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Page 1
Kearns-Sayre syndrome presenting as 2-oxoadipic aciduria.
Barshop BA, Nyhan WL, Naviaux RK, McGowan KA, Friedlander M, Haas RH. Barshop BA, et al. Among authors: naviaux rk. Mol Genet Metab. 2000 Jan;69(1):64-8. doi: 10.1006/mgme.1999.2946. Mol Genet Metab. 2000. PMID: 10655159
Mitochondrial DNA disorders.
Naviaux RK. Naviaux RK. Eur J Pediatr. 2000 Dec;159 Suppl 3:S219-26. doi: 10.1007/pl00014407. Eur J Pediatr. 2000. PMID: 11216904 Review.
Pyruvate carboxylase deficiency--insights from liver transplantation.
Nyhan WL, Khanna A, Barshop BA, Naviaux RK, Precht AF, Lavine JE, Hart MA, Hainline BE, Wappner RS, Nichols S, Haas RH. Nyhan WL, et al. Among authors: naviaux rk. Mol Genet Metab. 2002 Sep-Oct;77(1-2):143-9. doi: 10.1016/s1096-7192(02)00123-3. Mol Genet Metab. 2002. PMID: 12359142
Chronic treatment of mitochondrial disease patients with dichloroacetate.
Barshop BA, Naviaux RK, McGowan KA, Levine F, Nyhan WL, Loupis-Geller A, Haas RH. Barshop BA, et al. Among authors: naviaux rk. Mol Genet Metab. 2004 Sep-Oct;83(1-2):138-49. doi: 10.1016/j.ymgme.2004.06.009. Mol Genet Metab. 2004. PMID: 15464428 Clinical Trial.
119 results