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Specialty: Biochemistry
Condition: Encephalitis

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Total 4 results found since Jan 2013.

Myelin-associated glycoprotein activation triggers glutamate uptake by oligodendrocytes in vitro and contributes to ameliorate glutamate-mediated toxicity in vivo
CONCLUSIONS: MAG activation triggers Glu uptake into OLs under conditions of Glu overload and induces a robust protective antioxidant response.PMID:34954343 | DOI:10.1016/j.bbadis.2021.166324
Source: Biochimica et Biophysica Acta - December 26, 2021 Category: Biochemistry Authors: Ana L Vivinetto Clara Casta ñares Constanza Garcia-Keller Ana Lis Moyano Cristian Falcon Anabela Palandri Victoria Roz és-Salvador Juan I Rojas Liliana Patrucco Clara Monferran Liliana Cancela Edgardo Cristiano Ronald L Schnaar Pablo H H Lopez Source Type: research

Acute encephalopathy of the temporal lobes leading to m.3243A & gt;G. When MELAS is not always MELAS
Publication date: Available online 21 July 2016 Source:Mitochondrion Author(s): Elena Caldarazzo Ienco, Daniele Orsucci, Costanza Simoncini, Vincenzo Montano, Annalisa LoGerfo, Gabriele Siciliano, Ubaldo Bonuccelli, Michelangelo Mancuso MELAS syndrome (mitochondrial encephalopathy with lactic acidosis and stroke-like episodes) is a rare genetic condition whose differential diagnosis is often posed with juvenile stroke, but more rarely even with inflammatory/infectious encephalitis, causing diagnostic challenges. Here we report the case of a young man harbouring the m.3243A>G MELAS mutation presenting an ac...
Source: Mitochondrion - July 30, 2016 Category: Biochemistry Source Type: research

Acute encephalopathy of the temporal lobes leading to m3243A & gt;G. When MELAS is not always MELAS
Publication date: Available online 21 July 2016 Source:Mitochondrion Author(s): Elena Caldarazzo Ienco, Daniele Orsucci, Costanza Simoncini, Vincenzo Montano, Annalisa LoGerfo, Gabriele Siciliano, Ubaldo Bonuccelli, Michelangelo Mancuso MELAS syndrome (mitochondrial encephalopathy with lactic acidosis and stroke-like episodes) is a rare genetic condition whose differential diagnosis is often posed with juvenile stroke, but more rarely even with inflammatory/infectious encephalitis, causing diagnostic challenges. Here we report the case of a young man harbouring the m.3243A>G MELAS mutation presenting an ac...
Source: Mitochondrion - July 22, 2016 Category: Biochemistry Source Type: research