E-LIB Suche - Ergebnisse für: Tessa, A.

1

Deep neurological phenotyping in oculo-dento-digital syndro..:

Lopriore, P. ; Vista, M. ; Maritato, P....
Neurological Sciences. 45 (2024) 6 - p. 2853-2857 , 2024

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

2

Clinical and genetic features of dominant Essential Tremor ..:

Orsucci, D. ; Tessa, A. ; Caldarazzo Ienco, E....
Journal of the Neurological Sciences. 460 (2024) - p. 123012 , 2024

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

3

The complex phenotype of spinocerebellar ataxia type 48 in ..:

Lieto, M. ; Riso, V. ; Galatolo, D....
European Journal of Neurology. 27 (2019) 3 - p. 498-505 , 2019

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

4

Prevalence and phenotype of the c.1529C>T SPG7 variant in a..:

Mancini, C. ; Giorgio, E. ; Rubegni, A....
European Journal of Neurology. 26 (2018) 1 - p. 80-86 , 2018

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

5

Hereditary spastic paraplegia: Novel mutations and expansio..:

Masciullo, M. ; Tessa, A. ; Perazza, S....
European Journal of Paediatric Neurology. 20 (2016) 3 - p. 444-448 , 2016

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

6

Identification of mutations inAP4S1/SPG52 through next gene..:

Tessa, A. ; Battini, R. ; Rubegni, A....
European Journal of Neurology. 23 (2016) 10 - p. 1580-1587 , 2016

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

7

X-linked myotubular myopathy in females:

Fiorillo, C. ; Fattori, F. ; Astrea, G....
Neuromuscular Disorders. 25 (2015) - p. S274 , 2015

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

8

Ataxia with oculomotor apraxia type 2: not always an easy d..:

Mignarri, A. ; Tessa, A. ; Federico, A...
Neurological Sciences. 36 (2015) 8 - p. 1505-1507 , 2015

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

9

When atlastin meets spastin:

Di Fabio, R. ; Tessa, A. ; Marcotulli, C....
Clinical Genetics. 86 (2014) 5 - p. 504-505 , 2014

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

10

Large deletion mutation of SPAST in a multi‐generation fami..:

Racis, L. ; Di Fabio, R. ; Tessa, A....
European Journal of Neurology. 21 (2013) 6 - p. 935-938 , 2013

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

11

Do not jump to easy conclusions! Lessons from pitfall in th..:

Masciullo, M. ; Silvestri, G. ; Modoni, A....
Clinical Genetics. 86 (2013) 4 - p. 396-397 , 2013

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

12

Supratentorial and pontine MRI abnormalities characterize r..:

Prodi, E. ; Grisoli, M. ; Panzeri, M....
European Journal of Neurology. 20 (2012) 1 - p. 138-146 , 2012

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

13

Novel SACS mutations in two unrelated Italian patients with..:

Masciullo, M. ; Modoni, A. ; Tessa, A....
European Journal of Neurology. 19 (2012) 8 - p. , 2012

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

14

Myelinated retinal fibers in autosomal recessive spastic at..:

Vingolo, E. M. ; Di Fabio, R. ; Salvatore, S....
European Journal of Neurology. 18 (2011) 9 - p. 1187-1190 , 2011

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

15

Pontocerebellar hypoplasia: Clinical, pathologic, and genet..:

Cassandrini, D. ; Biancheri, R. ; Tessa, A....
Neurology. 75 (2010) 16 - p. 1459-1464 , 2010

Link: https://doi.org/10.1212/..