Caponnetto C - Search Results

1

T137A variant is a pathogenetic SOD1 mutation associated with a slowly progressive ALS phenotype.

Origone P, Caponnetto C, Verdiani S, Mantero V, Cichero E, Fossa P, Bellone E, Mancardi G, Mandich P. Origone P, et al. Among authors: caponnetto c. Amyotroph Lateral Scler. 2012 Jun;13(4):398-9. doi: 10.3109/17482968.2012.684216. Amyotroph Lateral Scler. 2012. PMID: 22632445 No abstract available.

2

Withdrawal of mechanical ventilation in amyotrophic lateral sclerosis patients: a multicenter Italian survey.

Moglia C, Palumbo F, Veronese S; M. N. D. Italian Study Group; Calvo A. Moglia C, et al. Neurol Sci. 2023 Dec;44(12):4349-4357. doi: 10.1007/s10072-023-06905-7. Epub 2023 Jul 7. Neurol Sci. 2023. PMID: 37418099 Free PMC article.

3

Six-minute walk test as outcome measure of fatigability in adults with spinal muscular atrophy treated with nusinersen.

Govoni A, Ricci G, Bonanno S, Bello L, Magri F, Meneri M, Torri F, Caponnetto C, Passamano L, Grandis M, Trojsi F, Cerri F, Gadaleta G, Capece G, Caumo L, Tanel R, Saccani E, Vacchiano V, Sorarù G, D'Errico E, Tramacere I, Bortolani S, Rolle E, Gellera C, Zanin R, Silvestrini M, Politano L, Schenone A, Previtali SC, Berardinelli A, Turri M, Verriello L, Coccia M, Mantegazza R, Liguori R, Filosto M, Maioli MA, Simone IL, Mongini T, Corti S, Manca ML, Pegoraro E, Siciliano G, Comi GP, Maggi L. Govoni A, et al. Among authors: caponnetto c. Muscle Nerve. 2024 Oct;70(4):816-823. doi: 10.1002/mus.28225. Epub 2024 Aug 2. Muscle Nerve. 2024. PMID: 39096012 Free article.

4

Correlation between PMP-22 messenger RNA expression and phenotype in hereditary neuropathy with liability to pressure palsies.

Schenone A, Nobbio L, Caponnetto C, Abbruzzese M, Mandich P, Bellone E, Ajmar F, Gherardi G, Windebank AJ, Mancardi G. Schenone A, et al. Among authors: caponnetto c. Ann Neurol. 1997 Dec;42(6):866-72. doi: 10.1002/ana.410420607. Ann Neurol. 1997. PMID: 9403478

5

An Italian dominant FALS Leu144Phe SOD1 mutation: genotype-phenotype correlation.

Ferrera L, Caponnetto C, Marini V, Rizzi D, Bordo D, Penco S, Amoroso A, Origone P, Garrè C. Ferrera L, et al. Among authors: caponnetto c. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Sep;4(3):167-70. doi: 10.1080/aml.4.3.167.170. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003. PMID: 13129804

6

SOD1 mutations in amyotrophic lateral sclerosis. Results from a multicenter Italian study.

Battistini S, Giannini F, Greco G, Bibbò G, Ferrera L, Marini V, Causarano R, Casula M, Lando G, Patrosso MC, Caponnetto C, Origone P, Marocchi A, Del Corona A, Siciliano G, Carrera P, Mascia V, Giagheddu M, Carcassi C, Orrù S, Garrè C, Penco S. Battistini S, et al. Among authors: caponnetto c. J Neurol. 2005 Jul;252(7):782-8. doi: 10.1007/s00415-005-0742-y. Epub 2005 Mar 29. J Neurol. 2005. PMID: 15789135

7

Detection of motor cortex thinning and corticospinal tract involvement by quantitative MRI in amyotrophic lateral sclerosis.

Roccatagliata L, Bonzano L, Mancardi G, Canepa C, Caponnetto C. Roccatagliata L, et al. Among authors: caponnetto c. Amyotroph Lateral Scler. 2009 Feb;10(1):47-52. doi: 10.1080/17482960802267530. Amyotroph Lateral Scler. 2009. PMID: 18622772

8

Enlarging clinical spectrum of FALS with TARDBP gene mutations: S393L variant in an Italian family showing phenotypic variability and relevance for genetic counselling.

Origone P, Caponnetto C, Bandettini Di Poggio M, Ghiglione E, Bellone E, Ferrandes G, Mancardi GL, Mandich P. Origone P, et al. Among authors: caponnetto c. Amyotroph Lateral Scler. 2010;11(1-2):223-7. doi: 10.3109/17482960903165039. Amyotroph Lateral Scler. 2010. PMID: 19714537

9

Heterozygous D90A-SOD1 mutation in an Italian ALS patient with atypical presentation.

Origone P, Caponnetto C, Mascolo M, Mandich P. Origone P, et al. Among authors: caponnetto c. Amyotroph Lateral Scler. 2009 Oct-Dec;10(5-6):492. doi: 10.3109/17482960903055966. Amyotroph Lateral Scler. 2009. PMID: 19922148 No abstract available.

10

Lack of association of PON polymorphisms with sporadic ALS in an Italian population.

Ricci C, Battistini S, Cozzi L, Benigni M, Origone P, Verriello L, Lunetta C, Cereda C, Milani P, Greco G, Patrosso MC, Causarano R, Caponnetto C, Giannini F, Corbo M, Penco S. Ricci C, et al. Among authors: caponnetto c. Neurobiol Aging. 2011 Mar;32(3):552.e7-13. doi: 10.1016/j.neurobiolaging.2010.02.010. Epub 2010 Apr 9. Neurobiol Aging. 2011. PMID: 20381198

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