Manta P - Search Results

1

Cognitive impairment and cerebellar atrophy in typical onset 4Q35 fascioscapulohumeral dystrophy.

Zouvelou V, Rentzos M, Zalonis I, Filippopolitis K, Manta P, Evdokimidis I. Zouvelou V, et al. Among authors: manta p. Muscle Nerve. 2008 Nov;38(5):1523-1524. doi: 10.1002/mus.21100. Muscle Nerve. 2008. PMID: 18816620 No abstract available.

2

Asymptomatic elevation of serum creatine kinase leading to the diagnosis of 4q35 facioscapulohumeral muscular dystrophy.

Zouvelou V, Manta P, Kalfakis N, Evdokimidis I, Vassilopoulos D. Zouvelou V, et al. Among authors: manta p. J Clin Neurosci. 2009 Sep;16(9):1218-9. doi: 10.1016/j.jocn.2008.12.004. Epub 2009 Jun 6. J Clin Neurosci. 2009. PMID: 19502063

3

Toward understanding cognitive impairment in patients with myotonic dystrophy type 1.

Zalonis I, Bonakis A, Christidi F, Vagiakis E, Papageorgiou SG, Kalfakis N, Manta P, Vassilopoulos D. Zalonis I, et al. Among authors: manta p. Arch Clin Neuropsychol. 2010 Jun;25(4):303-13. doi: 10.1093/arclin/acq016. Epub 2010 Mar 17. Arch Clin Neuropsychol. 2010. PMID: 20237049

4

Diabetes mellitus associated with glycogen storage disease type III.

Spengos K, Michelakakis H, Vontzalidis A, Zouvelou V, Manta P. Spengos K, et al. Among authors: manta p. Muscle Nerve. 2009 Jun;39(6):876-7. doi: 10.1002/mus.21201. Muscle Nerve. 2009. PMID: 19334047 No abstract available.

5

Phenotypic variability and molecular genetics in proximal myotonic myopathy.

Papadimas GK, Kekou K, Papadopoulos C, Kararizou E, Kanavakis E, Manta P. Papadimas GK, et al. Among authors: manta p. Muscle Nerve. 2015 May;51(5):686-91. doi: 10.1002/mus.24440. Epub 2015 Mar 31. Muscle Nerve. 2015. PMID: 25186227

6

Delayed contrast enhancement on cardiac MRI unmasks subclinical cardiomyopathy in a case of myotonic dystrophy type 2.

Spengos K, Gialafos E, Vassilopoulou S, Toulas P, Manta P. Spengos K, et al. Among authors: manta p. Hellenic J Cardiol. 2012 Jul-Aug;53(4):324-6. Hellenic J Cardiol. 2012. PMID: 22796821 Free article.

7

Bent spine syndrome in facioscapulohumeral muscular dystrophy.

Papadopoulos C, Papadimas GK, Spengos K, Manta P. Papadopoulos C, et al. Among authors: manta p. Muscle Nerve. 2011 Apr;43(4):615; author reply 615-6. doi: 10.1002/mus.21971. Muscle Nerve. 2011. PMID: 21404293 No abstract available.

8

Facioscapulohumeral muscular dystrophy molecular testing using a non radioactive protocol.

Kekou K, Fryssira H, Sophocleous C, Mavrou A, Manta P, Metaxotou C. Kekou K, et al. Among authors: manta p. Mol Cell Probes. 2005 Dec;19(6):422-4. doi: 10.1016/j.mcp.2005.06.003. Epub 2005 Sep 6. Mol Cell Probes. 2005. PMID: 16144755

9

Coinheritance of Noonan syndrome and Becker muscular dystrophy.

Dinopoulos A, Papadopoulou A, Manta P, Kekou K, Kanelopoulos T, Fretzayas A, Kitsiou S. Dinopoulos A, et al. Among authors: manta p. Neuromuscul Disord. 2010 Jan;20(1):61-3. doi: 10.1016/j.nmd.2009.08.008. Epub 2009 Oct 28. Neuromuscul Disord. 2010. PMID: 19875288

10

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

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