"

Claim this Profile
L
Low proportion of whole exon deletions causing phenylketonuria in Denmark and Germany.
Lisbeth Birk Møller, Anders O H Nygren, Patrick Scott, Pia Hougaard, Jytte Bieber Nielsen

Hum Mutat· February 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pre- and postnatal diagnosis of tyrosine hydroxylase deficiency.
Lisbeth Birk Møller, Anne Romstad, Marianne Paulsen, Pia Hougaard, Aida Ormazabal

Prenat Diagn· August 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Levodopa-responsive infantile parkinsonism due to a novel mutation in the tyrosine hydroxylase gene and exacerbation by viral infections.
Katharina Diepold, Barbara Schütz, Kevin Rostasy, Bernd Wilken, Pia Hougaard

Mov Disord· June 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis