BARBIERI, FABRIZIO
 Distribuzione geografica
Continente #
NA - Nord America 393
EU - Europa 146
AS - Asia 105
Totale 644
Nazione #
US - Stati Uniti d'America 385
CN - Cina 91
FI - Finlandia 37
IT - Italia 32
IE - Irlanda 30
DE - Germania 22
SE - Svezia 9
UA - Ucraina 9
CA - Canada 8
GB - Regno Unito 4
IR - Iran 4
VN - Vietnam 4
IN - India 3
NL - Olanda 2
TH - Thailandia 2
FR - Francia 1
KR - Corea 1
Totale 644
Città #
Chandler 148
Princeton 37
Millbury 34
Beijing 33
Boston 24
Nanjing 24
Jacksonville 13
Augusta 9
Houston 9
Napoli 9
Nanchang 8
Norwalk 8
Wilmington 8
Shenyang 7
Jiaxing 5
Ottawa 5
Boardman 4
Dong Ket 4
Hebei 4
Tianjin 4
Changsha 3
Edmonton 3
Falls Church 3
Indiana 3
Carrù 2
Des Moines 2
Leawood 2
Yellow Springs 2
Agropoli 1
Ardabil 1
Baltimore 1
Dallas 1
Hangzhou 1
Kunming 1
Mereto Di Tomba 1
Milan 1
Monmouth Junction 1
Mumbai 1
Naples 1
Nocera Inferiore 1
Orange 1
Palermo 1
Redwood City 1
Salerno 1
San Jose 1
San Mateo 1
Seattle 1
Simi Valley 1
Solopaca 1
Totale 438
Nome #
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study 36
Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family. 33
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. 33
A new POLG1 mutation with peo and severe axonal and demyelinating sensory-motor neuropathy. 31
Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy 27
Variable phenotype in a P102L Gerstmann-Straussler-Scheinker Italian family 26
A new case of Ullrich's disease. 25
A new case of Refsum's disease. A clinical, biochemical and ultrastructural study. 24
Clinical and CT-scan study of a case of cerebellar ataxia and progressive hearing loss: Lichtenstein-Knorr disease? 24
Sural nerve and epidermal vascular abnormalities in a case of POEMS syndrome. 23
A case of Dejerine-Sottas disease with prominent ataxia and brain stem involvement. A clinical, electrophysiological, otoneurologic, and ultrastructural study. 23
A family with tomaculous neuropathy mimicking Charcot-Marie-Tooth disease. 22
A new case of Ullrich's disease. 22
Efficacy of dopamine agonist treatment in delayed-onset parkinsonism due to midbrain hemorrhage. 22
Suppression of myoclonus in SCA2 by piracetam. 19
Early onset hereditary ataxias of unknown etiology. Review of a personal series. 19
Cerebellar ataxia and hypogonadism. A clinicopathological report. 19
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 18
Amiodarone-induced experimental acute neuropathy in rats. 18
Clinical and computerized tomographic study of a case of Schilder's disease. 17
Chronic inflammatory demyelinating polyradiculoneuropathy. A clinical, electrophysiological and biopsy study. 16
Association of ataxia-telangiectasia and progressive muscular dystrophy. Clinico-biological study of a case. 16
Clinical and genetic heterogeneity in early onset cerebellar ataxia with retained tendon reflexes. 16
Radiation myelopathy. Report of three cases. 16
Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family. 15
Friedreich's ataxia: electrophysiological and histological findings. 12
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. 11
Late onset recessive ataxia with Friedreich's disease phenotype. 11
Contribution to the problem of the adrenoleukomyeloneuropathy complex. Study of two Italian brothers with adrenoleukodystrophy and their mother with myeloneuropathy. 10
Recurrent frontal status epilepticus with polymorphic clinical features. A case report. 9
Hearing loss associated with progressive ataxia (Lichtenstein-Knorr disease?). Report of a sporadic case with peculiar neuroradiological findings. 9
Myotonic dystrophy and pilomatricomas: an unusual association. 9
Idiopathic intracranial hypertension in a patient with thyroid papillary carcinoma 9
Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family. 8
The distal type of hereditary motor neuropathy. Clinical and neurophysiological report of a dominant case. 8
Evidence that Charcot-Marie-tooth disease with tremor coincides with the Roussy-Levy syndrome. 8
Ischemic cerebral vasculopathy in young adults on an angiodysplastic base. 6
Totale 670
Categoria #
all - tutte 1548
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 1548


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/20184 0000 00 02 0020
2018/201928 0004 013 80 0003
2019/202097 43020 23 00 218225
2020/202168 2242 815 30 31226
2021/2022198 3000 06 06 35184783
2022/2023191 39321138 3536 00 0000
Totale 670