CATALOGO DEI PRODOTTI DELLA RICERCA

CAVALLARO, Tiziana
 Distribuzione geografica
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Continente #
NA - Nord America 6.243
EU - Europa 5.291
AS - Asia 3.866
SA - Sud America 620
Continente sconosciuto - Info sul continente non disponibili 149
AF - Africa 105
OC - Oceania 13
Totale 16.287
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Nazione #
US - Stati Uniti d'America 6.132
RU - Federazione Russa 2.012
SG - Singapore 1.510
CN - Cina 1.166
GB - Regno Unito 955
IT - Italia 544
BR - Brasile 494
SE - Svezia 383
FR - Francia 364
VN - Vietnam 357
HK - Hong Kong 334
DE - Germania 291
IE - Irlanda 251
FI - Finlandia 227
KR - Corea 143
UA - Ucraina 71
BD - Bangladesh 70
IN - India 66
CA - Canada 56
AR - Argentina 45
BE - Belgio 39
NL - Olanda 36
ID - Indonesia 35
JP - Giappone 32
ES - Italia 24
TR - Turchia 24
NG - Nigeria 22
ZA - Sudafrica 21
PL - Polonia 20
CO - Colombia 19
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
PY - Paraguay 9
AU - Australia 8
EG - Egitto 8
IR - Iran 8
RO - Romania 8
TG - Togo 8
AE - Emirati Arabi Uniti 7
DO - Repubblica Dominicana 7
KZ - Kazakistan 7
PK - Pakistan 7
CR - Costa Rica 6
PS - Palestinian Territory 6
AL - Albania 5
BJ - Benin 5
GR - Grecia 5
HN - Honduras 5
IL - Israele 5
LB - Libano 5
MY - Malesia 5
PH - Filippine 5
CH - Svizzera 4
JM - Giamaica 4
SK - Slovacchia (Repubblica Slovacca) 4
TH - Thailandia 4
TN - Tunisia 4
BO - Bolivia 3
DK - Danimarca 3
ET - Etiopia 3
GT - Guatemala 3
HR - Croazia 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
BB - Barbados 2
CI - Costa d'Avorio 2
CZ - Repubblica Ceca 2
DM - Dominica 2
IM - Isola di Man 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
AG - Antigua e Barbuda 1
AM - Armenia 1
Totale 16.115
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Città #
Southend 798
Singapore 758
Moscow 621
Ashburn 613
Dallas 604
Chandler 569
Jacksonville 553
San Jose 525
Woodbridge 383
Hong Kong 333
Dublin 249
Ann Arbor 237
Houston 235
Council Bluffs 224
Verona 218
Beijing 205
The Dalles 186
New York 128
Wilmington 114
Lawrence 107
Princeton 107
Ho Chi Minh City 104
Los Angeles 101
Jinan 88
Hanoi 86
Nanjing 72
Buffalo 62
Santa Clara 61
Shenyang 57
Hebei 53
Helsinki 51
Columbus 48
Sindelfingen 48
Munich 47
São Paulo 42
Redmond 41
Tianjin 41
Changsha 37
Redondo Beach 35
Nanchang 33
Ningbo 32
Milan 31
Hangzhou 30
Brussels 29
Orem 29
Zhengzhou 29
Tokyo 28
Falls Church 26
Guangzhou 26
Seoul 26
Frankfurt am Main 25
Jakarta 25
Chicago 24
Haikou 24
Lancaster 23
Florence 22
Montreal 21
Rio de Janeiro 21
Turku 21
Abuja 20
Kent 20
London 20
Taiyuan 20
Denver 19
Jiaxing 19
Rome 19
Seattle 18
Belo Horizonte 17
Taizhou 17
Warsaw 17
Chennai 16
Fairfield 16
Haiphong 15
Norwalk 15
Brooklyn 14
Da Nang 14
Detroit 14
Nuremberg 14
Paris 14
Phoenix 14
San Francisco 14
Atlanta 13
Bloomsbury 13
Bologna 12
Dong Ket 12
Lappeenranta 12
Stockholm 12
Boardman 11
Hải Dương 11
Clearwater 10
Poplar 10
Biên Hòa 9
Fuzhou 9
Kemerovo 9
Mumbai 9
Redwood City 9
Tashkent 9
Amman 8
Ankara 8
Falkenstein 8
Totale 9.926
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Nome #
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. 239
Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. 236
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 232
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy 220
A 58-year-old man with B-cell chronic lymphocytic leukemia and multiple strokes 214
Brentuximab vedotin: axonal microtubule's Apollyon 210
Alpha-synuclein seeds in olfactory mucosa and cerebrospinal fluid of patients with dementia with Lewy bodies 207
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease 205
RFC1 AAGGG repeat expansion masquerading as Chronic Idiopathic Axonal Polyneuropathy 201
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 196
Convergent pathological and ultrasound features in hereditary syndromic and non‐syndromic minifascicular neuropathy related to DHH 194
Congenital hypomyelination neuropathy with a novel mutation of PMP22 191
Aberrant splicing in GJB1 and the relevance of 5′ UTR in CMTX1 pathogenesis 189
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 188
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E 188
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. 187
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 185
Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients. 185
Anxiety and depression in Charcot-Marie-Tooth disease: data from the Italian CMT national registry 182
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family. 182
Axonal neuropathy due to myelin protein zero mutation misdiagnosed as amyloid neuropathy 181
QTc Prolongation in Patients with Dementia and Mild Cognitive Impairment: Neuropsychological and Brain Imaging Correlations 179
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial. 178
Endothelial adhesion molecule expression is unaltered in the peripheral nerve from patients with AIDS and distal sensory polyneuropathy 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 176
X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32 173
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 173
Sural nerve biopsy: current role and comparison with serum neurofilament light chain levels 173
Neuropathic pain in Charcot-Marie-Tooth Disease 173
Myelin uncompaction and axo-glial detachment in chronic ataxic neuropathy with monospecific IgM antibody to ganglioside GD1b 169
CIDP, CMT1B, or CMT1B plus CIDP? 169
Polyneuropathy with anti-sulfatide and anti-MAG antibodies: Clinical, neurophysiological, pathological features and response to treatment. 167
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 166
A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B 165
Atypical Alzheimer's disease: a case report. 164
Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 Notch3 gene mutation 163
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 163
The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study 163
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 162
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy 159
ATTRv amyloidosis Italian Registry: clinical and epidemiological data 159
Peripheral nerve enlargement on nerve ultrasound parallels neuropathological changes in adult-onset Krabbe disease 159
Sporadic hereditary neuropathies misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): pitfalls and red flags 157
Charcot-Marie-Tooth disease with giant axons:a clinicopathological and genetic study 155
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. 155
Cytoskeletal pathology in ataxia-telangiectasia. 154
Charcot-Marie-Tooth disease: new insights from skin biopsy 151
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy 148
hATTR pathology: nerve biopsy results from italian referral centers 147
Hereditary neuropathies, a pathological perspective 147
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H. 146
Pentraxin-3 and VEGF in POEMS syndrome: A 2-year longitudinal study. 146
Deoxysphingolipids as candidate biomarkers for a novel SPTLC1 mutation associated with HSAN-I 142
Primary neurolymphomatosis as clinical onset of chronic lymphocytic leukemia 141
Charcot-Marie-Tooth type 2B: a new phenotype associated with a novel RAB7A mutation and inhibited EGFR degradation 141
Clinical and pathological findings in HCV-related peripheral neuropathies 140
Segmental conduction abnormalities and myelin thickenings in Val102/fs null mutation of MPZ gene 139
I quadri neuropatologici delle sindromi paraneoplastiche 139
Clinical spectrum and frequency of Charcot-Marie-Tooth disease in Italy: Data from the National CMT Registry 128
Mechanisms of nerve damage in neuropathies associated with hematological diseases: lesson from nerve biopsies 128
Painful neuropathy vasculitis in 2 patients with long-standing human immunodeficiency virus-1 infection. 127
Neurolymphomatosis, a rare manifestation of peripheral nerve involvement in lymphomas: suggestive features and diagnostic challenges 126
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 125
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 123
Infectious neuropathies 123
Neuropatie immunitarie. 122
Neuropathy in eosinophilic granulomatosis with polyangiitis: a comparison study of 24 cases with or without prior leukotriene antagonist exposure. 122
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 118
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause a MERFF syndrome. 118
Overexpression of ErbB2 and ErbB3 receptors in Schwann cells of patients with Charcot-Marie-tooth disease type 1A 116
Focal lesions are a feature of chronic inflammatory demyelinating polyneuropathy (CIDP). 116
Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area 116
Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutation 114
Clinical and pathology characterization of small nerve fiber neuro(no)pathy in cerebellar ataxia with neuropathy and vestibular areflexia syndrome 113
Human immunodeficiency virus-associated peripheral neuropathies 113
Correlation between clinical/neurophysiological findings and quality of life in Charcot-Marie-Tooth type 1A 113
Four novel cases of periaxin-related neuropathy and review of the literature. 113
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling 113
Leprosy Neuropathy in a Non-Endemic Area: A Clinical and Pathological Study 112
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 112
La patologia delle neuropatie periferiche. 112
Phenotypic spectrum of myelin protein zero-related neuropathies: a large cohort study from five mutation clusters across Italy 112
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study. 111
Multineuropathy in a patient with HBV infection, polyarteritis nodosa and celiac disease. 111
Clinico-pathological findings in a patient with progressive cerebellar ataxia, autoimmune polyendocrine syndrome, hepatocellular carcinoma and anti-GAD autoantibodies. 110
Nerve ultrasound findings differentiate Charcot-Marie-Tooth disease (CMT) 1A from other demyelinating CMTs 110
Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: electrophysiological abnormalities and sural nerve biopsy 109
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome 108
Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias. 106
Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis. 104
Diabetic neuropathy 104
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 101
Pharmacological treatment for familial amyloid polyneuropathy 101
Neuropatie genetiche. 99
PiB-PET detects transthyretin-related cerebral amyloid angiopathy 99
Reply: Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot–Marie–Tooth disease 97
Nerve conduction velocity in CMT1A: what else can we tell? 95
Progressive brachial plexus enlargement in hereditary transthyretin amyloidosis 95
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life. 94
Pharmacological treatment for familial amyloid neuropathy 93
Totale 14.771
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Categoria #
all - tutte 57.881
article - articoli 52.281
book - libri 0
conference - conferenze 2.589
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 3.011
Totale 115.762
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022905 0 328 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
2025/20266.658 484 469 558 1.091 1.633 421 534 305 571 298 119 175
2026/2027297 132 165 0 0 0 0 0 0 0 0 0 0
Totale 16.287