CATALOGO DEI PRODOTTI DELLA RICERCA

CAVALLARO, Tiziana
 Distribuzione geografica
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Continente #
NA - Nord America 4.616
EU - Europa 3.941
AS - Asia 3.070
SA - Sud America 526
AF - Africa 63
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 2
Totale 12.230
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Nazione #
US - Stati Uniti d'America 4.545
SG - Singapore 1.183
CN - Cina 1.072
RU - Federazione Russa 968
GB - Regno Unito 931
BR - Brasile 445
SE - Svezia 379
FR - Francia 353
IT - Italia 346
HK - Hong Kong 310
DE - Germania 275
IE - Irlanda 249
FI - Finlandia 225
VN - Vietnam 204
KR - Corea 110
UA - Ucraina 64
CA - Canada 39
BE - Belgio 36
IN - India 35
AR - Argentina 34
ID - Indonesia 33
NL - Olanda 30
JP - Giappone 24
PL - Polonia 18
EC - Ecuador 14
ES - Italia 14
MX - Messico 14
ZA - Sudafrica 14
BD - Bangladesh 13
TR - Turchia 13
LT - Lituania 10
MA - Marocco 10
CL - Cile 9
AT - Austria 8
IR - Iran 8
SA - Arabia Saudita 8
AU - Australia 7
CO - Colombia 7
DZ - Algeria 7
EG - Egitto 7
IQ - Iraq 7
TG - Togo 7
AE - Emirati Arabi Uniti 6
KZ - Kazakistan 6
PY - Paraguay 6
RO - Romania 6
BJ - Benin 5
DO - Repubblica Dominicana 5
IL - Israele 5
PK - Pakistan 5
UZ - Uzbekistan 4
VE - Venezuela 4
CH - Svizzera 3
DK - Danimarca 3
GR - Grecia 3
NZ - Nuova Zelanda 3
SK - Slovacchia (Repubblica Slovacca) 3
TN - Tunisia 3
AL - Albania 2
AZ - Azerbaigian 2
BA - Bosnia-Erzegovina 2
BO - Bolivia 2
CZ - Repubblica Ceca 2
DM - Dominica 2
HN - Honduras 2
JO - Giordania 2
KG - Kirghizistan 2
LK - Sri Lanka 2
LV - Lettonia 2
MU - Mauritius 2
MZ - Mozambico 2
NO - Norvegia 2
NP - Nepal 2
PE - Perù 2
PS - Palestinian Territory 2
SN - Senegal 2
TH - Thailandia 2
UY - Uruguay 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AF - Afghanistan, Repubblica islamica di 1
AM - Armenia 1
AO - Angola 1
BB - Barbados 1
BG - Bulgaria 1
BY - Bielorussia 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
EE - Estonia 1
ET - Etiopia 1
EU - Europa 1
GE - Georgia 1
GF - Guiana Francese 1
GH - Ghana 1
GT - Guatemala 1
HR - Croazia 1
IM - Isola di Man 1
JM - Giamaica 1
KH - Cambogia 1
KN - Saint Kitts e Nevis 1
KW - Kuwait 1
Totale 12.217
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Città #
Southend 798
Dallas 600
Chandler 569
Jacksonville 553
Singapore 478
Woodbridge 383
Hong Kong 310
Ashburn 264
Dublin 247
Moscow 246
Ann Arbor 237
Houston 229
Beijing 196
Wilmington 114
Lawrence 107
Princeton 107
New York 97
Verona 92
Jinan 88
Los Angeles 83
The Dalles 73
Nanjing 72
Ho Chi Minh City 62
Shenyang 57
Buffalo 56
Hebei 53
Helsinki 50
Columbus 48
Sindelfingen 48
Munich 47
Hanoi 42
Redmond 41
Tianjin 40
Changsha 37
Redondo Beach 35
Santa Clara 34
Nanchang 33
Ningbo 31
São Paulo 31
Hangzhou 30
Brussels 29
Zhengzhou 29
Milan 27
Falls Church 26
Guangzhou 26
Seoul 25
Haikou 24
Jakarta 23
Lancaster 23
Chicago 22
Rio de Janeiro 21
Turku 21
Taiyuan 20
Tokyo 20
Florence 19
Jiaxing 19
Kent 19
Montreal 17
Taizhou 17
Belo Horizonte 16
Council Bluffs 16
Fairfield 16
Seattle 16
Warsaw 15
Frankfurt am Main 14
London 14
Norwalk 14
Bloomsbury 13
Detroit 12
Dong Ket 12
Nuremberg 12
San Francisco 12
Boardman 11
Brooklyn 11
Lappeenranta 11
Clearwater 10
Denver 10
Rome 10
Kemerovo 9
Redwood City 9
Stockholm 9
Bologna 8
Falkenstein 8
Fuzhou 8
Haiphong 8
Orem 8
Atlanta 7
Biên Hòa 7
Chennai 7
Hải Dương 7
Joinville 7
Lanzhou 7
Lomé 7
Paris 7
Phoenix 7
Riva 7
Washington 7
Boston 6
Cairo 6
Campinas 6
Totale 7.552
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Nome #
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. 199
Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. 181
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 180
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy 171
Brentuximab vedotin: axonal microtubule's Apollyon 162
A 58-year-old man with B-cell chronic lymphocytic leukemia and multiple strokes 159
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E 157
RFC1 AAGGG repeat expansion masquerading as Chronic Idiopathic Axonal Polyneuropathy 156
Clinical and pathological correlations in Charcot-Marie-Tooth neuropathy type 1A with the 17p11.2p12 duplication: a cross-sectional morphometric and immunohistochemical study in twenty cases 154
Congenital hypomyelination neuropathy with a novel mutation of PMP22 153
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. 153
Convergent pathological and ultrasound features in hereditary syndromic and non‐syndromic minifascicular neuropathy related to DHH 153
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family. 151
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease 150
Alpha-synuclein seeds in olfactory mucosa and cerebrospinal fluid of patients with dementia with Lewy bodies 150
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 147
Aberrant splicing in GJB1 and the relevance of 5′ UTR in CMTX1 pathogenesis 144
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 143
Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients. 143
X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32 141
Endothelial adhesion molecule expression is unaltered in the peripheral nerve from patients with AIDS and distal sensory polyneuropathy 141
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 140
Cytoskeletal pathology in ataxia-telangiectasia. 139
Axonal neuropathy due to myelin protein zero mutation misdiagnosed as amyloid neuropathy 139
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 136
QTc Prolongation in Patients with Dementia and Mild Cognitive Impairment: Neuropsychological and Brain Imaging Correlations 135
A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B 131
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 130
Are novel outcome measures for Charcot-Marie-Tooth disease sensitive to change? The 6-minute walk test and StepWatch™ Activity Monitor in a 12-month longitudinal study 130
Anxiety and depression in Charcot-Marie-Tooth disease: data from the Italian CMT national registry 127
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy 127
Sural nerve biopsy: current role and comparison with serum neurofilament light chain levels 127
Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 Notch3 gene mutation 126
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 125
CIDP, CMT1B, or CMT1B plus CIDP? 125
Segmental conduction abnormalities and myelin thickenings in Val102/fs null mutation of MPZ gene 124
Charcot-Marie-Tooth disease with giant axons:a clinicopathological and genetic study 124
Polyneuropathy with anti-sulfatide and anti-MAG antibodies: Clinical, neurophysiological, pathological features and response to treatment. 122
Atypical Alzheimer's disease: a case report. 122
Peripheral nerve enlargement on nerve ultrasound parallels neuropathological changes in adult-onset Krabbe disease 119
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy 118
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H. 118
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial. 118
Autosomal dominant limb girdle myopathy with ragged-red fibers and cardiomyopathy. A pedigree study by in vivo 31P-MR spectroscopy indicating a mutlisystem mitochondrial defect. 117
The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study 114
Sporadic hereditary neuropathies misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): pitfalls and red flags 114
Myelin uncompaction and axo-glial detachment in chronic ataxic neuropathy with monospecific IgM antibody to ganglioside GD1b 113
Clinical and pathological findings in HCV-related peripheral neuropathies 112
ATTRv amyloidosis Italian Registry: clinical and epidemiological data 112
I quadri neuropatologici delle sindromi paraneoplastiche 111
Pentraxin-3 and VEGF in POEMS syndrome: A 2-year longitudinal study. 109
Charcot-Marie-Tooth disease: new insights from skin biopsy 105
Deoxysphingolipids as candidate biomarkers for a novel SPTLC1 mutation associated with HSAN-I 105
Painful neuropathy vasculitis in 2 patients with long-standing human immunodeficiency virus-1 infection. 104
Hereditary neuropathies, a pathological perspective 104
Primary neurolymphomatosis as clinical onset of chronic lymphocytic leukemia 103
Charcot-Marie-Tooth type 2B: a new phenotype associated with a novel RAB7A mutation and inhibited EGFR degradation 103
hATTR pathology: nerve biopsy results from italian referral centers 102
Focal lesions are a feature of chronic inflammatory demyelinating polyneuropathy (CIDP). 101
Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutation 101
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 100
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause a MERFF syndrome. 98
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 96
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 95
Neuropathic pain in Charcot-Marie-Tooth Disease 95
Overexpression of ErbB2 and ErbB3 receptors in Schwann cells of patients with Charcot-Marie-tooth disease type 1A 94
Correlation between clinical/neurophysiological findings and quality of life in Charcot-Marie-Tooth type 1A 94
Neuropatie immunitarie. 94
Neuropathy in eosinophilic granulomatosis with polyangiitis: a comparison study of 24 cases with or without prior leukotriene antagonist exposure. 94
Infectious neuropathies 94
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling 94
Human immunodeficiency virus-associated peripheral neuropathies 93
Mechanisms of nerve damage in neuropathies associated with hematological diseases: lesson from nerve biopsies 93
Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: electrophysiological abnormalities and sural nerve biopsy 92
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome 92
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 92
La patologia delle neuropatie periferiche. 90
Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias. 88
Four novel cases of periaxin-related neuropathy and review of the literature. 88
Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis. 87
Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area 86
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study. 85
Nerve ultrasound findings differentiate Charcot-Marie-Tooth disease (CMT) 1A from other demyelinating CMTs 83
Clinico-pathological findings in a patient with progressive cerebellar ataxia, autoimmune polyendocrine syndrome, hepatocellular carcinoma and anti-GAD autoantibodies. 82
Multineuropathy in a patient with HBV infection, polyarteritis nodosa and celiac disease. 81
Reply: Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot–Marie–Tooth disease 80
Neuropatie genetiche. 79
Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study 78
Diabetic neuropathy 78
PiB-PET detects transthyretin-related cerebral amyloid angiopathy 77
Novel familial variant of the Desert Hedgehog Gene: clinical findings in two sisters with 46,XY gonadal dysgenesis or 46,XX karyotype and literature review 77
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life. 74
Neurolymphomatosis, a rare manifestation of peripheral nerve involvement in lymphomas: suggestive features and diagnostic challenges 73
Clinical spectrum and frequency of Charcot-Marie-Tooth disease in Italy: Data from the National CMT Registry 72
Clinical and pathology characterization of small nerve fiber neuro(no)pathy in cerebellar ataxia with neuropathy and vestibular areflexia syndrome 72
Hereditary neuropathy with liability to pressure palsies: Electrophysiological and genetic study of a family with carpal tunnel syndrome as only clinical manifestation 72
Nerve conduction velocity in CMT1A: what else can we tell? 72
Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. 72
Pharmacological treatment for familial amyloid neuropathy 71
Progressive brachial plexus enlargement in hereditary transthyretin amyloidosis 71
Totale 11.318
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Categoria #
all - tutte 45.968
article - articoli 41.447
book - libri 0
conference - conferenze 2.103
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 2.418
Totale 91.936
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021542 0 0 0 0 81 90 44 72 58 24 133 40
2021/2022995 90 328 9 96 31 68 11 47 42 26 78 169
2022/20231.690 125 160 178 311 138 403 26 113 174 11 32 19
2023/2024756 36 55 57 84 93 136 28 40 14 47 104 62
2024/20252.363 146 153 75 389 119 65 108 94 373 180 185 476
2025/20263.045 484 469 558 1.091 443 0 0 0 0 0 0 0
Totale 12.377