Late-Onset Pompe Disease with Nemaline Bodies von Greco, G., Rastelli, E., Giacanelli, Manlio, Terracciano, Chiara, Frezza, E., Massa, Roberto

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P26.8 Motor evoked potentials in conversion disorders. A case report von Petrucci, A, Lispi, L, Haggiag, S, Giacanelli, M

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An interrupted 34-CAG repeat SCA-2 allele in patients with sporadic spinocerebellar ataxia von COSTANZI-PORRINI, S, TESSAROLO, D, ABBRUZZESE, C, LIGUORI, M, ASHIZAWA, T, GIACANELLI, M

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Different entities of proximal spinal muscular atrophy within one family von WIRTH, B, TESSAROLO, D, HAHNEN, E, RUDNIK-SCHÖNEBORN, S, RASCHKE, H, LIGUORI, M, GIACANELLI, M, ZERRES, K

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Effect of Myotonic Dystrophy Trinucleotide Repeat Expansion on DMPK Transcription and Processing von Krahe, Ralf, Ashizawa, Tetsuo, Abbruzzese, Claudia, Roeder, Elizabeth, Carango, Paul, Giacanelli, Manlio, Funanage, Vicky L., Siciliano, Michael J.

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Instability of a premutation allele in homozygous patients with myotonic dystrophy type 1 von Abbruzzese, Claudia, Costanzi Porrini, Sandro, Mariani, Bruno, Gould, Fiona K., Mcabney, John P., Monckton, Darren G., Ashizawa, Tetsuo, Giacanelli, Manlio

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Iatrogenic Worsening of Hypokalemia and Neuromuscular Paralysis Associated with the Use of Glucose Solutions for Potassium Replacement in a Young Woman with Licorice Intoxication a... von Famularo, Giuseppe, Corsi, Fabio Massimo, Giacanelli, Manlio

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Detection of NAD+--malate dehydrogenase in human muscle von Giacanelli, M, Liguori, M, Tessarolo, D, Marcelli, M

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Myotonic dystrophy (Steinert disease): a morphologic and biochemical hair study von Amorosi, Beatrice, Giustini, Sandra, Rossi, Alfredo, Giacanelli, Manlio, Calvieri, Stefano

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Myotonic dystrophy phenotype without expansion of (CTG)n repeat : an entity distinct from proximal myotonic myopathy (PROMM) ? von ABBRUZZESE, C, KRAHE, R, LIGUORI, M, TESSAROLO, D, SICILIANO, M. J, ASHIZAWA, T, GIACANELLI, M

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Brain Connectomics' Modification to Clarify Motor and Nonmotor Features of Myotonic Dystrophy Type 1 von Serra, L, Mancini, M, Silvestri, G, Petrucci, A, Masciullo, M, Spano, B, Torso, M, Mastropasqua, C, Giacanelli, M, Caltagirone, C, Cercignani, M, Meola, G, Bozzali, M

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NAD+/NADP+-Dependent Malic Enzyme: Evidence of a NADP+ Preferring Activity in Human Skeletal Muscle von Liguori, M., Tessarolo, D., Abbruzzese, C., Giacanelli, M.

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Late-Onset Pompe Disease with Nemaline Bodies von Frezza, E, Terracciano, C, Giacanelli, M, Rastelli, E, Greco, G, Massa, R

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"I Know that You Know that I Know": Neural Substrates Associated with Social Cognition Deficits in DM1 Patients von Serra, L, Cercignani, M, Bruschini, M, Cipolotti, L, Mancini, M, Silvestri, G, Petrucci, A, Bucci, E, Antonini, G, Licchelli, L, Spano, B, Giacanelli, M, Caltagirone, C, Meola, G, Bozzali, M

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Human malic enzymes in heart and muscle: Evidence of a selective distribution von Tessarolo, D., Liguori, M., Giacanelli, M.

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Kearns-Sayre syndrome. A case of the complete syndrome with encephalic leukodystrophy and calcification of basal ganglia von Carboni, P., Giacanelli, M., Porro, G., Sideri, G., Paolella, A.

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Acute hypokalemic myopathy due to chronic licorice ingestion: report of a case von Corsi, F. M., Galgani, S., Gasparini, C., Giacanelli, M., Piazza, G.

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(CTG)n Triplet Mutation and Phenotype Manifestations in Myotonic Dystrophy Patients von Novelli, G., Gennarelli, M., Menegazzo, E., Mostacciuolo, M.L., Pizzuti, A., Fattorini, C., Tessarolo, D., Tomelleri, G., Giacanelli, M., Danieli, G.A., Rizzuto, N., Caskey, C.T., Angelini, C., Dallapiccola, B.

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Effects of myotonic dystrophy trinucleotide repeat expansion on DMPK transcription and processing von KRAHE, R, ASHIZAWA, T, ABBRUZZESE, C, ROEDER, E, CARANGO, P, GIACANELLI, M, FUNANAGE, V. L, SICILIANO, M. J

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Mapping of the Emery-Dreifuss gene through reconstruction of crossover points in two Italian pedigrees von ROMEO, G, RONCUZZI, L, SANGIORGI, S, GIACANELLI, M, LIGUORI, M, TESSAROLO, D, ROCCHI, M

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