Late-Onset Pompe Disease with Nemaline Bodies
Greco, G., Rastelli, E., Giacanelli, Manlio, Terracciano, Chiara, Frezza, E., Massa, Roberto
Published in Case reports in neurological medicine (01.01.2018)
Published in Case reports in neurological medicine (01.01.2018)
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An interrupted 34-CAG repeat SCA-2 allele in patients with sporadic spinocerebellar ataxia
Costanzi-Porrini, S, Tessarolo, D, Abbruzzese, C, Liguori, M, Ashizawa, T, Giacanelli, M
Published in Neurology (25.01.2000)
Published in Neurology (25.01.2000)
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Different entities of proximal spinal muscular atrophy within one family
WIRTH, B, TESSAROLO, D, HAHNEN, E, RUDNIK-SCHÖNEBORN, S, RASCHKE, H, LIGUORI, M, GIACANELLI, M, ZERRES, K
Published in Human genetics (01.10.1997)
Published in Human genetics (01.10.1997)
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Human malic enzymes in heart and muscle: Evidence of a selective distribution
Tessarolo, D., Liguori, M., Giacanelli, M.
Published in Biochemical medicine and metabolic biology (01.02.1991)
Published in Biochemical medicine and metabolic biology (01.02.1991)
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Acute hypokalemic myopathy due to chronic licorice ingestion: report of a case
Corsi, F M, Galgani, S, Gasparini, C, Giacanelli, M, Piazza, G
Published in Italian journal of neurological sciences (01.12.1983)
Published in Italian journal of neurological sciences (01.12.1983)
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Effect of Myotonic Dystrophy Trinucleotide Repeat Expansion on DMPK Transcription and Processing
Krahe, Ralf, Ashizawa, Tetsuo, Abbruzzese, Claudia, Roeder, Elizabeth, Carango, Paul, Giacanelli, Manlio, Funanage, Vicky L., Siciliano, Michael J.
Published in Genomics (San Diego, Calif.) (01.07.1995)
Published in Genomics (San Diego, Calif.) (01.07.1995)
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NAD+/NADP+-Dependent Malic Enzyme: Evidence of a NADP+ Preferring Activity in Human Skeletal Muscle
Liguori, M., Tessarolo, D., Abbruzzese, C., Giacanelli, M.
Published in Biochemical and molecular medicine (01.10.1995)
Published in Biochemical and molecular medicine (01.10.1995)
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(CTG)n Triplet Mutation and Phenotype Manifestations in Myotonic Dystrophy Patients
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.
Published in Biochemical medicine and metabolic biology (01.08.1993)
Published in Biochemical medicine and metabolic biology (01.08.1993)
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Instability of a premutation allele in homozygous patients with myotonic dystrophy type 1
Abbruzzese, Claudia, Costanzi Porrini, Sandro, Mariani, Bruno, Gould, Fiona K., Mcabney, John P., Monckton, Darren G., Ashizawa, Tetsuo, Giacanelli, Manlio
Published in Annals of neurology (01.10.2002)
Published in Annals of neurology (01.10.2002)
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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 and Furosemide Abuse
Famularo, Giuseppe, Corsi, Fabio Massimo, Giacanelli, Manlio
Published in Academic emergency medicine (01.09.1999)
Published in Academic emergency medicine (01.09.1999)
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Syndrome of continuous muscle fiber activity. Case report
Grassa, C, Figà-Talamanca, L, Lo Russo, F, Giacanelli, M, Pontesilli, R
Published in Italian journal of neurological sciences (01.12.1981)
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Published in Italian journal of neurological sciences (01.12.1981)
Journal Article
Late-Onset Pompe Disease with Nemaline Bodies
Frezza, E, Terracciano, C, Giacanelli, M, Rastelli, E, Greco, G, Massa, R
Published in Case reports in neurological medicine (01.01.2018)
Published in Case reports in neurological medicine (01.01.2018)
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Myotonic dystrophy phenotype without expansion of (CTG)n repeat: an entity distinct from proximal myotonic myopathy (PROMM)?
Abbruzzese, C, Krahe, R, Liguori, M, Tessarolo, D, Siciliano, M J, Ashizawa, T, Giacanelli, M
Published in Journal of neurology (01.10.1996)
Published in Journal of neurology (01.10.1996)
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