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Page 1
Renal manifestations of congenital lactic acidosis.
Neiberger RE, George JC, Perkins LA, Theriaque DW, Hutson AD, Stacpoole PW. Neiberger RE, et al. Among authors: stacpoole pw. Am J Kidney Dis. 2002 Jan;39(1):12-23. doi: 10.1053/ajkd.2002.29872. Am J Kidney Dis. 2002. PMID: 11774096
Controlled clinical trial of dichloroacetate for treatment of congenital lactic acidosis in children.
Stacpoole PW, Kerr DS, Barnes C, Bunch ST, Carney PR, Fennell EM, Felitsyn NM, Gilmore RL, Greer M, Henderson GN, Hutson AD, Neiberger RE, O'Brien RG, Perkins LA, Quisling RG, Shroads AL, Shuster JJ, Silverstein JH, Theriaque DW, Valenstein E. Stacpoole PW, et al. Pediatrics. 2006 May;117(5):1519-31. doi: 10.1542/peds.2005-1226. Pediatrics. 2006. PMID: 16651305 Clinical Trial.
Long-term safety of dichloroacetate in congenital lactic acidosis.
Abdelmalak M, Lew A, Ramezani R, Shroads AL, Coats BS, Langaee T, Shankar MN, Neiberger RE, Subramony SH, Stacpoole PW. Abdelmalak M, et al. Among authors: stacpoole pw. Mol Genet Metab. 2013 Jun;109(2):139-43. doi: 10.1016/j.ymgme.2013.03.019. Epub 2013 Apr 6. Mol Genet Metab. 2013. PMID: 23611579 Free PMC article.
Peripheral neuropathy in genetic mitochondrial diseases.
Stickler DE, Valenstein E, Neiberger RE, Perkins LA, Carney PR, Shuster JJ, Theriaque DW, Stacpoole PW. Stickler DE, et al. Among authors: stacpoole pw. Pediatr Neurol. 2006 Feb;34(2):127-31. doi: 10.1016/j.pediatrneurol.2005.08.006. Pediatr Neurol. 2006. PMID: 16458825
The spectrum of pyruvate dehydrogenase complex deficiency: clinical, biochemical and genetic features in 371 patients.
Patel KP, O'Brien TW, Subramony SH, Shuster J, Stacpoole PW. Patel KP, et al. Among authors: stacpoole pw. Mol Genet Metab. 2012 Jan;105(1):34-43. doi: 10.1016/j.ymgme.2011.09.032. Epub 2011 Oct 7. Mol Genet Metab. 2012. Corrected and republished in: Mol Genet Metab. 2012 Jul;106(3):385-94. doi: 10.1016/j.ymgme.2012.03.017 PMID: 22079328 Free PMC article. Corrected and republished. Review.
211 results