IRIS
PROCOPIO, RADHA
 Distribuzione geografica
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Continente #
NA - Nord America 216
EU - Europa 77
AS - Asia 75
Totale 368
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Nazione #
US - Stati Uniti d'America 216
SG - Singapore 65
IT - Italia 50
GB - Regno Unito 11
DE - Germania 9
CN - Cina 5
HK - Hong Kong 5
FI - Finlandia 2
AT - Austria 1
CZ - Repubblica Ceca 1
EE - Estonia 1
FR - Francia 1
NL - Olanda 1
Totale 368
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Città #
Santa Clara 46
Singapore 34
Chicago 13
London 11
Ashburn 10
Pasadena 10
Secaucus 10
Milan 9
Buffalo 5
Elk Grove Village 5
Hong Kong 5
Rome 5
Assago 4
Washington 4
Boardman 3
Munich 3
The Dalles 3
Bovisio-Masciago 2
Catanzaro 2
Cormons 2
Hanover 2
Helsinki 2
Lawrence 2
Naples 2
Palo del Colle 2
Pesaro 2
Pisa 2
Princeton 2
San Nicola Manfredi 2
Shenzhen 2
Turin 2
Vicopisano 2
Amsterdam 1
Cernusco sul Naviglio 1
Lamezia Terme 1
Messina 1
Miami 1
Olomouc 1
Pescara 1
Redmond 1
San Francisco 1
Trento 1
Vienna 1
Wilmington 1
Totale 222
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Nome #
Analysis of the LRP10 gene in patients with Parkinson’s disease and dementia with Lewy bodies from Southern Italy 29
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia 28
Glucose transporter-1 deficiency syndrome with extreme phenotypic variability in a five-generation family carrying a novel SLC2A1 variant 26
Idiopathic generalized epilepsy in a family with SCN4A-related myotonia 25
Mutation analysis of the ATP13A2 gene in patients with PD and MSA from Italy 24
A novel phenotype in an Italian family with a rare progranulin mutation 24
Selectivity of the CUBAN domain in the recognition of ubiquitin and NEDD8 23
ANXA1 mutation analysis in Italian patients with early onset PD 20
Neurological manifestations in patients and disease carriers in an Italian family with osteosclerosis 20
DCTN1 mutation analysis in Italian patients with PSP, MSA, and DLB 19
Analysis of the TMEM230 gene in patients with multiple system atrophy 18
Genetic mutation analysis of the COQ2 gene in Italian patients with multiple system atrophy 18
ANXA1 mutation analysis in Italian patients with early onset PD 17
Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria 17
Corrigendum to “A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy” [J. Neurol. Sci. 381C (2017) 209–212] (S0022510X17337528) (10.1016/j.jns.2017.08.3260)) 15
Analysis of the TMEM230 gene in familial Parkinson's disease from south Italy 15
Multiple system atrophy and C9orf72 hexanucleotide repeat expansions in a cohort of Italian patients 13
Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by Fragile X Tremor Ataxia Syndrome 12
Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria 11
Admixture analysis to define late onset Parkinson's disease: Moderating effect of the APOE gene 7
Hereditary Spastic Paraplegia Associated with Ultra-Rare Variant Enrichment Encompassing the SYNE1, CAPN1 and PGAP1 Genes 7
Two Novel Variants in the CHRNA2 and SCN2A Genes in Italian Patients with Febrile Seizures 5
Totale 393
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Categoria #
all - tutte 4.329
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 4.329
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202 0 0 0 0 0 0 0 0 0 0 2 0
2020/20212 0 0 0 0 2 0 0 0 0 0 0 0
2021/20222 0 0 0 0 0 0 0 2 0 0 0 0
2022/202359 4 0 0 0 1 21 4 6 7 4 6 6
2023/202489 22 11 5 12 9 17 0 0 0 0 5 8
2024/2025239 17 4 2 35 22 45 24 22 45 18 5 0
Totale 393