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

Year Number of Results
2005 2
2006 1
2007 1
2008 1
2009 1
2010 3
2011 3
2012 2
2024 0

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13 results

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Page 1
The struggle to model muscular dystrophy.
Kang PB. Kang PB. Muscle Nerve. 2011 Aug;44(2):157-9. doi: 10.1002/mus.22124. Epub 2011 Jun 9. Muscle Nerve. 2011. PMID: 21660989 No abstract available.
LGMD2I in a North American population.
Kang PB, Feener CA, Estrella E, Thorne M, White AJ, Darras BT, Amato AA, Kunkel LM. Kang PB, et al. BMC Musculoskelet Disord. 2007 Nov 24;8:115. doi: 10.1186/1471-2474-8-115. BMC Musculoskelet Disord. 2007. PMID: 18036232 Free PMC article.
Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores.
Boyden SE, Mahoney LJ, Kawahara G, Myers JA, Mitsuhashi S, Estrella EA, Duncan AR, Dey F, DeChene ET, Blasko-Goehringer JM, Bönnemann CG, Darras BT, Mendell JR, Lidov HG, Nishino I, Beggs AH, Kunkel LM, Kang PB. Boyden SE, et al. Neurogenetics. 2012 May;13(2):115-24. doi: 10.1007/s10048-012-0315-z. Epub 2012 Feb 28. Neurogenetics. 2012. PMID: 22371254 Free PMC article.
Novel MPZ mutations and congenital hypomyelinating neuropathy.
McMillan HJ, Santagata S, Shapiro F, Batish SD, Couchon L, Donnelly S, Kang PB. McMillan HJ, et al. Neuromuscul Disord. 2010 Nov;20(11):725-9. doi: 10.1016/j.nmd.2010.06.004. Neuromuscul Disord. 2010. PMID: 20621479 Free PMC article.
Congenital myasthenic syndrome with episodic apnea.
Mallory LA, Shaw JG, Burgess SL, Estrella E, Nurko S, Burpee TM, Agus MS, Darras BT, Kunkel LM, Kang PB. Mallory LA, et al. Pediatr Neurol. 2009 Jul;41(1):42-5. doi: 10.1016/j.pediatrneurol.2009.02.017. Pediatr Neurol. 2009. PMID: 19520274 Free PMC article.
13 results