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Nerve conduction velocity in CMT1A: what else can we tell?
Published in:
European Journal of Neurology, 2016, v. 23, n. 10, p. 1566, doi. 10.1111/ene.13079
By:
- Manganelli, F.;
- Pisciotta, C.;
- Reilly, M. M.;
- Tozza, S.;
- Schenone, A.;
- Fabrizi, G. M.;
- Cavallaro, T.;
- Vita, G.;
- Padua, L.;
- Gemignani, F.;
- Laurà, M.;
- Hughes, R. A. C.;
- Solari, A.;
- Pareyson, D.;
- Santoro, L.;
- Nolano, Maria;
- Iodice, Rosa;
- Grandis, Marina;
- Cabrini, Ilaria;
- Bertolasi, Laura
Publication type:
Article
Case of acute motor conduction block neuropathy (AMCBN)
Published in:
2009
By:
- Manganelli F;
- Pisciotta C;
- Iodice R;
- Calandro S;
- Dubbioso R;
- Ranieri A;
- Santoro L
Publication type:
Journal Article
Motor performance deterioration accelerates after 50 years of age in Charcot‐Marie‐Tooth type 1A patients.
Published in:
European Journal of Neurology, 2018, v. 25, n. 2, p. 301, doi. 10.1111/ene.13494
By:
- Tozza, S.;
- Bruzzese, D.;
- Pisciotta, C.;
- Iodice, R.;
- Esposito, M.;
- Dubbioso, R.;
- Ruggiero, L.;
- Topa, A.;
- Spina, E.;
- Santoro, L.;
- Manganelli, F.
Publication type:
Article
Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy.
Published in:
European Journal of Neurology, 2018, v. 25, n. 1, p. 154, doi. 10.1111/ene.13478
By:
- Cortese, A.;
- Laurà, M.;
- Casali, C.;
- Nishino, I.;
- Hayashi, Y. K.;
- Magri, S.;
- Taroni, F.;
- Stuani, C.;
- Saveri, P.;
- Moggio, M.;
- Ripolone, M.;
- Prelle, A.;
- Pisciotta, C.;
- Sagnelli, A.;
- Pichiecchio, A.;
- Reilly, M. M.;
- Buratti, E.;
- Pareyson, D.
Publication type:
Article
Two families with novel PMP22 point mutations: genotype-phenotype correlation.
Published in:
2009
By:
- Pisciotta C;
- Manganelli F;
- Iodice R;
- Bellone E;
- Geroldi A;
- Volpi N;
- Mandich P;
- Santoro L
Publication type:
Journal Article

Found: 5

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

Case of acute motor conduction block neuropathy (AMCBN)

Motor performance deterioration accelerates after 50 years of age in Charcot‐Marie‐Tooth type 1A patients.

Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy.

Two families with novel PMP22 point mutations: genotype-phenotype correlation.