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Darra, F.
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1

Clinical characteristics of 80 subjects with KCNQ2-related ..:

Cossu, A. ; Lo Barco, T. ; Proietti, J....
Epilepsy & Behavior.  142 (2023)  - p. 109153 , 2023
Link: https://doi.org/10.1016/..
 
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2

Stabilometry in patients with Dravet Syndrome to quantitati..:

Di Marco, R. ; Duso, M. ; Cesaletti, R....
Gait & Posture.  66 (2018)  - p. S15 , 2018
Link: https://doi.org/10.1016/..
 
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3

Electroclinical findings and long-term outcomes in epilepti..:

Matricardi, S. ; Darra, F. ; Spalice, A....
Acta Neurologica Scandinavica.  137 (2018)  6 - p. 575-581 , 2018
Link: https://doi.org/10.1111/..
 
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4

EEG findings during "paroxysmal hemiplegia" in a patient wi..:

Pellegrin, S. ; Cantalupo, G. ; Opri, R...
European Journal of Paediatric Neurology.  21 (2017)  3 - p. 580-582 , 2017
Link: https://doi.org/10.1016/..
 
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5

Is Aicardi Syndrome truly linked to a mutation on X-Chromos..:

Cavallin, M. ; Nitschké, P. ; Petit, J.B....
European Journal of Paediatric Neurology.  21 (2017)  - p. e61 , 2017
Link: https://doi.org/10.1016/..
 
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6

Gait patterns in Dravet syndrome: Preliminary data of a mul..:

Spagnolo, E. ; Benedetti, M.G. ; Rigato, A....
Gait & Posture.  49 (2016)  - p. S10-S11 , 2016
Link: https://doi.org/10.1016/..
 
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7

Somatic mosaicism of PCDH19 mutation in a family with low-p..:

Terracciano, A. ; Specchio, N. ; Darra, F....
neurogenetics.  13 (2012)  4 - p. 341-345 , 2012
Link: https://doi.org/10.1007/..
 
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8

Early‐onset absence epilepsy: SLC2A1 gene analysis and trea..:

Agostinelli, S. ; Traverso, M. ; Accorsi, P....
European Journal of Neurology.  20 (2012)  5 - p. 856-859 , 2012
Link: https://doi.org/10.1111/..
 
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9

2FC1.4 Epilepsy in girls with de novo protocadherin 19 muta..:

Specchio, N. ; Terracciano, A. ; Marini, C....
European Journal of Paediatric Neurology.  15 (2011)  - p. S18-S19 , 2011
Link: https://doi.org/10.1016/..
 
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10

Refining the phenotype associated with MEF2C haploinsuffici..:

Novara, F ; Beri, S ; Giorda, R...
Clinical Genetics.  78 (2010)  5 - p. 471-477 , 2010
Link: https://doi.org/10.1111/..
 
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11

Familial Ohtahara syndrome due to a novel ARX gene mutation:

Giordano, L. ; Sartori, S. ; Russo, S....
American Journal of Medical Genetics Part A.  152A (2010)  12 - p. 3133-3137 , 2010
Link: https://doi.org/10.1002/..
 
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12

Periventricular heterotopia in fragile X syndrome:

Moro, F. ; Pisano, T. ; Bernardina, B. Dalla...
Neurology.  67 (2006)  4 - p. 713-715 , 2006
Link: https://doi.org/10.1212/..
 
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13

Candidate biomarkers from the integration of methylation an..:

Perini S ; Filosi M ; Allibrio G...
info:eu-repo/semantics/altIdentifier/pmid/37012247.  , 2023
Link: https://hdl.handle.net/1..
 
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14

Clinical characteristics of 80 subjects with KCNQ2-related ..:

Cossu, A ; Lo Barco, T ; Proietti, J...
info:eu-repo/semantics/altIdentifier/pmid/36989566.  , 2023
Link: https://hdl.handle.net/1..
 
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15

Quantitative Characterization of Motor Control during Gait ..:

Bisi M. C ; Di Marco R ; Ragona F...
info:eu-repo/semantics/altIdentifier/pmid/35336311.  , 2022
Link: http://hdl.handle.net/11..
 
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