IRIS
ROMANO, ALFONSO
 Distribuzione geografica
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Continente #
NA - Nord America 723
EU - Europa 377
AS - Asia 190
AF - Africa 9
OC - Oceania 1
Totale 1.300
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Nazione #
US - Stati Uniti d'America 704
IT - Italia 146
SG - Singapore 104
CN - Cina 84
FR - Francia 60
UA - Ucraina 32
FI - Finlandia 30
IE - Irlanda 29
DE - Germania 26
NL - Olanda 22
CA - Canada 19
GB - Regno Unito 12
BG - Bulgaria 8
CI - Costa d'Avorio 8
RU - Federazione Russa 4
PL - Polonia 2
RS - Serbia 2
SE - Svezia 2
AU - Australia 1
BE - Belgio 1
IN - India 1
IR - Iran 1
MA - Marocco 1
RO - Romania 1
Totale 1.300
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Città #
Chandler 158
Santa Clara 91
Singapore 89
Jacksonville 35
Ashburn 34
Beijing 34
Millbury 33
Princeton 25
Woodbridge 23
Amsterdam 22
Naples 21
Nanjing 20
Boston 18
Ottawa 15
Wilmington 14
Houston 11
Napoli 11
Sofia 8
Des Moines 7
Lawrence 6
Milan 6
Nanchang 5
Pratola Peligna 5
Tianjin 5
Washington 5
Augusta 4
Helsinki 4
L’Aquila 4
Tübingen 4
Casalnuovo Di Napoli 3
Hebei 3
Kronberg 3
Los Angeles 3
Norwalk 3
Sassari 3
Adrano 2
Belgrade 2
Boardman 2
Cambridge 2
Campagna 2
Castell'alfero 2
Changsha 2
Dublin 2
Edinburgh 2
Enna 2
Falls Church 2
Genoa 2
Kraków 2
Leawood 2
Padova 2
Siracusa 2
Toronto 2
Villaricca 2
Ardabil 1
Atlanta 1
Bergamo 1
Bordolano 1
Brisbane 1
Brussels 1
Casoria 1
Changchun 1
Corigliano Calabro 1
Dearborn 1
Fairfield 1
Falkenstein 1
Ferrara 1
Frattamaggiore 1
Hefei 1
Jiaxing 1
Jinan 1
Kenitra 1
Kunming 1
Lappeenranta 1
London 1
Paris 1
Prineville 1
Pune 1
Quartu Sant'elena 1
Redwood City 1
Roccadaspide 1
Rome 1
San Giuliano Milanese 1
Seattle 1
Serramazzoni 1
Taranto 1
Teramo 1
Timisoara 1
Totale 805
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Nome #
A Chaperone Enhances Blood α-Glucosidase Activity in Pompe Disease Patients Treated With Enzyme Replacement Therapy 80
Familial white matter hypoplasia agenesis of the corpus callosum, mental retardation and growth deficiency: A new distinctive syndrome. 66
Approccio clinico alle macrocranie non familiari: presentazione di una casistica di 21 pazienti. 65
Long-term enzyme replacement therapy for Pompe disease with recombinant human alpha-glucosidase derived from chinese hamster ovary cells. 54
Long term follow-up to evaluate the efficacy of miglustat treatment in Italian patients with Niemann-Pick disease type C 54
Brain damage in glycogen storage disease type I 53
Neonatal urinary cotinine correlates with behavioural alterations due to maternal active and passive smoke during pregnancy . E129545 48
COVID-19-associated severe mono-hemispheric encephalitis in a young infant 48
Unexplained Bilateral Occipital Calcification and Reduced Vision. 46
The videofluoroscopic swallowing study shows a sustained improvement of dysphagia in children with Niemann-Pick disease type C after therapy with miglustat 46
Clinical Value of Perfusion Abnormalities of Brain on Technetium-99m HMPAO Single-Photon Emission Computed Tomography in Children With Sydenham Chorea 45
Megalocornea and mental retardation syndrome: two new cases. 44
Congenital fiber type disproportion myopathy. Report of a case with late onset and myalgia. 44
Functional gastrointestinal disorders in migrainous children: efficacy of flunarizine 43
Low-dose amitriptyline-induced acute dystonia in a patient with metachromatic leukodystrophy. 43
Disturbi da deficit dell'attenzione, percettivi e motori in età scolare. II. Risultati di uno studio effettuato su una popolazione di bambini della scuola elementare. 41
Cavitating and tigroid-like leukoencephalopathy in a case of NDUFA2-related disorder 41
The Pediatric Symptom Checklist as screening tool for neurological and psychosocial problems in a paediatric cohort of patients with coeliac disease. 40
A further contribution to the delineation of epileptic phenotype in PACS2-related syndrome 40
EEG findings in West syndrome a follow-up of 20 patients. 36
Sindrome di Miller-Dieker: osservazione di un caso con studio tomografico computerizzato. 35
Induzione enzimatica ed epatopatie da farmaci anticonvulsivanti. Studio retrospettivo su 20 bambini. 30
Disturbi da deficit dell'attenzione, percettivi e motori in età scolare. I. Aspetti della procedura di screening. 30
Steroid therapy in an alpha-dystroglycanopathy due to GMPPB gene mutations: A case report 30
Cerebellar dentate nuclei swelling: a new and early magnetic resonance imaging finding of beta-propeller protein-associated neurodegeneration 30
Electroencephalographic findings in ATRX syndrome: A new case series and review of literature 29
Acute inflammatory demyelinating polyradiculoneuropathy associated with perforin-deficient familial haemophagocytic lymphohistiocytosis. 26
Disturbi da deficit d'attenzione, percettivi e motori in età scolare. III. Aspetti neuroevolutivi. 25
Impact of malnutrition on gastrointestinal disorders and gross motor abilities in children with cerebral palsy. 25
Mild neurological phenotype in a family carrying a novel N-terminal null GRIN2A variant 25
La sindrome dell'X fragile. 24
Sindrome oro-facio-digitale tipo I. Descrizione di due casi. 19
A Novel Splicing SCN2A Mutation in an Adolescent With Low-Functioning Autism, Acute Dystonic Movement Disorder, and Late-Onset Generalized Epilepsy 17
null 12
Totale 1.334
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Categoria #
all - tutte 5.802
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 5.802
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202088 0 0 0 0 0 14 2 3 2 24 28 15
2020/2021107 10 8 6 8 17 22 7 0 14 1 14 0
2021/2022182 3 0 0 1 7 1 0 4 25 30 34 77
2022/2023316 37 39 18 16 36 36 0 35 54 22 19 4
2023/2024173 8 29 28 12 17 12 1 14 11 2 27 12
2024/2025229 45 49 5 11 52 67 0 0 0 0 0 0
Totale 1.334