CATALOGO DEI PRODOTTI DELLA RICERCA

CAVALLARO, Tiziana
 Distribuzione geografica
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Continente #
NA - Nord America 3.133
EU - Europa 2.638
AS - Asia 889
AF - Africa 7
SA - Sud America 7
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 2
Totale 6.681
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Nazione #
US - Stati Uniti d'America 3.128
GB - Regno Unito 891
CN - Cina 801
SE - Svezia 372
FR - Francia 333
IE - Irlanda 249
IT - Italia 245
DE - Germania 192
FI - Finlandia 186
UA - Ucraina 60
BE - Belgio 34
RU - Federazione Russa 29
VN - Vietnam 27
KR - Corea 20
NL - Olanda 20
IN - India 9
IR - Iran 8
HK - Hong Kong 7
RO - Romania 6
CA - Canada 5
CL - Cile 5
EG - Egitto 5
AU - Australia 4
ES - Italia 4
CH - Svizzera 3
IL - Israele 3
JP - Giappone 3
TR - Turchia 3
BR - Brasile 2
DK - Danimarca 2
GR - Grecia 2
NO - Norvegia 2
SK - Slovacchia (Repubblica Slovacca) 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AT - Austria 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
LV - Lettonia 1
MA - Marocco 1
MD - Moldavia 1
NZ - Nuova Zelanda 1
PL - Polonia 1
SA - Arabia Saudita 1
TH - Thailandia 1
TW - Taiwan 1
Totale 6.681
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Città #
Southend 798
Chandler 574
Jacksonville 553
Woodbridge 383
Dublin 249
Ann Arbor 237
Houston 222
Beijing 132
Ashburn 129
Wilmington 114
Lawrence 107
Princeton 107
Jinan 88
Verona 85
Nanjing 71
New York 71
Shenyang 56
Hebei 53
Sindelfingen 49
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
Milan 18
Fairfield 16
Taizhou 16
Norwalk 14
Bloomsbury 13
Chicago 13
Detroit 12
Dong Ket 12
Seattle 11
Clearwater 10
Los Angeles 10
Kemerovo 9
Redwood City 9
Fuzhou 8
Boardman 7
Bologna 7
Florence 7
Hong Kong 7
Lanzhou 7
Riva 7
San Diego 6
Waanrode 6
Washington 6
Cairo 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
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
Novokuznetsk 2
Philadelphia 2
Somma Vesuviana 2
Toronto 2
Udine 2
Yicheng 2
Almaty 1
Amsterdam 1
Totale 4.875
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Nome #
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. 133
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 104
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family. 102
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. 102
Cytoskeletal pathology in ataxia-telangiectasia. 99
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E 99
Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients. 99
Congenital hypomyelination neuropathy with a novel mutation of PMP22 97
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 88
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 85
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 85
Convergent pathological and ultrasound features in hereditary syndromic and non‐syndromic minifascicular neuropathy related to DHH 85
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H. 84
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy 83
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 83
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 83
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 82
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 82
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 82
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 81
Brentuximab vedotin: axonal microtubule's Apollyon 81
Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. 81
I quadri neuropatologici delle sindromi paraneoplastiche 80
null 77
Charcot-Marie-Tooth disease with giant axons:a clinicopathological and genetic study 74
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 73
Atypical Alzheimer's disease: a case report. 73
Correlation between clinical/neurophysiological findings and quality of life in Charcot-Marie-Tooth type 1A 71
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause a MERFF syndrome. 71
Polyneuropathy with anti-sulfatide and anti-MAG antibodies: Clinical, neurophysiological, pathological features and response to treatment. 71
Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutation 70
Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 Notch3 gene mutation 69
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. 69
A 58-year-old man with B-cell chronic lymphocytic leukemia and multiple strokes 69
Axonal neuropathy due to myelin protein zero mutation misdiagnosed as amyloid neuropathy 68
RFC1 AAGGG repeat expansion masquerading as Chronic Idiopathic Axonal Polyneuropathy 68
The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study 67
Overexpression of ErbB2 and ErbB3 receptors in Schwann cells of patients with Charcot-Marie-tooth disease type 1A 66
A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B 66
Deoxysphingolipids as candidate biomarkers for a novel SPTLC1 mutation associated with HSAN-I 65
Focal lesions are a feature of chronic inflammatory demyelinating polyneuropathy (CIDP). 64
Primary neurolymphomatosis as clinical onset of chronic lymphocytic leukemia 64
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 63
Sural nerve biopsy: current role and comparison with serum neurofilament light chain levels 63
Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias. 61
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial. 61
Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis. 61
Charcot-Marie-Tooth disease: new insights from skin biopsy 61
Infectious neuropathies 61
Neuropatie immunitarie. 60
Myelin uncompaction and axo-glial detachment in chronic ataxic neuropathy with monospecific IgM antibody to ganglioside GD1b 60
Alpha-synuclein seeds in olfactory mucosa and cerebrospinal fluid of patients with dementia with Lewy bodies 60
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 59
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 59
Reply: Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot–Marie–Tooth disease 59
Aberrant splicing in GJB1 and the relevance of 5′ UTR in CMTX1 pathogenesis 59
Painful neuropathy vasculitis in 2 patients with long-standing human immunodeficiency virus-1 infection. 58
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome 57
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
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 56
QTc Prolongation in Patients with Dementia and Mild Cognitive Impairment: Neuropsychological and Brain Imaging Correlations 56
Human immunodeficiency virus-associated peripheral neuropathies 55
Multineuropathy in a patient with HBV infection, polyarteritis nodosa and celiac disease. 55
Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: electrophysiological abnormalities and sural nerve biopsy 54
Clinico-pathological findings in a patient with progressive cerebellar ataxia, autoimmune polyendocrine syndrome, hepatocellular carcinoma and anti-GAD autoantibodies. 51
Four novel cases of periaxin-related neuropathy and review of the literature. 51
hATTR pathology: nerve biopsy results from italian referral centers 51
La patologia delle neuropatie periferiche. 50
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling 50
ATTRv amyloidosis Italian Registry: clinical and epidemiological data 49
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study. 48
Neuropatie genetiche. 48
Sporadic hereditary neuropathies misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): pitfalls and red flags 48
Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. 48
Peripheral nerve enlargement on nerve ultrasound parallels neuropathological changes in adult-onset Krabbe disease 47
CIDP, CMT1B, or CMT1B plus CIDP? 46
Mechanisms of nerve damage in neuropathies associated with hematological diseases: lesson from nerve biopsies 46
Hereditary neuropathy with liability to pressure palsies: Electrophysiological and genetic study of a family with carpal tunnel syndrome as only clinical manifestation 45
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life. 45
Neuropathy in eosinophilic granulomatosis with polyangiitis: a comparison study of 24 cases with or without prior leukotriene antagonist exposure. 45
Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study 44
Nerve conduction velocity in CMT1A: what else can we tell? 44
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
PiB-PET detects transthyretin-related cerebral amyloid angiopathy 43
Diabetic neuropathy 42
Hereditary neuropathies, a pathological perspective 42
Neuronal intranuclear inclusion disease: Polymerase chain reaction and ultrastructural study of rectal biopsy specimen in a new case 40
Neuropathic pain in Charcot-Marie-Tooth Disease 40
Pharmacological treatment for familial amyloid neuropathy 39
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 37
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 34
Is overwork weakness relevant in Charcot-Marie-Tooth disease? 33
Nerve ultrasound findings differentiate Charcot-Marie-Tooth disease (CMT) 1A from other demyelinating CMTs 33
Totale 6.497
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Categoria #
all - tutte 22.122
article - articoli 19.715
book - libri 0
conference - conferenze 1.154
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.253
Totale 44.244
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201912 0 0 0 0 0 0 0 0 0 0 2 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
2023/2024599 36 57 58 86 95 136 28 40 14 47 2 0
Totale 6.826