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Page 1
Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.
Parikh S, Goldstein A, Karaa A, Koenig MK, Anselm I, Brunel-Guitton C, Christodoulou J, Cohen BH, Dimmock D, Enns GM, Falk MJ, Feigenbaum A, Frye RE, Ganesh J, Griesemer D, Haas R, Horvath R, Korson M, Kruer MC, Mancuso M, McCormack S, Raboisson MJ, Reimschisel T, Salvarinova R, Saneto RP, Scaglia F, Shoffner J, Stacpoole PW, Sue CM, Tarnopolsky M, Van Karnebeek C, Wolfe LA, Cunningham ZZ, Rahman S, Chinnery PF. Parikh S, et al. Among authors: cohen bh. Genet Med. 2017 Dec;19(12):10.1038/gim.2017.107. doi: 10.1038/gim.2017.107. Epub 2017 Jul 27. Genet Med. 2017. PMID: 28749475 Free PMC article. Review.
Acute neurotoxicity of meperidine in an infant.
Saneto RP, Fitch JA, Cohen BH. Saneto RP, et al. Among authors: cohen bh. Pediatr Neurol. 1996 May;14(4):339-41. doi: 10.1016/0887-8994(96)00062-8. Pediatr Neurol. 1996. PMID: 8962593
The in-depth evaluation of suspected mitochondrial disease.
Mitochondrial Medicine Society's Committee on Diagnosis; Haas RH, Parikh S, Falk MJ, Saneto RP, Wolf NI, Darin N, Wong LJ, Cohen BH, Naviaux RK. Mitochondrial Medicine Society's Committee on Diagnosis, et al. Among authors: cohen bh. Mol Genet Metab. 2008 May;94(1):16-37. doi: 10.1016/j.ymgme.2007.11.018. Epub 2008 Feb 1. Mol Genet Metab. 2008. PMID: 18243024 Free PMC article. Review.
Metabolic testing in the pediatric epilepsy unit.
Parikh S, Cohen BH, Gupta A, Lachhwani DK, Wyllie E, Kotagal P. Parikh S, et al. Among authors: cohen bh. Pediatr Neurol. 2008 Mar;38(3):191-5. doi: 10.1016/j.pediatrneurol.2007.10.011. Pediatr Neurol. 2008. PMID: 18279754
Molecular and clinical genetics of mitochondrial diseases due to POLG mutations.
Wong LJ, Naviaux RK, Brunetti-Pierri N, Zhang Q, Schmitt ES, Truong C, Milone M, Cohen BH, Wical B, Ganesh J, Basinger AA, Burton BK, Swoboda K, Gilbert DL, Vanderver A, Saneto RP, Maranda B, Arnold G, Abdenur JE, Waters PJ, Copeland WC. Wong LJ, et al. Among authors: cohen bh. Hum Mutat. 2008 Sep;29(9):E150-72. doi: 10.1002/humu.20824. Hum Mutat. 2008. PMID: 18546365 Free PMC article.
A modern approach to the treatment of mitochondrial disease.
Parikh S, Saneto R, Falk MJ, Anselm I, Cohen BH, Haas R, Medicine Society TM. Parikh S, et al. Among authors: cohen bh. Curr Treat Options Neurol. 2009 Nov;11(6):414-30. doi: 10.1007/s11940-009-0046-0. Curr Treat Options Neurol. 2009. PMID: 19891905 Free PMC article.
Initial experience in the treatment of inherited mitochondrial disease with EPI-743.
Enns GM, Kinsman SL, Perlman SL, Spicer KM, Abdenur JE, Cohen BH, Amagata A, Barnes A, Kheifets V, Shrader WD, Thoolen M, Blankenberg F, Miller G. Enns GM, et al. Among authors: cohen bh. Mol Genet Metab. 2012 Jan;105(1):91-102. doi: 10.1016/j.ymgme.2011.10.009. Epub 2011 Oct 21. Mol Genet Metab. 2012. PMID: 22115768 Free article. Clinical Trial.
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