メチルクロトニルグリシン尿症
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English Journal
- Selective screening of glutaric acid acidurias by capillary electrophoresis-mass spectrometry.
- Fernández-Bravo J1, de Andrés F2, Zougagh M3, Ríos Á4.
- Journal of pharmaceutical and biomedical analysis.J Pharm Biomed Anal.2017 Jun 19;145:40-45. doi: 10.1016/j.jpba.2017.06.037. [Epub ahead of print]
- PMID 28648786
- Coupled brain and urine spectroscopy - in vivo metabolomic characterization of HMG-CoA lyase deficiency in 5 patients.
- Roland D1, Jissendi-Tchofo P2, Briand G3, Vamecq J4, Fontaine M5, Ultré V6, Acquaviva-Bourdain C7, Mention K8, Dobbelaere D9.
- Molecular genetics and metabolism.Mol Genet Metab.2017 Jun;121(2):111-118. doi: 10.1016/j.ymgme.2017.03.006. Epub 2017 Mar 30.
- PMID 28396157
- Induction of a Proinflammatory Response in Cortical Astrocytes by the Major Metabolites Accumulating in HMG-CoA Lyase Deficiency: the Role of ERK Signaling Pathway in Cytokine Release.
- Fernandes CG1, Rodrigues MDN1, Seminotti B1, Colín-González AL2, Santamaria A2, Quincozes-Santos A1, Wajner M3,4.
- Molecular neurobiology.Mol Neurobiol.2016 Aug;53(6):3586-3595. doi: 10.1007/s12035-015-9289-9. Epub 2015 Jun 23.
- PMID 26099308
Japanese Journal
- 3-hydroxy-3-methylglutaric aciduria : response to carnitine therapy and fat and leucine restriction
Related Links
- Each child with 3-hydroxy-3-methylglutaric aciduria (HMG) has a slightly different experience. Most affected children start to show signs of HMG between 3 months and 2 years of age. In a few cases, babies start to show signs of the ...
- Advocacy and Support Organizations Condition Specific Organizations Following organizations serve the condition "3-Hydroxy-3-methylglutaric aciduria" for support ... CLIMB - Children Living with Inherited Metabolic Diseases Climb ...
★リンクテーブル★
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- 英
- methylglutaric aciduria
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β-メチルクロトニルグリシン尿症