Caponnetto C - Search Results

1

Complexities of Genetic Counseling for ALS: A Case of Two Siblings with Discordant Genetic Test Results.

Mandich P, Mantero V, Verdiani S, Gotta F, Caponnetto C, Bellone E, Ferrandes G, Origone P. Mandich P, et al. Among authors: caponnetto c. J Genet Couns. 2015 Aug;24(4):553-7. doi: 10.1007/s10897-015-9831-y. Epub 2015 Apr 7. J Genet Couns. 2015. PMID: 25843563

2

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

3

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

4

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

5

[Amyotrophic lateral sclerosis: an assessment of the needs of patients and caregivers in the Liguria region of Italy].

Ferullo CM, Mascolo M, Ferrandes G, Caponnetto C. Ferullo CM, et al. Among authors: caponnetto c. G Ital Med Lav Ergon. 2009 Jan-Mar;31(1 Suppl A):A16-23. G Ital Med Lav Ergon. 2009. PMID: 19621534 Italian.

6

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

7

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.

8

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

9

I112M SOD1 mutation causes ALS with rapid progression and reduced penetrance in four Mediterranean families.

Gamez J, Caponnetto C, Ferrera L, Syriani E, Marini V, Morales M, Bordo D, Pirro C, Garre C, Origone P. Gamez J, et al. Among authors: caponnetto c. Amyotroph Lateral Scler. 2011 Jan;12(1):70-5. doi: 10.3109/17482968.2010.487906. Epub 2010 Jun 2. Amyotroph Lateral Scler. 2011. PMID: 20515426

10

Fast course ALS presenting with vocal cord paralysis: clinical features, bioinformatic and modelling analysis of the novel SOD1 Gly147Ser mutation.

Origone P, Caponnetto C, Mantero V, Cichero E, Fossa P, Geroldi A, Verdiani S, Bellone E, Mancardi G, Mandich P. Origone P, et al. Among authors: caponnetto c. Amyotroph Lateral Scler. 2012 Jan;13(1):144-8. doi: 10.3109/17482968.2011.614254. Epub 2011 Sep 19. Amyotroph Lateral Scler. 2012. PMID: 21929355

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