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Molecular Genetics and Metabolism Reports|December 2, 2016
Highlighting intrafamilial clinical heterogeneity in late-onset Pompe diseaseC Papadopoulos, G K Papadimas, H Michelakakis, et al.The American Journal of Sports Medicine|September 26, 1997
Arthroscopic transglenoid suture capsulolabral repair. Five-year followupJ P Manta, S Organ, R P Nirschl, et al.Journal of Neurology|July 1, 1990
McArdle's disease: two clinical expressions in the same pedigreeA Papadimitriou, P Manta, R Divari, et al.Acta Neurologica Scandinavica|March 1, 1991
Neuropathy following acute intoxication with Mecarbam (OP ester)E Stamboulis, A Psimaras, D Vassilopoulos, et al.The International Journal of Neuroscience|May 23, 2015
Electrodiagnosis and muscle biopsy in asymptomatic hyperckemiaP Kokotis, G K Papadimas, V Zouvelou, et al.Journal of Neuromuscular Diseases|November 18, 2016
GNE-Myopathy in a Greek Romani Family with Unusual Calf Phenotype and Protein Aggregation PathologyG K Papadimas, A Evilä, C Papadopoulos, et al.Functional Neurology|March 1, 1996
Type II glycogenosis and thyroxine binding globulin deficiency in the same familyP Manta, P Kontoleon, A Panousopoulou, et al.Functional Neurology|July 1, 1995
External ophthalmoplegia with ragged-red fibres and acetylcholine receptor antibodiesD Mitsikostas, P Manta, N Kalfakis, et al.Neurology|June 20, 1998
A new mitochondrial tRNA(Met) gene mutation in a patient with dystrophic muscle and exercise intoleranceJ Vissing, M B Salamon, P Arlien-Søborg, et al.Neuromuscular Disorders : NMD|February 24, 2012
Mutation spectrum and phenotypic manifestation in FSHD Greek patientsP Sakellariou, K Kekou, H Fryssira, et al.Pageof 3