MORGESE, GUIDO
 Distribuzione geografica
Continente #
EU - Europa 29
Totale 29
Nazione #
IT - Italia 29
Totale 29
Città #
Siena 29
Totale 29
Nome #
Efficacy and safety of levetiracetam: an add-on trial in children with refractory epilepsy, file e0feeaa5-f000-44d2-e053-6605fe0a8db0 4
Intractable reflex audiogenic seizures in Aicardi syndrome, file e0feeaa5-e917-44d2-e053-6605fe0a8db0 3
GM2 gangliosidosis variant B1 neuroradiological findings, file e0feeaa5-e9ae-44d2-e053-6605fe0a8db0 3
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria, file e0feeaa5-e815-44d2-e053-6605fe0a8db0 2
Craniofacial dyssynostosis: case report and review, file e0feeaa5-e9b1-44d2-e053-6605fe0a8db0 2
Aicardi syndrome with favorable outcome: case report and review, file e0feeaa5-f3d2-44d2-e053-6605fe0a8db0 2
Efficacy and safety of topiramate in infants according to epilepsy syndromes, file e0feeaa4-e428-44d2-e053-6605fe0a8db0 1
18q-syndrome and ectodermal dysplasia syndrome: description of a child and his family, file e0feeaa4-e7a2-44d2-e053-6605fe0a8db0 1
Efficacy and safety of topiramate in refractory epilepsy of childhood: long-term follow-up study, file e0feeaa4-f300-44d2-e053-6605fe0a8db0 1
Transient neonatal hypothyroidism after gestational exposure to amiodarone: a follow-up of two cases, file e0feeaa5-e7e0-44d2-e053-6605fe0a8db0 1
Selective mutism, speech delay, dysmorphisms, and deletion of the short arm of chromosome 18: a distinct entity?, file e0feeaa5-e7f6-44d2-e053-6605fe0a8db0 1
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss a provisionally unique genetic syndrome, file e0feeaa5-e90a-44d2-e053-6605fe0a8db0 1
Pontocerebellar hypoplasia type 2: further clinical characterization and evidence of positive response of dyskinesia to levodopa, file e0feeaa5-eac5-44d2-e053-6605fe0a8db0 1
Ethylmalonic encephalopathy: further clinical and neuroradiological characterization, file e0feeaa5-eed7-44d2-e053-6605fe0a8db0 1
Hot water epilepsy and focal malformation of the parietal cortex development, file e0feeaa5-ef22-44d2-e053-6605fe0a8db0 1
Central precocious puberty and abnormal chromosomal patterns, file e0feeaa5-f010-44d2-e053-6605fe0a8db0 1
De novo complete trisomy 5p clinical and neuroradiological findings, file e0feeaa5-f322-44d2-e053-6605fe0a8db0 1
Seizures and electroencephalographic findings in CDKL5 mutations: case report and review, file e0feeaa7-0beb-44d2-e053-6605fe0a8db0 1
Typical absence seizures associated with localization-related epilepsy: a clinical and electroencephalographic characterization, file e0feeaa7-3744-44d2-e053-6605fe0a8db0 1
Totale 29
Categoria #
all - tutte 977
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 977


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202118 0 0 0 0 0 0 0 0 0 0 15 3
2021/20224 0 0 0 0 0 0 0 4 0 0 0 0
Totale 29