IRIS
DI IORIO, Giuseppe
 Distribuzione geografica
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Continente #
EU - Europa 13.271
NA - Nord America 5.959
AS - Asia 4.265
SA - Sud America 803
AF - Africa 59
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 4
Totale 24.366
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Nazione #
RU - Federazione Russa 7.705
US - Stati Uniti d'America 5.904
SG - Singapore 1.740
IE - Irlanda 1.577
IT - Italia 984
UA - Ucraina 974
CN - Cina 930
HK - Hong Kong 835
BR - Brasile 686
GB - Regno Unito 682
DE - Germania 396
FI - Finlandia 263
TR - Turchia 228
SE - Svezia 204
VN - Vietnam 197
FR - Francia 187
GR - Grecia 161
IN - India 90
KR - Corea 85
AR - Argentina 44
BE - Belgio 30
BD - Bangladesh 28
MX - Messico 26
NL - Olanda 23
ID - Indonesia 21
JP - Giappone 20
CA - Canada 18
EC - Ecuador 18
ZA - Sudafrica 18
PL - Polonia 17
CO - Colombia 16
IR - Iran 16
AT - Austria 14
ES - Italia 12
UZ - Uzbekistan 12
IQ - Iraq 11
MA - Marocco 11
VE - Venezuela 9
HU - Ungheria 8
PK - Pakistan 8
PY - Paraguay 8
CL - Cile 7
EG - Egitto 7
IL - Israele 7
MY - Malesia 6
PE - Perù 6
BG - Bulgaria 5
CH - Svizzera 5
KE - Kenya 5
UY - Uruguay 5
AU - Australia 4
DK - Danimarca 4
DZ - Algeria 4
EU - Europa 4
RO - Romania 4
SN - Senegal 4
AE - Emirati Arabi Uniti 3
AO - Angola 3
AZ - Azerbaigian 3
BO - Bolivia 3
CZ - Repubblica Ceca 3
JO - Giordania 3
KZ - Kazakistan 3
LB - Libano 3
LT - Lituania 3
RS - Serbia 3
SA - Arabia Saudita 3
SV - El Salvador 3
TH - Thailandia 3
AL - Albania 2
DO - Repubblica Dominicana 2
GE - Georgia 2
JM - Giamaica 2
KG - Kirghizistan 2
OM - Oman 2
TN - Tunisia 2
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BW - Botswana 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
CY - Cipro 1
ET - Etiopia 1
GA - Gabon 1
HN - Honduras 1
KW - Kuwait 1
LY - Libia 1
MD - Moldavia 1
MN - Mongolia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PA - Panama 1
PT - Portogallo 1
SK - Slovacchia (Repubblica Slovacca) 1
SR - Suriname 1
TT - Trinidad e Tobago 1
Totale 24.366
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Città #
Moscow 2.611
Dublin 1.577
Jacksonville 1.466
Hong Kong 832
Chandler 694
Santa Clara 643
Singapore 544
Princeton 255
Ashburn 202
Medford 198
Roxbury 186
Beijing 158
Ann Arbor 154
Boardman 121
Wilmington 120
Caserta 107
The Dalles 98
Woodbridge 84
Seoul 79
Hefei 76
San Mateo 75
Ho Chi Minh City 68
Cambridge 63
Dallas 63
Des Moines 59
Bengaluru 55
Nanjing 51
São Paulo 50
Mountain View 46
Orange 45
Rome 45
Naples 44
New York 44
Düsseldorf 43
Milan 43
Napoli 35
Bremen 34
Munich 33
Hanoi 31
Brussels 28
Los Angeles 27
Kunming 22
Norwalk 22
Redwood City 21
Shanghai 21
Belo Horizonte 19
Dearborn 18
Helsinki 18
Nanchang 18
Hangzhou 17
Dong Ket 16
Florence 16
Tianjin 16
Salvador 15
Bologna 14
Houston 14
Nuremberg 14
Brasília 12
Porto Alegre 12
Rio de Janeiro 12
Tashkent 12
Turku 12
Auburn Hills 11
Changsha 11
Salerno 11
Verona 11
Brooklyn 10
Curitiba 10
Guangzhou 10
Jinan 10
Barano D'ischia 8
Ribeirão Preto 8
Seattle 8
Shenyang 8
Baghdad 7
Campinas 7
Da Nang 7
Dhaka 7
Eboli 7
Genoa 7
Johannesburg 7
Joinville 7
Ningbo 7
Paris 7
San Francisco 7
Vienna 7
Atlanta 6
Can Tho 6
Catania 6
Changchun 6
Chennai 6
Council Bluffs 6
Falls Church 6
Ferrara 6
Haiphong 6
Hortolândia 6
Ilhéus 6
Jakarta 6
Kuala Lumpur 6
Leawood 6
Totale 11.812
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Nome #
Le iperCKemie familiari 377
Risposta inabituale alla SLI in un paziente anziano: variante fotomioclonica o risposta fotoconvulsiva atipica? 278
Abnormal accumulation of tTGase products in muscle and erythrocytes of chorea-acanthocytosis patients 188
Modifications moleculaires au cours de la regeneration et reinnervation musculaires in vitro 167
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations 163
Identification and characterization of a novel member of the dystrobrevin gene family 154
A novel diagnostic method to detect truncated neurofibromin in Neurofibromatosis 1 154
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients. 154
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation 152
A novel GBE1 mutation and features of polyglucosan bodies autophagy in Adult Polyglucosan Body Disease. A novel GBE1 mutation and features of polyglucosan bodies autophagy in Adult Polyglucosan Body Disease 149
Synergistic Interplay between Curcumin and Polyphenol-Rich Foods in the Mediterranean Diet: Therapeutic Prospects for Neurofibromatosis 1 Patients 146
Biochemical and morphological evidences supporting the hypothesis of a role of TGase in the pathogenesis of chorea acanthocytosis (C-A) 146
Deterioramento cognitivo ed anticorpi linfocitotossici in pazienti con lupus eritematoso sistemico 145
A Unique Myopathy Syndrome in a Patient Disclosing Clinical, Laboratory, and Genetic Findings of Late-Onset Pompe Disease, Together with a Lack of Dysferlin on Muscle Biopsy 144
Adult polyglucosan body disease; novel homozygous missense mutation in the glycogen-branching enzyme gene in an italian patient. 142
A novel GBE1 mutation and features of polyglucosan bodies autophagy in adult polyglucosan body disease 141
Biochemical and morphological evidences supporting the hypothesis of a role of Tgase in the pathogeneisi of Chorea-Acanthocytosis 141
A coding variant in GRIN3A gene is associated with migraine in italian population. 141
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 139
Adult-onset brain tumors and neurodegeneration: Are polyphenols protective? 137
A case of diffuse lupus encephalopathy successfully treated with high-dose intravenous methylprednisolone 135
A comment on: 'Molecular diagnosis of transthyretin Met30 mutation in an Italian family with familial amyloidotic polyneuropathy' by Paola Strocchi et al., FEBS Letters 359 (1995) 203-205 135
Symptomatic heterozygosity due to definite GAA mutation in late onset Pompe disease 135
Neuro-Behçet’s Disease presenting as an isolated progressive cognitive and behavioral syndrome 135
Biochemical and morphological evidences supporting the hypothesis of a role of TGase in the pathogenesis of chorea acanthocytosis (C-A) 133
Malattie dei nervi periferici 133
A case of progressive frontal lobe syndrome in a sporadic form of Cerebral Amyloid Angiopathy: A singular overlap with fronto-temporal dementia? 133
A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis 132
Diagnostic contribution of magnetic resonance imaging in an atypical presentation of motor neuron disease 130
Analisi in istofluorescenza di densità e distribuzione dei recettori per ConA e WGA in corso di rigenerazione e re-innervazione nel muscolo scheletrico di ratto ischemizzato e denervato, reversibilmente o irreversibilmente 130
A novel and rapid method of determining truncated neurofibromin 1 to rapidly screen for neurofibromatosis type 1 (NF1) 129
Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship. 128
[Unusual histo-cytopathologic findings in a familial case of stiff spine syndrome] 128
[Aicardi's syndrome. Report of 2 cases] 126
19. Fitc-conjugated plant agglutinins as specific saccharide stains for fluorescence microscopy of normal and pathologic muscles: preliminary results 126
An unusual phenotype of familial motor and sensory neuropathy with morphological features of HMSN1 126
Lymphocytosis as a response biomarker of natalizumab therapeutic efficacy in multiple sclerosis 125
The Contursi kindred, a large family with autosomal dominant Parkinson's disease: implications of clinical and molecular studies 124
39. Density and distribution of ConA and WGA receptors determined by histofluorescence analysis during degeneration, regeneration and reinnervation of the rat skeletal muscle following ischemia and reversible or irreversible denervation. , : , 122
A large kindred with Paramyotonia Congenita 122
7. (2011). Exome sequencing approach to define the complex genetic substrate in a family with insulin resistance, left ventricular noncompaction (LVNC) and congenital fiber type disproportion (CFTD). In: XLII Congress of the Italian Neurological Society. NEUROLOGICAL SCIENCES, p. S285, ISSN: 1590-1874, Torino, 22-25 novembre, 2011 120
A case of Kohlmeier-Degos disease with dramatic neurological involvment 119
Brain involvement in Systemic Lupus Erythematosus evaluated by single photon emission computed tomography and magnetic resonance imaging 118
[Hunter's disease: genetic, clinical and biochemical study of a new family] 118
Myopathic changes in neurofibromatosis type 1 118
A cluster of progranulin C157KfsX97 mutation in southern Italy- clinical characterization and genetic correlations 118
A large kindred with autosomal dominant Parkinson's disease 117
[Neurological manifestations of systemic lupus erythematosus. Study of 53 cases] 116
[Introduction to neuroimmunology] 116
Interessamento del sistema nervoso centrale nel Lupus Eritematoso Sistemico. Studio prospettico di 51 pazienti con esordio in età pediatrica 116
Retrospective epidemiology of Duchenne muscular dystrophy in Molise 115
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease 115
[Cortical neuronal immaturity with agenesis of the major interhemispherical commissures and hypoplasia of the optico-pyramidal tracts in 3 children of the same family] 115
Associazione di distrofia muscolare congenita e malformazioni oculo-cerebrali : presentazione di un caso 115
A promoter deletion at the dystrophin gene in a severe muscular Duchenne-like phenotype 115
Foix-Chavany-Marie syndrome in a 17-year-old female with congenital cytomegalovirus infection. 113
[Ophthalmoplegia plus: clinical, metabolic and histochemical study of a new case] 113
[Peripheral nervous system involvement in HCV-related mixed cryoglobulinemia] 112
Autonomic neuropathy in mixed cryoglobulinemia 112
Towards genetic prevention of Adrenoleukodystrophy through early biochemical diagnosis of hemizygotes and heterozygotes in families at risk 111
Vacuolated PAS-positive lymphocytes as an hallmark of Pompe disease and other myopathies related to impaired autophagy. 111
Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility. 110
Interessamento del Sistema Nervoso in corso di Lupus Eritematoso Sistemico 110
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease 110
Crioglobulinemia mista essenziale: prevalenza e caratteri della neuropatia periferica 110
Symptomatic heterozygosity due to definite GAA mutations in late onset Pompe disease 109
Reperti isto e citopatologici del tutto peculiari riscontrati in un caso familiare di sindrome della spina rigida 108
Animal model to study factors influencing regeneration and direct innervation or neurotization of skeletal muscle 107
Utilità della SPECT cerebrale in pazienti con Lupus Eritematoso Sistemico 107
Lupus Eritematoso Sistemico e Sistema Nervoso: studio clinico-strumentale 107
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy. 106
Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophy 106
A peculiar report of rare multifocal "ganglio-glioneurocytoma" 106
Familial amyloidotic polyneuropathy: description of an Italian kindred 105
Increased cerebrospinal fluid levels of 3,3',5'-triiodothyronine in patients with Alzheimer's disease 105
Viral RNA in nerve tissues of patients with hepatitis C infection and peripheral neuropathy 105
La capacità rigenerativa del muscolo scheletrico danneggiato: studio sperimentale 105
Histopathological heterogeneity and cytopathological similarity of findings in different muscles of two brothers affected by rigid spine syndrome 104
Prostaglandin Synthesis Is Involved In The Induction Of MyoD Expression 104
Hemicorea-hemiballismus in a patient with non-ketotic hyperglicaemia mimicking basal ganglia hemorrage: a case report 104
Early posterior vitreous detachment is associated with LAMA5 dominant mutation 104
Lecithin-cholesterol acyltransferase in brain: Does oxidative stress influence the 24-hydroxycholesterol esterification? 103
LOPED Study: looking for an early diagnosis in a late onset Pompe Disease high-risk population” Journal of Neurology, Neurosurgery, and Psychiatry (submitted) 102
Heidenhain variant of Creutzfeldt-Jakob disease with the co-occurrence of two differents types of prion proteins 101
Novel autophagic vacuolar myopathies: phenotype and genotype features 101
A proposito di un nuovo caso di neuropatia ipertrofica familiare a trasmissione dominante, ad esordio precoce e ad evoluzione benigna 100
Does abnormal neuronal excitability exist in myotonic dystrophy? II. Effects of the antiarrhythmic drug hydroquinidine on apathy and hypersomnia 100
Clinical features and outcome measures during 1 year enzyme replacement therapy in late onset GSD II 99
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study 99
Postural and gait patterns assessed by 3D movement analysis in a late onset Pompe disease sibship 99
Is the accumulation of very long fatty acids in plasma sufficient test to be used for preclinical diagnosis and genetic prevention of adrenoleukodystrophy (ALD)? 98
Epidemiological study of inherited ataxias in Campania (a Region of Southern Italy) 98
Does abnormal neuronal excitability exist in myotonic dystrophy? I. Effects of the antiarrhythmic drug hydroquinidine on slow saccadic eye movements 97
Validity of single photon emission computed tomography to study central nervous system involvement in patients with systemic lupus erythematosus 97
Novel VCP mutations expand the mutational spectrum of frontotemporal dementia 97
A review of anatomy, pathology and clinical data on the nigrostriatal system 97
Genotype-phenotype correlation analysis in a large italian family with late-onset glycogenosis II. 97
Peripheral neuropathy in hepatitis-related mixed cryoglobulinemia: electrophysiologic follow-up study 96
Utilità di megadosi di corticosteroidi in un caso di encefalopatia lupica 95
Paternally inherited case of congenital DM1: Brain MRI and review of literature 94
Totale 12.370
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Categoria #
all - tutte 83.159
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 83.159
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.115 0 0 0 0 0 13 279 243 29 285 204 62
2021/20221.646 86 52 7 45 566 21 29 48 62 106 143 481
2022/20232.838 275 23 45 191 285 224 8 166 1.453 36 67 65
2023/20241.092 89 30 120 92 409 43 8 22 10 4 107 158
2024/20253.206 17 45 53 55 511 260 367 267 509 736 246 140
2025/202610.234 351 262 526 687 1.056 7.352 0 0 0 0 0 0
Totale 24.661