IRIS
DI IORIO, Giuseppe
 Distribuzione geografica
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Continente #
EU - Europa 13.778
NA - Nord America 8.228
AS - Asia 5.004
SA - Sud America 834
Continente sconosciuto - Info sul continente non disponibili 299
AF - Africa 65
OC - Oceania 6
Totale 28.214
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Nazione #
US - Stati Uniti d'America 8.124
RU - Federazione Russa 7.917
SG - Singapore 2.101
IE - Irlanda 1.580
IT - Italia 1.112
CN - Cina 997
UA - Ucraina 974
HK - Hong Kong 863
BR - Brasile 701
GB - Regno Unito 697
DE - Germania 413
VN - Vietnam 412
FI - Finlandia 327
TR - Turchia 229
SE - Svezia 209
FR - Francia 204
GR - Grecia 161
IN - India 104
KR - Corea 93
AR - Argentina 49
CA - Canada 49
NL - Olanda 38
BD - Bangladesh 37
JP - Giappone 32
MX - Messico 32
BE - Belgio 30
PL - Polonia 26
ID - Indonesia 24
EC - Ecuador 23
ZA - Sudafrica 19
CO - Colombia 18
ES - Italia 18
IR - Iran 16
AT - Austria 14
IQ - Iraq 14
MA - Marocco 14
UZ - Uzbekistan 13
PK - Pakistan 11
CL - Cile 9
EG - Egitto 9
PY - Paraguay 9
VE - Venezuela 9
CH - Svizzera 8
CZ - Repubblica Ceca 8
HU - Ungheria 8
IL - Israele 7
MY - Malesia 7
PE - Perù 7
TH - Thailandia 7
AU - Australia 5
BG - Bulgaria 5
JM - Giamaica 5
KE - Kenya 5
PH - Filippine 5
SA - Arabia Saudita 5
UY - Uruguay 5
AE - Emirati Arabi Uniti 4
DK - Danimarca 4
DZ - Algeria 4
EU - Europa 4
LT - Lituania 4
PT - Portogallo 4
RO - Romania 4
SN - Senegal 4
SV - El Salvador 4
AO - Angola 3
AZ - Azerbaigian 3
BO - Bolivia 3
JO - Giordania 3
KZ - Kazakistan 3
LB - Libano 3
RS - Serbia 3
AL - Albania 2
BA - Bosnia-Erzegovina 2
CR - Costa Rica 2
DO - Repubblica Dominicana 2
GE - Georgia 2
HN - Honduras 2
KG - Kirghizistan 2
OM - Oman 2
SK - Slovacchia (Repubblica Slovacca) 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
AM - Armenia 1
BH - Bahrain 1
BS - Bahamas 1
BW - Botswana 1
CI - Costa d'Avorio 1
CY - Cipro 1
ET - Etiopia 1
GA - Gabon 1
GD - Grenada 1
GP - Guadalupe 1
IM - Isola di Man 1
KW - Kuwait 1
KY - Cayman, isole 1
LV - Lettonia 1
LY - Libia 1
MD - Moldavia 1
MN - Mongolia 1
Totale 27.914
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Città #
Moscow 2.751
Dublin 1.580
Jacksonville 1.466
Hong Kong 856
Singapore 725
Chandler 694
Santa Clara 688
San Jose 644
Ashburn 526
Council Bluffs 511
Princeton 257
Medford 199
Roxbury 186
Beijing 164
Ann Arbor 154
Ho Chi Minh City 126
Boardman 121
Wilmington 121
Caserta 107
The Dalles 98
Hanoi 85
Seoul 85
Woodbridge 84
Helsinki 82
Hefei 76
San Mateo 75
New York 72
Dallas 70
Milan 67
Cambridge 63
Des Moines 59
Bengaluru 55
Rome 54
Nanjing 51
São Paulo 51
Naples 50
Mountain View 46
Orange 45
Düsseldorf 43
Los Angeles 41
Napoli 35
Bremen 34
Munich 33
Brussels 28
Atlanta 25
Kunming 22
Norwalk 22
Da Nang 21
Redwood City 21
Shanghai 21
Belo Horizonte 20
Frankfurt am Main 20
Bologna 19
Dearborn 18
Nanchang 18
Amsterdam 17
Florence 17
Hangzhou 17
Dong Ket 16
Tianjin 16
Houston 15
Salvador 15
Toronto 15
Haiphong 14
Nuremberg 14
Porto Alegre 14
Tokyo 14
Brooklyn 13
Rio de Janeiro 13
Tashkent 13
Verona 13
Brasília 12
Hải Dương 12
Turku 12
Auburn Hills 11
Catania 11
Changsha 11
Chicago 11
Orem 11
Salerno 11
Seattle 11
Can Tho 10
Curitiba 10
Guangzhou 10
Jinan 10
Turin 10
Chennai 9
Memphis 9
Miano 9
Montreal 9
Newark 9
Warsaw 9
Barano D'ischia 8
Biên Hòa 8
Mexico City 8
Ribeirão Preto 8
Salt Lake City 8
San Francisco 8
Shenyang 8
Vienna 8
Totale 14.102
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Nome #
Le iperCKemie familiari 389
Risposta inabituale alla SLI in un paziente anziano: variante fotomioclonica o risposta fotoconvulsiva atipica? 325
Abnormal accumulation of tTGase products in muscle and erythrocytes of chorea-acanthocytosis patients 209
Modifications moleculaires au cours de la regeneration et reinnervation musculaires in vitro 188
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations 184
A novel diagnostic method to detect truncated neurofibromin in Neurofibromatosis 1 174
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation 173
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients. 171
Identification and characterization of a novel member of the dystrobrevin gene family 169
Deterioramento cognitivo ed anticorpi linfocitotossici in pazienti con lupus eritematoso sistemico 166
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 166
Biochemical and morphological evidences supporting the hypothesis of a role of TGase in the pathogenesis of chorea acanthocytosis (C-A) 166
A novel GBE1 mutation and features of polyglucosan bodies autophagy in adult polyglucosan body disease 163
Synergistic Interplay between Curcumin and Polyphenol-Rich Foods in the Mediterranean Diet: Therapeutic Prospects for Neurofibromatosis 1 Patients 163
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 159
Biochemical and morphological evidences supporting the hypothesis of a role of Tgase in the pathogeneisi of Chorea-Acanthocytosis 158
Adult polyglucosan body disease; novel homozygous missense mutation in the glycogen-branching enzyme gene in an italian patient. 158
Diagnostic contribution of magnetic resonance imaging in an atypical presentation of motor neuron disease 156
A case of progressive frontal lobe syndrome in a sporadic form of Cerebral Amyloid Angiopathy: A singular overlap with fronto-temporal dementia? 156
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 155
A coding variant in GRIN3A gene is associated with migraine in italian population. 155
Adult-onset brain tumors and neurodegeneration: Are polyphenols protective? 154
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) 203-205 153
Lymphocytosis as a response biomarker of natalizumab therapeutic efficacy in multiple sclerosis 152
A case of diffuse lupus encephalopathy successfully treated with high-dose intravenous methylprednisolone 151
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 151
A cluster of progranulin C157KfsX97 mutation in southern Italy- clinical characterization and genetic correlations 151
A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis 149
Biochemical and morphological evidences supporting the hypothesis of a role of TGase in the pathogenesis of chorea acanthocytosis (C-A) 148
Symptomatic heterozygosity due to definite GAA mutation in late onset Pompe disease 148
Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship. 147
Neuro-Behçet’s Disease presenting as an isolated progressive cognitive and behavioral syndrome 146
[Unusual histo-cytopathologic findings in a familial case of stiff spine syndrome] 145
A novel and rapid method of determining truncated neurofibromin 1 to rapidly screen for neurofibromatosis type 1 (NF1) 143
Malattie dei nervi periferici 143
The Contursi kindred, a large family with autosomal dominant Parkinson's disease: implications of clinical and molecular studies 142
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease 142
Myopathic changes in neurofibromatosis type 1 142
[Introduction to neuroimmunology] 141
A large kindred with Paramyotonia Congenita 141
An unusual phenotype of familial motor and sensory neuropathy with morphological features of HMSN1 140
[Aicardi's syndrome. Report of 2 cases] 139
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 138
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. , : , 137
19. Fitc-conjugated plant agglutinins as specific saccharide stains for fluorescence microscopy of normal and pathologic muscles: preliminary results 135
Brain involvement in Systemic Lupus Erythematosus evaluated by single photon emission computed tomography and magnetic resonance imaging 133
[Neurological manifestations of systemic lupus erythematosus. Study of 53 cases] 133
[Hunter's disease: genetic, clinical and biochemical study of a new family] 133
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease 133
A case of Kohlmeier-Degos disease with dramatic neurological involvment 133
A promoter deletion at the dystrophin gene in a severe muscular Duchenne-like phenotype 132
[Peripheral nervous system involvement in HCV-related mixed cryoglobulinemia] 131
Interessamento del sistema nervoso centrale nel Lupus Eritematoso Sistemico. Studio prospettico di 51 pazienti con esordio in età pediatrica 131
Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility. 130
A large kindred with autosomal dominant Parkinson's disease 129
[Cortical neuronal immaturity with agenesis of the major interhemispherical commissures and hypoplasia of the optico-pyramidal tracts in 3 children of the same family] 129
Associazione di distrofia muscolare congenita e malformazioni oculo-cerebrali : presentazione di un caso 129
LOPED Study: looking for an early diagnosis in a late onset Pompe Disease high-risk population” Journal of Neurology, Neurosurgery, and Psychiatry (submitted) 128
Reperti isto e citopatologici del tutto peculiari riscontrati in un caso familiare di sindrome della spina rigida 127
Foix-Chavany-Marie syndrome in a 17-year-old female with congenital cytomegalovirus infection. 126
Retrospective epidemiology of Duchenne muscular dystrophy in Molise 126
[Ophthalmoplegia plus: clinical, metabolic and histochemical study of a new case] 126
Towards genetic prevention of Adrenoleukodystrophy through early biochemical diagnosis of hemizygotes and heterozygotes in families at risk 126
Interessamento del Sistema Nervoso in corso di Lupus Eritematoso Sistemico 125
Symptomatic heterozygosity due to definite GAA mutations in late onset Pompe disease 125
Novel VCP mutations expand the mutational spectrum of frontotemporal dementia 125
Utilità della SPECT cerebrale in pazienti con Lupus Eritematoso Sistemico 123
Autonomic neuropathy in mixed cryoglobulinemia 122
La capacità rigenerativa del muscolo scheletrico danneggiato: studio sperimentale 122
Vacuolated PAS-positive lymphocytes as an hallmark of Pompe disease and other myopathies related to impaired autophagy. 122
Early posterior vitreous detachment is associated with LAMA5 dominant mutation 122
Familial amyloidotic polyneuropathy: description of an Italian kindred 121
Viral RNA in nerve tissues of patients with hepatitis C infection and peripheral neuropathy 121
Lupus Eritematoso Sistemico e Sistema Nervoso: studio clinico-strumentale 121
Animal model to study factors influencing regeneration and direct innervation or neurotization of skeletal muscle 120
Crioglobulinemia mista essenziale: prevalenza e caratteri della neuropatia periferica 119
A peculiar report of rare multifocal "ganglio-glioneurocytoma" 119
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy. 118
Histopathological heterogeneity and cytopathological similarity of findings in different muscles of two brothers affected by rigid spine syndrome 118
Increased cerebrospinal fluid levels of 3,3',5'-triiodothyronine in patients with Alzheimer's disease 117
Lecithin-cholesterol acyltransferase in brain: Does oxidative stress influence the 24-hydroxycholesterol esterification? 117
Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophy 116
Prostaglandin Synthesis Is Involved In The Induction Of MyoD Expression 116
Paternally inherited case of congenital DM1: Brain MRI and review of literature 115
Heidenhain variant of Creutzfeldt-Jakob disease with the co-occurrence of two differents types of prion proteins 115
Does abnormal neuronal excitability exist in myotonic dystrophy? II. Effects of the antiarrhythmic drug hydroquinidine on apathy and hypersomnia 115
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study 115
Mapping of a gene for Parkinson's disease to chromosome 4q21-q23 114
Hemicorea-hemiballismus in a patient with non-ketotic hyperglicaemia mimicking basal ganglia hemorrage: a case report 114
A review of anatomy, pathology and clinical data on the nigrostriatal system 113
Genotype-phenotype correlation analysis in a large italian family with late-onset glycogenosis II. 113
A proposito di un nuovo caso di neuropatia ipertrofica familiare a trasmissione dominante, ad esordio precoce e ad evoluzione benigna 112
Novel autophagic vacuolar myopathies: phenotype and genotype features 112
Diffuse glioblastoma resembling acute hemorrhagic leukoencephalitis 110
Is the accumulation of very long fatty acids in plasma sufficient test to be used for preclinical diagnosis and genetic prevention of adrenoleukodystrophy (ALD)? 109
Epidemiological study of inherited ataxias in Campania (a Region of Southern Italy) 109
Miopatia oculo-faringea: meccanismi fisiopatologici ed aspetti diagnostici e terapeutici. Caso Clinico 108
Peripheral nervous system involvement in Klippel-Trenaunay syndrome 108
Peripheral neuropathy in hepatitis-related mixed cryoglobulinemia: electrophysiologic follow-up study 107
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) 107
Totale 14.021
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Categoria #
all - tutte 98.723
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 98.723
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.501 0 0 0 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
2025/202612.258 351 262 526 687 1.056 7.390 623 304 574 266 138 81
2026/20271.529 81 357 955 136 0 0 0 0 0 0 0 0
Totale 28.214