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Year | Number of Results |
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2005 | 2 |
2006 | 2 |
2009 | 2 |
2024 | 0 |
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Page 1
Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort.
Hum Mutat. 2009 Dec;30(12):1657-66. doi: 10.1002/humu.21114.
Hum Mutat. 2009.
PMID: 19937601
Free PMC article.
Discrepancy between neuroimaging findings and clinical phenotype in Alexander disease.
Dinopoulos A, Gorospe JR, Egelhoff JC, Cecil KM, Nicolaidou P, Morehart P, DeGrauw T.
Dinopoulos A, et al. Among authors: morehart p.
AJNR Am J Neuroradiol. 2006 Nov-Dec;27(10):2088-92.
AJNR Am J Neuroradiol. 2006.
PMID: 17110673
Free PMC article.
Review.
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Muscle coenzyme Q: a potential test for mitochondrial activity and redox status.
Miles L, Miles MV, Tang PH, Horn PS, Wong BL, DeGrauw TJ, Morehart PJ, Bove KE.
Miles L, et al. Among authors: morehart pj.
Pediatr Neurol. 2005 May;32(5):318-24. doi: 10.1016/j.pediatrneurol.2005.01.009.
Pediatr Neurol. 2005.
PMID: 15866432
Item in Clipboard
Progressive myofiber loss with extensive fibro-fatty replacement in a child with mitochondrial DNA depletion syndrome and novel thymidine kinase 2 gene mutations.
Collins J, Bove KE, Dimmock D, Morehart P, Wong LJ, Wong B.
Collins J, et al. Among authors: morehart p.
Neuromuscul Disord. 2009 Nov;19(11):784-7. doi: 10.1016/j.nmd.2009.08.002. Epub 2009 Sep 6.
Neuromuscul Disord. 2009.
PMID: 19736010
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Investigation of children for mitochondriopathy confirms need for strict patient selection, improved morphological criteria, and better laboratory methods.
Miles L, Wong BL, Dinopoulos A, Morehart PJ, Hofmann IA, Bove KE.
Miles L, et al. Among authors: morehart pj.
Hum Pathol. 2006 Feb;37(2):173-84. doi: 10.1016/j.humpath.2005.10.008. Epub 2005 Dec 20.
Hum Pathol. 2006.
PMID: 16426917
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