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

Year Number of Results
1983 1
1987 1
1988 1
1989 1
1990 1
1991 1
1993 1
1995 3
1996 2
1998 1
1999 2
2002 1
2003 1
2004 2
2005 2
2006 7
2007 6
2008 9
2009 8
2010 9
2011 8
2012 7
2013 3
2014 3
2015 3
2016 3
2020 1
2021 1
2024 0

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79 results

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Page 1
Caveolinopathies in Greece.
Papadopoulos C, Papadimas GK, Kekou K, Spengos K, Svigou M, Kitsiou-Tzeli S, Manta P. Papadopoulos C, et al. Among authors: manta p. Neurologist. 2015 Jul;20(1):8-12. doi: 10.1097/NRL.0000000000000036. Neurologist. 2015. PMID: 26185955
Electrodiagnosis and muscle biopsy in asymptomatic hyperckemia.
Kokotis P, Papadimas GK, Zouvelou V, Zambelis T, Manta P, Karandreas N. Kokotis P, et al. Among authors: manta p. Int J Neurosci. 2016 Jun;126(6):514-519. doi: 10.3109/00207454.2015.1038534. Epub 2015 Jul 14. Int J Neurosci. 2016. PMID: 26000931
OX40-OX40L expression in idiopathic inflammatory myopathies.
Papadopoulos C, Terzis G, Papadimas GK, Manta P. Papadopoulos C, et al. Among authors: manta p. Anal Quant Cytopathol Histpathol. 2013 Feb;35(1):17-26. Anal Quant Cytopathol Histpathol. 2013. PMID: 23469620
Throwing performance after resistance training and detraining.
Terzis G, Stratakos G, Manta P, Georgiadis G. Terzis G, et al. Among authors: manta p. J Strength Cond Res. 2008 Jul;22(4):1198-204. doi: 10.1519/JSC.0b013e31816d5c97. J Strength Cond Res. 2008. PMID: 18545188 Clinical Trial.
Body composition analysis in late-onset Pompe disease.
Papadimas GK, Terzis G, Methenitis S, Spengos K, Papadopoulos C, Vassilopoulou S, Kavouras S, Michelakakis H, Manta P. Papadimas GK, et al. Among authors: manta p. Mol Genet Metab. 2011 Jan;102(1):41-3. doi: 10.1016/j.ymgme.2010.09.002. Epub 2010 Sep 16. Mol Genet Metab. 2011. PMID: 20926325
Nucleo-cytoplasmic ratio in ageing skeletal muscle.
Manta P, Vassilopoulos D, Spengos M. Manta P, et al. Eur Arch Psychiatry Neurol Sci. 1987;236(4):235-6. doi: 10.1007/BF00383854. Eur Arch Psychiatry Neurol Sci. 1987. PMID: 3582433
Mutation spectrum and phenotypic manifestation in FSHD Greek patients.
Sakellariou P, Kekou K, Fryssira H, Sofocleous C, Manta P, Panousopoulou A, Gounaris K, Kanavakis E. Sakellariou P, et al. Among authors: manta p. Neuromuscul Disord. 2012 Apr;22(4):339-49. doi: 10.1016/j.nmd.2011.11.001. Epub 2012 Feb 21. Neuromuscul Disord. 2012. PMID: 22357364
79 results