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

MONTECCHIANI, CELESTE
 Distribuzione geografica
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Continente #
NA - Nord America 427
EU - Europa 254
AS - Asia 124
Continente sconosciuto - Info sul continente non disponibili 2
Totale 807
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Nazione #
US - Stati Uniti d'America 423
IE - Irlanda 90
IT - Italia 49
SG - Singapore 37
CN - Cina 33
HK - Hong Kong 32
AT - Austria 24
SE - Svezia 22
RU - Federazione Russa 21
VN - Vietnam 14
FI - Finlandia 11
FR - Francia 10
GB - Regno Unito 8
BE - Belgio 5
UA - Ucraina 5
CA - Canada 4
KR - Corea 4
PL - Polonia 3
CH - Svizzera 2
DK - Danimarca 2
EU - Europa 2
DE - Germania 1
JP - Giappone 1
LB - Libano 1
PH - Filippine 1
SK - Slovacchia (Repubblica Slovacca) 1
UZ - Uzbekistan 1
Totale 807
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Città #
Dublin 90
Chandler 77
San Mateo 68
Hong Kong 32
Singapore 25
Ann Arbor 24
Vienna 23
Beijing 21
Santa Clara 20
Boardman 19
Medford 19
Princeton 19
Wilmington 15
Dong Ket 14
Lawrence 14
Perugia 14
Altamura 13
Redmond 12
Saint Petersburg 6
Ashburn 5
Brussels 5
Helsinki 4
Winnipeg 4
Andover 3
Dallas 3
Los Angeles 2
Moscow 2
New York 2
Norwalk 2
Redwood City 2
Sciacca 2
Seoul 2
Woodbridge 2
Bratislava 1
Cattolica 1
Changsha 1
Chicago 1
Chongqing 1
Florence 1
Gimhae 1
Houston 1
Kunming 1
Nanjing 1
Quezon City 1
San Paolo di Civitate 1
Turek 1
Totale 578
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Nome #
Clinical and genetic study of an Italian family with complicated hereditary spastic paraplegia and Alzheimer's disease 86
Trans-crocetin improves amyloid-β degradation in monocytes from Alzheimer's Disease patients 72
ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease 67
Spastic paraplegia type 4: a novel SPAST splice site donor mutation and expansion of the phenotype variability 66
Spastic paraplegia type 4: A novel SPAST splice site donor mutation and expansion of the phenotype variability 61
A clinico-genetical study in a large cohort of patients with spastic paraplegia type 4 (SPG4) 53
Clinico-genetic study of two Japanese pedigrees with hereditary spastic paraparesis and Alzheimer’s disease 53
Hereditary spastic paraplegia and Alzheimer’s disease: clinical and genetic study of a Brazilian family 52
Spastic paraplegia type 4: a novel SPAST splice site donor mutation and expansion of the phenotype variability 50
SPG11-related parkinsonism: Clinical profile, molecular imaging and l-dopa response 50
Clinical and genetic study of a Japanese family with complicated hereditary spastic paraplegia and Alzheimer's disease 48
A new SPG4/SPAST mutation in an Italian family with hereditary spastic paraplegia and Alzheimer's disease 46
Identification of ALS5/SPG11/KIAA1840 Mutations in Patients with Autosomal Recessive Form of Charcot-Marie-Tooth Disease Type 2 45
SPG11 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease 44
Phenotype variability and allelic heterogeneity in KMT2B-Associated disease 40
Hereditary Spastic Paraplegia Type 4 (SPG4): A Clinico-Genetic Study in a Large Cohort of Patients with Spastic Paraplegia 39
Spastic paraplegia type 31: A novel REEP1 splice site donor variant and expansion of the phenotype variability 36
Spastic paraplegia type 4: A novel SPAST splice site donor mutation and expansion of the phenotype variability 36
SPG11 mutations cause widespread white matter and basal ganglia abnormalities, but restricted cortical damage 29
Totale 973
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Categoria #
all - tutte 4.429
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 4.429
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202044 0 0 0 0 1 1 5 1 1 21 4 10
2020/202198 9 1 3 1 37 7 11 2 5 3 2 17
2021/2022172 2 52 9 6 13 0 1 44 2 5 15 23
2022/2023262 21 32 13 6 27 25 1 16 115 0 4 2
2023/2024110 7 22 7 3 0 0 34 0 0 7 14 16
2024/202564 0 22 21 1 20 0 0 0 0 0 0 0
Totale 973