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Pia Hougaard

Research Profile

Chemicals & Drugs

Procedures

Disorders

Physiology

Mutation

Geographic Areas

Denmark

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Publications

TOP 3
Lisbeth Birk Møller; Anders O H Nygren; patrick scott; Pia Hougaard; Jytte Bieber Nielsen; Caroline Hartmann; Flemming Güttler; Linda Tyfield; Johannes Zschocke
Low proportion of whole exon deletions causing phenylketonuria in Denmark and Germany.
Lisbeth Birk Møller; Anne Romstad; Marianne Paulsen; Pia Hougaard; Aida Ormazabal; Manuel Pineda; Nenad Blau; Flemming Güttler; Rafael Artuch
Pre- and postnatal diagnosis of tyrosine hydroxylase deficiency.
Katharina Diepold; Barbara Schütz; Kevin Rostasy; Bernd Wilken; Pia Hougaard; Flemming Güttler; Anne Romstad; Lisbeth Birk Møller
Levodopa-responsive infantile parkinsonism due to a novel mutation in the tyrosine hydroxylase gene and exacerbation by viral infections.

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All Publications

2007: Lisbeth Birk Møller; Anders O H Nygren; patrick scott; Pia Hougaard; Jytte Bieber Nielsen; Caroline Hartmann; Flemming Güttler; Linda Tyfield; Johannes Zschocke
Low proportion of whole exon deletions causing phenylketonuria in Denmark and Germany.
Human mutation 2007;28(2):207.
2005: Lisbeth Birk Møller; Anne Romstad; Marianne Paulsen; Pia Hougaard; Aida Ormazabal; Manuel Pineda; Nenad Blau; Flemming Güttler; Rafael Artuch
Pre- and postnatal diagnosis of tyrosine hydroxylase deficiency.
Prenatal diagnosis 2005;25(8):671-5.
2005: Katharina Diepold; Barbara Schütz; Kevin Rostasy; Bernd Wilken; Pia Hougaard; Flemming Güttler; Anne Romstad; Lisbeth Birk Møller
Levodopa-responsive infantile parkinsonism due to a novel mutation in the tyrosine hydroxylase gene and exacerbation by viral infections.
Movement disorders : official journal of the Movement Disorder Society 2005;20(6):764-7.

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