IRIS
CATALDI, MATTEO
 Distribuzione geografica
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Continente #
EU - Europa 980
AS - Asia 18
NA - Nord America 2
SA - Sud America 1
Totale 1.001
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Nazione #
IT - Italia 980
CN - Cina 15
SG - Singapore 2
US - Stati Uniti d'America 2
EC - Ecuador 1
VN - Vietnam 1
Totale 1.001
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Città #
Genoa 629
Vado Ligure 131
Rapallo 116
Genova 100
Beijing 9
Bordighera 4
Ashburn 2
Phúc Yên 1
Yantzaza 1
Totale 993
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Nome #
Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutation 120
Musculoskeletal features without ataxia associated with a novel de novo mutation in KCNA1 impairing the voltage sensitivity of Kv1.1 channel 88
The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatment 87
On the role of REM sleep microstructure in suppressing interictal spikes in Electrical Status Epilepticus during Sleep 82
Multimodal approach in the pre-surgical evaluation of focal epilepsy surgery candidates: how far are we from a non-invasive ESI-based "sourcectomy"? 80
A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers 77
Comparison of Qualitative and Quantitative Analyses of MR-Arterial Spin Labeling Perfusion Data for the Assessment of Pediatric Patients with Focal Epilepsies 74
Sleep disorders in Prader-Willi syndrome, evidence from animal models and humans 71
Sleep disturbances in craniopharyngioma: a challenging diagnosis 68
Early Onset Inherited Peripheral Neuropathies: The Experience of a Specialized Referral Center for Genetic Diagnosis Achievement 65
Correction to: Sleep disturbances in craniopharyngioma: a challenging diagnosis (Journal of Neurology, (2021), 268, 11, (4362-4369), 10.1007/s00415-021-10794-1) 63
Quantitative sleep EEG biomarkers in Rett Syndrome: Sleep as a window to understand synaptic dysfunction. 55
Optimizing Integration with the Italian EHR: The Use of LOINC Codes 40
Recurrent Sensory-Motor Neuropathy Mimicking CIDP as Predominant Presentation of PDH Deficiency 39
Early-Onset Sensorimotor Axonal Neuropathy as Sole Manifestation of HADHA -Related Disorder/ Mitochondrial Trifunctional Protein Defect 11
Case Report: Parsonage-Turner syndrome due to SEPTIN9 mutation: report of an Italian family with childhood onset and review of the literature 6
Totale 1.026
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Categoria #
all - tutte 5.274
article - articoli 4.927
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 152
Totale 10.353
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202115 0 0 0 0 0 0 0 2 3 8 2 0
2021/202260 8 0 1 4 2 3 0 17 6 11 0 8
2022/2023131 8 12 1 13 19 16 0 10 21 2 29 0
2023/2024129 1 8 2 14 7 28 9 7 6 16 11 20
2024/2025420 13 22 7 26 44 36 53 72 37 23 43 44
2025/2026236 92 16 62 65 1 0 0 0 0 0 0 0
Totale 1.026