BARBIERI, FABRIZIO
 Distribuzione geografica
Continente #
NA - Nord America 656
AS - Asia 338
EU - Europa 292
AF - Africa 4
SA - Sud America 1
Totale 1.291
Nazione #
US - Stati Uniti d'America 648
SG - Singapore 149
CN - Cina 92
HK - Hong Kong 80
IT - Italia 66
NL - Olanda 60
FI - Finlandia 38
RU - Federazione Russa 35
IE - Irlanda 30
DE - Germania 28
CZ - Repubblica Ceca 10
SE - Svezia 9
UA - Ucraina 9
CA - Canada 8
GB - Regno Unito 5
IN - India 4
IR - Iran 4
VN - Vietnam 4
CI - Costa d'Avorio 2
TH - Thailandia 2
TR - Turchia 2
ZA - Sudafrica 2
BR - Brasile 1
FR - Francia 1
KR - Corea 1
PT - Portogallo 1
Totale 1.291
Città #
Chandler 151
Singapore 86
Hong Kong 80
Amsterdam 58
Santa Clara 47
Princeton 37
Millbury 34
Beijing 33
Naples 29
Boston 24
Nanjing 24
Ashburn 23
Jacksonville 13
Seattle 11
Brno 10
Augusta 9
Houston 9
Napoli 9
Nanchang 8
Norwalk 8
Wilmington 8
Shenyang 7
Jiaxing 5
Kronberg 5
Ottawa 5
Boardman 4
Dong Ket 4
Hebei 4
Tianjin 4
Changsha 3
Dallas 3
Edmonton 3
Falls Church 3
Indiana 3
Ankara 2
Cape Town 2
Carrù 2
Columbus 2
Des Moines 2
Leawood 2
Yellow Springs 2
Agropoli 1
Ardabil 1
Baltimore 1
Bauru 1
Brookline 1
Camposano 1
Clifton 1
Fort Worth 1
Handan 1
Hangzhou 1
Helsinki 1
Kunming 1
Lisbon 1
London 1
Mereto Di Tomba 1
Milan 1
Monmouth Junction 1
Mumbai 1
Nocera Inferiore 1
Nuremberg 1
Orange 1
Palermo 1
Pune 1
Redwood City 1
Rome 1
Salerno 1
San Jose 1
San Mateo 1
Simi Valley 1
Solopaca 1
Totale 808
Nome #
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study 59
A new POLG1 mutation with peo and severe axonal and demyelinating sensory-motor neuropathy. 55
Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy 55
Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family. 54
Variable phenotype in a P102L Gerstmann-Straussler-Scheinker Italian family 50
Sural nerve and epidermal vascular abnormalities in a case of POEMS syndrome. 49
A second family with hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibres, detected in the same geographic area as the first family. 48
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 45
A new case of Ullrich's disease. 45
Clinical and CT-scan study of a case of cerebellar ataxia and progressive hearing loss: Lichtenstein-Knorr disease? 44
A new case of Refsum's disease. A clinical, biochemical and ultrastructural study. 43
Efficacy of dopamine agonist treatment in delayed-onset parkinsonism due to midbrain hemorrhage. 43
A family with tomaculous neuropathy mimicking Charcot-Marie-Tooth disease. 40
Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family. 40
A new case of Ullrich's disease. 39
A case of Dejerine-Sottas disease with prominent ataxia and brain stem involvement. A clinical, electrophysiological, otoneurologic, and ultrastructural study. 38
Early onset hereditary ataxias of unknown etiology. Review of a personal series. 38
Amiodarone-induced experimental acute neuropathy in rats. 37
Suppression of myoclonus in SCA2 by piracetam. 36
Cerebellar ataxia and hypogonadism. A clinicopathological report. 36
Clinical and genetic heterogeneity in early onset cerebellar ataxia with retained tendon reflexes. 33
Clinical and computerized tomographic study of a case of Schilder's disease. 32
Association of ataxia-telangiectasia and progressive muscular dystrophy. Clinico-biological study of a case. 31
Chronic inflammatory demyelinating polyradiculoneuropathy. A clinical, electrophysiological and biopsy study. 29
Contribution to the problem of the adrenoleukomyeloneuropathy complex. Study of two Italian brothers with adrenoleukodystrophy and their mother with myeloneuropathy. 29
Radiation myelopathy. Report of three cases. 28
Friedreich's ataxia: electrophysiological and histological findings. 25
Myotonic dystrophy and pilomatricomas: an unusual association. 25
Idiopathic intracranial hypertension in a patient with thyroid papillary carcinoma 24
Evidence that Charcot-Marie-tooth disease with tremor coincides with the Roussy-Levy syndrome. 23
Is the sensory neuropathy in ataxia-telangiectasia distinguishable from that in Friedreich's ataxia? Morphometric and ultrastructural study of the sural nerve in a case of Louis Bar syndrome. 22
Late onset recessive ataxia with Friedreich's disease phenotype. 22
Recurrent frontal status epilepticus with polymorphic clinical features. A case report. 22
Ischemic cerebral vasculopathy in young adults on an angiodysplastic base. 22
The distal type of hereditary motor neuropathy. Clinical and neurophysiological report of a dominant case. 21
Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family. 18
Hearing loss associated with progressive ataxia (Lichtenstein-Knorr disease?). Report of a sporadic case with peculiar neuroradiological findings. 18
Totale 1.318
Categoria #
all - tutte 6.573
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 6.573


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202047 0 0 0 0 0 0 0 0 2 18 22 5
2020/202168 2 2 4 2 8 15 3 0 3 1 22 6
2021/2022198 3 0 0 0 0 6 0 6 35 18 47 83
2022/2023317 39 32 11 38 35 36 0 13 43 62 7 1
2023/2024188 6 42 45 5 7 3 10 20 0 0 34 16
2024/2025334 51 48 0 2 30 48 113 42 0 0 0 0
Totale 1.318