IRIS
DI IORIO, Giuseppe
 Distribuzione geografica
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Continente #
EU - Europa 5.371
NA - Nord America 5.070
AS - Asia 928
SA - Sud America 26
AF - Africa 5
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 11.406
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Nazione #
US - Stati Uniti d'America 5.058
IE - Irlanda 1.585
UA - Ucraina 966
IT - Italia 913
GB - Regno Unito 670
DE - Germania 364
CN - Cina 317
SG - Singapore 317
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 11
PL - Polonia 10
HU - Ungheria 8
ES - Italia 7
HK - Hong Kong 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
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 11.406
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Città #
Dublin 1.585
Jacksonville 1.465
Chandler 694
Santa Clara 257
Princeton 255
Medford 198
Roxbury 186
Singapore 181
Ann Arbor 154
Boardman 121
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
Hong Kong 4
Kraków 4
Lanzhou 4
Paris 4
Porto 4
Pune 4
Sacile 4
Siegen 4
Tabriz 4
Turin 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
Totale 6.748
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Nome #
Le iperCKemie familiari 337
Risposta inabituale alla SLI in un paziente anziano: variante fotomioclonica o risposta fotoconvulsiva atipica? 195
Abnormal accumulation of tTGase products in muscle and erythrocytes of chorea-acanthocytosis patients 97
Synergistic Interplay between Curcumin and Polyphenol-Rich Foods in the Mediterranean Diet: Therapeutic Prospects for Neurofibromatosis 1 Patients 89
Modifications moleculaires au cours de la regeneration et reinnervation musculaires in vitro 87
Neuro-Behçet’s Disease presenting as an isolated progressive cognitive and behavioral syndrome 86
Symptomatic heterozygosity due to definite GAA mutation in late onset Pompe disease 84
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations 84
Identification and characterization of a novel member of the dystrobrevin gene family 73
Biochemical and morphological evidences supporting the hypothesis of a role of Tgase in the pathogeneisi of Chorea-Acanthocytosis 72
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 68
Interessamento del sistema nervoso centrale nel Lupus Eritematoso Sistemico. Studio prospettico di 51 pazienti con esordio in età pediatrica 68
Towards genetic prevention of Adrenoleukodystrophy through early biochemical diagnosis of hemizygotes and heterozygotes in families at risk 67
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 66
A coding variant in GRIN3A gene is associated with migraine in italian population. 66
Deterioramento cognitivo ed anticorpi linfocitotossici in pazienti con lupus eritematoso sistemico 65
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation 65
Foix-Chavany-Marie syndrome in a 17-year-old female with congenital cytomegalovirus infection. 64
The Contursi kindred, a large family with autosomal dominant Parkinson's disease: implications of clinical and molecular studies 64
Malattie dei nervi periferici 64
Myopathic changes in neurofibromatosis type 1 64
Prostaglandin Synthesis Is Involved In The Induction Of MyoD Expression 64
Lupus Eritematoso Sistemico e Sistema Nervoso: studio clinico-strumentale 64
Symptomatic heterozygosity due to definite GAA mutations in late onset Pompe disease 63
Biochemical and morphological evidences supporting the hypothesis of a role of TGase in the pathogenesis of chorea acanthocytosis (C-A) 63
19. Fitc-conjugated plant agglutinins as specific saccharide stains for fluorescence microscopy of normal and pathologic muscles: preliminary results 62
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 62
Retrospective epidemiology of Duchenne muscular dystrophy in Molise 61
A novel GBE1 mutation and features of polyglucosan bodies autophagy in adult polyglucosan body disease 61
Reperti isto e citopatologici del tutto peculiari riscontrati in un caso familiare di sindrome della spina rigida 61
A novel diagnostic method to detect truncated neurofibromin in Neurofibromatosis 1 61
Familial amyloidotic polyneuropathy: description of an Italian kindred 60
Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility. 60
Biochemical and morphological evidences supporting the hypothesis of a role of TGase in the pathogenesis of chorea acanthocytosis (C-A) 60
Adult polyglucosan body disease; novel homozygous missense mutation in the glycogen-branching enzyme gene in an italian patient. 60
Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophy 59
Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship. 59
La capacità rigenerativa del muscolo scheletrico danneggiato: studio sperimentale 59
Vacuolated PAS-positive lymphocytes as an hallmark of Pompe disease and other myopathies related to impaired autophagy. 59
A case of diffuse lupus encephalopathy successfully treated with high-dose intravenous methylprednisolone 58
Animal model to study factors influencing regeneration and direct innervation or neurotization of skeletal muscle 58
Crioglobulinemia mista essenziale: prevalenza e caratteri della neuropatia periferica 57
An unusual phenotype of familial motor and sensory neuropathy with morphological features of HMSN1 57
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients. 57
LOPED Study: looking for an early diagnosis in a late onset Pompe Disease high-risk population” Journal of Neurology, Neurosurgery, and Psychiatry (submitted) 56
Brain involvement in Systemic Lupus Erythematosus evaluated by single photon emission computed tomography and magnetic resonance imaging 56
A review of anatomy, pathology and clinical data on the nigrostriatal system 56
Utilità della SPECT cerebrale in pazienti con Lupus Eritematoso Sistemico 55
Lymphocytosis as a response biomarker of natalizumab therapeutic efficacy in multiple sclerosis 55
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy. 54
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 54
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. , : , 54
Epidemiological study of inherited ataxias in Campania (a Region of Southern Italy) 53
Increased cerebrospinal fluid levels of 3,3',5'-triiodothyronine in patients with Alzheimer's disease 53
A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis 53
Miopatia oculo-faringea: meccanismi fisiopatologici ed aspetti diagnostici e terapeutici. Caso Clinico 53
[Unusual histo-cytopathologic findings in a familial case of stiff spine syndrome] 53
Histopathological heterogeneity and cytopathological similarity of findings in different muscles of two brothers affected by rigid spine syndrome 53
A novel and rapid method of determining truncated neurofibromin 1 to rapidly screen for neurofibromatosis type 1 (NF1) 53
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 53
A case of progressive frontal lobe syndrome in a sporadic form of Cerebral Amyloid Angiopathy: A singular overlap with fronto-temporal dementia? 53
Genotype-phenotype correlation analysis in a large italian family with late-onset glycogenosis II. 53
Viral RNA in nerve tissues of patients with hepatitis C infection and peripheral neuropathy 52
A large kindred with Paramyotonia Congenita 52
SPET cerebrale in pazienti con elevati valori sierici di anticorpi anticardiolipina 52
Neurologia clinica. Diagnosi e terapia 52
Inhibition of prostaglandin synthesis reduces the induction of MyoD expression in rat soleus muscle 51
Paternally inherited case of congenital DM1: Brain MRI and review of literature 51
Semeiotica strumentale: indagini morfologiche 51
Studio epidemiologico delle eredo-atassie cerebellari in Campania. Napoli, 26-27 Ottobre 51
Interessamento del Sistema Nervoso in corso di Lupus Eritematoso Sistemico 50
Utilità di megadosi di corticosteroidi in un caso di encefalopatia lupica 50
The neural control of skeletal muscle sarcolemma: preliminary results of different approaches to the study of a possible control of membrane-bound glycoconjugates 50
Disease phenotype and genetic profile of a large italian family with late-onset glycogenosis II 50
A cluster of progranulin C157KfsX97 mutation in southern Italy- clinical characterization and genetic correlations 50
Peripheral neuropathy in hepatitis-related mixed cryoglobulinemia: electrophysiologic follow-up study 49
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease 49
SPET cerebrale in pazienti con elevati livelli sierici di anticorpi antocardiolipina 49
Hemicorea-hemiballismus in a patient with non-ketotic hyperglicaemia mimicking basal ganglia hemorrage: a case report 49
Studio neurofisiologico in 17 casi di crioglobulinemia. Rivista Italiana di EEG e Neurofisiologia Clinica : , 48
Does abnormal neuronal excitability exist in myotonic dystrophy? I. Effects of the antiarrhythmic drug hydroquinidine on slow saccadic eye movements 48
Is the accumulation of very long fatty acids in plasma sufficient test to be used for preclinical diagnosis and genetic prevention of adrenoleukodystrophy (ALD)? 48
Clinical features and outcome measures during 1 year enzyme replacement therapy in late onset GSD II 48
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 48
[Cortical neuronal immaturity with agenesis of the major interhemispherical commissures and hypoplasia of the optico-pyramidal tracts in 3 children of the same family] 48
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease 48
Toward genetic prevention of adrenoleukodystrophy trough early biochemical diagnosis of hemizygotes and heterozygotes in families at risk. 48
Malattie mono e plurisistemiche 48
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 48
Nonhereditary amyloidosis presenting with a syringomyelia-like syndrome 48
Biochemical changes of gray and white matter in Creutzfeldt-Jacob disease 48
Congenital fibre type disproportion and non-compaction cardiomyopathy associated with insulin resistance 48
Cognitive impairment in systemic lupus erythematosus: a follow-up study 47
A proposito di un nuovo caso di neuropatia ipertrofica familiare a trasmissione dominante, ad esordio precoce e ad evoluzione benigna 47
[Aicardi's syndrome. Report of 2 cases] 47
Does abnormal neuronal excitability exist in myotonic dystrophy? II. Effects of the antiarrhythmic drug hydroquinidine on apathy and hypersomnia 47
A somatic-nervous syndrome related to Marinesco-Sjogren's disease with some manifestations of Strumpell Lorrain's disease. Clinical report on five siblings 47
Le malattie extrapiramidali 47
Vertigini 47
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) 47
Totale 6.138
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Categoria #
all - tutte 48.040
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 48.040
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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
2022/20232.848 275 23 45 191 286 224 8 166 1.461 36 68 65
2023/20241.100 91 31 120 92 412 45 8 22 10 4 107 158
2024/2025462 17 45 53 55 292 0 0 0 0 0 0 0
Totale 11.701