IRIS
PISCIOTTA, CHIARA
 Distribuzione geografica
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Continente #
NA - Nord America 751
EU - Europa 420
AS - Asia 233
AF - Africa 23
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
SA - Sud America 1
Totale 1.430
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Nazione #
US - Stati Uniti d'America 723
IT - Italia 224
SG - Singapore 108
CN - Cina 106
NL - Olanda 64
DE - Germania 33
FI - Finlandia 29
CA - Canada 28
IE - Irlanda 26
CI - Costa d'Avorio 23
GB - Regno Unito 12
SE - Svezia 11
UA - Ucraina 11
VN - Vietnam 8
BE - Belgio 5
FR - Francia 4
IR - Iran 4
TR - Turchia 3
HK - Hong Kong 2
IN - India 2
AU - Australia 1
BG - Bulgaria 1
BR - Brasile 1
EU - Europa 1
Totale 1.430
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Città #
Chandler 162
Singapore 92
Amsterdam 60
Naples 45
Santa Clara 40
Napoli 39
Millbury 36
Ashburn 31
Beijing 31
Nanjing 30
Princeton 30
Ottawa 28
Boston 23
Des Moines 22
Seattle 21
Wilmington 14
Jacksonville 13
Nanchang 11
Dong Ket 8
Tianjin 8
Buccinasco 7
Baronissi 6
Dearborn 6
Lawrence 6
Monmouth Junction 6
Dallas 5
Wuhan 5
Ardabil 4
Hebei 4
Redwood City 4
Shenyang 4
Waanrode 4
Woodbridge 4
Boardman 3
Changsha 3
Kronberg 3
Milan 3
Nocera Inferiore 3
Seregno 3
Bolzano 2
Campagna 2
Carrù 2
Cattolica 2
Cinisello Balsamo 2
Fort Worth 2
Guangzhou 2
Hong Kong 2
Houston 2
Laguna Woods 2
New York 2
Palermo 2
Parma 2
Poggiomarino 2
Rome 2
Rozzano 2
Salerno 2
Shanghai 2
Ankara 1
Ann Arbor 1
Arzano 1
Atella 1
Atena Lucana 1
Augusta 1
Avellino 1
Benevento 1
Böblingen 1
Caposele 1
Carinaro 1
Castellammare Di Stabia 1
Chengdu 1
Elk Grove Village 1
Essen 1
Fairfield 1
Falls Church 1
Feltham 1
Genoa 1
Genova 1
Hangzhou 1
Hefei 1
Helsinki 1
Jiaxing 1
Kunming 1
Lake Saint Louis 1
Leawood 1
Los Angeles 1
Mereto Di Tomba 1
Mumbai 1
Munich 1
Oderzo 1
Orta di Atella 1
Pompei 1
Pune 1
Quartu Sant'elena 1
San Mateo 1
San Pietro 1
Shenzhen 1
Sofia 1
Stockholm 1
Sydney 1
Torino 1
Totale 906
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Nome #
Novel mutations in dystonin provide clues to the pathomechanisms of HSAN-VI 97
Small nerve fiber involvement in CMT1A 73
Motor performance deterioration accelerates after 50 years of age in Charcot-Marie-Tooth type 1a patients 69
Electrophysiological characterization of adult-onset Niemann?Pick type C disease 64
Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population 51
Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy 48
Electrophysiological characterisation in hereditary spastic paraplegia type 5. 48
Early onset Charcot-Marie-Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2-related neuropathy 48
A case of congenital cataracts, facial dysmorphisms, neuropathy, and hyperkinetic movement disorder 46
Postural instability in Charcot-Marie-Tooth 1A disease 46
Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population 46
Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCs 44
Short-latency afferent inhibition in patients with Parkinson's disease and freezing of gait 43
Expanding the spectrum of genes responsible for hereditary motor neuropathies 42
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability. 41
Hirayama's disease: an Italian single center experience and review of the literature 41
Charcot-Marie-Tooth disease: New insights from skin biopsy 39
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial 39
A novel autosomal dominant GDAP1 mutation in an Italian CMT2 family. 38
Somatosensory Temporal Discrimination Threshold Is Increased in Patients with Cerebellar Atrophy. 38
Electrophysiological comparison between males and females in HNPP. 37
GDAP1 mutations in Italian axonal Charcot-Marie-Tooth patients: Phenotypic features and clinical course 37
Thermosensitive hereditary neuropathy with liability to pressure palsy. 35
Autonomic nervous system involvement in a new CMT2B family. 35
A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs) 34
Nerve conduction velocity in CMT1A: what else can we tell? 32
Reliability of clinical outcome measures in Charcot-Marie-Tooth disease. 31
A novel family with axonal Charcot-Marie-Tooth disease caused by a mutation in the EGR2 gene 28
Two families with novel PMP22 point mutations: genotype-phenotype correlation. 26
Nine-year case history of monofocal motor neuropathy. 26
PMP22 messenger RNA levels in skin biopsies: testing the effectiveness of a Charcot-Marie-Tooth 1A biomarker 26
A new Italian FHM2 family: Clinical aspects and functional analysis of the disease-associated mutation 25
Influence of comorbidities on the phenotype of patients affected by Charcot?Marie?Tooth neuropathy type 1A 25
Is overwork weakness relevant in Charcot-Marie-Tooth disease? 25
Phenotypic spectrum of myelin protein zero-related neuropathies: a large cohort study from five mutation clusters across Italy 24
Different nerve ultrasound patterns in charcot-marie-tooth types and hereditary neuropathy with liability to pressure palsies 24
Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease 19
Pregnancy in Charcot-Marie-Tooth disease Data from the Italian CMT national registry 16
Anxiety and depression in Charcot-Marie-Tooth disease: data from the Italian CMT national registry 12
Mutations in MYO9B are associated with CMT2 neuropathies and isolated optic atrophy 10
Totale 1.528
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Categoria #
all - tutte 6.646
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 6.646
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202091 0 0 0 0 3 10 12 1 4 26 22 13
2020/202192 12 4 6 3 9 16 3 3 3 4 21 8
2021/2022194 3 0 4 0 1 1 0 2 32 29 31 91
2022/2023376 41 45 2 33 38 40 1 31 57 62 19 7
2023/2024231 12 38 53 8 4 26 3 44 1 0 31 11
2024/2025183 56 48 16 10 53 0 0 0 0 0 0 0
Totale 1.528