Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

D. Battaglia · SciRah

Researcher profile · Semantic Scholar

D. Battaglia

Share profile

D. Battaglia — researcher profile on SciRah

h-index: 35
Works: 141
Citations: 3,594

Most-cited papers

Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype
M. Zollino, Daniela Orteschi, M. Murdolo, S. Lattante +6 more
2012Nature Genetics163 citations
Semantic Scholar
Cognitive development in Dravet syndrome: A retrospective, multicenter study of 26 patients
F. Ragona, T. Granata, B. Bernardina, Francesca Offredi +17 more
2011Epilepsia137 citations
Semantic Scholar
Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations
V. Cetica, S. Chiari, D. Mei, E. Parrini +15 more
2017Neurology124 citations Open access
Semantic Scholar
Protocadherin 19 mutations in girls with infantile-onset epilepsy
C. Marini, D. Mei, L. Parmeggiani, V. Norci +8 more
2010Neurology124 citations
Semantic Scholar
Sleep disorders in children with cerebral palsy: neurodevelopmental and behavioral correlates.
D. Romeo, Claudia Brogna, Michela Quintiliani, G. Baranello +11 more
2014Sleep Medicine115 citations
Semantic Scholar
PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine
C. Marini, V. Conti, D. Mei, D. Battaglia +5 more
2012Neurology110 citations Open access
Semantic Scholar
Electrical and autonomic cardiac function in patients with Dravet syndrome
A. Delogu, A. Spinelli, D. Battaglia, C. Dravet +5 more
2011Epilepsia87 citations Open access
Semantic Scholar
Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical review.
T. Schirinzi, Giacomo Garone, L. Travaglini, G. Vasco +13 more
2019Parkinsonism & Related Disorders79 citations
Semantic Scholar
Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy
S. Syrbe, F. L. Harms, E. Parrini, Martino Montomoli +40 more
2017Brain : a journal of neurology78 citations Open access
Semantic Scholar
Focal seizures with affective symptoms are a major feature of PCDH19 gene–related epilepsy
C. Marini, F. Darra, N. Specchio, D. Mei +21 more
2012Epilepsia78 citations Open access
Semantic Scholar
Neuropsychological development in children with Dravet syndrome.
D. Chieffo, D. Battaglia, D. Lettori, M. Del Re +4 more
2011Epilepsy Research73 citations
Semantic Scholar
The Pitt‐Hopkins syndrome: Report of 16 new patients and clinical diagnostic criteria
G. Marangi, S. Ricciardi, Daniela Orteschi, S. Lattante +22 more
2011American Journal of Medical Genetics. Part A72 citations
Semantic Scholar
Temporal lobe epilepsy surgery in children and adults: A multicenter study
C. Barba, M. Cossu, R. Guerrini, G. Di Gennaro +27 more
2020Epilepsia62 citations
Semantic Scholar
Trends in pediatric epilepsy surgery in Europe between 2008 and 2015: Country‐, center‐, and age‐specific variation
C. Barba, J. H. Cross, K. Braun, M. Cossu +66 more
2019Epilepsia61 citations Open access
Semantic Scholar
Sleep disturbances in preschool age children with cerebral palsy: a questionnaire study.
D. Romeo, Claudia Brogna, E. Musto, G. Baranello +9 more
2014Sleep Medicine56 citations
Semantic Scholar
Dravet syndrome: Early electroclinical findings and long‐term outcome in adolescents and adults
F. Darra, D. Battaglia, C. Dravet, Mara Patrini +9 more
2019Epilepsia55 citations Open access
Semantic Scholar
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real‐world study
N. Specchio, N. Pietrafusa, Viola Doccini, M. Trivisano +13 more
2020Epilepsia51 citations Open access
Semantic Scholar
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome
C. Cafiero, G. Marangi, Daniela Orteschi, M. Ali +12 more
2015European Journal of Human Genetics50 citations Open access
Semantic Scholar
Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype–phenotype correlations in a large cohort of patients
M. Zollino, G. Marangi, Emanuela Ponzi, Daniela Orteschi +26 more
2015Journal of Medical Genetics50 citations
Semantic Scholar
Defining the electroclinical phenotype and outcome of PCDH19‐related epilepsy: A multicenter study
M. Trivisano, N. Pietrafusa, A. Terracciano, C. Marini +36 more
2018Epilepsia49 citations
Semantic Scholar
Clinical‐genetic features and peculiar muscle histopathology in infantile DNM1L‐related mitochondrial epileptic encephalopathy
D. Verrigni, M. Di Nottia, A. Ardissone, E. Baruffini +23 more
2019Human Mutation48 citations Open access
Semantic Scholar
Early development in Dravet syndrome; visual function impairment precedes cognitive decline.
D. Chieffo, D. Ricci, G. Baranello, D. Martinelli +6 more
2011Epilepsy Research47 citations
Semantic Scholar
Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox–Gastaut Syndrome
L. Iannone, Gabriele Arena, D. Battaglia, F. Bisulli +38 more
2021Frontiers in Neurology44 citations Open access
Semantic Scholar
Interactions between antiepileptic and chemotherapeutic drugs in children with brain tumors: Is it time to change treatment?
A. Ruggiero, D. Rizzo, S. Mastrangelo, D. Battaglia +2 more
2010Pediatric Blood & Cancer44 citations
Semantic Scholar
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf‐Hirschhorn syndrome–associated seizures disorder
M. Zollino, Daniela Orteschi, Mariken Ruiter, R. Pfundt +11 more
2014Epilepsia39 citations Open access
Semantic Scholar
Chromosome 9p deletion syndrome and sex reversal: Novel findings and redefinition of the critically deleted regions
Roberta Onesimo, Daniela Orteschi, M. Scalzone, A. Rossodivita +6 more
2012American Journal of Medical Genetics. Part A37 citations Open access
Semantic Scholar
Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review
J. Garau, Vanessa Cavallera, Marialuisa Valente, D. Tonduti +35 more
2019Journal of Clinical Medicine36 citations Open access
Semantic Scholar
Congenital immunodeficiency in an individual with Wiedemann–Steiner syndrome due to a novel missense mutation in KMT2A
E. Stellacci, R. Onesimo, A. Bruselles, S. Pizzi +4 more
2016American Journal of Medical Genetics. Part A35 citations
Semantic Scholar
CHARGE‐like presentation, craniosynostosis and mild Mowat–Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases
T. Wenger, M. Harr, S. Ricciardi, E. Bhoj +20 more
2014American Journal of Medical Genetics. Part A35 citations
Semantic Scholar
Cognitive decline in Dravet syndrome: is there a cerebellar role?
D. Battaglia, D. Chieffo, R. Siracusano, C. de Waure +7 more
2013Epilepsy Research33 citations
Semantic Scholar
Increasing volume and complexity of pediatric epilepsy surgery with stable seizure outcome between 2008 and 2014: A nationwide multicenter study.
C. Barba, N. Specchio, R. Guerrini, L. Tassi +23 more
2017Epilepsy & Behavior32 citations
Semantic Scholar
Documentation of autonomic seizures and autonomic status epilepticus with ictal EEG in Panayiotopoulos syndrome.
N. Specchio, M. Trivisano, D. Claps, D. Battaglia +2 more
2010Epilepsy & Behavior32 citations
Semantic Scholar
Sturge-Weber syndrome: an update on the relevant issues for neurosurgeons
F. Bianchi, A. Auricchio, D. Battaglia, D. Chieffo +1 more
2020Child's Nervous System31 citations
Semantic Scholar
Glyburide ameliorates motor coordination and glucose homeostasis in a child with diabetes associated with the KCNJ11/S225T, del226-232 mutation
D. Battaglia, Yu-Wen Lin, Claudia Brogna, A. Crinò +9 more
2012Pediatric Diabetes30 citations Open access
Semantic Scholar
Surgery of children with frontal lobe lesional epilepsy: neuropsychological study.
D. Chieffo, D. Lettori, I. Contaldo, F. Perrino +7 more
2011Brain & development (Tokyo. 1979)30 citations
Semantic Scholar
Proposal of a clinical score for the molecular test for Pitt–Hopkins syndrome
G. Marangi, S. Ricciardi, Daniela Orteschi, R. Tenconi +6 more
2012American Journal of Medical Genetics. Part A29 citations
Semantic Scholar
Epilepsy and BRAF Mutations: Phenotypes, Natural History and Genotype-Phenotype Correlations
D. Battaglia, M. Gambardella, S. Veltri, Ilaria Contaldo +13 more
2021Genes24 citations Open access
Semantic Scholar
Spectral Domain Optical Coherence Tomography of Choroidal and Outer Retinal Layer Thickness in the Sturge Weber Syndrome
S. Abdolrahimzadeh, V. Scavella, D. Battaglia, S. Recupero
2016Current Eye Research24 citations
Semantic Scholar
Disorders of early language development in Dravet syndrome.
D. Chieffo, D. Battaglia, S. Lucibello, M. Gambardella +6 more
2016Epilepsy & Behavior23 citations
Semantic Scholar
Outlining a core neuropsychological phenotype for Dravet syndrome.
D. Battaglia, D. Ricci, D. Chieffo, F. Guzzetta
2016Epilepsy Research23 citations
Semantic Scholar
Cognitive-behavioral profiles in teenagers with Dravet syndrome.
G. Olivieri, D. Battaglia, D. Chieffo, Roberta Rubbino +5 more
2016Brain & development (Tokyo. 1979)23 citations
Semantic Scholar
Cortical Visual Impairment in CDKL5 Deficiency Disorder
Michela Quintiliani, D. Ricci, M. Petrianni, Simona Leone +9 more
2022Frontiers in Neurology22 citations Open access
Semantic Scholar
GABRA1‐Related Disorders: From Genetic to Functional Pathways
E. Musto, V. Liao, K. Johannesen, C. Fenger +44 more
2023Annals of Neurology21 citations Open access
Semantic Scholar
Rufinamide for the treatment of refractory epilepsy secondary to neuronal migration disorders.
R. Cusmai, A. Verrotti, R. Moavero, P. Curatolo +9 more
2014Epilepsy Research20 citations
Semantic Scholar
A registry for Dravet syndrome: The Italian experience
S. Balestrini, Viola Doccini, S. Giometto, E. Lucenteforte +43 more
2023Epilepsia Open19 citations Open access
Semantic Scholar
Sleep-potentiated epileptiform activity in early thalamic injuries: Study in a large series (60 cases).
E. Losito, D. Battaglia, D. Chieffo, M. Raponi +11 more
2015Epilepsy Research19 citations
Semantic Scholar
Phosphatase and tensin homolog (PTEN) variants and epilepsy: A multicenter case series.
N. Ronzano, M. Scala, E. Abiusi, Ilaria Contaldo +8 more
2022Seizure18 citations Open access
Semantic Scholar
Functional Characterization of a Novel KCNJ11 in Frame Mutation-Deletion Associated with Infancy-Onset Diabetes and a Mild Form of Intermediate DEND: A Battle between KATP Gain of Channel Activity and Loss of Channel Expression
Yu-Wen Lin, An-Long Li, V. Grasso, D. Battaglia +4 more
2013PLoS ONE18 citations Open access
Semantic Scholar
Early neurodevelopmental characterization in children with cobalamin C/defect
D. Ricci, D. Martinelli, Gloria Ferrantini, S. Lucibello +10 more
2020Journal of Inherited Metabolic Disease17 citations Open access
Semantic Scholar
Posterior resection for childhood lesional epilepsy: neuropsychological evolution.
D. Battaglia, D. Chieffo, G. Tamburrini, D. Lettori +8 more
2012Epilepsy & Behavior17 citations
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

E. Mercuri×14
Invite
E. Mercuri — researcher profile on SciRah
R. Guerrini×13
Invite
R. Guerrini — researcher profile on SciRah
D. Chieffo×11
Invite
D. Chieffo — researcher profile on SciRah
N. Specchio×11
Invite
N. Specchio — researcher profile on SciRah

×10

Invite

F. Guzzetta — researcher profile on SciRah

Invite

C. Dravet — researcher profile on SciRah

Invite

T. Granata — researcher profile on SciRah

Invite

I. Contaldo — researcher profile on SciRah

Invite

M. Zollino — researcher profile on SciRah

Daniela Orteschi×7

Invite

Daniela Orteschi — researcher profile on SciRah

Invite

G. Marangi — researcher profile on SciRah

Invite

F. Ragona — researcher profile on SciRah