CATALOGO DEI PRODOTTI DELLA RICERCA

CAVALLARO, Tiziana
 Distribuzione geografica
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Continente #
NA - Nord America 6.848
EU - Europa 5.328
AS - Asia 3.884
SA - Sud America 633
Continente sconosciuto - Info sul continente non disponibili 149
AF - Africa 106
OC - Oceania 13
Totale 16.961
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Nazione #
US - Stati Uniti d'America 6.715
RU - Federazione Russa 2.012
SG - Singapore 1.514
CN - Cina 1.169
GB - Regno Unito 964
IT - Italia 563
BR - Brasile 500
SE - Svezia 384
FR - Francia 366
VN - Vietnam 359
HK - Hong Kong 335
DE - Germania 292
IE - Irlanda 251
FI - Finlandia 227
KR - Corea 143
BD - Bangladesh 72
UA - Ucraina 71
IN - India 67
CA - Canada 66
AR - Argentina 46
BE - Belgio 39
NL - Olanda 36
ID - Indonesia 35
JP - Giappone 34
ES - Italia 25
CO - Colombia 24
TR - Turchia 24
NG - Nigeria 22
ZA - Sudafrica 21
PL - Polonia 20
MX - Messico 19
IQ - Iraq 18
EC - Ecuador 15
CL - Cile 14
VE - Venezuela 14
LT - Lituania 12
SA - Arabia Saudita 12
CR - Costa Rica 11
MA - Marocco 11
AT - Austria 10
DZ - Algeria 10
UZ - Uzbekistan 10
JO - Giordania 9
PY - Paraguay 9
AE - Emirati Arabi Uniti 8
AU - Australia 8
EG - Egitto 8
IR - Iran 8
RO - Romania 8
TG - Togo 8
DO - Repubblica Dominicana 7
KZ - Kazakistan 7
PK - Pakistan 7
JM - Giamaica 6
PH - Filippine 6
PS - Palestinian Territory 6
AL - Albania 5
BJ - Benin 5
DK - Danimarca 5
GR - Grecia 5
HN - Honduras 5
IL - Israele 5
LB - Libano 5
MY - Malesia 5
CH - Svizzera 4
SK - Slovacchia (Repubblica Slovacca) 4
TH - Thailandia 4
TN - Tunisia 4
BO - Bolivia 3
EE - Estonia 3
ET - Etiopia 3
GT - Guatemala 3
HR - Croazia 3
KE - Kenya 3
LV - Lettonia 3
NI - Nicaragua 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
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
PR - Porto Rico 2
SN - Senegal 2
SY - Repubblica araba siriana 2
A2 - ???statistics.table.value.countryCode.A2??? 1
Totale 16.788
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Città #
Southend 798
Singapore 759
Ashburn 740
San Jose 635
Dallas 628
Moscow 621
Chandler 569
Jacksonville 554
Woodbridge 383
Hong Kong 334
Dublin 249
Houston 238
Ann Arbor 237
Council Bluffs 224
Verona 218
Beijing 206
The Dalles 186
New York 135
Wilmington 114
Lawrence 107
Princeton 107
Ho Chi Minh City 105
Los Angeles 104
Jinan 88
Hanoi 86
Nanjing 72
Santa Clara 71
Buffalo 62
Shenyang 57
Hebei 53
Helsinki 51
Columbus 48
Sindelfingen 48
Munich 47
São Paulo 45
Redmond 41
Tianjin 41
Changsha 37
Redondo Beach 35
Milan 33
Nanchang 33
Ningbo 32
Orem 31
Hangzhou 30
Tokyo 30
Brussels 29
Zhengzhou 29
Chicago 27
Falls Church 26
Guangzhou 26
Seoul 26
Frankfurt am Main 25
Jakarta 25
Haikou 24
Lancaster 24
Atlanta 22
Denver 22
Florence 22
Montreal 22
Las Vegas 21
London 21
Rio de Janeiro 21
Turku 21
Abuja 20
Kent 20
Seattle 20
Taiyuan 20
Jiaxing 19
Rome 19
Phoenix 18
Belo Horizonte 17
Taizhou 17
Warsaw 17
Chennai 16
Detroit 16
Fairfield 16
Brooklyn 15
Haiphong 15
Norwalk 15
San Francisco 15
Da Nang 14
Nuremberg 14
Paris 14
Bloomsbury 13
Bologna 13
Stockholm 13
Dong Ket 12
Lappeenranta 12
Boardman 11
Hải Dương 11
Clearwater 10
Poplar 10
San Diego 10
Biên Hòa 9
Fuzhou 9
Kemerovo 9
Mumbai 9
Redwood City 9
Tashkent 9
Washington 9
Totale 10.270
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Nome #
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. 254
Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. 241
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 240
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy 224
A 58-year-old man with B-cell chronic lymphocytic leukemia and multiple strokes 222
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease 214
Brentuximab vedotin: axonal microtubule's Apollyon 214
Alpha-synuclein seeds in olfactory mucosa and cerebrospinal fluid of patients with dementia with Lewy bodies 214
RFC1 AAGGG repeat expansion masquerading as Chronic Idiopathic Axonal Polyneuropathy 207
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 205
Convergent pathological and ultrasound features in hereditary syndromic and non‐syndromic minifascicular neuropathy related to DHH 201
Congenital hypomyelination neuropathy with a novel mutation of PMP22 196
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 195
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E 195
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. 194
Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients. 193
Aberrant splicing in GJB1 and the relevance of 5′ UTR in CMTX1 pathogenesis 192
Anxiety and depression in Charcot-Marie-Tooth disease: data from the Italian CMT national registry 191
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 191
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family. 188
Axonal neuropathy due to myelin protein zero mutation misdiagnosed as amyloid neuropathy 187
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial. 185
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 184
QTc Prolongation in Patients with Dementia and Mild Cognitive Impairment: Neuropsychological and Brain Imaging Correlations 184
Endothelial adhesion molecule expression is unaltered in the peripheral nerve from patients with AIDS and distal sensory polyneuropathy 181
Neuropathic pain in Charcot-Marie-Tooth Disease 181
Sural nerve biopsy: current role and comparison with serum neurofilament light chain levels 179
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 178
X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32 177
CIDP, CMT1B, or CMT1B plus CIDP? 177
A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B 174
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 173
Polyneuropathy with anti-sulfatide and anti-MAG antibodies: Clinical, neurophysiological, pathological features and response to treatment. 173
Myelin uncompaction and axo-glial detachment in chronic ataxic neuropathy with monospecific IgM antibody to ganglioside GD1b 173
Atypical Alzheimer's disease: a case report. 171
Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 Notch3 gene mutation 170
The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study 170
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 169
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy 168
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 164
Peripheral nerve enlargement on nerve ultrasound parallels neuropathological changes in adult-onset Krabbe disease 164
Charcot-Marie-Tooth disease with giant axons:a clinicopathological and genetic study 163
Sporadic hereditary neuropathies misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): pitfalls and red flags 163
ATTRv amyloidosis Italian Registry: clinical and epidemiological data 163
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. 161
Cytoskeletal pathology in ataxia-telangiectasia. 160
Charcot-Marie-Tooth disease: new insights from skin biopsy 157
Hereditary neuropathies, a pathological perspective 155
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy 151
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H. 151
Pentraxin-3 and VEGF in POEMS syndrome: A 2-year longitudinal study. 150
hATTR pathology: nerve biopsy results from italian referral centers 150
Clinical and pathological findings in HCV-related peripheral neuropathies 148
Deoxysphingolipids as candidate biomarkers for a novel SPTLC1 mutation associated with HSAN-I 145
Charcot-Marie-Tooth type 2B: a new phenotype associated with a novel RAB7A mutation and inhibited EGFR degradation 145
Primary neurolymphomatosis as clinical onset of chronic lymphocytic leukemia 144
Mechanisms of nerve damage in neuropathies associated with hematological diseases: lesson from nerve biopsies 144
Segmental conduction abnormalities and myelin thickenings in Val102/fs null mutation of MPZ gene 143
I quadri neuropatologici delle sindromi paraneoplastiche 143
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 137
Clinical spectrum and frequency of Charcot-Marie-Tooth disease in Italy: Data from the National CMT Registry 136
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 131
Painful neuropathy vasculitis in 2 patients with long-standing human immunodeficiency virus-1 infection. 130
Neurolymphomatosis, a rare manifestation of peripheral nerve involvement in lymphomas: suggestive features and diagnostic challenges 130
Infectious neuropathies 126
Neuropathy in eosinophilic granulomatosis with polyangiitis: a comparison study of 24 cases with or without prior leukotriene antagonist exposure. 125
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 124
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause a MERFF syndrome. 124
Clinical and pathology characterization of small nerve fiber neuro(no)pathy in cerebellar ataxia with neuropathy and vestibular areflexia syndrome 123
Overexpression of ErbB2 and ErbB3 receptors in Schwann cells of patients with Charcot-Marie-tooth disease type 1A 123
Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area 123
Neuropatie immunitarie. 122
Focal lesions are a feature of chronic inflammatory demyelinating polyneuropathy (CIDP). 120
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling 120
Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutation 119
Correlation between clinical/neurophysiological findings and quality of life in Charcot-Marie-Tooth type 1A 119
Human immunodeficiency virus-associated peripheral neuropathies 118
Clinico-pathological findings in a patient with progressive cerebellar ataxia, autoimmune polyendocrine syndrome, hepatocellular carcinoma and anti-GAD autoantibodies. 118
Phenotypic spectrum of myelin protein zero-related neuropathies: a large cohort study from five mutation clusters across Italy 118
Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: electrophysiological abnormalities and sural nerve biopsy 117
Nerve ultrasound findings differentiate Charcot-Marie-Tooth disease (CMT) 1A from other demyelinating CMTs 117
Leprosy Neuropathy in a Non-Endemic Area: A Clinical and Pathological Study 116
Multineuropathy in a patient with HBV infection, polyarteritis nodosa and celiac disease. 116
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 116
Four novel cases of periaxin-related neuropathy and review of the literature. 116
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study. 113
La patologia delle neuropatie periferiche. 113
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome 111
Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis. 111
Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias. 109
Pharmacological treatment for familial amyloid polyneuropathy 107
Diabetic neuropathy 106
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 103
Progressive brachial plexus enlargement in hereditary transthyretin amyloidosis 103
PiB-PET detects transthyretin-related cerebral amyloid angiopathy 102
Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study 100
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life. 100
Neuropatie genetiche. 100
Reply: Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot–Marie–Tooth disease 100
Nerve conduction velocity in CMT1A: what else can we tell? 98
Totale 15.349
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Categoria #
all - tutte 60.301
article - articoli 54.481
book - libri 0
conference - conferenze 2.677
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 3.143
Totale 120.602
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022568 0 0 0 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
2026/2027971 132 184 309 346 0 0 0 0 0 0 0 0
Totale 16.961