IRIS
BARBIERI, FABRIZIO
 Distribuzione geografica
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Continente #
NA - Nord America 612
EU - Europa 251
AS - Asia 222
AF - Africa 4
Totale 1.089
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Nazione #
US - Stati Uniti d'America 604
SG - Singapore 112
CN - Cina 91
IT - Italia 64
NL - Olanda 60
FI - Finlandia 37
IE - Irlanda 30
DE - Germania 27
CZ - Repubblica Ceca 10
SE - Svezia 9
UA - Ucraina 9
CA - Canada 8
GB - Regno Unito 4
IN - India 4
IR - Iran 4
VN - Vietnam 4
CI - Costa d'Avorio 2
HK - Hong Kong 2
TH - Thailandia 2
TR - Turchia 2
ZA - Sudafrica 2
FR - Francia 1
KR - Corea 1
Totale 1.089
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Città #
Chandler 151
Singapore 86
Amsterdam 58
Princeton 37
Millbury 34
Beijing 33
Naples 28
Boston 24
Nanjing 24
Ashburn 23
Santa Clara 14
Jacksonville 13
Brno 10
Augusta 9
Houston 9
Napoli 9
Nanchang 8
Norwalk 8
Wilmington 8
Shenyang 7
Seattle 6
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
Des Moines 2
Hong Kong 2
Leawood 2
Yellow Springs 2
Agropoli 1
Ardabil 1
Baltimore 1
Brookline 1
Clifton 1
Fort Worth 1
Hangzhou 1
Kunming 1
Mereto Di Tomba 1
Milan 1
Monmouth Junction 1
Mumbai 1
Nocera Inferiore 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 682
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Nome #
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study 52
A new POLG1 mutation with peo and severe axonal and demyelinating sensory-motor neuropathy. 49
Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family. 49
Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy 48
Sural nerve and epidermal vascular abnormalities in a case of POEMS syndrome. 46
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. 43
Variable phenotype in a P102L Gerstmann-Straussler-Scheinker Italian family 42
A new case of Ullrich's disease. 41
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 40
Clinical and CT-scan study of a case of cerebellar ataxia and progressive hearing loss: Lichtenstein-Knorr disease? 39
A new case of Refsum's disease. A clinical, biochemical and ultrastructural study. 36
Early onset hereditary ataxias of unknown etiology. Review of a personal series. 36
A family with tomaculous neuropathy mimicking Charcot-Marie-Tooth disease. 35
A new case of Ullrich's disease. 35
Efficacy of dopamine agonist treatment in delayed-onset parkinsonism due to midbrain hemorrhage. 35
A case of Dejerine-Sottas disease with prominent ataxia and brain stem involvement. A clinical, electrophysiological, otoneurologic, and ultrastructural study. 33
Cerebellar ataxia and hypogonadism. A clinicopathological report. 32
Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family. 32
Amiodarone-induced experimental acute neuropathy in rats. 30
Clinical and genetic heterogeneity in early onset cerebellar ataxia with retained tendon reflexes. 30
Suppression of myoclonus in SCA2 by piracetam. 27
Association of ataxia-telangiectasia and progressive muscular dystrophy. Clinico-biological study of a case. 25
Clinical and computerized tomographic study of a case of Schilder's disease. 25
Chronic inflammatory demyelinating polyradiculoneuropathy. A clinical, electrophysiological and biopsy study. 24
Contribution to the problem of the adrenoleukomyeloneuropathy complex. Study of two Italian brothers with adrenoleukodystrophy and their mother with myeloneuropathy. 23
Radiation myelopathy. Report of three cases. 23
Myotonic dystrophy and pilomatricomas: an unusual association. 22
Idiopathic intracranial hypertension in a patient with thyroid papillary carcinoma 19
Friedreich's ataxia: electrophysiological and histological findings. 18
Late onset recessive ataxia with Friedreich's disease phenotype. 18
Evidence that Charcot-Marie-tooth disease with tremor coincides with the Roussy-Levy syndrome. 18
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. 17
Recurrent frontal status epilepticus with polymorphic clinical features. A case report. 17
Ischemic cerebral vasculopathy in young adults on an angiodysplastic base. 16
The distal type of hereditary motor neuropathy. Clinical and neurophysiological report of a dominant case. 14
Hearing loss associated with progressive ataxia (Lichtenstein-Knorr disease?). Report of a sporadic case with peculiar neuroradiological findings. 14
Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family. 12
Totale 1.115
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Categoria #
all - tutte 5.701
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 5.701
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202052 0 0 0 0 2 3 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
2024/2025131 51 48 0 2 30 0 0 0 0 0 0 0
Totale 1.115