IRIS
PALMERI, SILVIA
 Distribuzione geografica
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Continente #
NA - Nord America 5.645
EU - Europa 3.485
AS - Asia 2.017
SA - Sud America 279
AF - Africa 120
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 6
Totale 11.560
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Nazione #
US - Stati Uniti d'America 5.592
GB - Regno Unito 818
CN - Cina 817
RU - Federazione Russa 707
SG - Singapore 621
IE - Irlanda 503
UA - Ucraina 356
SE - Svezia 272
BR - Brasile 241
DE - Germania 229
FR - Francia 225
HK - Hong Kong 157
VN - Vietnam 150
FI - Finlandia 144
KR - Corea 122
IT - Italia 78
ZA - Sudafrica 73
ES - Italia 71
IN - India 42
CA - Canada 32
NG - Nigeria 20
BE - Belgio 19
PL - Polonia 18
JP - Giappone 15
TR - Turchia 15
AR - Argentina 13
IQ - Iraq 13
MX - Messico 12
NL - Olanda 12
BD - Bangladesh 11
PK - Pakistan 11
ID - Indonesia 8
SA - Arabia Saudita 7
AU - Australia 6
CI - Costa d'Avorio 6
KE - Kenya 6
VE - Venezuela 6
EG - Egitto 5
EU - Europa 5
IR - Iran 5
LT - Lituania 5
BG - Bulgaria 4
CO - Colombia 4
JO - Giordania 4
PT - Portogallo 4
AZ - Azerbaigian 3
CL - Cile 3
EC - Ecuador 3
HU - Ungheria 3
MA - Marocco 3
NP - Nepal 3
PA - Panama 3
PY - Paraguay 3
DK - Danimarca 2
GR - Grecia 2
HR - Croazia 2
LB - Libano 2
PE - Perù 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
UY - Uruguay 2
UZ - Uzbekistan 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AM - Armenia 1
AT - Austria 1
BO - Bolivia 1
BY - Bielorussia 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
GD - Grenada 1
GE - Georgia 1
GT - Guatemala 1
HN - Honduras 1
LA - Repubblica Popolare Democratica del Laos 1
LV - Lettonia 1
MD - Moldavia 1
MN - Mongolia 1
MU - Mauritius 1
MW - Malawi 1
MY - Malesia 1
NZ - Nuova Zelanda 1
PF - Polinesia Francese 1
PH - Filippine 1
PS - Palestinian Territory 1
QA - Qatar 1
RO - Romania 1
RS - Serbia 1
SR - Suriname 1
SV - El Salvador 1
TG - Togo 1
TH - Thailandia 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
Totale 11.560
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Città #
Menlo Park 723
Southend 718
Dallas 625
Fairfield 562
Dublin 503
Ashburn 386
Singapore 330
Chandler 317
Jacksonville 291
Houston 243
Woodbridge 236
Wilmington 229
Seattle 219
Santa Clara 212
Moscow 195
Cambridge 189
Beijing 177
Hong Kong 153
Ann Arbor 139
Seoul 122
Hefei 118
Princeton 111
Nanjing 99
San Jose 93
The Dalles 80
Johannesburg 68
Helsinki 65
Málaga 59
Los Angeles 57
Lauterbourg 51
Ho Chi Minh City 48
New York 47
Boardman 38
Nanchang 37
Hanoi 35
Munich 31
San Diego 31
Siena 31
Buffalo 28
Shenyang 27
Council Bluffs 24
Lancaster 23
London 23
Hebei 21
São Paulo 21
Tianjin 19
Abuja 17
Turku 17
Columbus 16
Shanghai 16
Brussels 15
Redondo Beach 15
Jinan 14
Orem 14
San Mateo 14
Changsha 13
Frankfurt am Main 13
Tokyo 13
Chennai 12
Kunming 12
Warsaw 12
Falls Church 11
Toronto 11
Montreal 10
Stockholm 10
Norwalk 9
Rio de Janeiro 9
San Francisco 9
Venezia 9
Atlanta 8
Brooklyn 8
Düsseldorf 8
Jiaxing 8
Ningbo 8
Dearborn 7
Guangzhou 7
Haiphong 7
Izmir 7
Phoenix 7
Washington 7
Abidjan 6
Bengaluru 6
Boston 6
Falkenstein 6
Hangzhou 6
Manchester 6
Mumbai 6
Nuremberg 6
Renton 6
Amsterdam 5
Baghdad 5
Belo Horizonte 5
Mexico City 5
Montespertoli 5
Saint Petersburg 5
Wroclaw 5
Amman 4
Bonndorf 4
Curitiba 4
Dhaka 4
Totale 8.332
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Nome #
A case of dystonia with onset during pregnancy 357
Antibodies to dorsal root ganglia and olfactory cells in a patient with chronic sensory neuropathy and anosmia 311
Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASIL. 293
Clinical Course of Two Italian Siblings with Ataxia-Telangiectasia-Like Disorder. 272
Ataxia, mental deterioration, epilepsy in a family with dominant enamel hypoplasia: a variant of Kohlschütter-Tönz syndrome? 251
Amiodarone induced lipidosis similar to Niemann-Pick C disease. Biochemical and morphological study 250
Peripheral neuropathy in late-onset Krabbe disease: report of three cases. 250
Chronic diarrhea associated with the A3243G mtDNA mutation 248
Neuronal intranuclear inclusion disease: neuropathologic study of a case 240
Type I sialidosis: a clinical, biochemical and neuroradiological study 240
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome C oxidase deficiency 235
Type 3 (chronic) GM1 gangliosidosis presenting as infanto-choreo-athetotic dementia, without epilepsy, in three sisters 232
Acanthocytosis, retinitis pigmentosa, pallidal degeneration. Report of two cases without serum lipid abnormalities 231
A syndrome of autosomal recessive pontocerebellar hypoplasia with white matter abnormalities and protracted course in two brothers 227
Characterization of the sialidase molecular defects in sialidosis patients suggests the structural organization of the lysosomal multienzyme complex 224
Juvenile Leigh syndrome with protracted course presenting as chronic sensory motor neuropathy, ataxia, deafness and retinitis pigmentosa: a clinicopathological report 224
Dementia, myoclonus, peripheral neuropathy, and lipid-like material in skin biopsy during psychotropic drug treatment 223
High-Dose Methylprednisolone For Bickerstaff’s Brainstem Encephalitis. 219
Neuro-Ophthalmological findings in two adult siblings with ataxiatelangiectasia– like disorder 218
Epilepsy with bilateral occipital calcifications: Sturge-Weber variant or a different encephalopathy? 217
Choreo-acanthocytosis like phenotype without acanthocytes: clinicopathological case report. A contribution to the knowledge of the functional pathology of the caudate nucleus 216
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy 211
Assessment of cognitive profile and visual spatial attention in autosomal dominant cerebellar ataxia type 2 (SCA2). Correlation between eye-tracking and neuroosychological studies. 208
Skin biopsies for cell cultures from Mediterranean free-ranging cetaceans 207
Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA) 207
Gliomatosis cerebri with oligodendrocytic components: description of 1 case 206
Assessment of cognitive profile and visual spatial attention in autosomal dominant cerebellar ataxia type 2 (SCA2). Correlation Between eye-tracking and neuropsychological studies. 200
Leukoencephalopathy as a rare complication of hepatitis C infection. 198
Congenital lactic acidosis due to a defect of pyruvate dehydrogenase complex (E1). Clinical, biochemical, nerve biopsy study and effect of therapy 194
PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation 193
Fluorescein retinal angiography in the early diagnosis of optic disc edema 190
Lung involvement in Niemann-Pick disease type C1: improvement with bronchoalveolar lavage 188
Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy 188
Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type 182
Hypoplasia of the corpus callosum in Niemann-Pick type C disease 176
Neurological presentation of Ehlers-Danlos syndrome type IV in a family with parental mosaicism 175
Imipramine induced lipidosis and dexamethasone effect: morphological and biochemical study in normal and chronic GM2 gangliosidosis fibroblasts 170
Human placental neuraminidase. Activation, stabilization and association with beta-galactosidase and its protective protein 165
The clinical aspects of adult hexosaminidase deficiencies 164
Increased lung surfactant phosphatidylcholine in patients affected by lysosomal storage diseases. 161
Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophy 160
Purification and partial characterization of lysosomal neuraminidase from human placenta 160
Palatal myoclonus and unusual MRI findings in a patient with membranous lipodystrophy 158
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations 157
Congenital oculo-facial paralysis (Moebius syndrome): evidence of dominant inheritance in two families 157
Neurophysiological study in chronic GM2 gangliosidosis (hexosaminidase A and B deficiency), with motor neuron disease phenotype 156
Kohlschütter-Tönz Syndrome: Mutations in ROGDI and Evidence of Genetic Heterogeneity. 154
Glycosaminoglycan and glycoprotein changes in subacute sclerosing leucoencephalitis 153
MRE11 mutations and impaired ATM-dependent responses in an Italian family with ataxia-telangiectasia-like disorder 151
Macrosomia and mental retardation: evidence of autosomal dominant inheritance in four generations 149
Infanto-juvenile encephaloneuropathy and pigmentary retinopathy in a girl associated with congenital adrenal insufficiency and altered plasma medium-chain fatty acid levels 144
Niemann-Pick type C disease: mutations of NPC1 gene and evidence of abnormal expression of some mutant alleles in fibroblasts 134
Galactosialidosis: molecular heterogeneity among distinct clinical phenotypes 130
Screening of ARHSP-TCC patients expand the spectrum of SPG11 mutations and includes a large scale gene deletion 128
null 120
Oculo-dento-digital syndrome (Gorlin's syndrome): clinical and genetical report of a new family 120
Neurocutaneous syndromes with pigmentary abnormalities and central nervous system involvement. II. Two cases with atypical incontinentia pigmenti 120
Molecular heterogeneity in human beta-galactosidase and neuraminidase deficiency 110
null 102
Selective bilateral amyotrophy of the anterior tibial muscle: a case report. 86
Long term follow-up to evaluate the efficacy of miglustat treatment in Italian patients with Niemann-Pick disease type C 82
Totale 11.592
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Categoria #
all - tutte 32.513
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 32.513
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021167 0 0 0 0 0 0 0 0 0 39 97 31
2021/2022708 48 110 24 43 32 14 50 27 28 84 72 176
2022/20231.136 67 86 158 161 93 226 9 87 126 68 37 18
2023/2024691 27 18 66 70 19 180 251 17 5 8 0 30
2024/20251.410 21 86 107 70 190 66 12 79 149 58 155 417
2025/20263.049 261 552 447 355 670 113 289 124 103 135 0 0
Totale 11.592