Effect of the branched-chain α-keto acids accumulating in maple syrup urine disease on S100B release from glial cells-Reference-Cited by-同舟云学术

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Effect of the branched-chain α-keto acids accumulating in maple syrup urine disease on S100B release from glial cells

Published:2007-09 Issue:1-2 Volume:260 Page:87-94
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Funchal Cláudia,Tramontina Francine,dos Santos André Quincozes,de Souza Daniela Fraga,Gonçalves Carlos Alberto,Pessoa-Pureur Regina,Wajner Moacir

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference83 articles.

1. Maple syrup urine disease (branched-chain ketoaciduria);Chuang,2001

2. Branched-chain organic acidurias;Ogier de Baulny;Semin Neonatol,2002

3. Maple syrup urine disease: branched-chain ketoaciduria;Nyhan,1984

4. Maple syrup urine disease: interrelationship between branched chain amino-, oxo-, and hydroxyacids; implications for treatment; association with CNS dysmelination;Treacy;J Inherit Metab Dis,1992

5. Metabolism of branched-chain amino acids in maple syrup urine disease;Schadewaldt;Eur J Pediatr,1997

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1. Metabolomic Profile of Posner–Schlossman Syndrome: A Gas Chromatography Time-of-Flight Mass Spectrometry-Based Approach Using Aqueous Humor;Frontiers in Pharmacology;2019-11-07

2. Divergent Induction of Branched-Chain Aminotransferases and Phosphorylation of Branched Chain Keto-Acid Dehydrogenase Is a Potential Mechanism Coupling Branched-Chain Keto-Acid–Mediated-Astrocyte Activation to Branched-Chain Amino Acid Depletion-Mediated Cognitive Deficit after Traumatic Brain Injury;Journal of Neurotrauma;2018-10-15

3. Long-term metabolic follow-up and clinical outcome of 35 patients with maple syrup urine disease;Journal of Inherited Metabolic Disease;2017-09-13

4. Two homozygous mutations in the exon 5 of BCKDHB gene that may cause the classic form of maple syrup urine disease;Metabolic Brain Disease;2017-02-15

5. Neonatal Screening for Inherited Metabolic Diseases in 2016;Seminars in Pediatric Neurology;2016-11

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