POLLINI, LUCA
 Distribuzione geografica
Continente #
NA - Nord America 248
EU - Europa 221
AS - Asia 85
AF - Africa 3
OC - Oceania 1
SA - Sud America 1
Totale 559
Nazione #
US - Stati Uniti d'America 242
IT - Italia 161
SG - Singapore 48
IN - India 14
CN - Cina 12
NL - Olanda 11
DE - Germania 10
BG - Bulgaria 9
ID - Indonesia 9
CA - Canada 6
FI - Finlandia 6
SE - Svezia 5
AL - Albania 3
BE - Belgio 3
FR - Francia 3
ES - Italia 2
GB - Regno Unito 2
IE - Irlanda 2
NG - Nigeria 2
AU - Australia 1
BR - Brasile 1
JP - Giappone 1
LI - Liechtenstein 1
MY - Malesia 1
NO - Norvegia 1
RO - Romania 1
UA - Ucraina 1
ZA - Sudafrica 1
Totale 559
Città #
Rome 52
Singapore 36
Fairfield 24
Chandler 23
Santa Clara 19
Seattle 13
Ashburn 12
Wilmington 12
Woodbridge 10
Jakarta 9
Sofia 9
Cambridge 8
Como 8
Boston 7
Princeton 7
Andover 6
New York 6
Houston 5
Milan 5
Torre del Greco 5
Norwalk 4
Palermo 4
San Paolo di Civitate 4
Ann Arbor 3
Bari 3
Beijing 3
Boardman 3
Brussels 3
Florence 3
Helsinki 3
Lawrence 3
Ottawa 3
Pune 3
Richmond 3
San Diego 3
Tirana 3
Toronto 3
Verona 3
Viterbo 3
Ancona 2
Bühl 2
Casalecchio di Reno 2
Dublin 2
Giugliano In Campania 2
Grafing 2
Hamburg 2
Lagos 2
Lappeenranta 2
Madrid 2
Mannheim 2
Millbury 2
Nocera Inferiore 2
Rotterdam 2
Americana 1
Bremen 1
Chicago 1
Chieti 1
Fort Worth 1
Frankfurt am Main 1
Groningen 1
Indiana 1
Kilburn 1
London 1
Los Angeles 1
Melbourne 1
Montecalvo Irpino 1
Muizenberg 1
Osaka 1
Oslo 1
Pathanamthitta 1
Phoenix 1
Plano 1
San Francisco 1
San Mateo 1
Schaan 1
Springfield 1
Stockholm 1
Turin 1
Washington 1
Totale 390
Nome #
KCND3-Related Neurological Disorders: From Old to Emerging Clinical Phenotypes 85
Attention in Parkinson’s disease with fatigue: evidence from the attention network test 72
Parkinsonism, Intellectual Disability, and Catatonia in a Young Male With MECP2 Variant 61
null 42
Expanding the phenotype of the rare neuronal ceroid lipofuscinoses (ncl) 10 42
A diagnosis of progressive myoclonic ataxia guided by blood biomarkers: Expert commentary 41
Neurophysiological assessment of juvenile parkinsonism due to primary monoamine neurotransmitter disorders 38
Fenotipo epilettico e gestione terapeutica in un paziente con deficit di succinico semialdeide deidrogenasi: evoluzione dall’ infanzia all’ età adulta 35
null 27
Improvement of Movement Disorder and Neurodevelopment under Selegiline in a CLTC-Deficient Patient 26
GNAO1 Haploinsufficiency: The Milder End of the GNAO1 Phenotypic Spectrum 26
Fever-Induced and Early Morning Paroxysmal Dyskinesia in a Man With GNB1 Encephalopathy 23
Multiple sclerosis and intracellular cobalamin defect (MMACHC/PRDX1) comorbidity in a young male 22
Delineating the neurological phenotype in children with defects in the ECHS1 or HIBCH gene 21
GNAO1-related movement disorder: An update on phenomenology, clinical course, and response to treatments 18
Motor, epileptic, and developmental phenotypes in genetic disorders affecting G protein coupled receptors-cAMP signaling 17
CACNA1G Causes Dominantly Inherited Myoclonus-Ataxia with Intellectual Disability: A Case Report 10
Totale 606
Categoria #
all - tutte 2.370
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 2.370


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202027 0 0 0 0 2 1 3 2 2 8 5 4
2020/2021107 2 21 16 4 10 3 5 17 11 7 0 11
2021/202292 0 2 1 2 10 6 0 5 28 5 23 10
2022/202391 12 11 2 13 13 9 6 6 15 0 4 0
2023/2024139 2 10 7 17 10 23 11 6 7 15 10 21
2024/2025134 11 25 16 46 36 0 0 0 0 0 0 0
Totale 606