Late-onset Pompe disease associated with polyneuropathy von Lamartine S.Monteiro, M., Remiche, G.

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Late-onset Pompe disease (LOPD) in Belgium: clinical characteristics and outcome measures von Vanherpe, P., Fieuws, S., D'Hondt, A., Bleyenheuft, C., Demaerel, P., De Bleecker, J., Van den Bergh, P., Baets, J., Remiche, G., Verhoeven, K., Delstanche, S., Toussaint, M., Buyse, B., Van Damme, P., Depuydt, C. E., Claeys, K. G.

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Electrophysiological evidence of spino-cortical proprioceptive tracts dysfunction in hereditary spastic paraplegia with thin corpus callosum von Lamartine Monteiro, M., Bourguignon, M., Sjogard, M., Remiche, G., Goldman, S., De Tiège, X., Naeije, G.

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Is late-onset type II glycogenosis underdiagnosed in Brussels and Wallonia (Belgium)? von Remiche, G, Abramowicz, M, Pandolfo, M

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G.P.297 von Remiche, G, Mavroudakis, N

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A novel NDUFV1 gene mutation in complex I deficiency in consanguineous siblings with brainstem lesions and Leigh syndrome von Vilain, C, Rens, C, Aeby, A, Balériaux, D, Van Bogaert, P, Remiche, G, Smet, J, Van Coster, R, Abramowicz, M, Pirson, I

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Database crossing allows better understanding of neuromuscular disorders epidemiology: The Belgian example von Bleyenheuft, C, Van Damme, P, Goemans, N, De Bleecker, J, Van Coster, R, De Jonghe, P, Beysen, D, Van den Bergh, P, Christiaens, F, Maertens de Noordhout, A, Haan, J, De Meirleir, L, Remiche, G, Deconinck, N, Depuijdt, E, Servais, L

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65P Striking periscapular muscle hypertrophy as the presenting symptom in a 5-month old infant diagnosed with a MYH7 congenital myopathy: report of a case von Deconinck, N., Coppens, S., Vilain, C., Remiche, G., Semal, B., Presiozi, M., Lecomte, S., Dontaine, P.

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G.P.297: Supramaximally stimulated complex A-waves are helpful to distinguish lower motor neurone disease from demyelinating neuropathies von Remiche, G., Mavroudakis, N.

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P.158 Is there a myopathic component in Urofacial (Ochoa) syndrome? von Remiche, G., Desmyter, L., Vandernoot, I., Kadhim, H., Coppens, S., Herbaut, A.

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EP.13Long-lasting corticosteroids-induced improvement in inclusion body myositis with prominent mitochondrial changes von Damien, C., Mavroudakis, N., Kadhim, H., Remiche, G.

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P.79 Late onset oculopharyngeal muscular dystrophy in a POLG1-related progressive external ophthalmoplegia (PEO), a diagnostic challenge von Remiche, G., Kadhim, H., Lecompte, S., Meneri, M., Ronchi, D., Comi, G., Seneca, S., Capiau, S., Stepman, H., Smits, G.

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CHANNELOPATHIES AND RELATED DISORDERS: EP.225 Autosomal dominant early onset vacuolar myopathy with granular material, without periodic paralysis, associated with c.1583C>A CACNA1S... von Bisciglia, M., Kadhim, H., Lecomte, S., Vandernoot, I., Desmyter, L., Remiche, G.

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CHANNELOPATHIES AND RELATED DISORDERS von Bisciglia, M., Kadhim, H., Lecomte, S., Vandernoot, I., Desmyter, L., Remiche, G.

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P424 Identify genetic modifiers controlling severity of collagen-6 related dystrophies (COL6-RD) von Bisciglia, M., Stojkovic, T., Nascimento, A., Vissing, J., Castiglioni, C., Claeys, K., Remiche, G., De Paepe, B., Butterfield, R., Deconinck, N.

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P.62 - Is late-onset type II glycogenosis underdiagnosed in Brussels and Wallonia (Belgium)? von Remiche, G., Abramowicz, M., Pandolfo, M.

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MYASTHENIA & RELATED DISORDERS: P.38 Autosomal recessive inheritance in hypokalaemic periodic paralysis due to a homozygous SCN4A gene mutation von Remiche, G., Desmyter, L., Grenet, M., Vandernoot, I., Devuyst, O., Smits, G., Potmans, V.

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MYASTHENIA & RELATED DISORDERS von Remiche, G., Desmyter, L., Grenet, M., Vandernoot, I., Devuyst, O., Smits, G., Potmans, V.

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MITOCHONDRIAL DISEASES & METABOLIC MYOPATHIES: P.321 Mitochondrial myopathy in X-linked creatine transporter deficiency due to a novel mutation of SLC6A8 gene von Bisciglia, M., Busson, A., Marangoni, M., David, P., Vandernoot, I., Michotte, A., Remiche, G.

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MITOCHONDRIAL DISEASES & METABOLIC MYOPATHIES von Bisciglia, M., Busson, A., Marangoni, M., David, P., Vandernoot, I., Michotte, A., Remiche, G.

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