CARLUCCIO, MARIA ALESSANDRA
 Distribuzione geografica
Continente #
NA - Nord America 1.178
EU - Europa 933
AS - Asia 125
SA - Sud America 4
OC - Oceania 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 2.243
Nazione #
US - Stati Uniti d'America 1.173
GB - Regno Unito 339
IE - Irlanda 149
IT - Italia 115
CN - Cina 92
DE - Germania 78
UA - Ucraina 72
SE - Svezia 65
FR - Francia 39
FI - Finlandia 25
RU - Federazione Russa 18
BE - Belgio 12
SG - Singapore 11
ES - Italia 9
TR - Turchia 8
VN - Vietnam 7
NL - Olanda 5
CA - Canada 4
CZ - Repubblica Ceca 4
JP - Giappone 3
AU - Australia 2
AL - Albania 1
AR - Argentina 1
BO - Bolivia 1
BY - Bielorussia 1
CL - Cile 1
EC - Ecuador 1
EU - Europa 1
IL - Israele 1
KR - Corea 1
KZ - Kazakistan 1
MX - Messico 1
RO - Romania 1
SA - Arabia Saudita 1
Totale 2.243
Città #
Southend 319
Fairfield 184
Menlo Park 180
Dublin 148
Ashburn 94
Woodbridge 78
Houston 71
Seattle 68
Wilmington 68
Cambridge 66
Chandler 63
Jacksonville 61
Ann Arbor 58
Siena 33
Nanjing 28
Beijing 26
Princeton 26
Helsinki 13
New York 10
Brussels 9
Málaga 9
Rome 8
San Diego 8
Boardman 7
Dong Ket 7
Izmir 7
Moscow 6
Shenyang 6
Hebei 5
Milan 5
Norwalk 5
Tianjin 5
Florence 4
London 4
San Mateo 4
Singapore 4
Brno 3
Changsha 3
Falls Church 3
Hefei 3
Kunming 3
Nürnberg 3
Washington 3
Atlanta 2
Daishinden 2
Dallas 2
Dearborn 2
Düsseldorf 2
Itri 2
Jinan 2
Lancaster 2
Munich 2
Nanchang 2
Nettuno 2
Palermo 2
Panicale 2
Pescara 2
Reggello 2
Shanghai 2
Stoney Creek 2
Waanrode 2
Almere Stad 1
Antrodoco 1
Berlin 1
Brunswick 1
Bussoleno 1
Canberra 1
Capergnanica 1
Chicago 1
Esslingen am Neckar 1
Fuzhou 1
Gelsenkirchen 1
Genova 1
Grosseto 1
Gunzenhausen 1
Hacienda El Triunfo 1
Haifa 1
Hangzhou 1
Hounslow 1
Iasi 1
Jiaxing 1
Kocaeli 1
Leawood 1
Lequile 1
Markham 1
Melbourne 1
Mestre 1
Minsk 1
Ningbo 1
Olomouc 1
Oral 1
Parma 1
Prato 1
Redmond 1
Redwood City 1
Rieti 1
Riyadh 1
Southwark 1
Sucre 1
Tappahannock 1
Totale 1.793
Nome #
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients 281
Cerebellum and neuropsychiatric disorders: insights from ARSACS 212
Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrum 206
Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsies. 190
Tarlov cysts: clinical evaluation of an italian cohort of patients. 182
null 182
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene. 177
A new thymidine phosphorylase mutation causing elongation of the protein underlies mitochondrial neurogastrointestinal encephalomyopathy 162
The first Italian patient with oculopharyngodistal myopathy: Case report and considerations on differential diagnosis. 155
Clinical and biochemical improvement following HSCT in a patient with MNGIE: 1-year follow-up. 146
Hand muscles corticomotor excitability in hereditary spastic paraparesis type 4. 135
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome 128
Neurophthalmologic and Orthoptic Ambulatory Assessments Reveal Ocular and Visual Changes in Patients With Early Alzheimer and Parkinson's Disease 83
Vitamin D levels in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) 43
Totale 2.282
Categoria #
all - tutte 6.025
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 6.025


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020429 0 22 34 84 33 41 39 54 57 27 16 22
2020/2021312 15 28 22 24 18 28 11 44 22 44 32 24
2021/2022208 17 33 6 9 19 6 18 6 13 19 21 41
2022/2023263 20 16 41 28 23 52 8 22 25 16 7 5
2023/2024259 4 2 27 18 7 71 90 7 5 10 2 16
2024/202522 5 17 0 0 0 0 0 0 0 0 0 0
Totale 2.282