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Dazzo, Emanuela
34  results:
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1

A de novo pathogenic variant in MICAL‐1 causes epilepsy wit..:

Bonanni, Paolo ; Giorda, Roberto ; Michelucci, Roberto..
Epilepsia Open.  9 (2024)  3 - p. 1083-1087 , 2024
Link: https://doi.org/10.1002/..
 
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2

Familial Mesial Temporal Lobe Epilepsy: Clinical Spectrum a..:

Harris, Rebekah V. ; Oliver, Karen L. ; Perucca, Piero...
Annals of Neurology.  94 (2023)  5 - p. 825-835 , 2023
Link: https://doi.org/10.1002/..
 
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3

Epilepsy-causing Reelin mutations result in impaired secret..:

Dazzo, Emanuela ; Nobile, Carlo
Human Molecular Genetics.  31 (2021)  5 - p. 665-673 , 2021
Link: https://doi.org/10.1093/..
 
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4

Autosomal dominant lateral temporal lobe epilepsy associate..:

Michelucci, Roberto ; Dazzo, Emanuela ; Volpi, Lilia...
Epileptic Disorders.  22 (2020)  4 - p. 443-448 , 2020
Link: https://doi.org/10.1684/..
 
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5

Mutations in MICAL‐1cause autosomal‐dominant lateral tempor..:

Dazzo, Emanuela ; Rehberg, Kati ; Michelucci, Roberto...
Annals of Neurology.  83 (2018)  3 - p. 483-493 , 2018
Link: https://doi.org/10.1002/..
 
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6

CNTNAP2 mutations and autosomal dominant epilepsy with audi..:

Leonardi, Emanuela ; Dazzo, Emanuela ; Aspromonte, Maria Cristina...
Epilepsy Research.  139 (2018)  - p. 51-53 , 2018
Link: https://doi.org/10.1016/..
 
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7

LGI1 tumor tissue expression and serum autoantibodies in pa..:

Dazzo, Emanuela ; Pasini, Elena ; Furlan, Sandra...
Clinical Neurology and Neurosurgery.  170 (2018)  - p. 27-33 , 2018
Link: https://doi.org/10.1016/..
 
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8

A novel murine model for arrhythmogenic cardiomyopathy poin..:

Calore, Martina ; Lorenzon, Alessandra ; Vitiello, Libero...
Cardiovascular Research.  115 (2018)  4 - p. 739-751 , 2018
Link: https://doi.org/10.1093/..
 
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9

The clinical phenotype of autosomal dominant lateral tempor..:

Michelucci, Roberto ; Pulitano, Patrizia ; Di Bonaventura, Carlo...
Epilepsy & Behavior.  68 (2017)  - p. 103-107 , 2017
Link: https://doi.org/10.1016/..
 
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10

Secretion-Positive LGI1 Mutations Linked to Lateral Tempora..:

Dazzo, Emanuela ; Leonardi, Emanuela ; Belluzzi, Elisa...
PLOS Genetics.  12 (2016)  10 - p. e1006376 , 2016
Link: https://doi.org/10.1371/..
 
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11

Autosomal dominant lateral temporal epilepsy (ADLTE): Novel..:

Dazzo, Emanuela ; Santulli, Lia ; Posar, Annio...
Epilepsy Research.  110 (2015)  - p. 132-138 , 2015
Link: https://doi.org/10.1016/..
 
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12

The novel S59P mutation in the TNFRSF1A gene identified in ..:

Greco, Eliana ; Aita, Ada ; Galozzi, Paola...
Arthritis Research & Therapy.  17 (2015)  1 - p. , 2015
Link: https://doi.org/10.1186/..
 
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13

DEPDC5 mutations are not a frequent cause of familial tempo..:

Striano, Pasquale ; Serioli, Elena ; Santulli, Lia...
Epilepsia.  56 (2015)  10 - p. , 2015
Link: https://doi.org/10.1111/..
 
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14

Suggestive linkage of familial mesial temporal lobe epileps..:

Fanciulli, Manuela ; Di Bonaventura, Carlo ; Egeo, Gabriella...
Epilepsy Research.  108 (2014)  2 - p. 232-240 , 2014
Link: https://doi.org/10.1016/..
 
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15

Low penetrance of autosomal dominant lateral temporal epile..:

Michelucci, Roberto ; Pasini, Elena ; Malacrida, Sandro...
Epilepsia.  54 (2013)  7 - p. 1288-1297 , 2013
Link: https://doi.org/10.1111/..
 
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