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Alessandro Iodice

Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care
2018 · Ivan Ivanovski, Olivera Djuric, et al. · Genetics in Medicine · 103
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ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients
2017 · Miryam Carecchio, Niccolò E. Mencacci, et al. · Parkinsonism & Related Disorders · 96
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Neuroimaging findings in Mowat–Wilson syndrome: a study of 54 patients
2016 · Livia Garavelli, Ivan Ivanovski, et al. · Genetics in Medicine · 59
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Signe du Depressor Anguli Oris (DAO) dans les parésies faciales. Comment le rechercher et libérer le sourire (note technique)
2012 · D. Labbé, L. Bénichou, et al. · Annales de Chirurgie Plastique Esthétique · 43
A comprehensive approach to long-standing facial paralysis based on lengthening temporalis myoplasty.
2012 · D Labbè, F Bussu, et al. · PubMed Central · 42
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Infantile neuroaxonal dystrophy and PLA2G6-associated neurodegeneration: An update for the diagnosis
2016 · Alessandro Iodice, Carlotta Spagnoli, et al. · Brain and Development · 36
The effects of lupus and antiphospholipid antibody syndrome on foetal outcomes
2014 · C Nalli, A Iodice, et al. · Lupus · 35
Long-term neurodevelopmental outcome of children born to prospectively followed pregnancies of women with systemic lupus erythematosus and/or antiphospholipid syndrome
2017 · C Nalli, A Iodice, et al. · Lupus · 29
Expanding phenotype of PRRT2 gene mutations: A new case with epilepsy and benign myoclonus of early infancy
2016 · Ilenia Maini, Alessandro Iodice, et al. · European Journal of Paediatric Neurology · 28
Pediatric Moyamoya Disease and Syndrome in Italy: A Multicenter Cohort
2022 · Chiara Po', Margherita Nosadini, et al. · Frontiers in Pediatrics · 25
CMV-associated axonal sensory-motor Guillain–Barré syndrome in a child: Case report and review of the literature
2015 · Carlotta Spagnoli, Alessandro Iodice, et al. · European Journal of Paediatric Neurology · 21
Mowat-Wilson syndrome: growth charts
2020 · Ivan Ivanovski, Olivera Djuric, et al. · Orphanet Journal of Rare Diseases · 20
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KCNQ2 encephalopathy: A case due to a de novo deletion
2017 · Carlotta Spagnoli, Grazia Gabriella Salerno, et al. · Brain and Development · 20
Status dystonicus: management and prevention in children at high risk.
2019 · Alessandro Iodice, Francesco Pisani · Acta bio-medica dell'Ateneo parmense/Acta biomedica · 16
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Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study
2016 · Marilena Vecchi, Carmen Barba, et al. · Epilepsia · 15
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Long-term follow-up in spastic paraplegia due to SPG56/CYP2U1: age-dependency rather than genetic variability?
2017 · Alessandro Iodice, Celeste Panteghini, et al. · Journal of Neurology · 11
Hereditary neuropathy with liability to pressure palsies in childhood: Case series and literature update
2016 · Carlotta Spagnoli, Alessandro Iodice, et al. · Neuromuscular Disorders · 10
Restless Legs Syndrome in NKX2-1-related chorea: An expansion of the disease spectrum
2018 · A. Iodice, M. Carecchio, et al. · Brain and Development · 9
Biallelic SZT2 mutation with early onset of focal status epilepticus: Useful diagnostic clues other than epilepsy, intellectual disability and macrocephaly
2019 · Alessandro Iodice, Carlotta Spagnoli, et al. · Seizure · 8
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Neurovisual Assessment in Children with Ataxia Telangiectasia
2017 · Jessica Galli, Anna Molinaro, et al. · Neuropediatrics · 8
Steroids efficacy in the acute management of seizure clusters in one case of PCDH19 female epilepsy
2015 · G. Bertani, C. Spagnoli, et al. · Seizure · 8
Children born to SLE and APS mothers
2014 · C Nalli, A Iodice, et al. · Lupus · 8
17p13.1 microdeletion: Genetic and clinical findings in a new patient with epilepsy and comparison with literature
2013 · Lucio Giordano, Filippo Palestra, et al. · American Journal of Medical Genetics Part A · 8
Myoclonic epilepsy of infancy related to YWHAG gene mutation: towards a better phenotypic characterization.
2021 · Alessandro Iodice, Costanza Giannelli, et al. · Seizure · 7
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PPP3CA gene-related developmental and epileptic encephalopathy: Expanding the electro-clinical phenotype
2024 · Jacopo Favaro, Alessandro Iodice, et al. · Seizure · 6
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Works count: 48
Citation count: 699
H-index: 15
I10-index: 17
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