Neuroimaging findings in children with paediatric neurotransmitter diseases. - Wikidata - awgldk - TriplyDB

Neuroimaging findings in children with paediatric neurotransmitter diseases.

Neuroimaging findings in children with paediatric neurotransmitter diseases.

http://www.wikidata.org/entity/Q37489614

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Aromatic L-amino acid decarboxylase (AADC) is crucial for brain development and motor functions A case of acute onset succinic semialdehyde dehydrogenase deficiency: neuroimaging findings and literature review.Should children with cerebral palsy and normal imaging undergo testing for inherited metabolic disorders?Parkinsonism and inborn errors of metabolism.Microstructural changes of brain in patients with aromatic L-amino acid decarboxylase deficiency.Parkinsonism in GTP cyclohydrolase 1-deficient DOPA-responsive dystonia.A novel mutation of ALDH5A1 gene associated with succinic semialdehyde dehydrogenase deficiency.

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Neuroimaging findings in children with paediatric neurotransmitter diseases.

http://www.wikidata.org/entity/Q37489614

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 20 May 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Neuroimaging findings in children with paediatric neurotransmitter diseases.

@en

Neuroimaging findings in children with paediatric neurotransmitter diseases.

@nl

type

label

Neuroimaging findings in children with paediatric neurotransmitter diseases.

@en

Neuroimaging findings in children with paediatric neurotransmitter diseases.

@nl

prefLabel

Neuroimaging findings in children with paediatric neurotransmitter diseases.

@en

Neuroimaging findings in children with paediatric neurotransmitter diseases.

@nl

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S10545-009-1106-Z

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Journal of Inherited Metabolic Disease

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Neuroimaging findings in children with paediatric neurotransmitter diseases

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Shinn-Forng Peng

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P2860

Proton MR spectroscopy in succinic semialdehyde dehydrogenase deficiency

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

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

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

Levodopa neurotoxicity: experimental studies versus clinical relevance.

Clinical spectrum of succinic semialdehyde dehydrogenase deficiency.

Dopamine transporter SPECT using fast kinetic ligands: 123I-FP-beta-CIT versus 99mTc-TRODAT-1.

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

Clinical and therapeutic observations in aromatic L-amino acid decarboxylase deficiency.

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

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s10545-009-1106-z

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361-370

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scholarly article

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10.1007/S10545-009-1106-Z

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3

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2009-05-20T00:00:00Z

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19455403

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neurotransmitter