CATALOGO DEI PRODOTTI DELLA RICERCA

CAVALLARO, Tiziana
 Distribuzione geografica
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Continente #
NA - Nord America 5.779
EU - Europa 5.242
AS - Asia 3.780
SA - Sud America 606
AF - Africa 105
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 2
Totale 15.527
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Nazione #
US - Stati Uniti d'America 5.687
RU - Federazione Russa 2.012
SG - Singapore 1.493
CN - Cina 1.148
GB - Regno Unito 954
IT - Italia 508
BR - Brasile 483
SE - Svezia 382
FR - Francia 364
VN - Vietnam 356
HK - Hong Kong 330
DE - Germania 291
IE - Irlanda 249
FI - Finlandia 227
KR - Corea 142
UA - Ucraina 70
IN - India 66
CA - Canada 48
AR - Argentina 44
BE - Belgio 36
NL - Olanda 36
ID - Indonesia 35
JP - Giappone 32
BD - Bangladesh 26
TR - Turchia 24
ES - Italia 22
NG - Nigeria 22
ZA - Sudafrica 21
PL - Polonia 20
CO - Colombia 18
IQ - Iraq 18
MX - Messico 18
EC - Ecuador 15
CL - Cile 14
VE - Venezuela 13
LT - Lituania 12
MA - Marocco 11
SA - Arabia Saudita 11
AT - Austria 10
DZ - Algeria 10
UZ - Uzbekistan 10
JO - Giordania 9
AU - Australia 8
EG - Egitto 8
IR - Iran 8
PY - Paraguay 8
RO - Romania 8
TG - Togo 8
AE - Emirati Arabi Uniti 7
DO - Repubblica Dominicana 7
KZ - Kazakistan 7
PK - Pakistan 7
PS - Palestinian Territory 6
BJ - Benin 5
IL - Israele 5
LB - Libano 5
MY - Malesia 5
AL - Albania 4
CH - Svizzera 4
CR - Costa Rica 4
GR - Grecia 4
PH - Filippine 4
SK - Slovacchia (Repubblica Slovacca) 4
TH - Thailandia 4
TN - Tunisia 4
BO - Bolivia 3
DK - Danimarca 3
ET - Etiopia 3
HR - Croazia 3
JM - Giamaica 3
LV - Lettonia 3
NZ - Nuova Zelanda 3
OM - Oman 3
PE - Perù 3
UY - Uruguay 3
AO - Angola 2
AZ - Azerbaigian 2
BA - Bosnia-Erzegovina 2
CI - Costa d'Avorio 2
CZ - Repubblica Ceca 2
DM - Dominica 2
GT - Guatemala 2
HN - Honduras 2
KE - Kenya 2
KG - Kirghizistan 2
LI - Liechtenstein 2
LK - Sri Lanka 2
MD - Moldavia 2
MU - Mauritius 2
MZ - Mozambico 2
NO - Norvegia 2
NP - Nepal 2
SN - Senegal 2
SY - Repubblica araba siriana 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AF - Afghanistan, Repubblica islamica di 1
AM - Armenia 1
BB - Barbados 1
BG - Bulgaria 1
BY - Bielorussia 1
Totale 15.505
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Città #
Southend 798
Singapore 753
Moscow 621
Dallas 601
Ashburn 576
Chandler 569
Jacksonville 553
San Jose 494
Woodbridge 383
Hong Kong 329
Dublin 247
Ann Arbor 237
Houston 232
Verona 217
Beijing 200
The Dalles 186
New York 117
Wilmington 114
Lawrence 107
Princeton 107
Ho Chi Minh City 104
Los Angeles 97
Jinan 88
Hanoi 85
Nanjing 72
Buffalo 58
Shenyang 57
Hebei 53
Helsinki 51
Columbus 48
Santa Clara 48
Sindelfingen 48
Munich 47
Redmond 41
Tianjin 41
São Paulo 40
Changsha 37
Redondo Beach 35
Nanchang 33
Ningbo 32
Hangzhou 30
Brussels 29
Zhengzhou 29
Milan 28
Orem 28
Tokyo 28
Falls Church 26
Guangzhou 26
Seoul 26
Frankfurt am Main 25
Jakarta 25
Chicago 24
Haikou 24
Lancaster 23
Florence 22
Council Bluffs 21
Montreal 21
Rio de Janeiro 21
Turku 21
Abuja 20
London 20
Taiyuan 20
Jiaxing 19
Kent 19
Seattle 18
Belo Horizonte 17
Taizhou 17
Warsaw 17
Chennai 16
Denver 16
Fairfield 16
Haiphong 15
Da Nang 14
Norwalk 14
Nuremberg 14
Paris 14
Rome 14
Bloomsbury 13
Brooklyn 13
Atlanta 12
Detroit 12
Dong Ket 12
Lappeenranta 12
San Francisco 12
Stockholm 12
Boardman 11
Hải Dương 11
Bologna 10
Clearwater 10
Poplar 10
Biên Hòa 9
Fuzhou 9
Kemerovo 9
Mumbai 9
Phoenix 9
Redwood City 9
Tashkent 9
Amman 8
Ankara 8
Falkenstein 8
Totale 9.570
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Nome #
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. 233
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 226
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy 217
Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. 213
A 58-year-old man with B-cell chronic lymphocytic leukemia and multiple strokes 209
Brentuximab vedotin: axonal microtubule's Apollyon 205
Alpha-synuclein seeds in olfactory mucosa and cerebrospinal fluid of patients with dementia with Lewy bodies 201
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease 195
RFC1 AAGGG repeat expansion masquerading as Chronic Idiopathic Axonal Polyneuropathy 194
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 191
Aberrant splicing in GJB1 and the relevance of 5′ UTR in CMTX1 pathogenesis 189
Congenital hypomyelination neuropathy with a novel mutation of PMP22 188
Convergent pathological and ultrasound features in hereditary syndromic and non‐syndromic minifascicular neuropathy related to DHH 187
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E 185
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. 185
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 184
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family. 180
Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients. 178
Axonal neuropathy due to myelin protein zero mutation misdiagnosed as amyloid neuropathy 177
QTc Prolongation in Patients with Dementia and Mild Cognitive Impairment: Neuropsychological and Brain Imaging Correlations 177
Anxiety and depression in Charcot-Marie-Tooth disease: data from the Italian CMT national registry 176
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 176
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 173
Endothelial adhesion molecule expression is unaltered in the peripheral nerve from patients with AIDS and distal sensory polyneuropathy 172
X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32 169
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 169
Sural nerve biopsy: current role and comparison with serum neurofilament light chain levels 169
CIDP, CMT1B, or CMT1B plus CIDP? 168
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 165
Polyneuropathy with anti-sulfatide and anti-MAG antibodies: Clinical, neurophysiological, pathological features and response to treatment. 164
A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B 163
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial. 162
Myelin uncompaction and axo-glial detachment in chronic ataxic neuropathy with monospecific IgM antibody to ganglioside GD1b 161
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 160
Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 Notch3 gene mutation 159
Atypical Alzheimer's disease: a case report. 159
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 158
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy 157
Peripheral nerve enlargement on nerve ultrasound parallels neuropathological changes in adult-onset Krabbe disease 157
ATTRv amyloidosis Italian Registry: clinical and epidemiological data 156
The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study 155
Charcot-Marie-Tooth disease with giant axons:a clinicopathological and genetic study 154
Cytoskeletal pathology in ataxia-telangiectasia. 153
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. 152
Sporadic hereditary neuropathies misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): pitfalls and red flags 152
Charcot-Marie-Tooth disease: new insights from skin biopsy 147
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy 146
Pentraxin-3 and VEGF in POEMS syndrome: A 2-year longitudinal study. 144
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H. 142
hATTR pathology: nerve biopsy results from italian referral centers 142
Hereditary neuropathies, a pathological perspective 142
Clinical and pathological findings in HCV-related peripheral neuropathies 139
Segmental conduction abnormalities and myelin thickenings in Val102/fs null mutation of MPZ gene 138
I quadri neuropatologici delle sindromi paraneoplastiche 137
Primary neurolymphomatosis as clinical onset of chronic lymphocytic leukemia 137
Deoxysphingolipids as candidate biomarkers for a novel SPTLC1 mutation associated with HSAN-I 137
Charcot-Marie-Tooth type 2B: a new phenotype associated with a novel RAB7A mutation and inhibited EGFR degradation 137
Neuropathic pain in Charcot-Marie-Tooth Disease 133
Mechanisms of nerve damage in neuropathies associated with hematological diseases: lesson from nerve biopsies 127
Clinical spectrum and frequency of Charcot-Marie-Tooth disease in Italy: Data from the National CMT Registry 124
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 121
Neuropatie immunitarie. 120
Painful neuropathy vasculitis in 2 patients with long-standing human immunodeficiency virus-1 infection. 118
Infectious neuropathies 117
Neurolymphomatosis, a rare manifestation of peripheral nerve involvement in lymphomas: suggestive features and diagnostic challenges 117
Neuropathy in eosinophilic granulomatosis with polyangiitis: a comparison study of 24 cases with or without prior leukotriene antagonist exposure. 116
Overexpression of ErbB2 and ErbB3 receptors in Schwann cells of patients with Charcot-Marie-tooth disease type 1A 115
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 115
Focal lesions are a feature of chronic inflammatory demyelinating polyneuropathy (CIDP). 114
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause a MERFF syndrome. 114
Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutation 113
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 112
Clinical and pathology characterization of small nerve fiber neuro(no)pathy in cerebellar ataxia with neuropathy and vestibular areflexia syndrome 111
Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area 111
Human immunodeficiency virus-associated peripheral neuropathies 110
La patologia delle neuropatie periferiche. 110
Correlation between clinical/neurophysiological findings and quality of life in Charcot-Marie-Tooth type 1A 109
Four novel cases of periaxin-related neuropathy and review of the literature. 109
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling 108
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 107
Leprosy Neuropathy in a Non-Endemic Area: A Clinical and Pathological Study 106
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome 106
Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: electrophysiological abnormalities and sural nerve biopsy 105
Clinico-pathological findings in a patient with progressive cerebellar ataxia, autoimmune polyendocrine syndrome, hepatocellular carcinoma and anti-GAD autoantibodies. 105
Nerve ultrasound findings differentiate Charcot-Marie-Tooth disease (CMT) 1A from other demyelinating CMTs 105
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study. 103
Multineuropathy in a patient with HBV infection, polyarteritis nodosa and celiac disease. 102
Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis. 102
Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias. 101
Diabetic neuropathy 99
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 97
Reply: Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot–Marie–Tooth disease 96
Pharmacological treatment for familial amyloid polyneuropathy 96
Neuropatie genetiche. 95
PiB-PET detects transthyretin-related cerebral amyloid angiopathy 95
Nerve conduction velocity in CMT1A: what else can we tell? 93
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life. 91
Progressive brachial plexus enlargement in hereditary transthyretin amyloidosis 91
Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study 88
Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. 88
Totale 14.276
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Categoria #
all - tutte 52.306
article - articoli 47.154
book - libri 0
conference - conferenze 2.395
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 2.757
Totale 104.612
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021197 0 0 0 0 0 0 0 0 0 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
2025/20266.342 484 469 558 1.091 1.633 421 534 305 571 276 0 0
Totale 15.674