IRIS
PALMERI, SILVIA
 Distribuzione geografica
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Continente #
NA - Nord America 5.433
EU - Europa 3.383
AS - Asia 1.697
SA - Sud America 256
AF - Africa 33
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 6
Totale 10.814
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Nazione #
US - Stati Uniti d'America 5.389
GB - Regno Unito 809
CN - Cina 737
RU - Federazione Russa 706
SG - Singapore 537
IE - Irlanda 503
UA - Ucraina 355
SE - Svezia 272
BR - Brasile 226
DE - Germania 217
FR - Francia 169
HK - Hong Kong 143
FI - Finlandia 141
KR - Corea 122
IT - Italia 72
ES - Italia 67
VN - Vietnam 59
CA - Canada 30
IN - India 25
BE - Belgio 18
PL - Polonia 14
TR - Turchia 14
JP - Giappone 13
ZA - Sudafrica 13
AR - Argentina 11
NL - Olanda 11
MX - Messico 8
IQ - Iraq 7
CI - Costa d'Avorio 6
ID - Indonesia 6
BD - Bangladesh 5
EU - Europa 5
LT - Lituania 5
PK - Pakistan 5
SA - Arabia Saudita 5
VE - Venezuela 5
AU - Australia 4
BG - Bulgaria 4
IR - Iran 4
PT - Portogallo 4
CO - Colombia 3
EC - Ecuador 3
EG - Egitto 3
KE - Kenya 3
AZ - Azerbaigian 2
DK - Danimarca 2
GR - Grecia 2
HU - Ungheria 2
JO - Giordania 2
LB - Libano 2
MA - Marocco 2
NG - Nigeria 2
PE - Perù 2
SK - Slovacchia (Repubblica Slovacca) 2
UY - Uruguay 2
UZ - Uzbekistan 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AT - Austria 1
BO - Bolivia 1
CH - Svizzera 1
CL - Cile 1
CZ - Repubblica Ceca 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
GE - Georgia 1
GT - Guatemala 1
HN - Honduras 1
HR - Croazia 1
LA - Repubblica Popolare Democratica del Laos 1
LV - Lettonia 1
MD - Moldavia 1
MW - Malawi 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PA - Panama 1
PF - Polinesia Francese 1
PH - Filippine 1
PS - Palestinian Territory 1
PY - Paraguay 1
QA - Qatar 1
RO - Romania 1
SN - Senegal 1
SR - Suriname 1
SV - El Salvador 1
TG - Togo 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
Totale 10.814
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Città #
Menlo Park 723
Southend 718
Dallas 623
Fairfield 562
Dublin 503
Ashburn 371
Chandler 317
Jacksonville 289
Singapore 273
Houston 243
Woodbridge 236
Wilmington 229
Seattle 219
Santa Clara 210
Moscow 195
Cambridge 189
Beijing 177
Hong Kong 143
Ann Arbor 139
Seoul 122
Princeton 111
Nanjing 99
Hefei 93
Helsinki 62
Málaga 59
Los Angeles 44
New York 44
Boardman 38
The Dalles 38
Nanchang 37
Munich 31
San Diego 31
Siena 31
Buffalo 28
Shenyang 27
Lancaster 23
London 23
Council Bluffs 21
Hebei 21
São Paulo 20
Ho Chi Minh City 19
Tianjin 19
Turku 17
Columbus 16
Shanghai 16
Redondo Beach 15
Brussels 14
Jinan 14
San Mateo 14
Changsha 13
Hanoi 12
Kunming 12
Falls Church 11
Tokyo 11
Toronto 11
Montreal 10
Stockholm 10
Warsaw 10
Norwalk 9
San Francisco 9
Venezia 9
Brooklyn 8
Düsseldorf 8
Jiaxing 8
Johannesburg 8
Ningbo 8
Rio de Janeiro 8
Atlanta 7
Chennai 7
Dearborn 7
Guangzhou 7
Izmir 7
Abidjan 6
Bengaluru 6
Falkenstein 6
Hangzhou 6
Phoenix 6
Renton 6
Washington 6
Belo Horizonte 5
Boston 5
Frankfurt am Main 5
Montespertoli 5
Nuremberg 5
Saint Petersburg 5
Amsterdam 4
Bonndorf 4
Curitiba 4
Haikou 4
Haiphong 4
João Pessoa 4
Mexico City 4
Newark 4
Orem 4
Roubaix 4
Santo André 4
Taizhou 4
Waanrode 4
Zhengzhou 4
Acton 3
Totale 7.847
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Nome #
A case of dystonia with onset during pregnancy 336
Antibodies to dorsal root ganglia and olfactory cells in a patient with chronic sensory neuropathy and anosmia 298
Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASIL. 274
Clinical Course of Two Italian Siblings with Ataxia-Telangiectasia-Like Disorder. 247
Ataxia, mental deterioration, epilepsy in a family with dominant enamel hypoplasia: a variant of Kohlschütter-Tönz syndrome? 237
Peripheral neuropathy in late-onset Krabbe disease: report of three cases. 236
Chronic diarrhea associated with the A3243G mtDNA mutation 235
Type I sialidosis: a clinical, biochemical and neuroradiological study 230
Amiodarone induced lipidosis similar to Niemann-Pick C disease. Biochemical and morphological study 226
Neuronal intranuclear inclusion disease: neuropathologic study of a case 223
Acanthocytosis, retinitis pigmentosa, pallidal degeneration. Report of two cases without serum lipid abnormalities 219
Juvenile Leigh syndrome with protracted course presenting as chronic sensory motor neuropathy, ataxia, deafness and retinitis pigmentosa: a clinicopathological report 216
Type 3 (chronic) GM1 gangliosidosis presenting as infanto-choreo-athetotic dementia, without epilepsy, in three sisters 215
Dementia, myoclonus, peripheral neuropathy, and lipid-like material in skin biopsy during psychotropic drug treatment 212
Characterization of the sialidase molecular defects in sialidosis patients suggests the structural organization of the lysosomal multienzyme complex 211
A syndrome of autosomal recessive pontocerebellar hypoplasia with white matter abnormalities and protracted course in two brothers 210
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome C oxidase deficiency 210
High-Dose Methylprednisolone For Bickerstaff’s Brainstem Encephalitis. 204
Choreo-acanthocytosis like phenotype without acanthocytes: clinicopathological case report. A contribution to the knowledge of the functional pathology of the caudate nucleus 204
Epilepsy with bilateral occipital calcifications: Sturge-Weber variant or a different encephalopathy? 202
Neuro-Ophthalmological findings in two adult siblings with ataxiatelangiectasia– like disorder 201
Assessment of cognitive profile and visual spatial attention in autosomal dominant cerebellar ataxia type 2 (SCA2). Correlation between eye-tracking and neuroosychological studies. 197
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy 196
Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA) 195
Skin biopsies for cell cultures from Mediterranean free-ranging cetaceans 194
Gliomatosis cerebri with oligodendrocytic components: description of 1 case 191
Leukoencephalopathy as a rare complication of hepatitis C infection. 187
Assessment of cognitive profile and visual spatial attention in autosomal dominant cerebellar ataxia type 2 (SCA2). Correlation Between eye-tracking and neuropsychological studies. 186
Congenital lactic acidosis due to a defect of pyruvate dehydrogenase complex (E1). Clinical, biochemical, nerve biopsy study and effect of therapy 182
Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy 181
PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation 178
Lung involvement in Niemann-Pick disease type C1: improvement with bronchoalveolar lavage 176
Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type 175
Fluorescein retinal angiography in the early diagnosis of optic disc edema 173
Hypoplasia of the corpus callosum in Niemann-Pick type C disease 169
Neurological presentation of Ehlers-Danlos syndrome type IV in a family with parental mosaicism 166
Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophy 155
Imipramine induced lipidosis and dexamethasone effect: morphological and biochemical study in normal and chronic GM2 gangliosidosis fibroblasts 154
The clinical aspects of adult hexosaminidase deficiencies 154
Increased lung surfactant phosphatidylcholine in patients affected by lysosomal storage diseases. 151
Human placental neuraminidase. Activation, stabilization and association with beta-galactosidase and its protective protein 151
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations 150
Neurophysiological study in chronic GM2 gangliosidosis (hexosaminidase A and B deficiency), with motor neuron disease phenotype 148
Purification and partial characterization of lysosomal neuraminidase from human placenta 146
Congenital oculo-facial paralysis (Moebius syndrome): evidence of dominant inheritance in two families 145
Palatal myoclonus and unusual MRI findings in a patient with membranous lipodystrophy 144
MRE11 mutations and impaired ATM-dependent responses in an Italian family with ataxia-telangiectasia-like disorder 143
Glycosaminoglycan and glycoprotein changes in subacute sclerosing leucoencephalitis 143
Macrosomia and mental retardation: evidence of autosomal dominant inheritance in four generations 141
Kohlschütter-Tönz Syndrome: Mutations in ROGDI and Evidence of Genetic Heterogeneity. 140
Infanto-juvenile encephaloneuropathy and pigmentary retinopathy in a girl associated with congenital adrenal insufficiency and altered plasma medium-chain fatty acid levels 136
Niemann-Pick type C disease: mutations of NPC1 gene and evidence of abnormal expression of some mutant alleles in fibroblasts 126
Galactosialidosis: molecular heterogeneity among distinct clinical phenotypes 122
null 120
Screening of ARHSP-TCC patients expand the spectrum of SPG11 mutations and includes a large scale gene deletion 117
Neurocutaneous syndromes with pigmentary abnormalities and central nervous system involvement. II. Two cases with atypical incontinentia pigmenti 114
Oculo-dento-digital syndrome (Gorlin's syndrome): clinical and genetical report of a new family 112
null 102
Molecular heterogeneity in human beta-galactosidase and neuraminidase deficiency 102
Selective bilateral amyotrophy of the anterior tibial muscle: a case report. 74
Long term follow-up to evaluate the efficacy of miglustat treatment in Italian patients with Niemann-Pick disease type C 64
Totale 10.846
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Categoria #
all - tutte 30.932
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 30.932
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021625 0 0 0 0 0 109 50 163 136 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
2025/20262.303 261 552 447 355 670 18 0 0 0 0 0 0
Totale 10.846