E-LIB Suche - Ergebnisse für: Rodolico, C.

1

A very late onset AChR and MuSK double positive myasthenia ..:

Pugliese, A. ; Nicocia, G. ; Messina, S...
Neuromuscular Disorders. 33 (2023) 2 - p. 145-147 , 2023

Link: https://doi.org/10.1016/..

2

VP.41 Congenital myasthenic syndrome: natural history of an..:

Gallone, A. ; Pugliese, A. ; Brugnoni, R....
Neuromuscular Disorders. 32 (2022) - p. S83 , 2022

Link: https://doi.org/10.1016/..

3

P.110Clinical, morphological and genetic data in Italian pa..:

Maggi, L. ; Verardo, M. ; Rubegni, A....
Neuromuscular Disorders. 29 (2019) - p. S80-S81 , 2019

Link: https://doi.org/10.1016/..

4

Value of insoluble PABPN1 accumulation in the diagnosis of ..:

Galimberti, V. ; Tironi, R. ; Lerario, A....
European Journal of Neurology. 27 (2019) 4 - p. 709-715 , 2019

Link: https://doi.org/10.1111/..

5

EP.126Congenital fiber type disproportion related to novel ..:

Fattori, F. ; D'Amico, A. ; Verardo, M....
Neuromuscular Disorders. 29 (2019) - p. S204 , 2019

Link: https://doi.org/10.1016/..

6

Expanding the histopathological spectrum of CFL2‐related my..:

Fattori, F. ; Fiorillo, C. ; Rodolico, C....
Clinical Genetics. 93 (2018) 6 - p. 1234-1239 , 2018

Link: https://doi.org/10.1111/..

7

Dilatative arterial malformations in patients with late ons..:

Toscano, A. ; Granata, F. ; Rodolico, C....
Neuromuscular Disorders. 27 (2017) - p. S162 , 2017

Link: https://doi.org/10.1016/..

8

Pseudo-dominant inheritance of a novel homozygous HACD1 mut..:

Toscano, A. ; Emmanuele, V. ; Savarese, M....
Neuromuscular Disorders. 27 (2017) - p. S173 , 2017

Link: https://doi.org/10.1016/..

9

Congenital myopathy with protein aggregates and nemaline bo..:

Fattori, F. ; Fiorillo, C. ; Rodolico, C....
Neuromuscular Disorders. 27 (2017) - p. S186 , 2017

Link: https://doi.org/10.1016/..

10

87. Electromyographic findings in patients with late-onset ..:

Marino, M. ; Terranova, C. ; Rizzo, V....
Clinical Neurophysiology. 128 (2017) 12 - p. e436 , 2017

Link: https://doi.org/10.1016/..

11

MicroRNA signatures predict dysregulated vitamin D receptor..:

Aguennouz, M. ; Lo Giudice, C. ; Licata, N....
Cell Biochemistry and Function. 34 (2016) 6 - p. 414-422 , 2016

Link: https://doi.org/10.1002/..

12

TRPV4 related scapuloperoneal spinal muscular atrophy: Repo..:

Biasini, F. ; Portaro, S. ; Mazzeo, A....
Neuromuscular Disorders. 26 (2016) 4-5 - p. 312-315 , 2016

Link: https://doi.org/10.1016/..

13

MYH7-related myopathies: clinical, histopathological and im..:

on behalf of the Italian Network on Congenital Myopathies ; Fiorillo, C. ; Astrea, G....
Orphanet Journal of Rare Diseases. 11 (2016) 1 - p. , 2016

Link: https://doi.org/10.1186/..

14

Intracranial arterial abnormalities in patients with late o..:

Toscano, A. ; Montagnese, F. ; Granata, F....
Neuromuscular Disorders. 25 (2015) - p. S190 , 2015

Link: https://doi.org/10.1016/..

15

Clinical and molecular aspects of 30 patients with late-ons..:

Montagnese, Federica ; Barca, E. ; Musumeci, O....
Journal of Neurology. 262 (2015) 4 - p. 968-978 , 2015

Link: https://doi.org/10.1007/..