IRIS
DI IORIO, Giuseppe
 Distribuzione geografica
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Continente #
EU - Europa 13.671
NA - Nord America 6.962
AS - Asia 4.817
SA - Sud America 825
AF - Africa 65
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 4
Totale 26.350
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Nazione #
RU - Federazione Russa 7.917
US - Stati Uniti d'America 6.884
SG - Singapore 1.949
IE - Irlanda 1.580
IT - Italia 1.031
CN - Cina 993
UA - Ucraina 974
HK - Hong Kong 853
BR - Brasile 699
GB - Regno Unito 692
VN - Vietnam 412
DE - Germania 402
FI - Finlandia 327
TR - Turchia 229
SE - Svezia 209
FR - Francia 201
GR - Grecia 161
IN - India 103
KR - Corea 87
AR - Argentina 48
NL - Olanda 37
CA - Canada 34
BD - Bangladesh 32
MX - Messico 31
BE - Belgio 30
PL - Polonia 26
JP - Giappone 25
ID - Indonesia 24
EC - Ecuador 19
ZA - Sudafrica 19
CO - Colombia 18
IR - Iran 16
ES - Italia 15
AT - Austria 14
IQ - Iraq 14
MA - Marocco 14
UZ - Uzbekistan 13
PK - Pakistan 10
EG - Egitto 9
PY - Paraguay 9
VE - Venezuela 9
CH - Svizzera 8
CL - Cile 8
CZ - Repubblica Ceca 8
HU - Ungheria 8
IL - Israele 7
MY - Malesia 7
TH - Thailandia 7
PE - Perù 6
AU - Australia 5
BG - Bulgaria 5
KE - Kenya 5
PH - Filippine 5
SA - Arabia Saudita 5
UY - Uruguay 5
DK - Danimarca 4
DZ - Algeria 4
EU - Europa 4
LT - Lituania 4
RO - Romania 4
SN - Senegal 4
SV - El Salvador 4
AE - Emirati Arabi Uniti 3
AO - Angola 3
AZ - Azerbaigian 3
BO - Bolivia 3
JM - Giamaica 3
JO - Giordania 3
KZ - Kazakistan 3
LB - Libano 3
PT - Portogallo 3
RS - Serbia 3
AL - Albania 2
DO - Repubblica Dominicana 2
GE - Georgia 2
KG - Kirghizistan 2
OM - Oman 2
TN - Tunisia 2
AM - Armenia 1
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
IM - Isola di Man 1
KW - Kuwait 1
LV - Lettonia 1
LY - Libia 1
MD - Moldavia 1
MN - Mongolia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PA - Panama 1
SK - Slovacchia (Repubblica Slovacca) 1
SR - Suriname 1
TT - Trinidad e Tobago 1
Totale 26.350
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Città #
Moscow 2.751
Dublin 1.580
Jacksonville 1.466
Hong Kong 847
Singapore 716
Chandler 694
Santa Clara 656
San Jose 515
Ashburn 328
Princeton 255
Medford 198
Roxbury 186
Beijing 160
Ann Arbor 154
Ho Chi Minh City 126
Boardman 121
Wilmington 120
Caserta 107
The Dalles 98
Hanoi 85
Woodbridge 84
Helsinki 82
Seoul 79
Hefei 76
San Mateo 75
New York 69
Dallas 68
Cambridge 63
Des Moines 59
Bengaluru 55
Nanjing 51
São Paulo 51
Naples 48
Rome 48
Milan 46
Mountain View 46
Orange 45
Düsseldorf 43
Napoli 35
Bremen 34
Los Angeles 34
Munich 33
Brussels 28
Atlanta 22
Kunming 22
Norwalk 22
Da Nang 21
Redwood City 21
Shanghai 21
Belo Horizonte 20
Dearborn 18
Nanchang 18
Hangzhou 17
Amsterdam 16
Bologna 16
Dong Ket 16
Florence 16
Tianjin 16
Houston 15
Salvador 15
Haiphong 14
Nuremberg 14
Porto Alegre 14
Toronto 14
Rio de Janeiro 13
Tashkent 13
Verona 13
Brasília 12
Brooklyn 12
Hải Dương 12
Turku 12
Auburn Hills 11
Changsha 11
Orem 11
Salerno 11
Can Tho 10
Curitiba 10
Guangzhou 10
Jinan 10
Chennai 9
Frankfurt am Main 9
Memphis 9
Seattle 9
Warsaw 9
Barano D'ischia 8
Biên Hòa 8
Catania 8
Council Bluffs 8
Ribeirão Preto 8
Shenyang 8
Turin 8
Baghdad 7
Campinas 7
Chicago 7
Dhaka 7
Eboli 7
Genoa 7
Johannesburg 7
Joinville 7
Mexico City 7
Totale 13.118
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Nome #
Le iperCKemie familiari 384
Risposta inabituale alla SLI in un paziente anziano: variante fotomioclonica o risposta fotoconvulsiva atipica? 318
Abnormal accumulation of tTGase products in muscle and erythrocytes of chorea-acanthocytosis patients 201
Modifications moleculaires au cours de la regeneration et reinnervation musculaires in vitro 182
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations 178
A novel diagnostic method to detect truncated neurofibromin in Neurofibromatosis 1 169
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation 166
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients. 164
Identification and characterization of a novel member of the dystrobrevin gene family 160
Biochemical and morphological evidences supporting the hypothesis of a role of TGase in the pathogenesis of chorea acanthocytosis (C-A) 160
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 159
Deterioramento cognitivo ed anticorpi linfocitotossici in pazienti con lupus eritematoso sistemico 157
A novel GBE1 mutation and features of polyglucosan bodies autophagy in adult polyglucosan body disease 155
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 154
Adult polyglucosan body disease; novel homozygous missense mutation in the glycogen-branching enzyme gene in an italian patient. 154
Synergistic Interplay between Curcumin and Polyphenol-Rich Foods in the Mediterranean Diet: Therapeutic Prospects for Neurofibromatosis 1 Patients 154
Adult-onset brain tumors and neurodegeneration: Are polyphenols protective? 150
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 149
Biochemical and morphological evidences supporting the hypothesis of a role of Tgase in the pathogeneisi of Chorea-Acanthocytosis 148
A coding variant in GRIN3A gene is associated with migraine in italian population. 148
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 146
A case of progressive frontal lobe syndrome in a sporadic form of Cerebral Amyloid Angiopathy: A singular overlap with fronto-temporal dementia? 146
A case of diffuse lupus encephalopathy successfully treated with high-dose intravenous methylprednisolone 145
Diagnostic contribution of magnetic resonance imaging in an atypical presentation of motor neuron disease 144
Symptomatic heterozygosity due to definite GAA mutation in late onset Pompe disease 143
A cluster of progranulin C157KfsX97 mutation in southern Italy- clinical characterization and genetic correlations 142
A novel and rapid method of determining truncated neurofibromin 1 to rapidly screen for neurofibromatosis type 1 (NF1) 140
Biochemical and morphological evidences supporting the hypothesis of a role of TGase in the pathogenesis of chorea acanthocytosis (C-A) 140
A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis 139
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) 203-205 139
[Unusual histo-cytopathologic findings in a familial case of stiff spine syndrome] 139
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease 138
Malattie dei nervi periferici 138
Myopathic changes in neurofibromatosis type 1 138
Neuro-Behçet’s Disease presenting as an isolated progressive cognitive and behavioral syndrome 138
Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship. 137
Lymphocytosis as a response biomarker of natalizumab therapeutic efficacy in multiple sclerosis 137
[Introduction to neuroimmunology] 136
An unusual phenotype of familial motor and sensory neuropathy with morphological features of HMSN1 135
[Aicardi's syndrome. Report of 2 cases] 134
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. , : , 133
The Contursi kindred, a large family with autosomal dominant Parkinson's disease: implications of clinical and molecular studies 132
19. Fitc-conjugated plant agglutinins as specific saccharide stains for fluorescence microscopy of normal and pathologic muscles: preliminary results 132
A large kindred with Paramyotonia Congenita 131
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 127
[Neurological manifestations of systemic lupus erythematosus. Study of 53 cases] 126
[Hunter's disease: genetic, clinical and biochemical study of a new family] 126
A case of Kohlmeier-Degos disease with dramatic neurological involvment 126
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease 125
LOPED Study: looking for an early diagnosis in a late onset Pompe Disease high-risk population” Journal of Neurology, Neurosurgery, and Psychiatry (submitted) 124
Brain involvement in Systemic Lupus Erythematosus evaluated by single photon emission computed tomography and magnetic resonance imaging 123
[Peripheral nervous system involvement in HCV-related mixed cryoglobulinemia] 123
A large kindred with autosomal dominant Parkinson's disease 123
Associazione di distrofia muscolare congenita e malformazioni oculo-cerebrali : presentazione di un caso 123
Interessamento del sistema nervoso centrale nel Lupus Eritematoso Sistemico. Studio prospettico di 51 pazienti con esordio in età pediatrica 123
Retrospective epidemiology of Duchenne muscular dystrophy in Molise 122
[Cortical neuronal immaturity with agenesis of the major interhemispherical commissures and hypoplasia of the optico-pyramidal tracts in 3 children of the same family] 122
A promoter deletion at the dystrophin gene in a severe muscular Duchenne-like phenotype 122
Reperti isto e citopatologici del tutto peculiari riscontrati in un caso familiare di sindrome della spina rigida 121
Symptomatic heterozygosity due to definite GAA mutations in late onset Pompe disease 120
Foix-Chavany-Marie syndrome in a 17-year-old female with congenital cytomegalovirus infection. 118
Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility. 118
[Ophthalmoplegia plus: clinical, metabolic and histochemical study of a new case] 118
Interessamento del Sistema Nervoso in corso di Lupus Eritematoso Sistemico 117
Autonomic neuropathy in mixed cryoglobulinemia 117
Novel VCP mutations expand the mutational spectrum of frontotemporal dementia 117
Towards genetic prevention of Adrenoleukodystrophy through early biochemical diagnosis of hemizygotes and heterozygotes in families at risk 117
Utilità della SPECT cerebrale in pazienti con Lupus Eritematoso Sistemico 117
Animal model to study factors influencing regeneration and direct innervation or neurotization of skeletal muscle 116
Vacuolated PAS-positive lymphocytes as an hallmark of Pompe disease and other myopathies related to impaired autophagy. 116
Crioglobulinemia mista essenziale: prevalenza e caratteri della neuropatia periferica 115
Lupus Eritematoso Sistemico e Sistema Nervoso: studio clinico-strumentale 115
La capacità rigenerativa del muscolo scheletrico danneggiato: studio sperimentale 114
A peculiar report of rare multifocal "ganglio-glioneurocytoma" 114
Viral RNA in nerve tissues of patients with hepatitis C infection and peripheral neuropathy 113
Lecithin-cholesterol acyltransferase in brain: Does oxidative stress influence the 24-hydroxycholesterol esterification? 113
Familial amyloidotic polyneuropathy: description of an Italian kindred 111
Heidenhain variant of Creutzfeldt-Jakob disease with the co-occurrence of two differents types of prion proteins 111
Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophy 111
Histopathological heterogeneity and cytopathological similarity of findings in different muscles of two brothers affected by rigid spine syndrome 110
Prostaglandin Synthesis Is Involved In The Induction Of MyoD Expression 110
Hemicorea-hemiballismus in a patient with non-ketotic hyperglicaemia mimicking basal ganglia hemorrage: a case report 110
Early posterior vitreous detachment is associated with LAMA5 dominant mutation 110
Does abnormal neuronal excitability exist in myotonic dystrophy? II. Effects of the antiarrhythmic drug hydroquinidine on apathy and hypersomnia 109
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy. 108
Increased cerebrospinal fluid levels of 3,3',5'-triiodothyronine in patients with Alzheimer's disease 108
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study 107
Genotype-phenotype correlation analysis in a large italian family with late-onset glycogenosis II. 107
Mapping of a gene for Parkinson's disease to chromosome 4q21-q23 106
A proposito di un nuovo caso di neuropatia ipertrofica familiare a trasmissione dominante, ad esordio precoce e ad evoluzione benigna 106
Epidemiological study of inherited ataxias in Campania (a Region of Southern Italy) 105
Paternally inherited case of congenital DM1: Brain MRI and review of literature 105
A review of anatomy, pathology and clinical data on the nigrostriatal system 105
Novel autophagic vacuolar myopathies: phenotype and genotype features 105
Miopatia oculo-faringea: meccanismi fisiopatologici ed aspetti diagnostici e terapeutici. Caso Clinico 104
Cerebral atrophy in SLE patients: a consequence of steroid treatment? 103
Postural and gait patterns assessed by 3D movement analysis in a late onset Pompe disease sibship 103
Is the accumulation of very long fatty acids in plasma sufficient test to be used for preclinical diagnosis and genetic prevention of adrenoleukodystrophy (ALD)? 102
Clinical features and outcome measures during 1 year enzyme replacement therapy in late onset GSD II 102
Slowly progressive JC positive multifocal leukoencephalopathy not associated with overt immunodeficency, oncohaematological disorder nor immunosoppressive therapies 102
Totale 13.323
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Categoria #
all - tutte 91.269
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 91.269
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202162 0 0 0 0 0 0 0 0 0 0 0 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
2025/202612.218 351 262 526 687 1.056 7.390 623 304 574 266 138 41
Totale 26.645