ORSINI, ALESSANDRO
 Distribuzione geografica
Continente #
EU - Europa 61
Totale 61
Nazione #
IT - Italia 61
Totale 61
Città #
Genoa 25
Genova 18
Rapallo 17
Bordighera 1
Totale 61
Nome #
Clinical features, disease evolution, ocular phenotype and electroretinogram abnormalities in Italian Lafora disease patients: a road to precision therapy, file e268c4ce-0b0b-a6b7-e053-3a05fe0adea1 26
Long-term dentoskeletal changes of class II growing patients' treatment with the propulseur universal light appliance. A prospective controlled study, file bde41bae-6ec8-47a4-88f7-93f70c67e874 16
Expanding Phenotype of Poirier–Bienvenu Syndrome: New Evidence from an Italian Multicentrical Cohort of Patients, file e268c4ce-a1d1-a6b7-e053-3a05fe0adea1 12
NovelAMPD2mutation in pontocerebellar hypoplasia, dysmorphisms, and teeth abnormalities, file e268c4cc-4895-a6b7-e053-3a05fe0adea1 1
Clinical spectrum and genotype-phenotype correlations in PRRT2 Italian patients, file e268c4cc-cbf8-a6b7-e053-3a05fe0adea1 1
Recent advances in epilepsy genetics, file e268c4cc-e285-a6b7-e053-3a05fe0adea1 1
The spectrum of intermediate SCN8A-related epilepsy, file e268c4cc-f07a-a6b7-e053-3a05fe0adea1 1
Medical management for neurosurgical related seizures, file e268c4cd-1cb8-a6b7-e053-3a05fe0adea1 1
The best evidence for progressive myoclonic epilepsy: A pathway to precision therapy, file e268c4cd-2489-a6b7-e053-3a05fe0adea1 1
Generalized epilepsy and mild intellectual disability associated with 13q34 deletion: A potential role for SOX1 and ARHGEF7, file e268c4cd-36df-a6b7-e053-3a05fe0adea1 1
Totale 61
Categoria #
all - tutte 378
article - articoli 249
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 627


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202110 0 0 0 0 0 0 2 0 0 4 1 3
2021/20228 1 1 2 0 0 0 0 0 2 1 1 0
2022/202320 0 1 0 0 1 10 0 3 1 2 2 0
2023/202423 3 2 0 1 2 0 8 3 2 2 0 0
Totale 61