PROCOPIO, RADHA
 Distribuzione geografica
Continente #
NA - Nord America 479
AS - Asia 167
EU - Europa 153
SA - Sud America 42
AF - Africa 2
Totale 843
Nazione #
US - Stati Uniti d'America 473
SG - Singapore 108
IT - Italia 63
DE - Germania 37
BR - Brasile 35
CN - Cina 29
FI - Finlandia 23
GB - Regno Unito 14
VN - Vietnam 11
HK - Hong Kong 6
AT - Austria 4
CA - Canada 3
ID - Indonesia 3
IN - India 3
PL - Polonia 3
CZ - Repubblica Ceca 2
EC - Ecuador 2
FR - Francia 2
IQ - Iraq 2
MX - Messico 2
NL - Olanda 2
TR - Turchia 2
VE - Venezuela 2
BD - Bangladesh 1
CO - Colombia 1
DM - Dominica 1
EE - Estonia 1
ES - Italia 1
IL - Israele 1
PS - Palestinian Territory 1
PY - Paraguay 1
SE - Svezia 1
TN - Tunisia 1
UY - Uruguay 1
ZA - Sudafrica 1
Totale 843
Città #
Dallas 141
Santa Clara 73
Singapore 72
Munich 28
Ashburn 25
Hefei 23
Secaucus 16
Turku 16
Chicago 15
London 12
Milan 10
Pasadena 10
Ho Chi Minh City 8
Rome 8
Buffalo 7
Helsinki 7
San Francisco 7
Columbus 6
Hong Kong 6
Elk Grove Village 5
Los Angeles 5
The Dalles 5
Assago 4
Boardman 4
São Paulo 4
Washington 4
Campinas 3
New York 3
Warsaw 3
Bovisio-Masciago 2
Brasília 2
Brooklyn 2
Catanzaro 2
Cormons 2
Denver 2
Genoa 2
Guarulhos 2
Hanover 2
Lawrence 2
Manaus 2
Miami 2
Montalto Uffugo 2
Naples 2
New Delhi 2
Olomouc 2
Palo del Colle 2
Pesaro 2
Phoenix 2
Pisa 2
Princeton 2
San Nicola Manfredi 2
Shenzhen 2
Turin 2
Vicopisano 2
Volla 2
Ad Dīwānīyah 1
Almont 1
Amsterdam 1
Ankara 1
Auriflama 1
Baghdad 1
Belo Horizonte 1
Bismarck 1
Biên Hòa 1
Boa Vista 1
Bom Jesus 1
Boston 1
Brockport 1
Camaçari 1
Caracas 1
Carney 1
Cartagena 1
Cernusco sul Naviglio 1
Charlotte 1
Ciudad del Este 1
Curitiba 1
Currais Novos 1
Eldorado dos Carajás 1
Formiga 1
Fronteira 1
Guayaquil 1
Hanoi 1
Jakarta 1
Johannesburg 1
Kairouan 1
Kediri 1
La Grita 1
Lamezia Terme 1
Londrina 1
Messina 1
Mexico City 1
Mogi das Cruzes 1
Montesilvano Marina 1
Montevideo 1
Mumbai 1
Mérida 1
Norfolk 1
Nova Iguaçu 1
Oklahoma City 1
Palermo 1
Totale 627
Nome #
Hereditary Transthyretin Amyloidosis: Genetic Characterization of the TTR P.Val142Ile Variant in a Calabrian Kindred 97
Mutation analysis of the ATP13A2 gene in patients with PD and MSA from Italy 51
Glucose transporter-1 deficiency syndrome with extreme phenotypic variability in a five-generation family carrying a novel SLC2A1 variant 51
Idiopathic generalized epilepsy in a family with SCN4A-related myotonia 47
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia 46
Analysis of the LRP10 gene in patients with Parkinson’s disease and dementia with Lewy bodies from Southern Italy 43
Selectivity of the CUBAN domain in the recognition of ubiquitin and NEDD8 42
A novel phenotype in an Italian family with a rare progranulin mutation 40
ANXA1 mutation analysis in Italian patients with early onset PD 38
Novel KCNQ2 Variants Related to a Variable Phenotypic Spectrum Ranging from Epilepsy with Auditory Features to Severe Developmental and Epileptic Encephalopathies 35
ANXA1 mutation analysis in Italian patients with early onset PD 34
Neurological manifestations in patients and disease carriers in an Italian family with osteosclerosis 34
DCTN1 mutation analysis in Italian patients with PSP, MSA, and DLB 33
Analysis of the TMEM230 gene in patients with multiple system atrophy 31
Analysis of the TMEM230 gene in familial Parkinson's disease from south Italy 29
Genetic mutation analysis of the COQ2 gene in Italian patients with multiple system atrophy 26
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)) 25
Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria 25
Identification of Ser71Arg mutation in RAB32 gene in familial Parkinson’s disease from Southern Italy 25
Multiple system atrophy and C9orf72 hexanucleotide repeat expansions in a cohort of Italian patients 22
Two Novel Variants in the CHRNA2 and SCN2A Genes in Italian Patients with Febrile Seizures 22
Admixture analysis to define late onset Parkinson's disease: Moderating effect of the APOE gene 18
Hereditary Spastic Paraplegia Associated with Ultra-Rare Variant Enrichment Encompassing the SYNE1, CAPN1 and PGAP1 Genes 18
Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by Fragile X Tremor Ataxia Syndrome 17
Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria 16
Genetic analysis of GBA1 gene in a cohort of patients with Parkinson's disease 5
MAPT Subhaplotypes in Different Progressive Supranuclear Palsy Phenotypes 3
Totale 873
Categoria #
all - tutte 6.975
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 6.975


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
2025/2026345 62 64 185 34 0 0 0 0 0 0 0 0
Totale 873