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216 related items for PubMed ID: 33951347
1. Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS-associated mtDNA mutations. Gramegna LL, Evangelisti S, Di Vito L, La Morgia C, Maresca A, Caporali L, Amore G, Talozzi L, Bianchini C, Testa C, Manners DN, Cortesi I, Valentino ML, Liguori R, Carelli V, Tonon C, Lodi R. Ann Clin Transl Neurol; 2021 Jun; 8(6):1200-1211. PubMed ID: 33951347 [Abstract] [Full Text] [Related]
6. A study of familial MELAS: evaluation of A3243G mutation, clinical phenotype, and magnetic resonance spectroscopy-monitored progression. Chen C, Xiong N, Wang Y, Xiong J, Huang J, Zhang Z, Wang T. Neurol India; 2012 Jun; 60(1):86-9. PubMed ID: 22406788 [Abstract] [Full Text] [Related]
7. Disease-causing mitochondrial heteroplasmy segregated within induced pluripotent stem cell clones derived from a patient with MELAS. Folmes CD, Martinez-Fernandez A, Perales-Clemente E, Li X, McDonald A, Oglesbee D, Hrstka SC, Perez-Terzic C, Terzic A, Nelson TJ. Stem Cells; 2013 Jul; 31(7):1298-308. PubMed ID: 23553816 [Abstract] [Full Text] [Related]
14. Evaluation of in vivo cerebral metabolism on proton magnetic resonance spectroscopy in patients with impaired glucose tolerance and type 2 diabetes mellitus. Sahin I, Alkan A, Keskin L, Cikim A, Karakas HM, Firat AK, Sigirci A. J Diabetes Complications; 2008 Aug 20; 22(4):254-60. PubMed ID: 18413166 [Abstract] [Full Text] [Related]