IRIS - Res&Arch Institutional Research Information System - Research & Archive

MONTECCHIANI, CELESTE
 Distribuzione geografica
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Continente #
NA - Nord America 466
EU - Europa 344
AS - Asia 175
SA - Sud America 18
Continente sconosciuto - Info sul continente non disponibili 2
AF - Africa 1
Totale 1.006
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Nazione #
US - Stati Uniti d'America 460
IE - Irlanda 103
SG - Singapore 78
RU - Federazione Russa 64
IT - Italia 56
CN - Cina 36
HK - Hong Kong 36
AT - Austria 30
SE - Svezia 22
BR - Brasile 17
FI - Finlandia 16
VN - Vietnam 14
FR - Francia 11
GB - Regno Unito 9
DE - Germania 8
UA - Ucraina 7
BE - Belgio 6
CA - Canada 5
KR - Corea 4
NL - Olanda 3
PL - Polonia 3
CH - Svizzera 2
DK - Danimarca 2
EU - Europa 2
JP - Giappone 2
UZ - Uzbekistan 2
AR - Argentina 1
KG - Kirghizistan 1
LB - Libano 1
LT - Lituania 1
MX - Messico 1
PH - Filippine 1
SK - Slovacchia (Repubblica Slovacca) 1
ZA - Sudafrica 1
Totale 1.006
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Città #
Dublin 103
Chandler 77
San Mateo 76
Singapore 40
Hong Kong 36
Ann Arbor 25
Santa Clara 25
Vienna 25
Boardman 23
Medford 23
Princeton 23
Moscow 22
Beijing 21
Perugia 16
Wilmington 16
Dong Ket 14
Lawrence 14
Altamura 13
Redmond 12
Saint Petersburg 7
Ashburn 6
Brussels 6
Nuremberg 6
Helsinki 5
Winnipeg 5
Rome 4
Andover 3
Dallas 3
Los Angeles 3
New York 2
Norwalk 2
Redwood City 2
Sciacca 2
Seoul 2
Woodbridge 2
Altamira 1
Amsterdam 1
Aparecida 1
Belo Horizonte 1
Berazategui 1
Bishkek 1
Blumenau 1
Boksburg 1
Bratislava 1
Camaquã 1
Campinas 1
Cattolica 1
Changsha 1
Chicago 1
Chongqing 1
Cuiabá 1
Den Haag 1
Düsseldorf 1
Florence 1
Gimhae 1
Houston 1
Jiutepec 1
Kunming 1
Maringá 1
Nanjing 1
Niterói 1
Quezon City 1
Ribeirão Preto 1
Ribeirão das Neves 1
Rio de Janeiro 1
Salto 1
San Paolo di Civitate 1
Santa Isabel 1
Shanghai 1
Sorocaba 1
São Paulo 1
Tashkent 1
The Dalles 1
Tokyo 1
Turek 1
Valinhos 1
Totale 705
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Nome #
Clinical and genetic study of an Italian family with complicated hereditary spastic paraplegia and Alzheimer's disease 91
Trans-crocetin improves amyloid-β degradation in monocytes from Alzheimer's Disease patients 83
ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease 71
Spastic paraplegia type 4: A novel SPAST splice site donor mutation and expansion of the phenotype variability 70
Spastic paraplegia type 4: a novel SPAST splice site donor mutation and expansion of the phenotype variability 69
Hereditary spastic paraplegia and Alzheimer’s disease: clinical and genetic study of a Brazilian family 62
SPG11-related parkinsonism: Clinical profile, molecular imaging and l-dopa response 61
Clinico-genetic study of two Japanese pedigrees with hereditary spastic paraparesis and Alzheimer’s disease 60
A clinico-genetical study in a large cohort of patients with spastic paraplegia type 4 (SPG4) 59
SPG11 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease 55
Spastic paraplegia type 4: a novel SPAST splice site donor mutation and expansion of the phenotype variability 54
A new SPG4/SPAST mutation in an Italian family with hereditary spastic paraplegia and Alzheimer's disease 52
Identification of ALS5/SPG11/KIAA1840 Mutations in Patients with Autosomal Recessive Form of Charcot-Marie-Tooth Disease Type 2 50
Clinical and genetic study of a Japanese family with complicated hereditary spastic paraplegia and Alzheimer's disease 50
Phenotype variability and allelic heterogeneity in KMT2B-Associated disease 48
Hereditary Spastic Paraplegia Type 4 (SPG4): A Clinico-Genetic Study in a Large Cohort of Patients with Spastic Paraplegia 45
Spastic paraplegia type 4: A novel SPAST splice site donor mutation and expansion of the phenotype variability 40
Spastic paraplegia type 31: A novel REEP1 splice site donor variant and expansion of the phenotype variability 38
Epidemiological, clinical, and genetic study in a large cohort of patients with spastic paraplegia 31
SPG11 mutations cause widespread white matter and basal ganglia abnormalities, but restricted cortical damage 31
Clinical and genetic study of a large SPG4 Italian family with hereditary spastic paraplegia and early-onset familial Alzheimer’s disease 28
Hereditary spastic paraplegia and Alzheimer's disease: hypothesis of a founder effect of a SPG4/SPAST mutation 27
Clinical and genetic study in a large cohort of patients with spastic paraplegia 26
Hereditary spastic paraplegia type 4 (SPG4): an international multicenter clinical and genetic study. 24
Totale 1.225
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Categoria #
all - tutte 6.076
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 6.076
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202035 0 0 0 0 0 0 0 0 0 21 4 10
2020/2021106 9 1 3 1 45 7 11 2 5 3 2 17
2021/2022193 2 56 9 6 13 0 1 54 3 6 16 27
2022/2023280 25 32 13 6 27 25 1 17 128 0 4 2
2023/2024119 7 22 7 3 1 0 36 0 0 7 19 17
2024/2025237 1 26 21 1 24 39 14 19 83 9 0 0
Totale 1.225