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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1954 2
1955 1
1956 2
1959 3
1960 2
1962 2
1963 4
1964 2
1965 1
1966 3
1967 1
1968 5
1969 2
1970 4
1971 2
1972 2
1973 1
1974 2
1975 3
1976 3
1977 4
1978 2
1980 9
1982 2
1984 7
1985 8
1986 5
1987 6
1988 6
1989 4
1990 7
1991 4
1992 5
1993 5
1994 2
1995 4
1996 3
1997 1
1998 3
1999 2
2000 4
2001 4
2002 2
2003 3
2004 1
2005 2
2006 2
2007 3
2008 5
2009 2
2010 6
2011 5
2012 6
2013 9
2014 4
2015 8
2016 6
2017 4
2018 7
2019 4
2020 12
2021 8
2022 7
2023 4

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239 results

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Page 1
Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.
Parikh S, Goldstein A, Koenig MK, Scaglia F, Enns GM, Saneto R, Anselm I, Cohen BH, Falk MJ, Greene C, Gropman AL, Haas R, Hirano M, Morgan P, Sims K, Tarnopolsky M, Van Hove JL, Wolfe L, DiMauro S. Parikh S, et al. Among authors: cohen bh. Genet Med. 2015 Sep;17(9):689-701. doi: 10.1038/gim.2014.177. Epub 2014 Dec 11. Genet Med. 2015. PMID: 25503498 Free PMC article. Review.
POLG-Related Disorders.
Cohen BH, Chinnery PF, Copeland WC. Cohen BH, et al. 2010 Mar 16 [updated 2018 Mar 1]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. 2010 Mar 16 [updated 2018 Mar 1]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. PMID: 20301791 Free Books & Documents. Review.
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.
Alpers-Huttenlocher syndrome.
Saneto RP, Cohen BH, Copeland WC, Naviaux RK. Saneto RP, et al. Among authors: cohen bh. Pediatr Neurol. 2013 Mar;48(3):167-78. doi: 10.1016/j.pediatrneurol.2012.09.014. Pediatr Neurol. 2013. PMID: 23419467 Free PMC article. Review.
Coding for Headaches.
Victorio MC, Cohen BH. Victorio MC, et al. Among authors: cohen bh. Continuum (Minneap Minn). 2015 Aug;21(4 Headache):1157-64. doi: 10.1212/CON.0000000000000202. Continuum (Minneap Minn). 2015. PMID: 26252599 No abstract available.
Coding for neuro-oncology.
Cohen BH. Cohen BH. Continuum (Minneap Minn). 2015 Apr;21(2 Neuro-oncology):487-98. doi: 10.1212/01.CON.0000464184.12452.15. Continuum (Minneap Minn). 2015. PMID: 25837909 No abstract available.
Mitochondrial and Metabolic Myopathies.
Cohen BH. Cohen BH. Continuum (Minneap Minn). 2019 Dec;25(6):1732-1766. doi: 10.1212/CON.0000000000000805. Continuum (Minneap Minn). 2019. PMID: 31794469 Review.
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.
Fetal anomaly diagnosis and termination of pregnancy.
Graf WD, Cohen BH, Kalsner L, Pearl PL, Sarnat HB, Epstein LG; Ethics Committee of the Child Neurology Society. Graf WD, et al. Among authors: cohen bh. Dev Med Child Neurol. 2023 Jul;65(7):900-907. doi: 10.1111/dmcn.15528. Epub 2023 Feb 2. Dev Med Child Neurol. 2023. PMID: 36732680 Review.
Diagnosis of 'possible' mitochondrial disease: an existential crisis.
Parikh S, Karaa A, Goldstein A, Bertini ES, Chinnery PF, Christodoulou J, Cohen BH, Davis RL, Falk MJ, Fratter C, Horvath R, Koenig MK, Mancuso M, McCormack S, McCormick EM, McFarland R, Nesbitt V, Schiff M, Steele H, Stockler S, Sue C, Tarnopolsky M, Thorburn DR, Vockley J, Rahman S. Parikh S, et al. Among authors: cohen bh. J Med Genet. 2019 Mar;56(3):123-130. doi: 10.1136/jmedgenet-2018-105800. Epub 2019 Jan 25. J Med Genet. 2019. PMID: 30683676 Review.
239 results