IRIS
DI IORIO, Giuseppe
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 5.365
NA - Nord America 4.811
AS - Asia 910
SA - Sud America 26
AF - Africa 5
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 11.123
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 4.799
IE - Irlanda 1.588
UA - Ucraina 966
IT - Italia 905
GB - Regno Unito 670
DE - Germania 364
CN - Cina 317
SG - Singapore 303
FI - Finlandia 249
TR - Turchia 216
SE - Svezia 201
FR - Francia 170
GR - Grecia 160
BE - Belgio 30
KR - Corea 20
VN - Vietnam 16
IR - Iran 15
BR - Brasile 14
IN - India 11
NL - Olanda 10
PL - Polonia 10
HU - Ungheria 8
ES - Italia 7
CA - Canada 6
MX - Messico 6
CH - Svizzera 5
DK - Danimarca 4
EU - Europa 4
IL - Israele 4
RO - Romania 4
CL - Cile 3
CZ - Repubblica Ceca 3
EG - Egitto 3
HK - Hong Kong 3
RU - Federazione Russa 3
AR - Argentina 2
AT - Austria 2
CO - Colombia 2
DZ - Algeria 2
EC - Ecuador 2
JP - Giappone 2
AE - Emirati Arabi Uniti 1
AU - Australia 1
BG - Bulgaria 1
BO - Bolivia 1
ID - Indonesia 1
KZ - Kazakistan 1
LT - Lituania 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PE - Perù 1
PT - Portogallo 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
VE - Venezuela 1
Totale 11.123
Salva come PNG Salva come JPEG
Città #
Dublin 1.588
Jacksonville 1.465
Chandler 694
Princeton 255
Medford 198
Roxbury 186
Singapore 168
Ann Arbor 154
Boardman 122
Wilmington 120
Caserta 107
Ashburn 92
Beijing 92
Woodbridge 84
San Mateo 75
Cambridge 63
Des Moines 59
Nanjing 49
Mountain View 46
Orange 45
Düsseldorf 43
Rome 41
Bremen 35
Napoli 35
New York 34
Milan 31
Brussels 28
Kunming 22
Norwalk 22
Redwood City 21
Munich 20
Naples 20
Hefei 19
Los Angeles 19
Dearborn 18
Nanchang 18
Dong Ket 16
Helsinki 16
Bologna 14
Florence 14
Houston 14
Seoul 14
Auburn Hills 11
Hangzhou 11
Salerno 11
Verona 11
Jinan 10
Tianjin 10
Dallas 9
Barano D'ischia 8
Shanghai 8
Eboli 7
Ningbo 7
Seattle 7
Shenyang 7
Catania 6
Changsha 6
Falls Church 6
Ferrara 6
Genoa 6
Leawood 6
Palermo 6
Vicenza 6
Barcelona 5
Cagliari 5
Changchun 5
Lecce 5
Radomsko 5
St Louis 5
Taiyuan 5
Torino 5
Trento 5
Zanjan 5
Buscoldo 4
Cockeysville 4
Guangzhou 4
Kraków 4
Lanzhou 4
Paris 4
Porto 4
Pune 4
Sacile 4
Siegen 4
Tabriz 4
Ancona 3
Andover 3
Ariano Irpino 3
Avellino 3
Brno 3
Brusciano 3
Castel Mella 3
Dalmine 3
Duncan 3
Ercolano 3
Favara 3
Hebei 3
London 3
Marcianise 3
Mestre 3
Monfalcone 3
Totale 6.483
Salva come PNG Salva come JPEG
Nome #
Le iperCKemie familiari 336
Risposta inabituale alla SLI in un paziente anziano: variante fotomioclonica o risposta fotoconvulsiva atipica? 192
Abnormal accumulation of tTGase products in muscle and erythrocytes of chorea-acanthocytosis patients 96
Synergistic Interplay between Curcumin and Polyphenol-Rich Foods in the Mediterranean Diet: Therapeutic Prospects for Neurofibromatosis 1 Patients 88
Modifications moleculaires au cours de la regeneration et reinnervation musculaires in vitro 86
Neuro-Behçet’s Disease presenting as an isolated progressive cognitive and behavioral syndrome 85
Symptomatic heterozygosity due to definite GAA mutation in late onset Pompe disease 83
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations 80
Identification and characterization of a novel member of the dystrobrevin gene family 71
Biochemical and morphological evidences supporting the hypothesis of a role of Tgase in the pathogeneisi of Chorea-Acanthocytosis 71
Interessamento del sistema nervoso centrale nel Lupus Eritematoso Sistemico. Studio prospettico di 51 pazienti con esordio in età pediatrica 67
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 66
Towards genetic prevention of Adrenoleukodystrophy through early biochemical diagnosis of hemizygotes and heterozygotes in families at risk 66
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 65
A coding variant in GRIN3A gene is associated with migraine in italian population. 65
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation 64
Foix-Chavany-Marie syndrome in a 17-year-old female with congenital cytomegalovirus infection. 63
Deterioramento cognitivo ed anticorpi linfocitotossici in pazienti con lupus eritematoso sistemico 63
The Contursi kindred, a large family with autosomal dominant Parkinson's disease: implications of clinical and molecular studies 63
Malattie dei nervi periferici 63
Myopathic changes in neurofibromatosis type 1 63
Prostaglandin Synthesis Is Involved In The Induction Of MyoD Expression 63
Lupus Eritematoso Sistemico e Sistema Nervoso: studio clinico-strumentale 63
Symptomatic heterozygosity due to definite GAA mutations in late onset Pompe disease 62
Biochemical and morphological evidences supporting the hypothesis of a role of TGase in the pathogenesis of chorea acanthocytosis (C-A) 62
19. Fitc-conjugated plant agglutinins as specific saccharide stains for fluorescence microscopy of normal and pathologic muscles: preliminary results 61
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 61
Retrospective epidemiology of Duchenne muscular dystrophy in Molise 60
A novel GBE1 mutation and features of polyglucosan bodies autophagy in adult polyglucosan body disease 60
Reperti isto e citopatologici del tutto peculiari riscontrati in un caso familiare di sindrome della spina rigida 60
Familial amyloidotic polyneuropathy: description of an Italian kindred 59
Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility. 59
Biochemical and morphological evidences supporting the hypothesis of a role of TGase in the pathogenesis of chorea acanthocytosis (C-A) 59
Adult polyglucosan body disease; novel homozygous missense mutation in the glycogen-branching enzyme gene in an italian patient. 59
A novel diagnostic method to detect truncated neurofibromin in Neurofibromatosis 1 59
Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophy 58
Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship. 58
La capacità rigenerativa del muscolo scheletrico danneggiato: studio sperimentale 58
Vacuolated PAS-positive lymphocytes as an hallmark of Pompe disease and other myopathies related to impaired autophagy. 58
A case of diffuse lupus encephalopathy successfully treated with high-dose intravenous methylprednisolone 57
Animal model to study factors influencing regeneration and direct innervation or neurotization of skeletal muscle 57
Crioglobulinemia mista essenziale: prevalenza e caratteri della neuropatia periferica 56
An unusual phenotype of familial motor and sensory neuropathy with morphological features of HMSN1 56
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients. 56
LOPED Study: looking for an early diagnosis in a late onset Pompe Disease high-risk population” Journal of Neurology, Neurosurgery, and Psychiatry (submitted) 55
A review of anatomy, pathology and clinical data on the nigrostriatal system 55
Brain involvement in Systemic Lupus Erythematosus evaluated by single photon emission computed tomography and magnetic resonance imaging 54
Utilità della SPECT cerebrale in pazienti con Lupus Eritematoso Sistemico 54
Lymphocytosis as a response biomarker of natalizumab therapeutic efficacy in multiple sclerosis 54
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy. 53
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 53
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. , : , 53
Epidemiological study of inherited ataxias in Campania (a Region of Southern Italy) 52
Increased cerebrospinal fluid levels of 3,3',5'-triiodothyronine in patients with Alzheimer's disease 52
A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis 52
Miopatia oculo-faringea: meccanismi fisiopatologici ed aspetti diagnostici e terapeutici. Caso Clinico 52
[Unusual histo-cytopathologic findings in a familial case of stiff spine syndrome] 52
Viral RNA in nerve tissues of patients with hepatitis C infection and peripheral neuropathy 51
Histopathological heterogeneity and cytopathological similarity of findings in different muscles of two brothers affected by rigid spine syndrome 51
A novel and rapid method of determining truncated neurofibromin 1 to rapidly screen for neurofibromatosis type 1 (NF1) 51
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 51
A large kindred with Paramyotonia Congenita 51
A case of progressive frontal lobe syndrome in a sporadic form of Cerebral Amyloid Angiopathy: A singular overlap with fronto-temporal dementia? 51
SPET cerebrale in pazienti con elevati valori sierici di anticorpi anticardiolipina 51
Neurologia clinica. Diagnosi e terapia 51
Inhibition of prostaglandin synthesis reduces the induction of MyoD expression in rat soleus muscle 50
Paternally inherited case of congenital DM1: Brain MRI and review of literature 50
Semeiotica strumentale: indagini morfologiche 50
Studio epidemiologico delle eredo-atassie cerebellari in Campania. Napoli, 26-27 Ottobre 50
Genotype-phenotype correlation analysis in a large italian family with late-onset glycogenosis II. 50
Interessamento del Sistema Nervoso in corso di Lupus Eritematoso Sistemico 49
Utilità di megadosi di corticosteroidi in un caso di encefalopatia lupica 49
The neural control of skeletal muscle sarcolemma: preliminary results of different approaches to the study of a possible control of membrane-bound glycoconjugates 49
Disease phenotype and genetic profile of a large italian family with late-onset glycogenosis II 49
A cluster of progranulin C157KfsX97 mutation in southern Italy- clinical characterization and genetic correlations 49
Peripheral neuropathy in hepatitis-related mixed cryoglobulinemia: electrophysiologic follow-up study 48
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease 48
SPET cerebrale in pazienti con elevati livelli sierici di anticorpi antocardiolipina 48
Hemicorea-hemiballismus in a patient with non-ketotic hyperglicaemia mimicking basal ganglia hemorrage: a case report 48
Studio neurofisiologico in 17 casi di crioglobulinemia. Rivista Italiana di EEG e Neurofisiologia Clinica : , 47
Does abnormal neuronal excitability exist in myotonic dystrophy? I. Effects of the antiarrhythmic drug hydroquinidine on slow saccadic eye movements 47
Is the accumulation of very long fatty acids in plasma sufficient test to be used for preclinical diagnosis and genetic prevention of adrenoleukodystrophy (ALD)? 47
Clinical features and outcome measures during 1 year enzyme replacement therapy in late onset GSD II 47
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 47
[Cortical neuronal immaturity with agenesis of the major interhemispherical commissures and hypoplasia of the optico-pyramidal tracts in 3 children of the same family] 47
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease 47
Toward genetic prevention of adrenoleukodystrophy trough early biochemical diagnosis of hemizygotes and heterozygotes in families at risk. 47
Malattie mono e plurisistemiche 47
Nonhereditary amyloidosis presenting with a syringomyelia-like syndrome 47
Biochemical changes of gray and white matter in Creutzfeldt-Jacob disease 47
Congenital fibre type disproportion and non-compaction cardiomyopathy associated with insulin resistance 47
Cognitive impairment in systemic lupus erythematosus: a follow-up study 46
A proposito di un nuovo caso di neuropatia ipertrofica familiare a trasmissione dominante, ad esordio precoce e ad evoluzione benigna 46
[Aicardi's syndrome. Report of 2 cases] 46
Does abnormal neuronal excitability exist in myotonic dystrophy? II. Effects of the antiarrhythmic drug hydroquinidine on apathy and hypersomnia 46
A somatic-nervous syndrome related to Marinesco-Sjogren's disease with some manifestations of Strumpell Lorrain's disease. Clinical report on five siblings 46
Le malattie extrapiramidali 46
Vertigini 46
Rigenerazione e reinnervazione del muscolo scheletrico di ratto ischemizzato e, reversibilmente o irreversibilmente, denervato: osservazioni in istofluorescenza della densità e distribuzione dei recettori per ConA e WGA 46
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) 46
Totale 6.021
Salva come PNG Salva come JPEG
Categoria #
all - tutte 46.982
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 46.982
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020886 0 0 0 0 249 47 302 56 98 52 54 28
2020/20211.968 214 7 264 70 298 13 279 243 29 285 204 62
2021/20221.646 86 52 7 45 566 21 29 48 62 106 143 481
2022/20232.851 275 23 45 191 287 224 8 166 1.463 36 68 65
2023/20241.102 91 31 120 92 413 45 8 22 10 4 107 159
2024/2025174 17 45 53 56 3 0 0 0 0 0 0 0
Totale 11.418