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Polymorphic variants in the human mitochondrial cytochrome b gene.
Andreu AL, Bruno C, Hadjigeorgiou GM, Shanske S, DiMauro S. Andreu AL, et al. Among authors: hadjigeorgiou gm. Mol Genet Metab. 1999 May;67(1):49-52. doi: 10.1006/mgme.1999.2843. Mol Genet Metab. 1999. PMID: 10329023 Free article.
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene.
Andreu AL, Tanji K, Bruno C, Hadjigeorgiou GM, Sue CM, Jay C, Ohnishi T, Shanske S, Bonilla E, DiMauro S. Andreu AL, et al. Among authors: hadjigeorgiou gm. Ann Neurol. 1999 Jun;45(6):820-3. doi: 10.1002/1531-8249(199906)45:6<820::aid-ana22>3.0.co;2-w. Ann Neurol. 1999. PMID: 10360780
Molecular characterization of McArdle's disease in two large Finnish families.
Bruno C, Löfberg M, Tamburino L, Jänkälä H, Hadjigeorgiou GM, Andreu AL, Shanske S, Somer H, DiMauro S. Bruno C, et al. Among authors: hadjigeorgiou gm. J Neurol Sci. 1999 Jun 1;165(2):121-5. doi: 10.1016/s0022-510x(99)00091-x. J Neurol Sci. 1999. PMID: 10450796 Free article.
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations.
Nishino I, Spinazzola A, Papadimitriou A, Hammans S, Steiner I, Hahn CD, Connolly AM, Verloes A, Guimarães J, Maillard I, Hamano H, Donati MA, Semrad CE, Russell JA, Andreu AL, Hadjigeorgiou GM, Vu TH, Tadesse S, Nygaard TG, Nonaka I, Hirano I, Bonilla E, Rowland LP, DiMauro S, Hirano M. Nishino I, et al. Among authors: hadjigeorgiou gm. Ann Neurol. 2000 Jun;47(6):792-800. Ann Neurol. 2000. PMID: 10852545
258 results