CATALOGO DEI PRODOTTI DELLA RICERCA

CAVALLARO, Tiziana
 Distribuzione geografica
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Continente #
NA - Nord America 4.357
EU - Europa 3.241
AS - Asia 2.709
SA - Sud America 426
AF - Africa 50
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 2
Totale 10.797
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Nazione #
US - Stati Uniti d'America 4.308
SG - Singapore 1.040
CN - Cina 986
GB - Regno Unito 915
BR - Brasile 376
SE - Svezia 375
FR - Francia 351
IT - Italia 341
RU - Federazione Russa 319
HK - Hong Kong 310
DE - Germania 271
IE - Irlanda 249
FI - Finlandia 225
VN - Vietnam 109
KR - Corea 102
UA - Ucraina 63
BE - Belgio 36
IN - India 30
NL - Olanda 29
ID - Indonesia 26
CA - Canada 24
AR - Argentina 18
JP - Giappone 17
EC - Ecuador 11
ES - Italia 11
MA - Marocco 10
MX - Messico 10
TR - Turchia 10
BD - Bangladesh 9
ZA - Sudafrica 9
AT - Austria 8
CL - Cile 8
IR - Iran 8
SA - Arabia Saudita 8
AU - Australia 7
EG - Egitto 7
LT - Lituania 7
PL - Polonia 7
TG - Togo 7
AE - Emirati Arabi Uniti 6
IQ - Iraq 6
RO - Romania 6
DZ - Algeria 5
IL - Israele 5
KZ - Kazakistan 5
PK - Pakistan 5
DO - Repubblica Dominicana 4
UZ - Uzbekistan 4
CH - Svizzera 3
CO - Colombia 3
DK - Danimarca 3
GR - Grecia 3
NZ - Nuova Zelanda 3
PY - Paraguay 3
SK - Slovacchia (Repubblica Slovacca) 3
AL - Albania 2
AZ - Azerbaigian 2
BA - Bosnia-Erzegovina 2
CZ - Repubblica Ceca 2
DM - Dominica 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
PS - Palestinian Territory 2
SN - Senegal 2
TH - Thailandia 2
TN - Tunisia 2
UY - Uruguay 2
VE - Venezuela 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AF - Afghanistan, Repubblica islamica di 1
AM - Armenia 1
AO - Angola 1
BB - Barbados 1
BO - Bolivia 1
BY - Bielorussia 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
EE - Estonia 1
ET - Etiopia 1
EU - Europa 1
GF - Guiana Francese 1
GH - Ghana 1
HN - Honduras 1
HR - Croazia 1
IM - Isola di Man 1
JM - Giamaica 1
KH - Cambogia 1
KN - Saint Kitts e Nevis 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LC - Santa Lucia 1
MD - Moldavia 1
ME - Montenegro 1
OM - Oman 1
Totale 10.788
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Città #
Southend 798
Dallas 600
Chandler 569
Jacksonville 553
Singapore 472
Woodbridge 383
Hong Kong 310
Dublin 247
Ann Arbor 237
Houston 224
Ashburn 182
Beijing 166
Wilmington 114
Lawrence 107
Princeton 107
Verona 92
Jinan 88
New York 83
The Dalles 73
Nanjing 72
Los Angeles 58
Shenyang 57
Buffalo 54
Hebei 53
Helsinki 50
Columbus 48
Sindelfingen 48
Munich 47
Redmond 41
Tianjin 38
Changsha 37
Nanchang 33
Santa Clara 33
Ningbo 31
Redondo Beach 31
Hangzhou 30
Ho Chi Minh City 30
Brussels 29
Zhengzhou 29
Milan 27
Falls Church 26
Guangzhou 26
Seoul 25
Haikou 24
Lancaster 23
São Paulo 23
Jakarta 22
Turku 21
Taiyuan 20
Chicago 19
Florence 19
Jiaxing 19
Kent 19
Hanoi 18
Taizhou 17
Belo Horizonte 16
Council Bluffs 16
Fairfield 16
Rio de Janeiro 15
Frankfurt am Main 14
Norwalk 14
Seattle 14
Bloomsbury 13
Tokyo 13
Detroit 12
Dong Ket 12
Nuremberg 12
Boardman 11
Lappeenranta 11
Moscow 11
San Francisco 11
Clearwater 10
Rome 10
Brooklyn 9
Kemerovo 9
Redwood City 9
Bologna 8
Fuzhou 8
Lanzhou 7
Lomé 7
Montreal 7
Paris 7
Riva 7
Washington 7
Cairo 6
Joinville 6
London 6
San Diego 6
Waanrode 6
Campinas 5
Curitiba 5
Dongguan 5
Gorizia 5
Haiphong 5
Midelt 5
New Delhi 5
Phoenix 5
Ponta Grossa 5
Quito 5
Stockholm 5
Totale 7.003
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Nome #
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. 175
Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. 165
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy 156
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 149
RFC1 AAGGG repeat expansion masquerading as Chronic Idiopathic Axonal Polyneuropathy 145
Congenital hypomyelination neuropathy with a novel mutation of PMP22 140
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family. 138
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. 137
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E 136
Cytoskeletal pathology in ataxia-telangiectasia. 134
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease 133
A 58-year-old man with B-cell chronic lymphocytic leukemia and multiple strokes 132
X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32 130
Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients. 128
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 127
Convergent pathological and ultrasound features in hereditary syndromic and non‐syndromic minifascicular neuropathy related to DHH 127
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 126
Endothelial adhesion molecule expression is unaltered in the peripheral nerve from patients with AIDS and distal sensory polyneuropathy 125
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 124
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 124
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 123
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy 122
Brentuximab vedotin: axonal microtubule's Apollyon 122
Alpha-synuclein seeds in olfactory mucosa and cerebrospinal fluid of patients with dementia with Lewy bodies 122
Segmental conduction abnormalities and myelin thickenings in Val102/fs null mutation of MPZ gene 119
A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B 118
Axonal neuropathy due to myelin protein zero mutation misdiagnosed as amyloid neuropathy 118
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 116
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 116
Aberrant splicing in GJB1 and the relevance of 5′ UTR in CMTX1 pathogenesis 115
Charcot-Marie-Tooth disease with giant axons:a clinicopathological and genetic study 113
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy 112
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H. 112
Anxiety and depression in Charcot-Marie-Tooth disease: data from the Italian CMT national registry 111
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 111
CIDP, CMT1B, or CMT1B plus CIDP? 111
Atypical Alzheimer's disease: a case report. 109
Polyneuropathy with anti-sulfatide and anti-MAG antibodies: Clinical, neurophysiological, pathological features and response to treatment. 108
Sural nerve biopsy: current role and comparison with serum neurofilament light chain levels 106
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial. 105
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. 104
Clinical and pathological findings in HCV-related peripheral neuropathies 103
I quadri neuropatologici delle sindromi paraneoplastiche 103
Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 Notch3 gene mutation 102
Myelin uncompaction and axo-glial detachment in chronic ataxic neuropathy with monospecific IgM antibody to ganglioside GD1b 100
The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study 99
ATTRv amyloidosis Italian Registry: clinical and epidemiological data 99
QTc Prolongation in Patients with Dementia and Mild Cognitive Impairment: Neuropsychological and Brain Imaging Correlations 97
Focal lesions are a feature of chronic inflammatory demyelinating polyneuropathy (CIDP). 96
Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutation 95
Pentraxin-3 and VEGF in POEMS syndrome: A 2-year longitudinal study. 95
Painful neuropathy vasculitis in 2 patients with long-standing human immunodeficiency virus-1 infection. 94
Charcot-Marie-Tooth disease: new insights from skin biopsy 94
Deoxysphingolipids as candidate biomarkers for a novel SPTLC1 mutation associated with HSAN-I 94
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause a MERFF syndrome. 93
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 93
Primary neurolymphomatosis as clinical onset of chronic lymphocytic leukemia 91
Charcot-Marie-Tooth type 2B: a new phenotype associated with a novel RAB7A mutation and inhibited EGFR degradation 91
Correlation between clinical/neurophysiological findings and quality of life in Charcot-Marie-Tooth type 1A 90
Overexpression of ErbB2 and ErbB3 receptors in Schwann cells of patients with Charcot-Marie-tooth disease type 1A 89
hATTR pathology: nerve biopsy results from italian referral centers 88
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling 88
Hereditary neuropathies, a pathological perspective 88
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome 87
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 87
Infectious neuropathies 87
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 86
Human immunodeficiency virus-associated peripheral neuropathies 86
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 85
Neuropatie immunitarie. 85
Neuropathy in eosinophilic granulomatosis with polyangiitis: a comparison study of 24 cases with or without prior leukotriene antagonist exposure. 84
Sporadic hereditary neuropathies misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): pitfalls and red flags 84
Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis. 83
Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias. 82
Four novel cases of periaxin-related neuropathy and review of the literature. 82
Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area 81
Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: electrophysiological abnormalities and sural nerve biopsy 80
La patologia delle neuropatie periferiche. 80
Neuropathic pain in Charcot-Marie-Tooth Disease 80
Mechanisms of nerve damage in neuropathies associated with hematological diseases: lesson from nerve biopsies 78
Clinico-pathological findings in a patient with progressive cerebellar ataxia, autoimmune polyendocrine syndrome, hepatocellular carcinoma and anti-GAD autoantibodies. 77
Reply: Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot–Marie–Tooth disease 76
Peripheral nerve enlargement on nerve ultrasound parallels neuropathological changes in adult-onset Krabbe disease 76
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study. 75
Multineuropathy in a patient with HBV infection, polyarteritis nodosa and celiac disease. 74
PiB-PET detects transthyretin-related cerebral amyloid angiopathy 73
Diabetic neuropathy 72
Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study 70
Nerve ultrasound findings differentiate Charcot-Marie-Tooth disease (CMT) 1A from other demyelinating CMTs 70
Hereditary neuropathy with liability to pressure palsies: Electrophysiological and genetic study of a family with carpal tunnel syndrome as only clinical manifestation 69
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life. 69
Neuropatie genetiche. 69
Nerve conduction velocity in CMT1A: what else can we tell? 67
Pharmacological treatment for familial amyloid polyneuropathy 67
Neurolymphomatosis, a rare manifestation of peripheral nerve involvement in lymphomas: suggestive features and diagnostic challenges 67
Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. 67
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 65
Progressive brachial plexus enlargement in hereditary transthyretin amyloidosis 65
Neuronal intranuclear inclusion disease: Polymerase chain reaction and ultrastructural study of rectal biopsy specimen in a new case 64
Pharmacological treatment for familial amyloid neuropathy 64
Totale 10.039
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Categoria #
all - tutte 42.712
article - articoli 38.480
book - libri 0
conference - conferenze 1.972
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 2.260
Totale 85.424
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021604 0 0 0 62 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
2025/20261.612 484 469 558 101 0 0 0 0 0 0 0 0
Totale 10.944