IRIS
BIANCHI, SILVIA
 Distribuzione geografica
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Continente #
NA - Nord America 156
EU - Europa 71
AS - Asia 21
AF - Africa 4
OC - Oceania 2
SA - Sud America 1
Totale 255
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Nazione #
US - Stati Uniti d'America 154
IT - Italia 32
IE - Irlanda 20
HK - Hong Kong 7
FR - Francia 6
VN - Vietnam 6
JP - Giappone 5
ZA - Sudafrica 4
DE - Germania 3
GB - Regno Unito 3
NL - Olanda 3
AU - Australia 2
CA - Canada 2
IN - India 2
SE - Svezia 2
AE - Emirati Arabi Uniti 1
BR - Brasile 1
GR - Grecia 1
LT - Lituania 1
Totale 255
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Città #
Fairfield 21
Dublin 19
Siena 19
Santa Cruz 12
Seattle 12
Ashburn 11
Woodbridge 11
Central 7
Dong Ket 6
Buffalo 5
Chapel Hill 5
Boardman 4
Cambridge 4
Chicago 4
Houston 4
Las Vegas 4
New York 4
Milan 3
Muizenberg 3
Naples 3
San Diego 3
Southend 3
Wilmington 3
Ann Arbor 2
Lake Forest 2
San Francisco 2
Stockholm 2
Sydney 2
Turin 2
Atlanta 1
Boisar 1
Büdelsdorf 1
Casoria 1
Cedar Knolls 1
Council Bluffs 1
Florence 1
Hartford 1
Henderson 1
Munich 1
Phoenix 1
Ponta Grossa 1
Pune 1
Rome 1
San Mateo 1
Silverton 1
Thessaloniki 1
Tokyo 1
Toronto 1
Totale 201
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Nome #
Location, number and factors associated with cerebral microbleeds in an Italian-British cohort of CADASIL patients, file e0feeaa7-e520-44d2-e053-6605fe0a8db0 122
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: Update on clinical, diagnostic, and management aspects, file e0feeaa6-2617-44d2-e053-6605fe0a8db0 72
Circulating Biomarkers in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Patients, file e0feeaa6-22bc-44d2-e053-6605fe0a8db0 23
Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease, file e0feeaab-c246-44d2-e053-6605fe0a8db0 23
Location, number and factors associated with cerebral microbleeds in an Italian-British cohort of CADASIL patients, file e0feeaa7-e535-44d2-e053-6605fe0a8db0 15
Blood–brain barrier permeability in a patient with Labrune syndrome due to SNORD118 mutations, file e0feeaa7-a367-44d2-e053-6605fe0a8db0 3
CADASIL in central Italy: a retrospective clinical and genetic study in 229 patients, file e0feeaa4-bc72-44d2-e053-6605fe0a8db0 1
Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients., file e0feeaa4-c1f1-44d2-e053-6605fe0a8db0 1
Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL, exon 2 mutation., file e0feeaa4-e2ac-44d2-e053-6605fe0a8db0 1
Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy., file e0feeaa4-ea59-44d2-e053-6605fe0a8db0 1
Human peripheral blood lymphocytes and fibroblasts as Notch3 expression models., file e0feeaa4-f37c-44d2-e053-6605fe0a8db0 1
Adult Alexander disease with de novo c.1193C>T heterozygous variant in GFAP gene, file e0feeaa5-9fab-44d2-e053-6605fe0a8db0 1
Totale 264
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Categoria #
all - tutte 2.315
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 2.315
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201919 0 0 0 0 0 0 0 0 0 6 7 6
2019/202031 3 3 2 4 2 3 3 3 3 2 1 2
2020/202140 2 1 1 2 0 3 5 2 1 9 5 9
2021/202254 3 5 2 0 3 1 3 0 1 8 22 6
2022/202371 3 5 14 9 9 15 3 8 1 0 4 0
2023/202439 3 0 2 4 2 7 15 6 0 0 0 0
Totale 264