CATALOGO DEI PRODOTTI DELLA RICERCA

CAVALLARO, Tiziana
 Distribuzione geografica
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Continente #
NA - Nord America 3.273
EU - Europa 2.994
AS - Asia 1.414
AF - Africa 23
SA - Sud America 14
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 2
Totale 7.726
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Nazione #
US - Stati Uniti d'America 3.266
CN - Cina 909
GB - Regno Unito 893
SG - Singapore 390
SE - Svezia 372
FR - Francia 333
RU - Federazione Russa 313
IT - Italia 296
IE - Irlanda 250
DE - Germania 198
FI - Finlandia 189
UA - Ucraina 60
BE - Belgio 35
VN - Vietnam 27
NL - Olanda 21
KR - Corea 20
ID - Indonesia 16
IN - India 14
BR - Brasile 8
HK - Hong Kong 8
IR - Iran 8
MA - Marocco 8
TG - Togo 7
RO - Romania 6
AU - Australia 5
CA - Canada 5
CL - Cile 5
EG - Egitto 5
IL - Israele 5
JP - Giappone 5
ES - Italia 4
CH - Svizzera 3
DK - Danimarca 3
TR - Turchia 3
AT - Austria 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
BA - Bosnia-Erzegovina 1
BD - Bangladesh 1
BO - Bolivia 1
DZ - Algeria 1
EE - Estonia 1
EU - Europa 1
HR - Croazia 1
IM - Isola di Man 1
JM - Giamaica 1
KG - Kirghizistan 1
KH - Cambogia 1
KZ - Kazakistan 1
LK - Sri Lanka 1
LT - Lituania 1
MD - Moldavia 1
MX - Messico 1
NZ - Nuova Zelanda 1
PL - Polonia 1
SA - Arabia Saudita 1
SN - Senegal 1
TH - Thailandia 1
TW - Taiwan 1
ZA - Sudafrica 1
Totale 7.726
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Città #
Southend 798
Chandler 574
Jacksonville 553
Woodbridge 383
Singapore 323
Dublin 250
Ann Arbor 237
Houston 222
Ashburn 150
Beijing 150
Wilmington 114
Lawrence 107
Princeton 107
Verona 90
Jinan 88
Nanjing 71
New York 71
Shenyang 56
Hebei 53
Sindelfingen 49
Redmond 41
Helsinki 39
Changsha 37
Tianjin 36
Nanchang 33
Ningbo 31
Zhengzhou 29
Brussels 28
Hangzhou 28
Falls Church 26
Haikou 24
Guangzhou 23
Lancaster 23
Milan 21
Santa Clara 20
Seoul 20
Taiyuan 20
Jiaxing 19
Kent 19
Taizhou 17
Fairfield 16
Jakarta 15
Florence 14
Norwalk 14
Bloomsbury 13
Chicago 13
Detroit 12
Dong Ket 12
Los Angeles 12
Dallas 11
Moscow 11
Seattle 11
Boardman 10
Clearwater 10
Kemerovo 9
Redwood City 9
Rome 9
Fuzhou 8
Hong Kong 8
Bologna 7
Lanzhou 7
Lappeenranta 7
Lomé 7
Riva 7
San Diego 6
Waanrode 6
Washington 6
Cairo 5
Gorizia 5
Midelt 5
Paris 5
Belo Horizonte 4
Dearborn 4
Dongguan 4
Düsseldorf 4
Edinburgh 4
Pescara 4
Vicenza 4
Auburn Hills 3
Castelfidardo 3
Des Moines 3
Frankfurt am Main 3
Mehlingen 3
Munich 3
Pavia 3
Phoenix 3
Sacramento 3
San Francisco 3
Serio 3
Tokyo 3
Trieste 3
Aarau 2
Amsterdam 2
Ardabil 2
Barcelona 2
Büdelsdorf 2
Cambridge 2
Canberra 2
Catanzaro 2
Duncan 2
Totale 5.355
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Nome #
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. 147
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy 117
RFC1 AAGGG repeat expansion masquerading as Chronic Idiopathic Axonal Polyneuropathy 114
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family. 112
X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32 112
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. 110
Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients. 110
Cytoskeletal pathology in ataxia-telangiectasia. 107
Congenital hypomyelination neuropathy with a novel mutation of PMP22 107
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E 107
Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. 107
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease 105
Endothelial adhesion molecule expression is unaltered in the peripheral nerve from patients with AIDS and distal sensory polyneuropathy 100
Segmental conduction abnormalities and myelin thickenings in Val102/fs null mutation of MPZ gene 100
Convergent pathological and ultrasound features in hereditary syndromic and non‐syndromic minifascicular neuropathy related to DHH 100
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy 98
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 96
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 95
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 93
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 93
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy 92
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H. 92
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 92
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 92
NERVE ULTRASOUND FINDINGS IN A COHORT OF PATIENTS WITH MPZ-RELATED CHARCOT-MARIE-TOOTH NEUROPATHIES 91
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 90
I quadri neuropatologici delle sindromi paraneoplastiche 89
Brentuximab vedotin: axonal microtubule's Apollyon 88
Charcot-Marie-Tooth disease with giant axons:a clinicopathological and genetic study 86
Atypical Alzheimer's disease: a case report. 81
A 58-year-old man with B-cell chronic lymphocytic leukemia and multiple strokes 80
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 79
Polyneuropathy with anti-sulfatide and anti-MAG antibodies: Clinical, neurophysiological, pathological features and response to treatment. 79
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause a MERFF syndrome. 78
Alpha-synuclein seeds in olfactory mucosa and cerebrospinal fluid of patients with dementia with Lewy bodies 78
null 77
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. 77
Axonal neuropathy due to myelin protein zero mutation misdiagnosed as amyloid neuropathy 77
Sural nerve biopsy: current role and comparison with serum neurofilament light chain levels 77
A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B 76
Correlation between clinical/neurophysiological findings and quality of life in Charcot-Marie-Tooth type 1A 76
Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 Notch3 gene mutation 76
Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutation 75
Overexpression of ErbB2 and ErbB3 receptors in Schwann cells of patients with Charcot-Marie-tooth disease type 1A 73
Primary neurolymphomatosis as clinical onset of chronic lymphocytic leukemia 73
The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study 73
Infectious neuropathies 72
Focal lesions are a feature of chronic inflammatory demyelinating polyneuropathy (CIDP). 71
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial. 71
Deoxysphingolipids as candidate biomarkers for a novel SPTLC1 mutation associated with HSAN-I 71
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 70
Myelin uncompaction and axo-glial detachment in chronic ataxic neuropathy with monospecific IgM antibody to ganglioside GD1b 70
Aberrant splicing in GJB1 and the relevance of 5′ UTR in CMTX1 pathogenesis 70
Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis. 68
Neuropatie immunitarie. 67
Reply: Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot–Marie–Tooth disease 67
Charcot-Marie-Tooth disease: new insights from skin biopsy 67
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 67
QTc Prolongation in Patients with Dementia and Mild Cognitive Impairment: Neuropsychological and Brain Imaging Correlations 67
Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias. 66
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 65
Pentraxin-3 and VEGF in POEMS syndrome: A 2-year longitudinal study. 65
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 64
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome 64
Painful neuropathy vasculitis in 2 patients with long-standing human immunodeficiency virus-1 infection. 64
La patologia delle neuropatie periferiche. 62
Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area 62
Human immunodeficiency virus-associated peripheral neuropathies 60
Multineuropathy in a patient with HBV infection, polyarteritis nodosa and celiac disease. 60
ATTRv amyloidosis Italian Registry: clinical and epidemiological data 60
hATTR pathology: nerve biopsy results from italian referral centers 60
Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: electrophysiological abnormalities and sural nerve biopsy 58
Sporadic hereditary neuropathies misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): pitfalls and red flags 58
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling 58
Clinico-pathological findings in a patient with progressive cerebellar ataxia, autoimmune polyendocrine syndrome, hepatocellular carcinoma and anti-GAD autoantibodies. 57
Four novel cases of periaxin-related neuropathy and review of the literature. 56
Neuropathy in eosinophilic granulomatosis with polyangiitis: a comparison study of 24 cases with or without prior leukotriene antagonist exposure. 56
Peripheral nerve enlargement on nerve ultrasound parallels neuropathological changes in adult-onset Krabbe disease 56
Neuropatie genetiche. 55
Hereditary neuropathies, a pathological perspective 55
CIDP, CMT1B, or CMT1B plus CIDP? 54
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study. 53
Charcot-Marie-Tooth type 2B: a new phenotype associated with a novel RAB7A mutation and inhibited EGFR degradation 53
Mechanisms of nerve damage in neuropathies associated with hematological diseases: lesson from nerve biopsies 53
Pharmacological treatment for familial amyloid polyneuropathy 51
Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. 51
Hereditary neuropathy with liability to pressure palsies: Electrophysiological and genetic study of a family with carpal tunnel syndrome as only clinical manifestation 50
Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study 50
Diabetic neuropathy 50
PiB-PET detects transthyretin-related cerebral amyloid angiopathy 49
Nerve conduction velocity in CMT1A: what else can we tell? 49
Neuropathic pain in Charcot-Marie-Tooth Disease 49
Anxiety and depression in Charcot-Marie-Tooth disease: data from the Italian CMT national registry 48
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life. 48
Neurolymphomatosis, a rare manifestation of peripheral nerve involvement in lymphomas: suggestive features and diagnostic challenges 46
Neuronal intranuclear inclusion disease: Polymerase chain reaction and ultrastructural study of rectal biopsy specimen in a new case 44
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 43
Pharmacological treatment for familial amyloid neuropathy 43
Responsiveness of clinical outcome measures in Charcot-Marie-Tooth disease 41
Progressive brachial plexus enlargement in hereditary transthyretin amyloidosis 41
Totale 7.372
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Categoria #
all - tutte 29.183
article - articoli 26.122
book - libri 0
conference - conferenze 1.445
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.616
Totale 58.366
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020672 0 0 0 0 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
2024/2025879 147 154 76 393 109 0 0 0 0 0 0 0
Totale 7.872