CNR Institutional Research Information System

DI PALMA, GEMMA
 Distribuzione geografica
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Continente #
AS - Asia 1.890
NA - Nord America 937
EU - Europa 623
SA - Sud America 378
AF - Africa 35
OC - Oceania 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 3.866
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Nazione #
US - Stati Uniti d'America 890
SG - Singapore 768
CN - Cina 453
BR - Brasile 317
IT - Italia 262
VN - Vietnam 212
HK - Hong Kong 163
FR - Francia 126
NL - Olanda 93
JP - Giappone 81
KR - Corea 73
IN - India 45
DE - Germania 26
GB - Regno Unito 25
FI - Finlandia 23
AR - Argentina 22
CA - Canada 18
BD - Bangladesh 16
ID - Indonesia 13
IL - Israele 13
IE - Irlanda 12
MX - Messico 12
EC - Ecuador 11
CO - Colombia 10
RU - Federazione Russa 9
ZA - Sudafrica 9
PL - Polonia 8
TR - Turchia 8
VE - Venezuela 7
AE - Emirati Arabi Uniti 6
JO - Giordania 6
KE - Kenya 6
UA - Ucraina 6
AT - Austria 5
MA - Marocco 5
SA - Arabia Saudita 5
TN - Tunisia 5
DO - Repubblica Dominicana 4
ES - Italia 4
IQ - Iraq 4
PY - Paraguay 4
SE - Svezia 4
SK - Slovacchia (Repubblica Slovacca) 4
AZ - Azerbaigian 3
CL - Cile 3
CR - Costa Rica 3
CZ - Repubblica Ceca 3
DZ - Algeria 3
EG - Egitto 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
PE - Perù 2
UZ - Uzbekistan 2
AU - Australia 1
BZ - Belize 1
CG - Congo 1
CH - Svizzera 1
CI - Costa d'Avorio 1
ET - Etiopia 1
GR - Grecia 1
HN - Honduras 1
HR - Croazia 1
JM - Giamaica 1
KH - Cambogia 1
KW - Kuwait 1
KZ - Kazakistan 1
LB - Libano 1
LT - Lituania 1
LV - Lettonia 1
MD - Moldavia 1
MT - Malta 1
MY - Malesia 1
NG - Nigeria 1
NI - Nicaragua 1
NO - Norvegia 1
PA - Panama 1
PF - Polinesia Francese 1
PH - Filippine 1
PR - Porto Rico 1
SI - Slovenia 1
SV - El Salvador 1
TT - Trinidad e Tobago 1
TW - Taiwan 1
XK - ???statistics.table.value.countryCode.XK??? 1
YE - Yemen 1
Totale 3.866
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Città #
Singapore 457
Santa Clara 373
Hefei 170
Hong Kong 163
San Jose 95
Lauterbourg 84
Ho Chi Minh City 81
Seoul 72
Tokyo 71
Beijing 70
Naples 66
Ashburn 53
Hanoi 45
Dallas 43
Los Angeles 38
São Paulo 26
Catania 18
Milan 18
New York 18
Bari 17
Buffalo 16
Dublin 12
Frankfurt am Main 11
Helsinki 11
Rome 10
Taranto 10
Amsterdam 9
Bengaluru 8
Bologna 8
Minamishinagawa 8
Brooklyn 7
Da Nang 7
Lappeenranta 7
London 7
Paris 7
Rio de Janeiro 7
Amman 6
Bắc Ninh 6
Haiphong 6
Montreal 6
Mumbai 6
Porto Alegre 6
Anoia Superiore 5
Council Bluffs 5
Lấp Vò 5
Orem 5
Thái Bình 5
Turin 5
Volta Redonda 5
Warsaw 5
Atlanta 4
Biên Hòa 4
Brasília 4
Chennai 4
Fortaleza 4
Goiânia 4
Hyderabad 4
Hải Dương 4
Johannesburg 4
Messina 4
Quito 4
Toronto 4
Vienna 4
Abu Dhabi 3
Asunción 3
Baku 3
Barquisimeto 3
Belo Horizonte 3
Boardman 3
Bratislava 3
Can Tho 3
Catanduva 3
Cosenza 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
Nairobi 3
Newark 3
Ourinhos 3
Phủ Lý 3
Pieve Emanuele 3
Poplar 3
Querétaro 3
Quảng Ninh 3
Quận Bình Thạnh 3
Quận Hai 3
Quận Một 3
Salvador 3
San José 3
Springfield 3
Sumaré 3
São José do Rio Preto 3
Totale 2.362
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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 122
Exploring the FKRP Gene in Calabrian Patients with Duchenne/Becker-like Phenotype 105
Genomics landscape of mitochondrial DNA variations in patients from South Italy affected by mitochondriopathies 95
A novel homozygous variant in DYSF gene is associated with Autosomal Recessive Limb Girdle Muscular Dystrophy R2/2B 86
Associazione tra la subunità 2B del recettore NMDA (gene GRIN2B) e la malattia di Alzheimer 83
Identificato in un paziente del Sud Italia la variante Arg596Gly in omozigosi associata a Distrofia Muscolare dei Cingoli recessiva di tipo 8 82
A new mutation detected by NGS in MT-ATP6 gene associated with MELAS and in silico 3D protein analysis 81
Cst3: fattore di rischio genetico per la Malattia di Alzheimer sporadica? 80
NOS2A AS CANDIDATE GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS: AN HAPLOTYPE STUDY BY USING A SUBSETS OF SNPs. 78
Sex and APOE genotype modulate neuropsychological profile and depression in temporal lobe epilepsy 77
Molecular Study of the Fukutin-Related Protein (FKRP) Gene in Patients from Southern Italy with Duchenne/Becker-like Phenotype 75
A NEW CYS1678TYR MUTATION RESPONSIBLE OF LGMD2B IDENTIFIED IN A FAMILY FROM SOUTHERN ITALY 74
ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION 72
HOMOZYGOUS R596G VARIANT IN TRIM32 GENE RELATED TO LGMD IN A NON-HUTTERITE PATIENT 72
Arg143Ser is the most frequent variant in Limb Girdle Muscular Dystrophy-R9 in southern Italy 71
Serotonin receptor 2a gene variant influences age at onset but not cognitive performance in patients with temporal lobe epilepsy. 70
Disturbo di Alzheimer e tono dell'umore 70
Interruptions of the FXN GAA repeat tract delay the age at onset of Friedreich's ataxia in a location dependent manner. 67
A WHOLE mtDNA NGS APPROACH TO IDENTIFY NOVEL VARIANTS IN PATIENTS AFFECTED BY MITOCHONDRIAL DISEASES 66
Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease 57
Targeted Next Generation Sequencing is a valuable diagnostic tool for Inherited Peripheral Neuropathies 57
Ruolo del gene Neuregulin 1 (NRG1) nella Sclerosi Multipla 53
The DRD2 TaqIA polymorphism associated with changed midbrain volumes in healthy individuals. 50
Kinesins in neurological inherited diseases: a novel motor-domain mutation in KIF5A gene in a patient from Southern Italy affected by hereditary spastic paraplegia. 50
NEUROFIBROMATOSIS TYPE 2 (NF2) IN A CHILD UNDER 1 YEAR OF AGE: A CLINICAL AND MOLECULAR STUDY 48
Role of the Neuregulin 1 gene (NRG1) in multiple sclerosis 48
Next-generation sequencing: identificazione di varianti geniche con effetto additivo nell'espressione del fenotipo patologico LGMD e cardiomiopatia dilatativa. 46
ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION 43
Usefulness of routine MRI to differentiate Progressive supranuclear palsy from Parkinson?s disease and Multiple System Atrophy 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 40
Serum levels of interleukin-6 and interleukin-8 are elevated in patients with partial epilepsy 40
Mutation analysis of the GRIN2B gene in Alzheimer's disease 40
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1 40
D678N mutation in a patient with an early-onset Alzheimer's Disease 38
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
Caratterizzazione dei portatori sani SMA con Real time PCR 36
Preliminary evidences of a NOS2A protective effect from Relapsing-Remitting Multiple Sclerosis 35
PERIPHERAL MRNA EXPRESSION OF BRAIN-DERIVED NEUROTROPHIC FACTOR VAL66MET POLYMORPHISM IN PATIENTS WITH RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS). 35
Studio clinico e genetico di una famiglia italiana affetta da una nuova forma di Paraparesi Spastica autosomica dominante complicata 34
Depression and epilepsy 33
Depression and Parkinson's disease 32
Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification 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
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1. 31
Depression and Parkinson's disease:a neuropsychological view 31
Screening for MELAS mutations in Italian patients having stroke-like episodes. 31
Leber s hereditary optic neuropathy associated with multiple sclerosis like picture in a man. 31
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy 31
Two SNPs in the Fas gene on chromosome 10 are not associated with Sporadic Alzheimer s Disease in southern Italy. 31
Preliminary evidences of a NOS2A protective effect from relapsing-remitting multiple sclerosis. 30
Molecular characterization of the APP gene in Italian patients with familial Alzheimer disease. 30
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
Cognitive impairment in Multiple Sclerosis 29
Myelin basic protein and Multiple Sclerosis 29
Analisi mutazionale del gene OPA1 in una famiglia affetta da atrofia ottica autosomica dominante. 29
Presenilin Enhancer-2 Gene mutations and Familial Alzheimer s Disease 29
Elam-1 genotyping in Italian population with Multiple Sclerosis : molecular characterization of A561C variation. 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
NOTCH3 gene mutations in twins with CADASIL 27
LRP1- LRPAP1 polymorphisms and risk of sporadic Alzheimer s disease. 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
Gene symbol: PSEN2. Disease: Alzheimer disease. 26
Mutational analysis of the mitochondrial tRNAleu gene In Italian patients with stroke-like episodes of undetermined origin. 26
A new quantitative PCR assay for rapid detection of aploid deletion of exon 7 in SMA health carriers 26
Caspase-9 gene C93T polymorphism and Multiple Sclerosis patients from Southern Italy 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
Preliminary evidence of NOS2A protective effect in patients with Relapsing-Remitting Multiple Sclerosis 24
Clinical and genetic study of an Italian Family with a new form of Autosomal Dominant Complicated Spastic Paraplegia 24
BK channel b4 subunit gene (KCNMB4) and Temporal Lobe Epilepsy 24
No association between estrogen receptor 1 gene polymorphisms and susceptibility to multiple sclerosis 24
Antigene Fas e malattia di Alzheimer sporadica: valutazione analitica di due polimorfismi nel gene TNFRSF6. 23
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. 23
Fabry disease: Enzymatic diagnosis 22
A novel Notch3 gene mutation in a patient with CADASIL from Southern Italy 22
Mutational Screening of the Notch3 Gene in Patients from Southern Italy Affected by CADASIL: Identification of Four Novel Pathogenic Mutations 22
Diagnosis of haploid and triploid based on measurement of gene copy number in CMT and HNPP 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
NOS2A as candidate gene in Relapsing-Remitting Multiple Sclerosis: an haplotype study by using a subsets of SNPs. 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
NOS2A as a candidate gene in Relapsing-Remitting Multiple Sclerosis: a haplotype study using selected subsets of single nucleotide polymorphisms. 19
Genetic variation of serotonin receptor 2a gene may influence age at onset but not cognitive performance in patients with temporal lobe epilepsy. 15
Totale 3.919
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Categoria #
all - tutte 11.910
article - articoli 4.015
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 15.925
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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
2024/20251.598 29 7 143 53 409 64 36 45 66 101 349 296
2025/20262.309 128 281 210 362 396 92 340 128 176 146 50 0
Totale 3.919