IRIS
PROCOPIO, RADHA
 Distribuzione geografica
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Continente #
NA - Nord America 273
EU - Europa 114
AS - Asia 111
SA - Sud America 4
Totale 502
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Nazione #
US - Stati Uniti d'America 271
SG - Singapore 98
IT - Italia 51
DE - Germania 26
FI - Finlandia 15
GB - Regno Unito 13
CN - Cina 5
HK - Hong Kong 5
BR - Brasile 4
AT - Austria 2
CZ - Repubblica Ceca 2
CA - Canada 1
EE - Estonia 1
FR - Francia 1
IL - Israele 1
IQ - Iraq 1
MX - Messico 1
NL - Olanda 1
PL - Polonia 1
SE - Svezia 1
VN - Vietnam 1
Totale 502
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Città #
Singapore 67
Santa Clara 61
Munich 20
Secaucus 15
Chicago 14
Turku 13
London 12
Ashburn 10
Pasadena 10
Milan 9
Buffalo 6
San Francisco 6
Elk Grove Village 5
Hong Kong 5
Rome 5
The Dalles 5
Assago 4
Washington 4
Boardman 3
Los Angeles 3
Bovisio-Masciago 2
Catanzaro 2
Columbus 2
Cormons 2
Hanover 2
Helsinki 2
Lawrence 2
Miami 2
Naples 2
Olomouc 2
Palo del Colle 2
Pesaro 2
Pisa 2
Princeton 2
San Nicola Manfredi 2
Shenzhen 2
Turin 2
Vicopisano 2
Ad Dīwānīyah 1
Almont 1
Amsterdam 1
Bismarck 1
Brockport 1
Campinas 1
Cernusco sul Naviglio 1
Denver 1
Ho Chi Minh City 1
Lamezia Terme 1
Messina 1
Mexico City 1
New York 1
Norfolk 1
Oklahoma City 1
Palermo 1
Passa e Fica 1
Peoria 1
Pescara 1
Porto Alegre 1
Redmond 1
Saint Neots 1
San Jose 1
Stockholm 1
Tel Aviv 1
Trento 1
Ubatuba 1
Vienna 1
Warsaw 1
Wilmington 1
Totale 343
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Nome #
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia 39
Idiopathic generalized epilepsy in a family with SCN4A-related myotonia 37
Glucose transporter-1 deficiency syndrome with extreme phenotypic variability in a five-generation family carrying a novel SLC2A1 variant 34
Analysis of the LRP10 gene in patients with Parkinson’s disease and dementia with Lewy bodies from Southern Italy 33
Mutation analysis of the ATP13A2 gene in patients with PD and MSA from Italy 31
A novel phenotype in an Italian family with a rare progranulin mutation 29
Selectivity of the CUBAN domain in the recognition of ubiquitin and NEDD8 28
ANXA1 mutation analysis in Italian patients with early onset PD 27
DCTN1 mutation analysis in Italian patients with PSP, MSA, and DLB 27
Analysis of the TMEM230 gene in patients with multiple system atrophy 25
ANXA1 mutation analysis in Italian patients with early onset PD 24
Neurological manifestations in patients and disease carriers in an Italian family with osteosclerosis 24
Analysis of the TMEM230 gene in familial Parkinson's disease from south Italy 21
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)) 20
Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria 20
Genetic mutation analysis of the COQ2 gene in Italian patients with multiple system atrophy 20
Hereditary Spastic Paraplegia Associated with Ultra-Rare Variant Enrichment Encompassing the SYNE1, CAPN1 and PGAP1 Genes 15
Multiple system atrophy and C9orf72 hexanucleotide repeat expansions in a cohort of Italian patients 15
Two Novel Variants in the CHRNA2 and SCN2A Genes in Italian Patients with Febrile Seizures 14
Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria 13
Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by Fragile X Tremor Ataxia Syndrome 13
Admixture analysis to define late onset Parkinson's disease: Moderating effect of the APOE gene 12
Identification of Ser71Arg mutation in RAB32 gene in familial Parkinson’s disease from Southern Italy 7
Totale 528
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Categoria #
all - tutte 5.858
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 5.858
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2024/2025374 17 4 2 35 22 45 24 22 45 18 53 87
Totale 528