IRIS
PALMERI, SILVIA
 Distribuzione geografica
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Continente #
NA - Nord America 4.165
EU - Europa 2.720
AS - Asia 514
AF - Africa 7
SA - Sud America 7
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 4
Totale 7.423
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Nazione #
US - Stati Uniti d'America 4.147
GB - Regno Unito 789
IE - Irlanda 502
CN - Cina 396
UA - Ucraina 350
SE - Svezia 263
RU - Federazione Russa 196
DE - Germania 181
FR - Francia 153
FI - Finlandia 116
SG - Singapore 94
IT - Italia 67
ES - Italia 60
BE - Belgio 17
CA - Canada 17
TR - Turchia 9
NL - Olanda 8
CI - Costa d'Avorio 6
EU - Europa 5
IR - Iran 4
AU - Australia 3
BG - Bulgaria 3
HK - Hong Kong 3
IN - India 3
PT - Portogallo 3
GR - Grecia 2
HU - Ungheria 2
JP - Giappone 2
PE - Perù 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AZ - Azerbaigian 1
BO - Bolivia 1
BR - Brasile 1
CH - Svizzera 1
CL - Cile 1
CO - Colombia 1
CZ - Repubblica Ceca 1
EC - Ecuador 1
HR - Croazia 1
ID - Indonesia 1
LA - Repubblica Popolare Democratica del Laos 1
LT - Lituania 1
LV - Lettonia 1
MA - Marocco 1
MD - Moldavia 1
NZ - Nuova Zelanda 1
PA - Panama 1
PL - Polonia 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 7.423
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Città #
Menlo Park 723
Southend 718
Fairfield 562
Dublin 502
Chandler 317
Ashburn 314
Jacksonville 288
Houston 239
Woodbridge 236
Wilmington 228
Seattle 217
Cambridge 189
Ann Arbor 139
Princeton 111
Nanjing 99
Beijing 88
Singapore 62
Málaga 59
Helsinki 54
Boardman 38
Nanchang 37
San Diego 31
Siena 31
Shenyang 27
Lancaster 23
Hebei 21
Tianjin 19
Moscow 18
New York 17
London 14
San Mateo 14
Brussels 13
Shanghai 13
Jinan 12
Kunming 12
Changsha 11
Falls Church 11
Norwalk 9
Venezia 9
Düsseldorf 8
Jiaxing 8
Munich 8
Ningbo 8
Toronto 8
Dearborn 7
Izmir 7
Abidjan 6
Hangzhou 6
Los Angeles 6
Renton 6
San Francisco 6
Montespertoli 5
Saint Petersburg 5
Washington 5
Bonndorf 4
Haikou 4
Taizhou 4
Waanrode 4
Zhengzhou 4
Acton 3
Changchun 3
Guangzhou 3
Hong Kong 3
Hounslow 3
Mississauga 3
Montreal 3
Shaoxing 3
Sofia 3
Tappahannock 3
Canberra 2
Costa Mesa 2
Dallas 2
Domodossola 2
Falkenstein 2
Indiana 2
Kilburn 2
Lanzhou 2
Lappeenranta 2
Lima 2
Lisbon 2
Mestre 2
New Orleans 2
Newark 2
Ottawa 2
Philadelphia 2
Redwood City 2
Southwark 2
Zanjan 2
Amsterdam 1
Andover 1
Antrodoco 1
Atlanta 1
Auckland 1
Bad Bellingen 1
Baku 1
Bend 1
Boston 1
Bratislava 1
Brunflo 1
Budapest 1
Totale 5.724
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Nome #
Type I sialidosis: a clinical, biochemical and neuroradiological study 192
A case of dystonia with onset during pregnancy 191
Peripheral neuropathy in late-onset Krabbe disease: report of three cases. 187
Juvenile Leigh syndrome with protracted course presenting as chronic sensory motor neuropathy, ataxia, deafness and retinitis pigmentosa: a clinicopathological report 186
Antibodies to dorsal root ganglia and olfactory cells in a patient with chronic sensory neuropathy and anosmia 183
Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASIL. 161
Ataxia, mental deterioration, epilepsy in a family with dominant enamel hypoplasia: a variant of Kohlschütter-Tönz syndrome? 160
Clinical Course of Two Italian Siblings with Ataxia-Telangiectasia-Like Disorder. 155
Neuronal intranuclear inclusion disease: neuropathologic study of a case 154
Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type 151
Amiodarone induced lipidosis similar to Niemann-Pick C disease. Biochemical and morphological study 147
Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy 146
Chronic diarrhea associated with the A3243G mtDNA mutation 144
Type 3 (chronic) GM1 gangliosidosis presenting as infanto-choreo-athetotic dementia, without epilepsy, in three sisters 142
Neuro-Ophthalmological findings in two adult siblings with ataxiatelangiectasia– like disorder 140
Acanthocytosis, retinitis pigmentosa, pallidal degeneration. Report of two cases without serum lipid abnormalities 138
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy 134
Dementia, myoclonus, peripheral neuropathy, and lipid-like material in skin biopsy during psychotropic drug treatment 133
The clinical aspects of adult hexosaminidase deficiencies 133
Characterization of the sialidase molecular defects in sialidosis patients suggests the structural organization of the lysosomal multienzyme complex 131
Lung involvement in Niemann-Pick disease type C1: improvement with bronchoalveolar lavage 131
Gliomatosis cerebri with oligodendrocytic components: description of 1 case 130
High-Dose Methylprednisolone For Bickerstaff’s Brainstem Encephalitis. 128
A syndrome of autosomal recessive pontocerebellar hypoplasia with white matter abnormalities and protracted course in two brothers 128
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome C oxidase deficiency 128
Assessment of cognitive profile and visual spatial attention in autosomal dominant cerebellar ataxia type 2 (SCA2). Correlation Between eye-tracking and neuropsychological studies. 127
Leukoencephalopathy as a rare complication of hepatitis C infection. 127
Assessment of cognitive profile and visual spatial attention in autosomal dominant cerebellar ataxia type 2 (SCA2). Correlation between eye-tracking and neuroosychological studies. 125
Neurological presentation of Ehlers-Danlos syndrome type IV in a family with parental mosaicism 125
Choreo-acanthocytosis like phenotype without acanthocytes: clinicopathological case report. A contribution to the knowledge of the functional pathology of the caudate nucleus 124
Neurophysiological study in chronic GM2 gangliosidosis (hexosaminidase A and B deficiency), with motor neuron disease phenotype 123
Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA) 123
PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation 122
Epilepsy with bilateral occipital calcifications: Sturge-Weber variant or a different encephalopathy? 122
Skin biopsies for cell cultures from Mediterranean free-ranging cetaceans 121
Increased lung surfactant phosphatidylcholine in patients affected by lysosomal storage diseases. 120
null 120
Macrosomia and mental retardation: evidence of autosomal dominant inheritance in four generations 117
Hypoplasia of the corpus callosum in Niemann-Pick type C disease 116
Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophy 116
Purification and partial characterization of lysosomal neuraminidase from human placenta 116
Imipramine induced lipidosis and dexamethasone effect: morphological and biochemical study in normal and chronic GM2 gangliosidosis fibroblasts 115
Palatal myoclonus and unusual MRI findings in a patient with membranous lipodystrophy 112
Fluorescein retinal angiography in the early diagnosis of optic disc edema 112
Human placental neuraminidase. Activation, stabilization and association with beta-galactosidase and its protective protein 111
Infanto-juvenile encephaloneuropathy and pigmentary retinopathy in a girl associated with congenital adrenal insufficiency and altered plasma medium-chain fatty acid levels 109
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations 107
Kohlschütter-Tönz Syndrome: Mutations in ROGDI and Evidence of Genetic Heterogeneity. 103
null 102
MRE11 mutations and impaired ATM-dependent responses in an Italian family with ataxia-telangiectasia-like disorder 101
Congenital lactic acidosis due to a defect of pyruvate dehydrogenase complex (E1). Clinical, biochemical, nerve biopsy study and effect of therapy 101
Glycosaminoglycan and glycoprotein changes in subacute sclerosing leucoencephalitis 100
Congenital oculo-facial paralysis (Moebius syndrome): evidence of dominant inheritance in two families 84
Neurocutaneous syndromes with pigmentary abnormalities and central nervous system involvement. II. Two cases with atypical incontinentia pigmenti 81
Screening of ARHSP-TCC patients expand the spectrum of SPG11 mutations and includes a large scale gene deletion 80
Oculo-dento-digital syndrome (Gorlin's syndrome): clinical and genetical report of a new family 78
Galactosialidosis: molecular heterogeneity among distinct clinical phenotypes 73
Molecular heterogeneity in human beta-galactosidase and neuraminidase deficiency 72
Niemann-Pick type C disease: mutations of NPC1 gene and evidence of abnormal expression of some mutant alleles in fibroblasts 71
Long term follow-up to evaluate the efficacy of miglustat treatment in Italian patients with Niemann-Pick disease type C 28
Selective bilateral amyotrophy of the anterior tibial muscle: a case report. 18
Totale 7.455
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Categoria #
all - tutte 22.098
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 22.098
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020899 0 0 0 0 106 111 133 195 115 125 24 90
2020/2021941 43 133 16 97 27 109 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
2024/2025322 21 86 107 70 38 0 0 0 0 0 0 0
Totale 7.455