CATALOGO DEI PRODOTTI DELLA RICERCA

CAVALLARO, Tiziana
 Distribuzione geografica
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Continente #
EU - Europa 5.000
NA - Nord America 4.731
AS - Asia 3.124
SA - Sud America 536
AF - Africa 64
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 2
Totale 13.469
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Nazione #
US - Stati Uniti d'America 4.657
RU - Federazione Russa 2.009
SG - Singapore 1.206
CN - Cina 1.085
GB - Regno Unito 932
BR - Brasile 447
SE - Svezia 382
FR - Francia 354
IT - Italia 347
HK - Hong Kong 310
DE - Germania 280
IE - Irlanda 249
FI - Finlandia 225
VN - Vietnam 205
KR - Corea 113
UA - Ucraina 65
CA - Canada 40
AR - Argentina 37
BE - Belgio 36
IN - India 36
ID - Indonesia 33
NL - Olanda 30
JP - Giappone 25
PL - Polonia 18
BD - Bangladesh 16
ES - Italia 15
TR - Turchia 15
ZA - Sudafrica 15
EC - Ecuador 14
MX - Messico 14
CL - Cile 11
LT - Lituania 11
MA - Marocco 10
AT - Austria 9
CO - Colombia 8
IR - Iran 8
SA - Arabia Saudita 8
AE - Emirati Arabi Uniti 7
AU - Australia 7
DZ - Algeria 7
EG - Egitto 7
IQ - Iraq 7
KZ - Kazakistan 7
PY - Paraguay 7
TG - Togo 7
RO - Romania 6
BJ - Benin 5
DO - Repubblica Dominicana 5
IL - Israele 5
PK - Pakistan 5
VE - Venezuela 5
UZ - Uzbekistan 4
AL - Albania 3
CH - Svizzera 3
DK - Danimarca 3
GR - Grecia 3
LB - Libano 3
NZ - Nuova Zelanda 3
PS - Palestinian Territory 3
SK - Slovacchia (Repubblica Slovacca) 3
TH - Thailandia 3
TN - Tunisia 3
AZ - Azerbaigian 2
BA - Bosnia-Erzegovina 2
BO - Bolivia 2
CZ - Repubblica Ceca 2
DM - Dominica 2
GT - Guatemala 2
HN - Honduras 2
JM - Giamaica 2
JO - Giordania 2
KG - Kirghizistan 2
LI - Liechtenstein 2
LK - Sri Lanka 2
LV - Lettonia 2
MU - Mauritius 2
MZ - Mozambico 2
NO - Norvegia 2
NP - Nepal 2
PE - Perù 2
SN - Senegal 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
HR - Croazia 1
IM - Isola di Man 1
KH - Cambogia 1
Totale 13.454
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Città #
Southend 798
Moscow 621
Dallas 600
Chandler 569
Jacksonville 553
Singapore 492
Woodbridge 383
Hong Kong 310
Ashburn 299
Dublin 247
Ann Arbor 237
Houston 230
Beijing 196
The Dalles 117
Wilmington 114
Lawrence 107
Princeton 107
New York 100
Verona 92
Jinan 88
Los Angeles 88
Nanjing 72
Ho Chi Minh City 62
Buffalo 57
Shenyang 57
Hebei 53
Helsinki 50
Columbus 48
Sindelfingen 48
Munich 47
Hanoi 43
Redmond 41
Tianjin 40
Changsha 37
Santa Clara 37
Redondo Beach 35
Nanchang 33
São Paulo 32
Ningbo 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
Tokyo 21
Turku 21
Taiyuan 20
Florence 19
Jiaxing 19
Kent 19
Montreal 18
Frankfurt am Main 17
Seattle 17
Taizhou 17
Belo Horizonte 16
Council Bluffs 16
Fairfield 16
Warsaw 15
London 14
Norwalk 14
Nuremberg 14
Bloomsbury 13
Brooklyn 12
Detroit 12
Dong Ket 12
San Francisco 12
Stockholm 12
Boardman 11
Denver 11
Lappeenranta 11
Clearwater 10
Orem 10
Rome 10
Kemerovo 9
Redwood City 9
Bologna 8
Falkenstein 8
Fuzhou 8
Haiphong 8
Paris 8
Phoenix 8
Atlanta 7
Biên Hòa 7
Chennai 7
Hải Dương 7
Johannesburg 7
Joinville 7
Lanzhou 7
Lomé 7
Poplar 7
Riva 7
Washington 7
Ankara 6
Totale 8.054
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Nome #
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. 215
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 200
Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. 196
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy 189
Brentuximab vedotin: axonal microtubule's Apollyon 186
A 58-year-old man with B-cell chronic lymphocytic leukemia and multiple strokes 179
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E 172
RFC1 AAGGG repeat expansion masquerading as Chronic Idiopathic Axonal Polyneuropathy 172
Congenital hypomyelination neuropathy with a novel mutation of PMP22 171
Alpha-synuclein seeds in olfactory mucosa and cerebrospinal fluid of patients with dementia with Lewy bodies 171
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 170
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease 168
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. 168
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family. 166
Convergent pathological and ultrasound features in hereditary syndromic and non‐syndromic minifascicular neuropathy related to DHH 166
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 163
Aberrant splicing in GJB1 and the relevance of 5′ UTR in CMTX1 pathogenesis 163
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 159
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 158
Endothelial adhesion molecule expression is unaltered in the peripheral nerve from patients with AIDS and distal sensory polyneuropathy 156
QTc Prolongation in Patients with Dementia and Mild Cognitive Impairment: Neuropsychological and Brain Imaging Correlations 155
Axonal neuropathy due to myelin protein zero mutation misdiagnosed as amyloid neuropathy 154
Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients. 154
Anxiety and depression in Charcot-Marie-Tooth disease: data from the Italian CMT national registry 153
X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32 152
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 147
A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B 147
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 147
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 147
CIDP, CMT1B, or CMT1B plus CIDP? 145
Sural nerve biopsy: current role and comparison with serum neurofilament light chain levels 144
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 143
Cytoskeletal pathology in ataxia-telangiectasia. 142
Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 Notch3 gene mutation 142
Atypical Alzheimer's disease: a case report. 142
Charcot-Marie-Tooth disease with giant axons:a clinicopathological and genetic study 138
Peripheral nerve enlargement on nerve ultrasound parallels neuropathological changes in adult-onset Krabbe disease 136
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy 133
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. 133
Polyneuropathy with anti-sulfatide and anti-MAG antibodies: Clinical, neurophysiological, pathological features and response to treatment. 133
Myelin uncompaction and axo-glial detachment in chronic ataxic neuropathy with monospecific IgM antibody to ganglioside GD1b 132
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial. 131
ATTRv amyloidosis Italian Registry: clinical and epidemiological data 129
Segmental conduction abnormalities and myelin thickenings in Val102/fs null mutation of MPZ gene 128
The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study 128
Sporadic hereditary neuropathies misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): pitfalls and red flags 128
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H. 124
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy 122
Pentraxin-3 and VEGF in POEMS syndrome: A 2-year longitudinal study. 122
Charcot-Marie-Tooth disease: new insights from skin biopsy 121
Hereditary neuropathies, a pathological perspective 121
Clinical and pathological findings in HCV-related peripheral neuropathies 119
Deoxysphingolipids as candidate biomarkers for a novel SPTLC1 mutation associated with HSAN-I 119
I quadri neuropatologici delle sindromi paraneoplastiche 118
Primary neurolymphomatosis as clinical onset of chronic lymphocytic leukemia 117
hATTR pathology: nerve biopsy results from italian referral centers 117
Charcot-Marie-Tooth type 2B: a new phenotype associated with a novel RAB7A mutation and inhibited EGFR degradation 114
Neuropathic pain in Charcot-Marie-Tooth Disease 111
Mechanisms of nerve damage in neuropathies associated with hematological diseases: lesson from nerve biopsies 108
Painful neuropathy vasculitis in 2 patients with long-standing human immunodeficiency virus-1 infection. 107
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 107
Focal lesions are a feature of chronic inflammatory demyelinating polyneuropathy (CIDP). 106
Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutation 105
Neuropatie immunitarie. 105
Infectious neuropathies 105
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 104
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause a MERFF syndrome. 103
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 101
Overexpression of ErbB2 and ErbB3 receptors in Schwann cells of patients with Charcot-Marie-tooth disease type 1A 98
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome 98
Human immunodeficiency virus-associated peripheral neuropathies 98
Correlation between clinical/neurophysiological findings and quality of life in Charcot-Marie-Tooth type 1A 98
Neuropathy in eosinophilic granulomatosis with polyangiitis: a comparison study of 24 cases with or without prior leukotriene antagonist exposure. 98
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling 97
Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: electrophysiological abnormalities and sural nerve biopsy 96
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 96
La patologia delle neuropatie periferiche. 96
Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias. 94
Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis. 93
Four novel cases of periaxin-related neuropathy and review of the literature. 92
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study. 90
Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area 90
Neurolymphomatosis, a rare manifestation of peripheral nerve involvement in lymphomas: suggestive features and diagnostic challenges 90
Clinical and pathology characterization of small nerve fiber neuro(no)pathy in cerebellar ataxia with neuropathy and vestibular areflexia syndrome 89
Nerve ultrasound findings differentiate Charcot-Marie-Tooth disease (CMT) 1A from other demyelinating CMTs 87
Clinical spectrum and frequency of Charcot-Marie-Tooth disease in Italy: Data from the National CMT Registry 86
Multineuropathy in a patient with HBV infection, polyarteritis nodosa and celiac disease. 86
Reply: Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot–Marie–Tooth disease 86
Clinico-pathological findings in a patient with progressive cerebellar ataxia, autoimmune polyendocrine syndrome, hepatocellular carcinoma and anti-GAD autoantibodies. 85
Neuropatie genetiche. 85
Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study 83
Diabetic neuropathy 83
Leprosy Neuropathy in a Non-Endemic Area: A Clinical and Pathological Study 82
PiB-PET detects transthyretin-related cerebral amyloid angiopathy 82
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 82
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life. 79
Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. 78
Nerve conduction velocity in CMT1A: what else can we tell? 77
Pharmacological treatment for familial amyloid neuropathy 77
Pharmacological treatment for familial amyloid polyneuropathy 76
Totale 12.454
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Categoria #
all - tutte 48.062
article - articoli 43.317
book - libri 0
conference - conferenze 2.220
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 2.525
Totale 96.124
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021461 0 0 0 0 0 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
2025/20264.284 484 469 558 1.091 1.633 49 0 0 0 0 0 0
Totale 13.616