(Q43144358)

14 November 2017

Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutation (English)

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14 November 2017

2

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4

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13

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14 November 2017

7

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14 November 2017

Roser Pons

1

1 reference

14 November 2017

Aida Ormazabal

3

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14 November 2017

Angels Garcia-Cazorla

5

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14 November 2017

Estela Area

6

1 reference

14 November 2017

Emmanuel Kanavakis

8

1 reference

14 November 2017

Kaliopi Drakaki

9

1 reference

14 November 2017

Aristotelis Giannakopoulos

10

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14 November 2017

Irene Orfanou

11

1 reference

14 November 2017

Sotiris Youroukos

12

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14 November 2017

Rafael Artuch

14

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14 November 2017

language of work or name

English

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publication date

1 June 2010

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14 November 2017

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14 November 2017

25

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14 November 2017

8

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14 November 2017

1086-1090

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

14 November 2017

1 reference

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

21 January 2018

1 reference

Aromatic L-amino acid decarboxylase deficiency: clinical features, diagnosis, and treatment of a new inborn error of neurotransmitter amine synthesis

21 January 2018

1 reference

Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment, and prognosis

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MDS.23002

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14 November 2017

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