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Items: 1 to 50 of 115

1.

Inherited motor-sensory neuropathy with upper limb predominance associated with the tropomyosin-receptor kinase fused gene.

Fabrizi GM, Høyer H, Taioli F, Cavallaro T, Hilmarsen HT, Squintani GM, Zanette G, Braathen GJ.

Neuromuscul Disord. 2020 Jan 17. pii: S0960-8966(20)30001-8. doi: 10.1016/j.nmd.2019.12.007. [Epub ahead of print]

PMID:
32085962
2.

Sporadic hereditary neuropathies misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy: Pitfalls and red flags.

Campagnolo M, Taioli F, Cacciavillani M, Ruiz M, Luigetti M, Salvalaggio A, Castellani F, Testi S, Ferrarini M, Cavallaro T, Gasparotti R, Fabrizi GM, Briani C.

J Peripher Nerv Syst. 2020 Mar;25(1):19-26. doi: 10.1111/jns.12362. Epub 2020 Jan 14.

PMID:
31919945
3.

Myelin uncompaction and axo-glial detachment in chronic ataxic neuropathy with monospecific IgM antibody to ganglioside GD1b.

Tagliapietra M, Zanusso G, Ferrari S, Orlandi R, Bertolasi L, Cavallaro T, Monaco S.

J Peripher Nerv Syst. 2020 Mar;25(1):54-59. doi: 10.1111/jns.12359. Epub 2019 Dec 19.

PMID:
31837178
4.

Deoxysphingolipids as candidate biomarkers for a novel SPTLC1 mutation associated with HSAN-I.

Boso F, Armirotti A, Taioli F, Ferrarini M, Nobbio L, Cavallaro T, Fabrizi GM.

Neurol Genet. 2019 Oct 8;5(6):e365. doi: 10.1212/NXG.0000000000000365. eCollection 2019 Dec. No abstract available.

5.

QTc Prolongation in Patients with Dementia and Mild Cognitive Impairment: Neuropsychological and Brain Imaging Correlations.

Danese A, Federico A, Martini A, Mantovani E, Zucchella C, Tagliapietra M, Tamburin S, Cavallaro T, Marafioti V, Monaco S, Turri G.

J Alzheimers Dis. 2019;72(4):1241-1249. doi: 10.3233/JAD-190632.

PMID:
31683480
6.

Nerve size correlates with clinical severity in Charcot-Marie-Tooth disease 1A.

Zanette G, Tamburin S, Taioli F, Lauriola MF, Badari A, Ferrarini M, Cavallaro T, Fabrizi GM.

Muscle Nerve. 2019 Dec;60(6):744-748. doi: 10.1002/mus.26688. Epub 2019 Sep 10.

PMID:
31469427
7.

Saposin B deficiency as a cause of adult-onset metachromatic leukodystrophy.

Fenu S, Castellotti B, Farina L, Cavallaro T, Di Bella D, Benzoni C, Gellera C, Pareyson D, Taroni F, Salsano E.

Neurology. 2019 Aug 13;93(7):310-312. doi: 10.1212/WNL.0000000000007951. Epub 2019 Jul 9. No abstract available.

PMID:
31289144
8.

Are novel outcome measures for Charcot-Marie-Tooth disease sensitive to change? The 6-minute walk test and StepWatch™ Activity Monitor in a 12-month longitudinal study.

Pazzaglia C, Padua L, Pareyson D, Schenone A, Aiello A, Fabrizi GM, Cavallaro T, Santoro L, Manganelli F, Coraci D, Gemignani F, Vitetta F, Quattrone A, Mazzeo A, Russo M, Vita G; CMT-TRIAAL Group.

Neuromuscul Disord. 2019 Apr;29(4):310-316. doi: 10.1016/j.nmd.2019.01.009. Epub 2019 Feb 2.

PMID:
30926199
9.

Peripheral nervous system involvement in lymphomas.

Briani C, Visentin A, Campagnolo M, Salvalaggio A, Ferrari S, Cavallaro T, Manara R, Gasparotti R, Piazza F.

J Peripher Nerv Syst. 2019 Mar;24(1):5-18. doi: 10.1111/jns.12295. Epub 2019 Jan 8. Review.

PMID:
30556258
10.

Nerve ultrasound findings differentiate Charcot-Marie-Tooth disease (CMT) 1A from other demyelinating CMTs.

Zanette G, Fabrizi GM, Taioli F, Lauriola MF, Badari A, Ferrarini M, Cavallaro T, Tamburin S.

Clin Neurophysiol. 2018 Nov;129(11):2259-2267. doi: 10.1016/j.clinph.2018.08.016. Epub 2018 Sep 1.

PMID:
30216910
11.

Reply to "Relationship between age and nerve dimensions in Charcot-Marie-Tooth disease. Do we know the reality?"

Fabrizi GM, Tamburin S, Cavallaro T, Zanette G.

Clin Neurophysiol. 2018 Jun;129(6):1335-1336. doi: 10.1016/j.clinph.2018.03.003. Epub 2018 Mar 22. No abstract available.

PMID:
29615307
12.

Novel Familial Variant of the Desert Hedgehog Gene: Clinical Findings in Two Sisters with 46,XY Gonadal Dysgenesis or 46,XX Karyotype and Literature Review.

Baldinotti F, Cavallaro T, Dati E, Baroncelli GI, Bertini V, Valetto A, Massart F, Fabrizi GM, Zanette G, Peroni D, Bertelloni S.

Horm Res Paediatr. 2018;89(3):141-149. doi: 10.1159/000485507. Epub 2018 Feb 22. Review.

PMID:
29471294
13.

The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study.

Fabrizi GM, Tamburin S, Cavallaro T, Cabrini I, Ferrarini M, Taioli F, Magrinelli F, Zanette G.

Clin Neurophysiol. 2018 Jan;129(1):21-32. doi: 10.1016/j.clinph.2017.09.117. Epub 2017 Oct 20.

PMID:
29136549
14.

Primary neurolymphomatosis as clinical onset of chronic lymphocytic leukemia.

Briani C, Visentin A, Cavallaro T, Cacciavillani M, Cabrini I, Ferrari S, Zambello R, Trentin L.

Ann Hematol. 2017 Jan;96(1):159-161. doi: 10.1007/s00277-016-2852-2. Epub 2016 Oct 19. No abstract available.

PMID:
27761605
15.

PiB-PET detects transthyretin-related cerebral amyloid angiopathy.

Cavallaro T, Klunk W.

Neurology. 2016 Aug 23;87(8):750-1. doi: 10.1212/WNL.0000000000003018. Epub 2016 Jul 27. No abstract available.

PMID:
27466476
16.

Nerve conduction velocity in CMT1A: what else can we tell?

Manganelli F, Pisciotta C, Reilly MM, Tozza S, Schenone A, Fabrizi GM, Cavallaro T, Vita G, Padua L, Gemignani F, Laurà M, Hughes RA, Solari A, Pareyson D, Santoro L; CMT-TRIAAL and CMT-TRAUK Group.

Eur J Neurol. 2016 Oct;23(10):1566-71. doi: 10.1111/ene.13079. Epub 2016 Jul 14.

17.

Predictive role of early milestones-related psychomotor profiles and long-term neurodevelopmental pitfalls in preterm infants.

Di Rosa G, Cavallaro T, Alibrandi A, Marseglia L, Lamberti M, Giaimo E, Nicotera A, Bonsignore M, Gagliano A.

Early Hum Dev. 2016 Oct;101:49-55. doi: 10.1016/j.earlhumdev.2016.04.012. Epub 2016 Jul 9.

PMID:
27405056
18.

Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling.

Gregianin E, Pallafacchina G, Zanin S, Crippa V, Rusmini P, Poletti A, Fang M, Li Z, Diano L, Petrucci A, Lispi L, Cavallaro T, Fabrizi GM, Muglia M, Boaretto F, Vettori A, Rizzuto R, Mostacciuolo ML, Vazza G.

Hum Mol Genet. 2016 Sep 1;25(17):3741-3753. doi: 10.1093/hmg/ddw220. Epub 2016 Jul 8.

PMID:
27402882
19.

Novel outcome measures for Charcot-Marie-Tooth disease: validation and reliability of the 6-min walk test and StepWatch(™) Activity Monitor and identification of the walking features related to higher quality of life.

Padua L, Pazzaglia C, Pareyson D, Schenone A, Aiello A, Fabrizi GM, Cavallaro T, Santoro L, Manganelli F, Gemignani F, Vitetta F, Quattrone A, Mazzeo A, Russo M, Vita G; CMT-TRIAAL Group.

Eur J Neurol. 2016 Aug;23(8):1343-50. doi: 10.1111/ene.13033. Epub 2016 May 10.

PMID:
27160471
20.

Erratum to: Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area.

Cortese A, Vita G, Luigetti M, Russo M, Bisogni G, Sabatelli M, Manganelli F, Santoro L, Cavallaro T, Fabrizi GM, Schenone A, Grandis M, Gemelli C, Mauro A, Pradotto LG, Gentile L, Stancanelli C, Lozza A, Perlini S, Piscosquito G, Calabrese D, Mazzeo A, Obici L, Pareyson D.

J Neurol. 2016 May;263(5):925-926. doi: 10.1007/s00415-016-8116-1. No abstract available.

PMID:
27098978
21.

Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area.

Cortese A, Vita G, Luigetti M, Russo M, Bisogni G, Sabatelli M, Manganelli F, Santoro L, Cavallaro T, Fabrizi GM, Schenone A, Grandis M, Gemelli C, Mauro A, Pradotto LG, Gentile L, Stancanelli C, Lozza A, Perlini S, Piscosquito G, Calabrese D, Mazzeo A, Obici L, Pareyson D.

J Neurol. 2016 May;263(5):916-924. doi: 10.1007/s00415-016-8064-9. Epub 2016 Mar 16. Erratum in: J Neurol. 2016 May;263(5):925-926.

PMID:
26984605
22.

Magnetic resonance parkinsonism index in progressive supranuclear palsy and vascular parkinsonism.

Mostile G, Nicoletti A, Cicero CE, Cavallaro T, Bruno E, Dibilio V, Luca A, Sciacca G, Raciti L, Contrafatto D, Chiaramonte I, Zappia M.

Neurol Sci. 2016 Apr;37(4):591-5. doi: 10.1007/s10072-016-2489-x. Epub 2016 Jan 28.

PMID:
26820655
23.

Charcot-Marie-Tooth disease: New insights from skin biopsy.

Manganelli F, Nolano M, Pisciotta C, Provitera V, Fabrizi GM, Cavallaro T, Stancanelli A, Caporaso G, Shy ME, Santoro L.

Neurology. 2015 Oct 6;85(14):1202-8. doi: 10.1212/WNL.0000000000001993. Epub 2015 Sep 11.

24.

Brentuximab vedotin: axonal microtubule's Apollyon.

Mariotto S, Ferrari S, Sorio M, Benedetti F, Tridente G, Cavallaro T, Gajofatto A, Monaco S.

Blood Cancer J. 2015 Aug 28;5:e343. doi: 10.1038/bcj.2015.72. No abstract available.

25.

Responsiveness of clinical outcome measures in Charcot-Marie-Tooth disease.

Piscosquito G, Reilly MM, Schenone A, Fabrizi GM, Cavallaro T, Santoro L, Manganelli F, Vita G, Quattrone A, Padua L, Gemignani F, Visioli F, Laurà M, Calabrese D, Hughes RA, Radice D, Solari A, Pareyson D; CMT-TRIAAL Group; CMT-TRAUK Group.

Eur J Neurol. 2015 Dec;22(12):1556-63. doi: 10.1111/ene.12783. Epub 2015 Jul 31.

PMID:
26227902
26.

Neuroimaging in diagnosis of atypical polyradiculoneuropathies: report of three cases and review of the literature.

Gasparotti R, Lucchetta M, Cacciavillani M, Neri W, Guidi C, Cavallaro T, Ferrari S, Padua L, Briani C.

J Neurol. 2015 Jul;262(7):1714-23. doi: 10.1007/s00415-015-7770-z. Epub 2015 May 10. Review.

PMID:
25957643
27.

Polyneuropathy with anti-sulfatide and anti-MAG antibodies: clinical, neurophysiological, pathological features and response to treatment.

Campagnolo M, Ferrari S, Dalla Torre C, Cabrini I, Cacciavillani M, Lucchetta M, Ruggero S, Toffanin E, Cavallaro T, Briani C.

J Neuroimmunol. 2015 Apr 15;281:1-4. doi: 10.1016/j.jneuroim.2015.02.009. Epub 2015 Mar 3.

PMID:
25867460
28.

Mononeuritis multiplex associated with primary livedoid vasculopathy: neuropathological evidence of ischemic nerve damage.

Malaguti MC, Cavallaro T, Speziali L, Zorzi MG, Marangoni S, Morini A.

J Neurol Sci. 2015 Apr 15;351(1-2):214-215. doi: 10.1016/j.jns.2015.03.013. Epub 2015 Mar 14. No abstract available.

PMID:
25798525
29.

Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family.

Stancanelli C, Fabrizi GM, Ferrarini M, Cavallaro T, Taioli F, Di Leo R, Russo M, Gentile L, Toscano A, Vita G, Mazzeo A.

Neurol Sci. 2015 Jun;36(6):1003-6. doi: 10.1007/s10072-014-2050-8. Epub 2014 Dec 30.

PMID:
25547330
30.

Pentraxin-3 and VEGF in POEMS syndrome: a 2-year longitudinal study.

Briani C, Dalla Torre C, Lessi F, Cavallaro T, Scarlato M, Ferrari S, Campagnolo M, Lucchetta M, Cabrini I, Morbin M, Lauria G, Adami F, Manfredi AA.

J Neuroimmunol. 2014 Dec 15;277(1-2):189-92. doi: 10.1016/j.jneuroim.2014.09.021. Epub 2014 Oct 5.

PMID:
25447599
31.

Neuropathy in eosinophilic granulomatosis with polyangiitis: a comparison study of 24 cases with or without prior leukotriene antagonist exposure.

Giusti Del Giardino L, Cavallaro T, Anzola GP, Lombardi C, Ferrari S.

Eur Ann Allergy Clin Immunol. 2014 Nov;46(6):201-9.

PMID:
25398163
32.

Is overwork weakness relevant in Charcot-Marie-Tooth disease?

Piscosquito G, Reilly MM, Schenone A, Fabrizi GM, Cavallaro T, Santoro L, Vita G, Quattrone A, Padua L, Gemignani F, Visioli F, Laurà M, Calabrese D, Hughes RA, Radice D, Solari A, Pareyson D; CMT-TRIAAL & CMT-TRAUK Group.

J Neurol Neurosurg Psychiatry. 2014 Dec;85(12):1354-8. doi: 10.1136/jnnp-2014-307598. Epub 2014 Mar 21.

PMID:
24659795
33.

Guillain-barré syndrome associated with acute onset bilateral facial nerve palsies. A case report and literature review.

D'Amore A, Viglianesi A, Cavallaro T, Chiaramonte R, Muscoso EG, Giuffrida S, Chiaramonte I, Ettorre GC.

Neuroradiol J. 2012 Dec 20;25(6):665-70. Epub 2012 Dec 20.

PMID:
24029178
34.

Vascular cerebral anomalies associated with Septo-Optic Dysplasia. A case report.

Chiaramonte I, Cappello G, Uccello A, Guarrera V, D'Amore A, Cavallaro T, Chiaramonte R, Ettorre GC.

Neuroradiol J. 2013 Feb;26(1):66-70. Epub 2013 Mar 8.

35.

Traumatic labyrinthine concussion in a patient with sensorineural hearing loss.

Chiaramonte R, Bonfiglio M, D'Amore A, Viglianesi A, Cavallaro T, Chiaramonte I.

Neuroradiol J. 2013 Feb;26(1):52-5. Epub 2013 Mar 8.

36.

Executive dysfunctions in migraine with and without aura: what is the role of white matter lesions?

Le Pira F, Reggio E, Quattrocchi G, Sanfilippo C, Maci T, Cavallaro T, Zappia M.

Headache. 2014 Jan;54(1):125-30. doi: 10.1111/head.12158. Epub 2013 Jun 28.

PMID:
23808818
37.

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats.

van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theuns J, Engelborghs S, Philtjens S, Vandenbulcke M, Sleegers K, Sieben A, Bäumer V, Maes G, Corsmit E, Borroni B, Padovani A, Archetti S, Perneczky R, Diehl-Schmid J, de Mendonça A, Miltenberger-Miltenyi G, Pereira S, Pimentel J, Nacmias B, Bagnoli S, Sorbi S, Graff C, Chiang HH, Westerlund M, Sanchez-Valle R, Llado A, Gelpi E, Santana I, Almeida MR, Santiago B, Frisoni G, Zanetti O, Bonvicini C, Synofzik M, Maetzler W, Vom Hagen JM, Schöls L, Heneka MT, Jessen F, Matej R, Parobkova E, Kovacs GG, Ströbel T, Sarafov S, Tournev I, Jordanova A, Danek A, Arzberger T, Fabrizi GM, Testi S, Salmon E, Santens P, Martin JJ, Cras P, Vandenberghe R, De Deyn PP, Cruts M, Van Broeckhoven C, van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theuns J, Philtjens S, Sleegers K, Bäumer V, Maes G, Corsmit E, Cruts M, Van Broeckhoven C, van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Philtjens S, Theuns J, Sleegers K, Bäumer V, Maes G, Cruts M, Van Broeckhoven C, Engelborghs S, De Deyn PP, Cras P, Engelborghs S, De Deyn PP, Vandenbulcke M, Vandenbulcke M, Borroni B, Padovani A, Archetti S, Perneczky R, Diehl-Schmid J, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, de Mendonça A, Miltenberger-Miltenyi G, Pereira S, Firmo C, Pimentel J, Sanchez-Valle R, Llado A, Antonell A, Molinuevo J, Gelpi E, Graff C, Chiang HH, Westerlund M, Graff C, Kinhult Ståhlbom A, Thonberg H, Nennesmo I, Börjesson-Hanson A, Nacmias B, Bagnoli S, Sorbi S, Bessi V, Piaceri I, Santana I, Santiago B, Santana I, Helena Ribeiro M, Rosário Almeida M, Oliveira C, Massano J, Garret C, Pires P, Frisoni G, Zanetti O, Bonvicini C, Sarafov S, Tournev I, Jordanova A, Tournev I, Kovacs GG, Ströbel T, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, Jessen F, Matej R, Parobkova E, Danel A, Arzberger T, Maria Fabrizi G, Testi S, Ferrari S, Cavallaro T, Salmon E, Santens P, Cras P; European Early-Onset Dementia Consortium.

Hum Mutat. 2013 Feb;34(2):363-73. doi: 10.1002/humu.22244. Epub 2013 Jan 4.

38.

An occult spinal neurenteric cyst associated with congenital hemivertebrae. A case report.

Guarrera V, Conte G, Cavallaro T, Chiaramonte R, D'Amore A, Caltabiano R, Chiaramonte I.

Neuroradiol J. 2012 Jul;25(3):368-73. Epub 2012 Jun 26.

PMID:
24028992
39.

Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis.

Briani C, Cavallaro T, Ferrari S, Taioli F, Calamelli S, Verga L, Adami F, Fabrizi GM.

J Neurol. 2012 Oct;259(10):2226-8. doi: 10.1007/s00415-012-6529-z. Epub 2012 May 12. No abstract available.

PMID:
22580845
40.

Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients.

Cappellari M, Cavallaro T, Ferrarini M, Cabrini I, Taioli F, Ferrari S, Merlini G, Obici L, Briani C, Fabrizi GM.

J Peripher Nerv Syst. 2011 Jun;16(2):119-29. doi: 10.1111/j.1529-8027.2011.00331.x.

PMID:
21692911
41.

Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene.

Taioli F, Cabrini I, Cavallaro T, Simonati A, Testi S, Fabrizi GM.

J Peripher Nerv Syst. 2011 Mar;16(1):59-64. doi: 10.1111/j.1529-8027.2011.00319.x.

PMID:
21504504
42.

Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial.

Pareyson D, Reilly MM, Schenone A, Fabrizi GM, Cavallaro T, Santoro L, Vita G, Quattrone A, Padua L, Gemignani F, Visioli F, Laurà M, Radice D, Calabrese D, Hughes RA, Solari A; CMT-TRIAAL; CMT-TRAUK groups.

Lancet Neurol. 2011 Apr;10(4):320-8. doi: 10.1016/S1474-4422(11)70025-4.

43.

Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias.

Briani C, Fabrizi GM, Ruggero S, Torre CD, Ferrarini M, Campagnolo M, Cavallaro T, Ferrari S, Scarlato M, Taioli F, Adami F.

Muscle Nerve. 2011 Feb;43(2):164-7. doi: 10.1002/mus.21872. Epub 2010 Nov 16.

PMID:
21254078
44.

Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene.

Taioli F, Cabrini I, Cavallaro T, Acler M, Fabrizi GM.

Brain. 2011 Feb;134(Pt 2):608-17. doi: 10.1093/brain/awq374. Epub 2011 Jan 19.

PMID:
21252112
45.

Four novel cases of periaxin-related neuropathy and review of the literature.

Marchesi C, Milani M, Morbin M, Cesani M, Lauria G, Scaioli V, Piccolo G, Fabrizi GM, Cavallaro T, Taroni F, Pareyson D.

Neurology. 2010 Nov 16;75(20):1830-8. doi: 10.1212/WNL.0b013e3181fd6314. Review.

PMID:
21079185
46.

Atypical Alzheimer's disease: a case report.

Iemolo F, Cavallaro T, Rizzuto N.

Neurol Sci. 2010 Oct;31(5):643-6. doi: 10.1007/s10072-010-0334-1. Epub 2010 Jun 15.

PMID:
20552242
47.

Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation.

Boaretto F, Vettori A, Casarin A, Vazza G, Muglia M, Rossetto MG, Cavallaro T, Rizzuto N, Carelli V, Salviati L, Mostacciuolo ML, Martinuzzi A.

Neurology. 2010 Jun 8;74(23):1919-21. doi: 10.1212/WNL.0b013e3181e240f9. No abstract available.

PMID:
20530328
48.

Outcome of psychiatric symptoms presenting at onset of multiple sclerosis: a retrospective study.

Lo Fermo S, Barone R, Patti F, Laisa P, Cavallaro TL, Nicoletti A, Zappia M.

Mult Scler. 2010 Jun;16(6):742-8. doi: 10.1177/1352458510365157. Epub 2010 Mar 29.

PMID:
20350959
49.

Clinico-pathological findings in a patient with progressive cerebellar ataxia, autoimmune polyendocrine syndrome, hepatocellular carcinoma and anti-GAD autoantibodies.

Piccolo G, Tavazzi E, Cavallaro T, Romani A, Scelsi R, Martino G.

J Neurol Sci. 2010 Mar 15;290(1-2):148-9. doi: 10.1016/j.jns.2009.12.006. Epub 2010 Jan 6.

PMID:
20056249
50.

Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life.

Padua L, Pareyson D, Aprile I, Cavallaro T, Quattrone DA, Rizzuto N, Vita G, Tonali P, Schenone A.

Neurol Sci. 2010 Apr;31(2):175-8. doi: 10.1007/s10072-009-0202-z. Epub 2009 Dec 17.

PMID:
20016922

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