IRIS
DI IORIO, Giuseppe
 Distribuzione geografica
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Continente #
EU - Europa 5.271
NA - Nord America 4.786
AS - Asia 594
SA - Sud America 21
AF - Africa 5
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 10.683
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Nazione #
US - Stati Uniti d'America 4.777
IE - Irlanda 1.588
UA - Ucraina 966
IT - Italia 852
GB - Regno Unito 670
DE - Germania 340
CN - Cina 309
FI - Finlandia 240
TR - Turchia 216
SE - Svezia 201
FR - Francia 170
GR - Grecia 160
BE - Belgio 30
VN - Vietnam 16
IR - Iran 15
IN - India 11
NL - Olanda 10
PL - Polonia 10
SG - Singapore 10
BR - Brasile 9
HU - Ungheria 8
ES - Italia 7
KR - Corea 7
CA - Canada 6
CH - Svizzera 5
EU - Europa 4
CL - Cile 3
EG - Egitto 3
HK - Hong Kong 3
MX - Messico 3
RU - Federazione Russa 3
AR - Argentina 2
AT - Austria 2
CO - Colombia 2
DK - Danimarca 2
DZ - Algeria 2
EC - Ecuador 2
IL - Israele 2
JP - Giappone 2
RO - Romania 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
SK - Slovacchia (Repubblica Slovacca) 1
VE - Venezuela 1
Totale 10.683
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Città #
Dublin 1.588
Jacksonville 1.465
Chandler 694
Princeton 255
Medford 198
Roxbury 186
Ann Arbor 154
Wilmington 120
Boardman 116
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 37
Bremen 35
Napoli 35
New York 34
Brussels 28
Milan 27
Kunming 22
Norwalk 22
Redwood City 21
Hefei 19
Dearborn 18
Nanchang 18
Dong Ket 16
Los Angeles 15
Bologna 14
Houston 14
Florence 13
Naples 13
Auburn Hills 11
Hangzhou 11
Salerno 11
Verona 11
Jinan 10
Tianjin 10
Barano D'ischia 8
Shanghai 8
Eboli 7
Helsinki 7
Ningbo 7
Seattle 7
Shenyang 7
Catania 6
Changsha 6
Falls Church 6
Ferrara 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
Brusciano 3
Castel Mella 3
Dalmine 3
Duncan 3
Ercolano 3
Hebei 3
London 3
Marcianise 3
Mestre 3
Monfalcone 3
Orvieto 3
Rimini 3
Santa Maria a Vico 3
Staffolo 3
Taizhou 3
Venice 3
Agrate Brianza 2
Totale 6.245
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Nome #
Le iperCKemie familiari 334
Risposta inabituale alla SLI in un paziente anziano: variante fotomioclonica o risposta fotoconvulsiva atipica? 147
Abnormal accumulation of tTGase products in muscle and erythrocytes of chorea-acanthocytosis patients 89
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 84
Neuro-Behçet’s Disease presenting as an isolated progressive cognitive and behavioral syndrome 84
Symptomatic heterozygosity due to definite GAA mutation in late onset Pompe disease 82
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations 75
Identification and characterization of a novel member of the dystrobrevin gene family 69
Biochemical and morphological evidences supporting the hypothesis of a role of Tgase in the pathogeneisi of Chorea-Acanthocytosis 68
Towards genetic prevention of Adrenoleukodystrophy through early biochemical diagnosis of hemizygotes and heterozygotes in families at risk 65
Interessamento del sistema nervoso centrale nel Lupus Eritematoso Sistemico. Studio prospettico di 51 pazienti con esordio in età pediatrica 64
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 63
Foix-Chavany-Marie syndrome in a 17-year-old female with congenital cytomegalovirus infection. 62
Malattie dei nervi periferici 62
Deterioramento cognitivo ed anticorpi linfocitotossici in pazienti con lupus eritematoso sistemico 61
Symptomatic heterozygosity due to definite GAA mutations in late onset Pompe disease 61
Myopathic changes in neurofibromatosis type 1 61
Prostaglandin Synthesis Is Involved In The Induction Of MyoD Expression 61
19. Fitc-conjugated plant agglutinins as specific saccharide stains for fluorescence microscopy of normal and pathologic muscles: preliminary results 60
A coding variant in GRIN3A gene is associated with migraine in italian population. 60
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 60
Biochemical and morphological evidences supporting the hypothesis of a role of TGase in the pathogenesis of chorea acanthocytosis (C-A) 60
Reperti isto e citopatologici del tutto peculiari riscontrati in un caso familiare di sindrome della spina rigida 59
Lupus Eritematoso Sistemico e Sistema Nervoso: studio clinico-strumentale 59
Familial amyloidotic polyneuropathy: description of an Italian kindred 58
Retrospective epidemiology of Duchenne muscular dystrophy in Molise 58
A novel GBE1 mutation and features of polyglucosan bodies autophagy in adult polyglucosan body disease 58
Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility. 58
The Contursi kindred, a large family with autosomal dominant Parkinson's disease: implications of clinical and molecular studies 58
Adult polyglucosan body disease; novel homozygous missense mutation in the glycogen-branching enzyme gene in an italian patient. 58
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation 58
La capacità rigenerativa del muscolo scheletrico danneggiato: studio sperimentale 57
Vacuolated PAS-positive lymphocytes as an hallmark of Pompe disease and other myopathies related to impaired autophagy. 57
Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophy 56
Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship. 56
Biochemical and morphological evidences supporting the hypothesis of a role of TGase in the pathogenesis of chorea acanthocytosis (C-A) 56
Animal model to study factors influencing regeneration and direct innervation or neurotization of skeletal muscle 56
A case of diffuse lupus encephalopathy successfully treated with high-dose intravenous methylprednisolone 55
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 55
Crioglobulinemia mista essenziale: prevalenza e caratteri della neuropatia periferica 55
A novel diagnostic method to detect truncated neurofibromin in Neurofibromatosis 1 55
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients. 55
LOPED Study: looking for an early diagnosis in a late onset Pompe Disease high-risk population” Journal of Neurology, Neurosurgery, and Psychiatry (submitted) 54
A review of anatomy, pathology and clinical data on the nigrostriatal system 53
Brain involvement in Systemic Lupus Erythematosus evaluated by single photon emission computed tomography and magnetic resonance imaging 52
An unusual phenotype of familial motor and sensory neuropathy with morphological features of HMSN1 52
Utilità della SPECT cerebrale in pazienti con Lupus Eritematoso Sistemico 52
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy. 51
Increased cerebrospinal fluid levels of 3,3',5'-triiodothyronine in patients with Alzheimer's disease 51
Miopatia oculo-faringea: meccanismi fisiopatologici ed aspetti diagnostici e terapeutici. Caso Clinico 51
Lymphocytosis as a response biomarker of natalizumab therapeutic efficacy in multiple sclerosis 51
Epidemiological study of inherited ataxias in Campania (a Region of Southern Italy) 50
Viral RNA in nerve tissues of patients with hepatitis C infection and peripheral neuropathy 50
A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis 50
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 50
Semeiotica strumentale: indagini morfologiche 50
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. , : , 50
A large kindred with Paramyotonia Congenita 50
SPET cerebrale in pazienti con elevati valori sierici di anticorpi anticardiolipina 50
Neurologia clinica. Diagnosi e terapia 50
Inhibition of prostaglandin synthesis reduces the induction of MyoD expression in rat soleus muscle 49
Paternally inherited case of congenital DM1: Brain MRI and review of literature 49
A novel and rapid method of determining truncated neurofibromin 1 to rapidly screen for neurofibromatosis type 1 (NF1) 49
Studio epidemiologico delle eredo-atassie cerebellari in Campania. Napoli, 26-27 Ottobre 49
Genotype-phenotype correlation analysis in a large italian family with late-onset glycogenosis II. 49
Disease phenotype and genetic profile of a large italian family with late-onset glycogenosis II 48
Peripheral neuropathy in hepatitis-related mixed cryoglobulinemia: electrophysiologic follow-up study 47
Interessamento del Sistema Nervoso in corso di Lupus Eritematoso Sistemico 47
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease 47
Utilità di megadosi di corticosteroidi in un caso di encefalopatia lupica 47
The neural control of skeletal muscle sarcolemma: preliminary results of different approaches to the study of a possible control of membrane-bound glycoconjugates 47
A case of progressive frontal lobe syndrome in a sporadic form of Cerebral Amyloid Angiopathy: A singular overlap with fronto-temporal dementia? 47
SPET cerebrale in pazienti con elevati livelli sierici di anticorpi antocardiolipina 47
Hemicorea-hemiballismus in a patient with non-ketotic hyperglicaemia mimicking basal ganglia hemorrage: a case report 47
Studio neurofisiologico in 17 casi di crioglobulinemia. Rivista Italiana di EEG e Neurofisiologia Clinica : , 46
Does abnormal neuronal excitability exist in myotonic dystrophy? I. Effects of the antiarrhythmic drug hydroquinidine on slow saccadic eye movements 46
Is the accumulation of very long fatty acids in plasma sufficient test to be used for preclinical diagnosis and genetic prevention of adrenoleukodystrophy (ALD)? 46
Clinical features and outcome measures during 1 year enzyme replacement therapy in late onset GSD II 46
A proposito di un nuovo caso di neuropatia ipertrofica familiare a trasmissione dominante, ad esordio precoce e ad evoluzione benigna 46
[Cortical neuronal immaturity with agenesis of the major interhemispherical commissures and hypoplasia of the optico-pyramidal tracts in 3 children of the same family] 46
Toward genetic prevention of adrenoleukodystrophy trough early biochemical diagnosis of hemizygotes and heterozygotes in families at risk. 46
Malattie mono e plurisistemiche 46
Biochemical changes of gray and white matter in Creutzfeldt-Jacob disease 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
Congenital fibre type disproportion and non-compaction cardiomyopathy associated with insulin resistance 46
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 45
Does abnormal neuronal excitability exist in myotonic dystrophy? II. Effects of the antiarrhythmic drug hydroquinidine on apathy and hypersomnia 45
[Unusual histo-cytopathologic findings in a familial case of stiff spine syndrome] 45
A somatic-nervous syndrome related to Marinesco-Sjogren's disease with some manifestations of Strumpell Lorrain's disease. Clinical report on five siblings 45
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease 45
Le malattie extrapiramidali 45
Vertigini 45
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 45
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 45
Nonhereditary amyloidosis presenting with a syringomyelia-like syndrome 45
A cluster of progranulin C157KfsX97 mutation in southern Italy- clinical characterization and genetic correlations 45
Cognitive impairment in systemic lupus erythematosus: a follow-up study 44
Autonomic neuropathy in mixed cryoglobulinemia 44
Histopathological heterogeneity and cytopathological similarity of findings in different muscles of two brothers affected by rigid spine syndrome 44
Totale 5.776
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Categoria #
all - tutte 37.792
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 37.792
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201942 0 0 0 0 0 0 0 0 0 0 15 27
2019/20201.499 278 273 38 24 249 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
2023/2024836 91 31 120 92 413 45 8 22 10 4 0 0
Totale 10.978