IRIS
DI IORIO, Giuseppe
 Distribuzione geografica
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Continente #
EU - Europa 7.775
NA - Nord America 5.929
AS - Asia 4.178
SA - Sud America 795
AF - Africa 57
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 4
Totale 18.743
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Nazione #
US - Stati Uniti d'America 5.877
RU - Federazione Russa 2.213
SG - Singapore 1.692
IE - Irlanda 1.577
IT - Italia 981
UA - Ucraina 974
CN - Cina 925
HK - Hong Kong 835
GB - Regno Unito 682
BR - Brasile 680
DE - Germania 396
FI - Finlandia 263
TR - Turchia 228
SE - Svezia 204
FR - Francia 187
VN - Vietnam 171
GR - Grecia 161
IN - India 89
KR - Corea 85
AR - Argentina 44
BE - Belgio 30
BD - Bangladesh 26
MX - Messico 25
NL - Olanda 23
ID - Indonesia 21
JP - Giappone 20
CA - Canada 18
EC - Ecuador 18
ZA - Sudafrica 18
PL - Polonia 17
IR - Iran 16
CO - Colombia 15
AT - Austria 13
ES - Italia 12
MA - Marocco 11
IQ - Iraq 10
UZ - Uzbekistan 10
VE - Venezuela 9
HU - Ungheria 8
PK - Pakistan 8
CL - Cile 7
EG - Egitto 7
IL - Israele 7
PY - Paraguay 7
PE - Perù 6
BG - Bulgaria 5
CH - Svizzera 5
KE - Kenya 5
MY - Malesia 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
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
AO - Angola 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
KW - Kuwait 1
LY - Libia 1
MD - Moldavia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PT - Portogallo 1
SK - Slovacchia (Repubblica Slovacca) 1
SR - Suriname 1
TT - Trinidad e Tobago 1
Totale 18.743
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Città #
Dublin 1.577
Jacksonville 1.466
Hong Kong 832
Chandler 694
Moscow 692
Santa Clara 643
Singapore 496
Princeton 255
Medford 198
Roxbury 186
Ashburn 178
Beijing 158
Ann Arbor 154
Boardman 121
Wilmington 120
Caserta 107
The Dalles 98
Woodbridge 84
Seoul 79
Hefei 76
San Mateo 75
Cambridge 63
Dallas 63
Ho Chi Minh City 63
Des Moines 59
Bengaluru 55
Nanjing 51
São Paulo 49
Mountain View 46
Orange 45
Rome 45
Naples 44
New York 44
Düsseldorf 43
Milan 43
Napoli 35
Bremen 34
Munich 33
Brussels 28
Hanoi 27
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
Bologna 14
Houston 14
Nuremberg 14
Salvador 14
Brasília 12
Porto Alegre 12
Rio de Janeiro 12
Turku 12
Auburn Hills 11
Changsha 11
Salerno 11
Verona 11
Brooklyn 10
Curitiba 10
Guangzhou 10
Jinan 10
Tashkent 10
Barano D'ischia 8
Ribeirão Preto 8
Seattle 8
Shenyang 8
Baghdad 7
Campinas 7
Dhaka 7
Eboli 7
Genoa 7
Johannesburg 7
Joinville 7
Ningbo 7
Paris 7
San Francisco 7
Vienna 7
Can Tho 6
Catania 6
Changchun 6
Chennai 6
Council Bluffs 6
Falls Church 6
Ferrara 6
Hortolândia 6
Ilhéus 6
Jakarta 6
Leawood 6
Mexico City 6
Palermo 6
Pelotas 6
Shijiazhuang 6
Totale 9.807
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Nome #
Le iperCKemie familiari 356
Risposta inabituale alla SLI in un paziente anziano: variante fotomioclonica o risposta fotoconvulsiva atipica? 256
Abnormal accumulation of tTGase products in muscle and erythrocytes of chorea-acanthocytosis patients 150
Modifications moleculaires au cours de la regeneration et reinnervation musculaires in vitro 134
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations 130
Synergistic Interplay between Curcumin and Polyphenol-Rich Foods in the Mediterranean Diet: Therapeutic Prospects for Neurofibromatosis 1 Patients 121
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation 119
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 117
Neuro-Behçet’s Disease presenting as an isolated progressive cognitive and behavioral syndrome 115
Identification and characterization of a novel member of the dystrobrevin gene family 114
A novel diagnostic method to detect truncated neurofibromin in Neurofibromatosis 1 113
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients. 113
Deterioramento cognitivo ed anticorpi linfocitotossici in pazienti con lupus eritematoso sistemico 112
Symptomatic heterozygosity due to definite GAA mutation in late onset Pompe disease 112
A coding variant in GRIN3A gene is associated with migraine in italian population. 109
Malattie dei nervi periferici 108
Biochemical and morphological evidences supporting the hypothesis of a role of Tgase in the pathogeneisi of Chorea-Acanthocytosis 108
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 106
A novel GBE1 mutation and features of polyglucosan bodies autophagy in adult polyglucosan body disease 104
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 104
Adult polyglucosan body disease; novel homozygous missense mutation in the glycogen-branching enzyme gene in an italian patient. 103
Biochemical and morphological evidences supporting the hypothesis of a role of TGase in the pathogenesis of chorea acanthocytosis (C-A) 103
A case of diffuse lupus encephalopathy successfully treated with high-dose intravenous methylprednisolone 102
The Contursi kindred, a large family with autosomal dominant Parkinson's disease: implications of clinical and molecular studies 101
A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis 101
[Unusual histo-cytopathologic findings in a familial case of stiff spine syndrome] 99
Biochemical and morphological evidences supporting the hypothesis of a role of TGase in the pathogenesis of chorea acanthocytosis (C-A) 99
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 98
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 98
Lymphocytosis as a response biomarker of natalizumab therapeutic efficacy in multiple sclerosis 97
A case of progressive frontal lobe syndrome in a sporadic form of Cerebral Amyloid Angiopathy: A singular overlap with fronto-temporal dementia? 96
Diagnostic contribution of magnetic resonance imaging in an atypical presentation of motor neuron disease 95
Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship. 94
A novel and rapid method of determining truncated neurofibromin 1 to rapidly screen for neurofibromatosis type 1 (NF1) 93
An unusual phenotype of familial motor and sensory neuropathy with morphological features of HMSN1 93
Interessamento del sistema nervoso centrale nel Lupus Eritematoso Sistemico. Studio prospettico di 51 pazienti con esordio in età pediatrica 93
19. Fitc-conjugated plant agglutinins as specific saccharide stains for fluorescence microscopy of normal and pathologic muscles: preliminary results 92
Vacuolated PAS-positive lymphocytes as an hallmark of Pompe disease and other myopathies related to impaired autophagy. 92
Adult-onset brain tumors and neurodegeneration: Are polyphenols protective? 92
Foix-Chavany-Marie syndrome in a 17-year-old female with congenital cytomegalovirus infection. 91
Retrospective epidemiology of Duchenne muscular dystrophy in Molise 91
Brain involvement in Systemic Lupus Erythematosus evaluated by single photon emission computed tomography and magnetic resonance imaging 91
Symptomatic heterozygosity due to definite GAA mutations in late onset Pompe disease 91
A cluster of progranulin C157KfsX97 mutation in southern Italy- clinical characterization and genetic correlations 91
Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility. 90
A large kindred with autosomal dominant Parkinson's disease 90
Myopathic changes in neurofibromatosis type 1 90
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease 89
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. , : , 89
A large kindred with Paramyotonia Congenita 89
A case of Kohlmeier-Degos disease with dramatic neurological involvment 89
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy. 88
[Aicardi's syndrome. Report of 2 cases] 88
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease 88
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 88
Animal model to study factors influencing regeneration and direct innervation or neurotization of skeletal muscle 88
Towards genetic prevention of Adrenoleukodystrophy through early biochemical diagnosis of hemizygotes and heterozygotes in families at risk 88
Interessamento del Sistema Nervoso in corso di Lupus Eritematoso Sistemico 87
Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophy 87
Reperti isto e citopatologici del tutto peculiari riscontrati in un caso familiare di sindrome della spina rigida 87
Histopathological heterogeneity and cytopathological similarity of findings in different muscles of two brothers affected by rigid spine syndrome 86
[Hunter's disease: genetic, clinical and biochemical study of a new family] 86
[Introduction to neuroimmunology] 86
La capacità rigenerativa del muscolo scheletrico danneggiato: studio sperimentale 86
Lupus Eritematoso Sistemico e Sistema Nervoso: studio clinico-strumentale 86
Increased cerebrospinal fluid levels of 3,3',5'-triiodothyronine in patients with Alzheimer's disease 85
[Peripheral nervous system involvement in HCV-related mixed cryoglobulinemia] 84
[Neurological manifestations of systemic lupus erythematosus. Study of 53 cases] 84
[Cortical neuronal immaturity with agenesis of the major interhemispherical commissures and hypoplasia of the optico-pyramidal tracts in 3 children of the same family] 84
Associazione di distrofia muscolare congenita e malformazioni oculo-cerebrali : presentazione di un caso 84
Familial amyloidotic polyneuropathy: description of an Italian kindred 83
Prostaglandin Synthesis Is Involved In The Induction Of MyoD Expression 83
LOPED Study: looking for an early diagnosis in a late onset Pompe Disease high-risk population” Journal of Neurology, Neurosurgery, and Psychiatry (submitted) 82
Heidenhain variant of Creutzfeldt-Jakob disease with the co-occurrence of two differents types of prion proteins 82
Autonomic neuropathy in mixed cryoglobulinemia 82
Hemicorea-hemiballismus in a patient with non-ketotic hyperglicaemia mimicking basal ganglia hemorrage: a case report 82
Lecithin-cholesterol acyltransferase in brain: Does oxidative stress influence the 24-hydroxycholesterol esterification? 82
Early posterior vitreous detachment is associated with LAMA5 dominant mutation 82
A proposito di un nuovo caso di neuropatia ipertrofica familiare a trasmissione dominante, ad esordio precoce e ad evoluzione benigna 81
Crioglobulinemia mista essenziale: prevalenza e caratteri della neuropatia periferica 81
Does abnormal neuronal excitability exist in myotonic dystrophy? I. Effects of the antiarrhythmic drug hydroquinidine on slow saccadic eye movements 80
Epidemiological study of inherited ataxias in Campania (a Region of Southern Italy) 80
Viral RNA in nerve tissues of patients with hepatitis C infection and peripheral neuropathy 80
Novel VCP mutations expand the mutational spectrum of frontotemporal dementia 80
A promoter deletion at the dystrophin gene in a severe muscular Duchenne-like phenotype 80
Peripheral nervous system involvement in Klippel-Trenaunay syndrome 79
[Ophthalmoplegia plus: clinical, metabolic and histochemical study of a new case] 79
A review of anatomy, pathology and clinical data on the nigrostriatal system 79
Is the accumulation of very long fatty acids in plasma sufficient test to be used for preclinical diagnosis and genetic prevention of adrenoleukodystrophy (ALD)? 78
Clinical features and outcome measures during 1 year enzyme replacement therapy in late onset GSD II 78
Does abnormal neuronal excitability exist in myotonic dystrophy? II. Effects of the antiarrhythmic drug hydroquinidine on apathy and hypersomnia 78
Utilità della SPECT cerebrale in pazienti con Lupus Eritematoso Sistemico 78
Genotype-phenotype correlation analysis in a large italian family with late-onset glycogenosis II. 78
Validity of single photon emission computed tomography to study central nervous system involvement in patients with systemic lupus erythematosus 77
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study 77
SPET cerebrale in pazienti con elevati valori sierici di anticorpi anticardiolipina 77
Peripheral neuropathy in hepatitis-related mixed cryoglobulinemia: electrophysiologic follow-up study 76
Paternally inherited case of congenital DM1: Brain MRI and review of literature 76
Long-term follow-up effects on enzyme replacement treatment of adult form of acid maltase deficiency myopathy. 76
Studio neurofisiologico in 17 casi di crioglobulinemia. Rivista Italiana di EEG e Neurofisiologia Clinica : , 75
Totale 9.644
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Categoria #
all - tutte 75.299
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 75.299
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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
2025/20264.611 351 262 526 687 1.056 1.729 0 0 0 0 0 0
Totale 19.038