CNR Institutional Research Information System

DI PALMA, GEMMA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
AS - Asia 1.848
NA - Nord America 1.065
EU - Europa 649
SA - Sud America 381
Continente sconosciuto - Info sul continente non disponibili 64
AF - Africa 36
OC - Oceania 2
Totale 4.045
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 998
SG - Singapore 756
CN - Cina 423
BR - Brasile 317
IT - Italia 289
VN - Vietnam 214
HK - Hong Kong 161
FR - Francia 125
NL - Olanda 91
JP - Giappone 78
KR - Corea 65
IN - India 44
BD - Bangladesh 28
CA - Canada 28
DE - Germania 26
GB - Regno Unito 26
AR - Argentina 22
FI - Finlandia 22
ID - Indonesia 13
EC - Ecuador 12
IE - Irlanda 12
IL - Israele 12
MX - Messico 12
CO - Colombia 11
PL - Polonia 9
RU - Federazione Russa 9
ZA - Sudafrica 9
TR - Turchia 8
VE - Venezuela 8
CR - Costa Rica 7
AE - Emirati Arabi Uniti 6
JO - Giordania 6
KE - Kenya 6
TN - Tunisia 6
UA - Ucraina 6
AT - Austria 5
ES - Italia 5
MA - Marocco 5
SA - Arabia Saudita 5
DO - Repubblica Dominicana 4
IQ - Iraq 4
PY - Paraguay 4
SE - Svezia 4
SK - Slovacchia (Repubblica Slovacca) 4
AZ - Azerbaigian 3
CL - Cile 3
CZ - Repubblica Ceca 3
DZ - Algeria 3
EG - Egitto 3
NI - Nicaragua 3
OM - Oman 3
PK - Pakistan 3
TH - Thailandia 3
AL - Albania 2
BB - Barbados 2
BO - Bolivia 2
BY - Bielorussia 2
KG - Kirghizistan 2
MY - Malesia 2
PA - Panama 2
PE - Perù 2
TT - Trinidad e Tobago 2
UZ - Uzbekistan 2
AU - Australia 1
BQ - ???statistics.table.value.countryCode.BQ??? 1
BZ - Belize 1
CG - Congo 1
CH - Svizzera 1
CI - Costa d'Avorio 1
ET - Etiopia 1
GR - Grecia 1
GT - Guatemala 1
HN - Honduras 1
HR - Croazia 1
JM - Giamaica 1
KH - Cambogia 1
KW - Kuwait 1
KY - Cayman, isole 1
KZ - Kazakistan 1
LB - Libano 1
LT - Lituania 1
LV - Lettonia 1
MD - Moldavia 1
MT - Malta 1
NG - Nigeria 1
NO - Norvegia 1
PF - Polinesia Francese 1
PH - Filippine 1
PR - Porto Rico 1
SI - Slovenia 1
SV - El Salvador 1
TW - Taiwan 1
XK - ???statistics.table.value.countryCode.XK??? 1
YE - Yemen 1
Totale 3.983
Salva come PNG Salva come JPEG
Città #
Singapore 447
Santa Clara 371
Hong Kong 161
Hefei 146
San Jose 93
Lauterbourg 83
Ho Chi Minh City 82
Beijing 69
Tokyo 69
Naples 67
Seoul 64
Ashburn 54
Dallas 46
Hanoi 45
Los Angeles 39
São Paulo 26
New York 23
Milan 21
Catania 20
Bari 17
Buffalo 16
Rome 14
Dublin 12
Frankfurt am Main 11
Helsinki 10
Taranto 10
Amsterdam 9
Bologna 9
Brooklyn 9
London 8
Bengaluru 7
Da Nang 7
Lappeenranta 7
Minamishinagawa 7
Montreal 7
Paris 7
Rio de Janeiro 7
San José 7
Amman 6
Boardman 6
Bắc Ninh 6
Haiphong 6
Mumbai 6
Porto Alegre 6
Anoia Superiore 5
Council Bluffs 5
Genoa 5
Lấp Vò 5
Orem 5
Quito 5
Thái Bình 5
Toronto 5
Turin 5
Warsaw 5
Atlanta 4
Biên Hòa 4
Brasília 4
Chennai 4
Cincinnati 4
Dhaka 4
Fortaleza 4
Goiânia 4
Hyderabad 4
Hải Dương 4
Johannesburg 4
Messina 4
Newark 4
Vienna 4
Volta Redonda 4
Abu Dhabi 3
Asunción 3
Baku 3
Barquisimeto 3
Belo Horizonte 3
Bratislava 3
Can Tho 3
Catanduva 3
Chicago 3
Cosenza 3
Denver 3
Fazenda Rio Grande 3
Florianópolis 3
Formosa 3
Guangzhou 3
Guarulhos 3
Guayaquil 3
Ha Long 3
Houston 3
Juiz de Fora 3
Maceió 3
Manaus 3
Milwaukee 3
Nairobi 3
Nashville 3
Ourinhos 3
Phoenix 3
Phủ Lý 3
Pieve Emanuele 3
Poplar 3
Querétaro 3
Totale 2.346
Salva come PNG Salva come JPEG
Nome #
MALDI-ISD mass spectrometry analysis as a simple and reliable tool to detect post-translational modifications of hemoglobin variants: the case of Hb Raleigh 126
Exploring the FKRP Gene in Calabrian Patients with Duchenne/Becker-like Phenotype 112
Genomics landscape of mitochondrial DNA variations in patients from South Italy affected by mitochondriopathies 98
A new mutation detected by NGS in MT-ATP6 gene associated with MELAS and in silico 3D protein analysis 95
A novel homozygous variant in DYSF gene is associated with Autosomal Recessive Limb Girdle Muscular Dystrophy R2/2B 92
Identificato in un paziente del Sud Italia la variante Arg596Gly in omozigosi associata a Distrofia Muscolare dei Cingoli recessiva di tipo 8 89
Associazione tra la subunità 2B del recettore NMDA (gene GRIN2B) e la malattia di Alzheimer 85
Cst3: fattore di rischio genetico per la Malattia di Alzheimer sporadica? 82
Sex and APOE genotype modulate neuropsychological profile and depression in temporal lobe epilepsy 81
A NEW CYS1678TYR MUTATION RESPONSIBLE OF LGMD2B IDENTIFIED IN A FAMILY FROM SOUTHERN ITALY 78
Molecular Study of the Fukutin-Related Protein (FKRP) Gene in Patients from Southern Italy with Duchenne/Becker-like Phenotype 78
Arg143Ser is the most frequent variant in Limb Girdle Muscular Dystrophy-R9 in southern Italy 77
HOMOZYGOUS R596G VARIANT IN TRIM32 GENE RELATED TO LGMD IN A NON-HUTTERITE PATIENT 75
A WHOLE mtDNA NGS APPROACH TO IDENTIFY NOVEL VARIANTS IN PATIENTS AFFECTED BY MITOCHONDRIAL DISEASES 75
ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION 73
Serotonin receptor 2a gene variant influences age at onset but not cognitive performance in patients with temporal lobe epilepsy. 72
Disturbo di Alzheimer e tono dell'umore 72
Interruptions of the FXN GAA repeat tract delay the age at onset of Friedreich's ataxia in a location dependent manner. 70
Targeted Next Generation Sequencing is a valuable diagnostic tool for Inherited Peripheral Neuropathies 61
Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease 59
Ruolo del gene Neuregulin 1 (NRG1) nella Sclerosi Multipla 56
Kinesins in neurological inherited diseases: a novel motor-domain mutation in KIF5A gene in a patient from Southern Italy affected by hereditary spastic paraplegia. 55
The DRD2 TaqIA polymorphism associated with changed midbrain volumes in healthy individuals. 54
Role of the Neuregulin 1 gene (NRG1) in multiple sclerosis 53
Next-generation sequencing: identificazione di varianti geniche con effetto additivo nell'espressione del fenotipo patologico LGMD e cardiomiopatia dilatativa. 53
NEUROFIBROMATOSIS TYPE 2 (NF2) IN A CHILD UNDER 1 YEAR OF AGE: A CLINICAL AND MOLECULAR STUDY 48
ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION 45
Mutation analysis of the GRIN2B gene in Alzheimer's disease 45
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1 44
Usefulness of routine MRI to differentiate Progressive supranuclear palsy from Parkinson?s disease and Multiple System Atrophy 43
Serum levels of interleukin-6 and interleukin-8 are elevated in patients with partial epilepsy 42
Molecular characterization of the APP gene in italian patients with familial Alzheimer disease. 41
Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease 41
D678N mutation in a patient with an early-onset Alzheimer's Disease 40
PERIPHERAL MRNA EXPRESSION OF BRAIN-DERIVED NEUROTROPHIC FACTOR VAL66MET POLYMORPHISM IN PATIENTS WITH RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS). 38
Preliminary evidences of a NOS2A protective effect from Relapsing-Remitting Multiple Sclerosis 37
Caratterizzazione dei portatori sani SMA con Real time PCR 37
APP gene mutation (D678N) in a patient with an Early-Onset Alzheimer's Disease 37
Familial Alzheimer's disease with amyloid precursor protein D678N mutation: a case report 37
Depression and epilepsy 35
Screening for MELAS mutations in Italian patients having stroke-like episodes. 34
Studio clinico e genetico di una famiglia italiana affetta da una nuova forma di Paraparesi Spastica autosomica dominante complicata 34
Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification 34
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1. 33
Depression and Parkinson's disease:a neuropsychological view 33
Depression and Parkinson's disease 33
Two SNPs in the Fas gene on chromosome 10 are not associated with Sporadic Alzheimer s Disease in southern Italy. 33
Preliminary evidences of a NOS2A protective effect from relapsing-remitting multiple sclerosis. 32
Cognitive impairment in Multiple Sclerosis 32
Molecular characterization of the APP gene in Italian patients with familial Alzheimer disease. 32
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy 32
Analisi molecolare del promotore del gene PSEN-2 nella Malattia di Alzheimer: uno studio di associazione nella popolazione calabrese 32
Trauma cranico e genotipo APO-E: causa o rischio di malatia di Alzheimer? 32
The association of the regulatory region of the PS-2 gene with Alzheimer s disease. 31
Leber s hereditary optic neuropathy associated with multiple sclerosis like picture in a man. 31
Presenilin Enhancer-2 Gene mutations and Familial Alzheimer s Disease 31
Genetic screening of Alzheimer's disease genes in Italian samples yields novel mutations in Presenilin-enhancer 2. 30
Identification of four novel pathogenic mutations in patients from Southern Italy with CADASIL 30
Analisi mutazionale del gene OPA1 in una famiglia affetta da atrofia ottica autosomica dominante. 30
LRP1- LRPAP1 polymorphisms and risk of sporadic Alzheimer s disease. 29
Myelin basic protein and Multiple Sclerosis 29
Elam-1 genotyping in Italian population with Multiple Sclerosis : molecular characterization of A561C variation. 28
Mutational analysis of the mitochondrial tRNAleu gene In Italian patients with stroke-like episodes of undetermined origin. 28
CFS levels of myelin basic protein in multiple sclerosis 28
Twenty novel mutations revealed by DHPLC analysis of the Neurofibromatosis Type 1 (NF1) gene in Southern Italian NF1 Patients 28
Clinical and genetic study of an Italian family with CADASIL: a novel Notch3 mutation not involving a cysteine residue 28
CASP-9 exon 1 polymorphism in patients with Multiple Sclerosis. 28
Caspase-9 gene C93T polymorphism and Multiple Sclerosis patients from Southern Italy 28
NOTCH3 gene mutations in twins with CADASIL 27
Variations in two lipid metabolizing genes and susceptibility to sporadic Alzheimer s disease. 27
Identificazione di marcatori nel gene della presenilina-2 predittivi di malattia di alzheimer familiare. 27
Identification of Pen-2 gene mutations in Italian patients with Familial Alzheimer s Disease 27
A new quantitative PCR assay for rapid detection of aploid deletion of exon 7 in SMA health carriers 27
Gene symbol: PSEN2. Disease: Alzheimer disease. 26
Preliminary evidence of NOS2A protective effect in patients with Relapsing-Remitting Multiple Sclerosis 26
Clinical and genetic study of an Italian Family with a new form of Autosomal Dominant Complicated Spastic Paraplegia 26
Associazione genetica tra un polimorfismo funzionale nel promotore del gene trasportatore della serotonina (5-HTT) e l epilessia del lobo temoprale: risultati di uno studio caso-controllo. 26
The association of single nucleotide E-selectin gene polymorphism with Multiple Sclerosis . 25
Diagnosi di CMT e HNPP con PCR quantitativa Real time 25
BK channel b4 subunit gene (KCNMB4) and Temporal Lobe Epilepsy 25
No association between estrogen receptor 1 gene polymorphisms and susceptibility to multiple sclerosis 24
Diagnosis of haploid and triploid based on measurement of gene copy number in CMT and HNPP 24
Antigene Fas e malattia di Alzheimer sporadica: valutazione analitica di due polimorfismi nel gene TNFRSF6. 23
Fabry disease: Enzymatic diagnosis 22
A novel Notch3 gene mutation in a patient with CADASIL from Southern Italy 22
NOS2A as a candidate gene in Relapsing-Remitting Multiple Sclerosis: a haplotype study using selected subsets of single nucleotide polymorphisms. 22
Mutational Screening of the Notch3 Gene in Patients from Southern Italy Affected by CADASIL: Identification of Four Novel Pathogenic Mutations 22
NOS2A as candidate gene in Relapsing-Remitting Multiple Sclerosis: an haplotype study by using a subsets of SNPs. 22
A mutation screening of PSEN2: genetic study of Italian patients with familial Alzheimer's disease. 21
The presence of M129V of PRNP gene influences mild temporal lobe epilepsy in women. 20
Clinical and genetic study in an Italian family with neurofibromatosis type 1. 20
No role of BDNF genetic variation on cognitive functions in patients with temporal lobe epilepsy. 20
Relapsing-remitting multiple sclerosis and protective effect of a NOS2A gene variant 19
Clinical and genetic study in an Italian family with neurofibromatosis type 1. 19
Genetic variation of serotonin receptor 2a gene may influence age at onset but not cognitive performance in patients with temporal lobe epilepsy. 15
Genomics landscape of mitochondrial DNA variations in patients from South Italy affected by mitochondriopathies 14
Serum Vitamin E Levels in Multiple Sclerosis: Association with Diagnosis, Cognitive Function, Disability, and Depressive Symptoms 4
Age at natural menopause, reproductive lifespan and Alzheimer’s disease in females: is APOE ε4 the missing link? 4
Totale 4.045
Salva come PNG Salva come JPEG
Categoria #
all - tutte 13.296
article - articoli 4.527
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 17.823
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202412 0 0 0 0 0 0 0 0 2 0 10 0
2024/20251.573 29 7 141 53 404 64 36 45 66 99 339 290
2025/20262.310 120 265 205 352 392 91 335 127 174 145 54 50
2026/2027150 147 3 0 0 0 0 0 0 0 0 0 0
Totale 4.045