IRIS
PALMERI, SILVIA
 Distribuzione geografica
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Continente #
NA - Nord America 6.110
EU - Europa 3.779
AS - Asia 2.075
SA - Sud America 298
AF - Africa 121
Continente sconosciuto - Info sul continente non disponibili 38
OC - Oceania 8
Totale 12.429
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Nazione #
US - Stati Uniti d'America 6.042
CN - Cina 822
GB - Regno Unito 821
RU - Federazione Russa 707
SG - Singapore 637
IE - Irlanda 503
IT - Italia 366
UA - Ucraina 356
SE - Svezia 272
BR - Brasile 252
DE - Germania 229
FR - Francia 226
HK - Hong Kong 160
VN - Vietnam 154
FI - Finlandia 144
KR - Corea 122
ZA - Sudafrica 73
ES - Italia 71
IN - India 44
CA - Canada 42
BD - Bangladesh 26
NG - Nigeria 20
BE - Belgio 19
PL - Polonia 18
JP - Giappone 16
TR - Turchia 15
AR - Argentina 14
IQ - Iraq 13
MX - Messico 13
NL - Olanda 12
PK - Pakistan 12
ID - Indonesia 11
CO - Colombia 8
VE - Venezuela 8
SA - Arabia Saudita 7
AU - Australia 6
CI - Costa d'Avorio 6
KE - Kenya 6
EG - Egitto 5
EU - Europa 5
IR - Iran 5
LT - Lituania 5
MY - Malesia 5
NP - Nepal 5
BG - Bulgaria 4
CL - Cile 4
JO - Giordania 4
PT - Portogallo 4
AZ - Azerbaigian 3
EC - Ecuador 3
HU - Ungheria 3
MA - Marocco 3
PA - Panama 3
PY - Paraguay 3
DK - Danimarca 2
GR - Grecia 2
HR - Croazia 2
JM - Giamaica 2
LB - Libano 2
PE - Perù 2
RO - Romania 2
RS - Serbia 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
TH - Thailandia 2
UY - Uruguay 2
UZ - Uzbekistan 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
AL - Albania 1
AM - Armenia 1
AT - Austria 1
BO - Bolivia 1
BY - Bielorussia 1
CG - Congo 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
NZ - Nuova Zelanda 1
PF - Polinesia Francese 1
PH - Filippine 1
PS - Palestinian Territory 1
QA - Qatar 1
SR - Suriname 1
SV - El Salvador 1
TG - Togo 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
VC - Saint Vincent e Grenadine 1
Totale 12.396
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Città #
Menlo Park 723
Southend 718
Dallas 629
Fairfield 562
Dublin 503
Ashburn 441
Singapore 334
Chandler 317
Jacksonville 291
Houston 244
Santa Clara 242
Woodbridge 236
Wilmington 229
Seattle 221
Moscow 195
Cambridge 189
San Jose 182
Beijing 179
Milan 162
Hong Kong 156
Ann Arbor 139
Seoul 122
Hefei 118
Princeton 112
Council Bluffs 109
Nanjing 99
The Dalles 80
Johannesburg 68
Helsinki 65
New York 62
Los Angeles 61
Málaga 59
Rome 54
Lauterbourg 51
Ho Chi Minh City 50
Boardman 38
Hanoi 37
Nanchang 37
San Diego 32
Columbus 31
Munich 31
Siena 31
Buffalo 28
Shenyang 27
Lancaster 23
London 23
São Paulo 22
Hebei 21
Tianjin 19
Figino 18
Abuja 17
Shanghai 17
Turku 17
Brussels 15
Redondo Beach 15
Jinan 14
Orem 14
San Mateo 14
Tokyo 14
Brooklyn 13
Changsha 13
Frankfurt am Main 13
Toronto 13
Chennai 12
Kunming 12
Montreal 12
Warsaw 12
Falls Church 11
Rio de Janeiro 10
Stockholm 10
Atlanta 9
Norwalk 9
San Francisco 9
Venezia 9
Boston 8
Düsseldorf 8
Jiaxing 8
Ningbo 8
Phoenix 8
Turin 8
Dearborn 7
Guangzhou 7
Haiphong 7
Izmir 7
Mumbai 7
Naples 7
Washington 7
Abidjan 6
Belo Horizonte 6
Bengaluru 6
Falkenstein 6
Hangzhou 6
Manchester 6
Mexico City 6
Nuremberg 6
Renton 6
Amsterdam 5
Baghdad 5
Chicago 5
Montespertoli 5
Totale 8.895
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Nome #
A case of dystonia with onset during pregnancy 368
Antibodies to dorsal root ganglia and olfactory cells in a patient with chronic sensory neuropathy and anosmia 332
Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASIL. 301
Clinical Course of Two Italian Siblings with Ataxia-Telangiectasia-Like Disorder. 280
Peripheral neuropathy in late-onset Krabbe disease: report of three cases. 280
Amiodarone induced lipidosis similar to Niemann-Pick C disease. Biochemical and morphological study 274
Ataxia, mental deterioration, epilepsy in a family with dominant enamel hypoplasia: a variant of Kohlschütter-Tönz syndrome? 273
Neuronal intranuclear inclusion disease: neuropathologic study of a case 260
Chronic diarrhea associated with the A3243G mtDNA mutation 257
Type I sialidosis: a clinical, biochemical and neuroradiological study 248
Characterization of the sialidase molecular defects in sialidosis patients suggests the structural organization of the lysosomal multienzyme complex 247
Type 3 (chronic) GM1 gangliosidosis presenting as infanto-choreo-athetotic dementia, without epilepsy, in three sisters 245
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome C oxidase deficiency 243
A syndrome of autosomal recessive pontocerebellar hypoplasia with white matter abnormalities and protracted course in two brothers 242
Acanthocytosis, retinitis pigmentosa, pallidal degeneration. Report of two cases without serum lipid abnormalities 240
Choreo-acanthocytosis like phenotype without acanthocytes: clinicopathological case report. A contribution to the knowledge of the functional pathology of the caudate nucleus 237
Juvenile Leigh syndrome with protracted course presenting as chronic sensory motor neuropathy, ataxia, deafness and retinitis pigmentosa: a clinicopathological report 235
Dementia, myoclonus, peripheral neuropathy, and lipid-like material in skin biopsy during psychotropic drug treatment 233
High-Dose Methylprednisolone For Bickerstaff’s Brainstem Encephalitis. 231
Neuro-Ophthalmological findings in two adult siblings with ataxiatelangiectasia– like disorder 230
Gliomatosis cerebri with oligodendrocytic components: description of 1 case 226
Epilepsy with bilateral occipital calcifications: Sturge-Weber variant or a different encephalopathy? 226
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy 225
Assessment of cognitive profile and visual spatial attention in autosomal dominant cerebellar ataxia type 2 (SCA2). Correlation between eye-tracking and neuroosychological studies. 224
Skin biopsies for cell cultures from Mediterranean free-ranging cetaceans 223
Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA) 223
Congenital lactic acidosis due to a defect of pyruvate dehydrogenase complex (E1). Clinical, biochemical, nerve biopsy study and effect of therapy 215
Assessment of cognitive profile and visual spatial attention in autosomal dominant cerebellar ataxia type 2 (SCA2). Correlation Between eye-tracking and neuropsychological studies. 211
Leukoencephalopathy as a rare complication of hepatitis C infection. 208
PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation 207
Infanto-juvenile encephaloneuropathy and pigmentary retinopathy in a girl associated with congenital adrenal insufficiency and altered plasma medium-chain fatty acid levels 206
Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy 202
Fluorescein retinal angiography in the early diagnosis of optic disc edema 200
Lung involvement in Niemann-Pick disease type C1: improvement with bronchoalveolar lavage 197
Hypoplasia of the corpus callosum in Niemann-Pick type C disease 190
Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type 190
Imipramine induced lipidosis and dexamethasone effect: morphological and biochemical study in normal and chronic GM2 gangliosidosis fibroblasts 183
Neurological presentation of Ehlers-Danlos syndrome type IV in a family with parental mosaicism 183
Purification and partial characterization of lysosomal neuraminidase from human placenta 180
The clinical aspects of adult hexosaminidase deficiencies 178
Human placental neuraminidase. Activation, stabilization and association with beta-galactosidase and its protective protein 176
Increased lung surfactant phosphatidylcholine in patients affected by lysosomal storage diseases. 173
Kohlschütter-Tönz Syndrome: Mutations in ROGDI and Evidence of Genetic Heterogeneity. 172
MRE11 mutations and impaired ATM-dependent responses in an Italian family with ataxia-telangiectasia-like disorder 171
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations 170
Palatal myoclonus and unusual MRI findings in a patient with membranous lipodystrophy 170
Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophy 169
Glycosaminoglycan and glycoprotein changes in subacute sclerosing leucoencephalitis 166
Neurophysiological study in chronic GM2 gangliosidosis (hexosaminidase A and B deficiency), with motor neuron disease phenotype 166
Congenital oculo-facial paralysis (Moebius syndrome): evidence of dominant inheritance in two families 162
Macrosomia and mental retardation: evidence of autosomal dominant inheritance in four generations 157
Galactosialidosis: molecular heterogeneity among distinct clinical phenotypes 147
Niemann-Pick type C disease: mutations of NPC1 gene and evidence of abnormal expression of some mutant alleles in fibroblasts 143
Screening of ARHSP-TCC patients expand the spectrum of SPG11 mutations and includes a large scale gene deletion 138
Oculo-dento-digital syndrome (Gorlin's syndrome): clinical and genetical report of a new family 133
Neurocutaneous syndromes with pigmentary abnormalities and central nervous system involvement. II. Two cases with atypical incontinentia pigmenti 130
Molecular heterogeneity in human beta-galactosidase and neuraminidase deficiency 123
null 120
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Long term follow-up to evaluate the efficacy of miglustat treatment in Italian patients with Niemann-Pick disease type C 94
Selective bilateral amyotrophy of the anterior tibial muscle: a case report. 94
Totale 12.429
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Categoria #
all - tutte 35.867
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 35.867
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022550 0 0 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
2025/20263.430 261 552 447 355 670 113 289 124 103 154 47 315
2026/2027456 137 140 179 0 0 0 0 0 0 0 0 0
Totale 12.429