CATALOGO DEI PRODOTTI DELLA RICERCA

CAVALLARO, Tiziana
 Distribuzione geografica
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Continente #
NA - Nord America 5.998
EU - Europa 5.276
AS - Asia 3.836
SA - Sud America 612
AF - Africa 105
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 2
Totale 15.842
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Nazione #
US - Stati Uniti d'America 5.896
RU - Federazione Russa 2.012
SG - Singapore 1.500
CN - Cina 1.151
GB - Regno Unito 955
IT - Italia 532
BR - Brasile 488
SE - Svezia 382
FR - Francia 364
VN - Vietnam 356
HK - Hong Kong 333
DE - Germania 291
IE - Irlanda 251
FI - Finlandia 227
KR - Corea 143
UA - Ucraina 71
BD - Bangladesh 68
IN - India 66
CA - Canada 53
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 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
CR - Costa Rica 5
GR - Grecia 5
IL - Israele 5
LB - Libano 5
MY - Malesia 5
AL - Albania 4
CH - Svizzera 4
JM - Giamaica 4
PH - Filippine 4
SK - Slovacchia (Repubblica Slovacca) 4
TH - Thailandia 4
TN - Tunisia 4
BO - Bolivia 3
DK - Danimarca 3
ET - Etiopia 3
HN - Honduras 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
CI - Costa d'Avorio 2
CZ - Repubblica Ceca 2
DM - Dominica 2
GT - Guatemala 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 15.818
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Città #
Southend 798
Singapore 756
Moscow 621
Dallas 603
Ashburn 594
Chandler 569
Jacksonville 553
San Jose 522
Woodbridge 383
Hong Kong 332
Dublin 249
Ann Arbor 237
Houston 234
Verona 218
Beijing 201
The Dalles 186
New York 127
Council Bluffs 118
Wilmington 114
Lawrence 107
Princeton 107
Ho Chi Minh City 104
Los Angeles 101
Jinan 88
Hanoi 85
Nanjing 72
Buffalo 61
Shenyang 57
Hebei 53
Helsinki 51
Santa Clara 51
Columbus 48
Sindelfingen 48
Munich 47
Redmond 41
São Paulo 41
Tianjin 41
Changsha 37
Redondo Beach 35
Nanchang 33
Ningbo 32
Hangzhou 30
Brussels 29
Milan 29
Zhengzhou 29
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
Montreal 21
Rio de Janeiro 21
Turku 21
Abuja 20
London 20
Taiyuan 20
Jiaxing 19
Kent 19
Seattle 18
Belo Horizonte 17
Denver 17
Taizhou 17
Warsaw 17
Chennai 16
Fairfield 16
Rome 16
Haiphong 15
Da Nang 14
Norwalk 14
Nuremberg 14
Paris 14
San Francisco 14
Bloomsbury 13
Brooklyn 13
Atlanta 12
Detroit 12
Dong Ket 12
Lappeenranta 12
Stockholm 12
Boardman 11
Bologna 11
Hải Dương 11
Clearwater 10
Phoenix 10
Poplar 10
Biên Hòa 9
Fuzhou 9
Kemerovo 9
Mumbai 9
Redwood City 9
Tashkent 9
Amman 8
Ankara 8
Falkenstein 8
Totale 9.756
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Nome #
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. 236
Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. 234
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 230
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy 218
A 58-year-old man with B-cell chronic lymphocytic leukemia and multiple strokes 211
Brentuximab vedotin: axonal microtubule's Apollyon 209
Alpha-synuclein seeds in olfactory mucosa and cerebrospinal fluid of patients with dementia with Lewy bodies 202
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease 200
RFC1 AAGGG repeat expansion masquerading as Chronic Idiopathic Axonal Polyneuropathy 200
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 193
Convergent pathological and ultrasound features in hereditary syndromic and non‐syndromic minifascicular neuropathy related to DHH 191
Congenital hypomyelination neuropathy with a novel mutation of PMP22 189
Aberrant splicing in GJB1 and the relevance of 5′ UTR in CMTX1 pathogenesis 189
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E 186
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. 186
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 185
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family. 180
Axonal neuropathy due to myelin protein zero mutation misdiagnosed as amyloid neuropathy 180
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 180
Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients. 180
Anxiety and depression in Charcot-Marie-Tooth disease: data from the Italian CMT national registry 178
QTc Prolongation in Patients with Dementia and Mild Cognitive Impairment: Neuropsychological and Brain Imaging Correlations 177
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial. 175
Endothelial adhesion molecule expression is unaltered in the peripheral nerve from patients with AIDS and distal sensory polyneuropathy 173
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
X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32 170
Sural nerve biopsy: current role and comparison with serum neurofilament light chain levels 170
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 169
CIDP, CMT1B, or CMT1B plus CIDP? 168
Polyneuropathy with anti-sulfatide and anti-MAG antibodies: Clinical, neurophysiological, pathological features and response to treatment. 166
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 165
A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B 163
Myelin uncompaction and axo-glial detachment in chronic ataxic neuropathy with monospecific IgM antibody to ganglioside GD1b 163
Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 Notch3 gene mutation 161
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 161
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 160
The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study 160
Atypical Alzheimer's disease: a case report. 159
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy 158
ATTRv amyloidosis Italian Registry: clinical and epidemiological data 158
Peripheral nerve enlargement on nerve ultrasound parallels neuropathological changes in adult-onset Krabbe disease 157
Sporadic hereditary neuropathies misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): pitfalls and red flags 156
Charcot-Marie-Tooth disease with giant axons:a clinicopathological and genetic study 154
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. 154
Cytoskeletal pathology in ataxia-telangiectasia. 153
Charcot-Marie-Tooth disease: new insights from skin biopsy 149
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy 146
hATTR pathology: nerve biopsy results from italian referral centers 146
Hereditary neuropathies, a pathological perspective 146
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H. 145
Pentraxin-3 and VEGF in POEMS syndrome: A 2-year longitudinal study. 144
Clinical and pathological findings in HCV-related peripheral neuropathies 139
Primary neurolymphomatosis as clinical onset of chronic lymphocytic leukemia 139
Deoxysphingolipids as candidate biomarkers for a novel SPTLC1 mutation associated with HSAN-I 139
Charcot-Marie-Tooth type 2B: a new phenotype associated with a novel RAB7A mutation and inhibited EGFR degradation 139
Segmental conduction abnormalities and myelin thickenings in Val102/fs null mutation of MPZ gene 138
I quadri neuropatologici delle sindromi paraneoplastiche 137
Neuropathic pain in Charcot-Marie-Tooth Disease 136
Mechanisms of nerve damage in neuropathies associated with hematological diseases: lesson from nerve biopsies 128
Clinical spectrum and frequency of Charcot-Marie-Tooth disease in Italy: Data from the National CMT Registry 127
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 122
Neurolymphomatosis, a rare manifestation of peripheral nerve involvement in lymphomas: suggestive features and diagnostic challenges 122
Painful neuropathy vasculitis in 2 patients with long-standing human immunodeficiency virus-1 infection. 121
Neuropatie immunitarie. 120
Infectious neuropathies 120
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause a MERFF syndrome. 118
Neuropathy in eosinophilic granulomatosis with polyangiitis: a comparison study of 24 cases with or without prior leukotriene antagonist exposure. 118
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 116
Overexpression of ErbB2 and ErbB3 receptors in Schwann cells of patients with Charcot-Marie-tooth disease type 1A 115
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 114
Focal lesions are a feature of chronic inflammatory demyelinating polyneuropathy (CIDP). 114
Clinical and pathology characterization of small nerve fiber neuro(no)pathy in cerebellar ataxia with neuropathy and vestibular areflexia syndrome 113
Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutation 113
Correlation between clinical/neurophysiological findings and quality of life in Charcot-Marie-Tooth type 1A 112
Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area 112
Four novel cases of periaxin-related neuropathy and review of the literature. 111
La patologia delle neuropatie periferiche. 111
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling 111
Leprosy Neuropathy in a Non-Endemic Area: A Clinical and Pathological Study 110
Human immunodeficiency virus-associated peripheral neuropathies 110
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 110
Multineuropathy in a patient with HBV infection, polyarteritis nodosa and celiac disease. 109
Clinico-pathological findings in a patient with progressive cerebellar ataxia, autoimmune polyendocrine syndrome, hepatocellular carcinoma and anti-GAD autoantibodies. 109
Phenotypic spectrum of myelin protein zero-related neuropathies: a large cohort study from five mutation clusters across Italy 109
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome 108
Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: electrophysiological abnormalities and sural nerve biopsy 107
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study. 107
Nerve ultrasound findings differentiate Charcot-Marie-Tooth disease (CMT) 1A from other demyelinating CMTs 107
Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias. 103
Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis. 102
Diabetic neuropathy 101
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 99
Pharmacological treatment for familial amyloid polyneuropathy 98
PiB-PET detects transthyretin-related cerebral amyloid angiopathy 97
Neuropatie genetiche. 96
Reply: Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot–Marie–Tooth disease 96
Nerve conduction velocity in CMT1A: what else can we tell? 94
Progressive brachial plexus enlargement in hereditary transthyretin amyloidosis 93
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life. 92
Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study 90
Totale 14.508
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Categoria #
all - tutte 55.516
article - articoli 50.080
book - libri 0
conference - conferenze 2.518
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 2.918
Totale 111.032
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202140 0 0 0 0 0 0 0 0 0 0 0 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
2025/20266.657 484 469 558 1.091 1.633 421 534 305 571 298 119 174
Totale 15.989