CATALOGO DEI PRODOTTI DELLA RICERCA

CAVALLARO, Tiziana
 Distribuzione geografica
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Continente #
NA - Nord America 3.172
EU - Europa 2.653
AS - Asia 994
AF - Africa 13
SA - Sud America 7
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 2
Totale 6.847
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Nazione #
US - Stati Uniti d'America 3.167
GB - Regno Unito 892
CN - Cina 826
SE - Svezia 372
FR - Francia 333
IT - Italia 251
IE - Irlanda 250
DE - Germania 194
FI - Finlandia 186
SG - Singapore 76
UA - Ucraina 60
BE - Belgio 34
RU - Federazione Russa 31
VN - Vietnam 27
NL - Olanda 21
KR - Corea 20
IN - India 10
HK - Hong Kong 8
IR - Iran 8
MA - Marocco 7
RO - Romania 6
AU - Australia 5
CA - Canada 5
CL - Cile 5
EG - Egitto 5
ES - Italia 4
JP - Giappone 4
CH - Svizzera 3
IL - Israele 3
TR - Turchia 3
AT - Austria 2
BR - Brasile 2
DK - Danimarca 2
GR - Grecia 2
LV - Lettonia 2
NO - Norvegia 2
SK - Slovacchia (Repubblica Slovacca) 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
AL - Albania 1
BD - Bangladesh 1
DZ - Algeria 1
EU - Europa 1
HR - Croazia 1
ID - Indonesia 1
KG - Kirghizistan 1
KH - Cambogia 1
KZ - Kazakistan 1
MD - Moldavia 1
NZ - Nuova Zelanda 1
PL - Polonia 1
SA - Arabia Saudita 1
TH - Thailandia 1
TW - Taiwan 1
Totale 6.847
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Città #
Southend 798
Chandler 574
Jacksonville 553
Woodbridge 383
Dublin 250
Ann Arbor 237
Houston 222
Beijing 146
Ashburn 140
Wilmington 114
Lawrence 107
Princeton 107
Verona 90
Jinan 88
Nanjing 71
New York 71
Shenyang 56
Hebei 53
Sindelfingen 49
Singapore 47
Redmond 41
Helsinki 39
Changsha 37
Tianjin 36
Nanchang 33
Ningbo 31
Hangzhou 28
Zhengzhou 28
Brussels 27
Falls Church 26
Haikou 23
Lancaster 23
Guangzhou 22
Seoul 20
Taiyuan 20
Jiaxing 19
Kent 19
Milan 18
Fairfield 16
Taizhou 16
Norwalk 14
Bloomsbury 13
Chicago 13
Detroit 12
Dong Ket 12
Seattle 11
Boardman 10
Clearwater 10
Los Angeles 10
Kemerovo 9
Redwood City 9
Fuzhou 8
Hong Kong 8
Bologna 7
Florence 7
Lanzhou 7
Riva 7
San Diego 6
Waanrode 6
Washington 6
Cairo 5
Midelt 5
Paris 5
Rome 5
Dearborn 4
Dongguan 4
Düsseldorf 4
Edinburgh 4
Lappeenranta 4
Vicenza 4
Auburn Hills 3
Castelfidardo 3
Des Moines 3
Mehlingen 3
Pavia 3
Phoenix 3
Sacramento 3
San Francisco 3
Serio 3
Trieste 3
Aarau 2
Amsterdam 2
Ardabil 2
Barcelona 2
Büdelsdorf 2
Cambridge 2
Canberra 2
Catanzaro 2
Duncan 2
Falkenstein 2
Frankfurt am Main 2
Grezzana 2
Groningen 2
Gunzenhausen 2
Markham 2
Meran 2
Moscow 2
Munich 2
Novokuznetsk 2
Philadelphia 2
Totale 4.977
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Nome #
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. 138
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy 109
X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32 105
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family. 103
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. 103
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E 100
Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients. 100
Cytoskeletal pathology in ataxia-telangiectasia. 99
Congenital hypomyelination neuropathy with a novel mutation of PMP22 99
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease 95
Segmental conduction abnormalities and myelin thickenings in Val102/fs null mutation of MPZ gene 92
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy 91
Endothelial adhesion molecule expression is unaltered in the peripheral nerve from patients with AIDS and distal sensory polyneuropathy 89
Convergent pathological and ultrasound features in hereditary syndromic and non‐syndromic minifascicular neuropathy related to DHH 89
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 87
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H. 86
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 86
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 85
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy 84
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 84
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 84
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 84
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 82
Brentuximab vedotin: axonal microtubule's Apollyon 82
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 82
Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. 82
I quadri neuropatologici delle sindromi paraneoplastiche 81
null 77
Charcot-Marie-Tooth disease with giant axons:a clinicopathological and genetic study 76
RFC1 AAGGG repeat expansion masquerading as Chronic Idiopathic Axonal Polyneuropathy 75
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 74
Atypical Alzheimer's disease: a case report. 73
Correlation between clinical/neurophysiological findings and quality of life in Charcot-Marie-Tooth type 1A 72
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause a MERFF syndrome. 72
Polyneuropathy with anti-sulfatide and anti-MAG antibodies: Clinical, neurophysiological, pathological features and response to treatment. 72
A 58-year-old man with B-cell chronic lymphocytic leukemia and multiple strokes 71
Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutation 70
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. 70
Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 Notch3 gene mutation 69
The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study 69
Axonal neuropathy due to myelin protein zero mutation misdiagnosed as amyloid neuropathy 68
A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B 67
Overexpression of ErbB2 and ErbB3 receptors in Schwann cells of patients with Charcot-Marie-tooth disease type 1A 66
Primary neurolymphomatosis as clinical onset of chronic lymphocytic leukemia 66
Deoxysphingolipids as candidate biomarkers for a novel SPTLC1 mutation associated with HSAN-I 66
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 65
Focal lesions are a feature of chronic inflammatory demyelinating polyneuropathy (CIDP). 64
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial. 64
Sural nerve biopsy: current role and comparison with serum neurofilament light chain levels 64
Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias. 63
Infectious neuropathies 63
Neuropatie immunitarie. 62
Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis. 62
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 61
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 61
Charcot-Marie-Tooth disease: new insights from skin biopsy 61
Myelin uncompaction and axo-glial detachment in chronic ataxic neuropathy with monospecific IgM antibody to ganglioside GD1b 61
Aberrant splicing in GJB1 and the relevance of 5′ UTR in CMTX1 pathogenesis 61
Reply: Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot–Marie–Tooth disease 60
Alpha-synuclein seeds in olfactory mucosa and cerebrospinal fluid of patients with dementia with Lewy bodies 60
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome 59
Painful neuropathy vasculitis in 2 patients with long-standing human immunodeficiency virus-1 infection. 59
Multineuropathy in a patient with HBV infection, polyarteritis nodosa and celiac disease. 58
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 58
Pentraxin-3 and VEGF in POEMS syndrome: A 2-year longitudinal study. 57
Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area 57
QTc Prolongation in Patients with Dementia and Mild Cognitive Impairment: Neuropsychological and Brain Imaging Correlations 57
Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: electrophysiological abnormalities and sural nerve biopsy 56
Human immunodeficiency virus-associated peripheral neuropathies 55
Clinico-pathological findings in a patient with progressive cerebellar ataxia, autoimmune polyendocrine syndrome, hepatocellular carcinoma and anti-GAD autoantibodies. 53
La patologia delle neuropatie periferiche. 53
Four novel cases of periaxin-related neuropathy and review of the literature. 52
Neuropatie genetiche. 52
ATTRv amyloidosis Italian Registry: clinical and epidemiological data 52
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling 52
Sporadic hereditary neuropathies misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): pitfalls and red flags 51
hATTR pathology: nerve biopsy results from italian referral centers 51
Peripheral nerve enlargement on nerve ultrasound parallels neuropathological changes in adult-onset Krabbe disease 50
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study. 49
Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. 48
Neuropathy in eosinophilic granulomatosis with polyangiitis: a comparison study of 24 cases with or without prior leukotriene antagonist exposure. 47
CIDP, CMT1B, or CMT1B plus CIDP? 47
Mechanisms of nerve damage in neuropathies associated with hematological diseases: lesson from nerve biopsies 47
Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study 46
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life. 46
Hereditary neuropathy with liability to pressure palsies: Electrophysiological and genetic study of a family with carpal tunnel syndrome as only clinical manifestation 45
PiB-PET detects transthyretin-related cerebral amyloid angiopathy 45
Nerve conduction velocity in CMT1A: what else can we tell? 45
Pharmacological treatment for familial amyloid polyneuropathy 44
Charcot-Marie-Tooth type 2B: a new phenotype associated with a novel RAB7A mutation and inhibited EGFR degradation 44
Diabetic neuropathy 43
Hereditary neuropathies, a pathological perspective 43
Neuropathic pain in Charcot-Marie-Tooth Disease 42
Neuronal intranuclear inclusion disease: Polymerase chain reaction and ultrastructural study of rectal biopsy specimen in a new case 40
Novel outcome measures for Charcot-Marie-Tooth disease: validation and reliability of the 6-min walk test and StepWatch(™) Activity Monitor and identification of the walking features related to higher quality of life 39
Pharmacological treatment for familial amyloid neuropathy 39
Neurolymphomatosis, a rare manifestation of peripheral nerve involvement in lymphomas: suggestive features and diagnostic challenges 36
Responsiveness of clinical outcome measures in Charcot-Marie-Tooth disease 35
Nerve ultrasound findings differentiate Charcot-Marie-Tooth disease (CMT) 1A from other demyelinating CMTs 35
Is overwork weakness relevant in Charcot-Marie-Tooth disease? 34
Totale 6.627
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Categoria #
all - tutte 23.826
article - articoli 21.273
book - libri 0
conference - conferenze 1.212
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.341
Totale 47.652
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201910 0 0 0 0 0 0 0 0 0 0 0 10
2019/2020869 110 5 7 75 78 98 101 67 43 107 53 125
2020/2021869 91 129 45 62 81 90 44 72 58 24 133 40
2021/2022995 90 328 9 96 31 68 11 47 42 26 78 169
2022/20231.704 125 160 178 317 138 408 26 114 176 11 32 19
2023/2024766 36 57 58 86 95 136 28 40 14 47 106 63
Totale 6.993