Secondary abnormalities of neurotransmitters in infants with neurological disorders-Reference-Cited by-同舟云学术

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Secondary abnormalities of neurotransmitters in infants with neurological disorders

Published:2007-10 Issue:10 Volume:49 Page:740-744
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:

Author:

García-Cazorla A,Serrano M,Pérez-Dueñas B,González V,Ormazábal A,Pineda M,Fernández-álvarez E,Campistol J M D,Artuch R M D

Publisher

Wiley

Subject

Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.2007.00740.x/fullpdf

Reference24 articles.

1. Neurotransmitters and neuromodulators during early human development;Herlenius;Early Hum Dev,2001

2. Mutations in the sepiapterin reductase gene cause a novel tetrahydrobioptern-dependent monoamine-neurotransmitter deficiency without hyperphenylalaninemia;Bonafé;Am J Hum Genet,2001

3. Decreased homovanillic acid concentrations in cerebrospinal fluid in children without a known defect in dopamine metabolism;Van der Heyden;Eur J Ped Neurol,2003

4. Cerebrospinal fluid and serum levels of dopa, catechols, and monoamine metabolites in patients with epilepsy;Devinsky;Epilepsia,1992

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1. Bioanalytical validation and clinical application of a liquid chromatography-tandem mass spectrometry method for the quantification of 3-orthomethyldopa, 5-hydroxytryptophan, 5-hydroxyindolacetic acid and homovanillic acid in human cerebrospinal fluid;Journal of Pharmaceutical and Biomedical Analysis;2024-09

2. Diagnostic Yield of CSF Testing in Infants for Disorders of Biogenic Amine Neurotransmitter Metabolism;Neurology;2024-05

3. Cerebrospinal Fluid Concentrations of Neurotransmitters in a Greek Pediatric Reference Population;Neuropediatrics;2022-11-28

4. Monoamine neurotransmitters in early epileptic encephalopathies: New insights into pathophysiology and therapy;Developmental Medicine & Child Neurology;2022-01-31

5. Mitofusin 2: The missing link between mtDNA maintenance defects and neurotransmitter disorders;Mitochondrion;2021-11

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