(Q51543419)

6 April 2018

title

Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiency. (English)

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author

Joannie Hui

4

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author name string

Wai-Lan Yeung

1

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Virginia C N Wong

2

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Kwok-Yin Chan

3

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Cheuk-Wing Fung

5

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Eric Yau

6

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Chun-Hung Ko

7

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Ching-Wan Lam

8

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Chloe M Mak

9

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Simon Siu

10

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Louis Low

11

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publication date

7 September 2010

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Journal of Child Neurology

published in

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volume

26

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issue

2

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page(s)

179-187

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The pediatric neurotransmitter disorders

cites work

1 reference

https://api.crossref.org/works/10.1177%2F0883073810377014

L-dopa-responsive infantile hypokinetic rigid parkinsonism due to tyrosine hydroxylase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810377014

Tyrosine hydroxylase deficiency: clinical manifestations of catecholamine insufficiency in infancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810377014

Dopa-responsive dystonia due to mild tyrosine hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810377014

Long-term course of L-dopa-responsive dystonia caused by tyrosine hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810377014

Tyrosine hydroxylase deficiency causes progressive encephalopathy and dopa-nonresponsive dystonia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810377014

Dopa-responsive dystonia simulating spastic paraplegia due to tyrosine hydroxylase (TH) gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810377014

Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810377014

Galactorrhea-a strong clinical clue towards the diagnosis of neurotransmitter disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810377014

Dystonia with motor delay in compound heterozygotes for GTP-cyclohydrolase I gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810377014

Tyrosine hydroxylase deficiency with severe clinical course: clinical and biochemical investigations and optimization of therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810377014

Atypical presentation of dopa-responsive dystonia: generalized hypotonia and proximal weakness

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810377014

A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810377014

L-dopa and selegiline for tyrosine hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810377014

21 January 2018

Identifiers

DOI

10.1177/0883073810377014

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6 April 2018

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6 April 2018