IRIS
TONDUTI, DAVIDE
 Distribuzione geografica
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Continente #
NA - Nord America 436
EU - Europa 239
AS - Asia 56
OC - Oceania 2
SA - Sud America 1
Totale 734
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Nazione #
US - Stati Uniti d'America 434
IE - Irlanda 146
CN - Cina 48
FI - Finlandia 29
IT - Italia 25
DE - Germania 14
BE - Belgio 10
SE - Svezia 6
IN - India 5
GB - Regno Unito 4
AU - Australia 2
CA - Canada 2
PT - Portogallo 2
BR - Brasile 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
HK - Hong Kong 1
KZ - Kazakistan 1
MD - Moldavia 1
SG - Singapore 1
Totale 734
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Città #
Chandler 157
Dublin 146
Ashburn 35
Wilmington 25
Helsinki 24
Ann Arbor 20
Lawrence 18
Medford 18
Princeton 18
Shanghai 13
New York 12
Beijing 11
Brussels 10
Jacksonville 10
Nanjing 9
Falls Church 8
Milan 7
Los Angeles 6
Washington 6
Shenyang 5
Norwalk 4
Pavia 4
Pune 4
Tianjin 3
Amadora 2
Brescia 2
Changsha 2
Osimo 2
Toronto 2
Tronzano Vercellese 2
Adliswil 1
Almaty 1
Andover 1
Berlin 1
Chisinau 1
Des Moines 1
Fairfield 1
Falkenstein 1
Garbagnate Milanese 1
Hebei 1
Hunters Hill 1
London 1
Melbourne 1
Nanchang 1
Olomouc 1
Padova 1
Redmond 1
Rio Saliceto 1
Rome 1
Singapore 1
Woodbridge 1
Totale 606
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Nome #
A novel mutation in COL4A1 gene: A possible cause of early postnatal cerebrovascular events 58
Neuroradiologic patterns and novel imaging findings in Aicardi-Goutières syndrome 56
cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing 54
Encephalopathies with intracranial calcification in children: Clinical and genetic characterization 50
Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review 47
Cortical malformations and COL4A1 mutation: Three new cases 46
Altered PLP1 splicing causes hypomyelination of early myelinating structures 44
The epileptology of Aicardi-Goutières syndrome: electro-clinical-radiological findings 42
Neurodevelopmental outcome of preterm very low birth weight infants admitted to an Italian tertiary center over an 11-year period 41
KARS-related diseases: Progressive leukoencephalopathy with brainstem and spinal cord calcifications as new phenotype and a review of literature 39
Genetic and phenotypic spectrum associated with IFIH1 gain-of-function 38
Expanding the phenotypic spectrum of Allan–Herndon–Dudley syndrome in patients with SLC16A2 mutations 38
TUBB4A-related hypomyelinating leukodystrophy: New insights from a series of 12 patients 37
Novel and emerging treatments for Aicardi-Goutières syndrome 37
Late-Onset Aicardi-Goutières Syndrome: A Characterization of Presenting Clinical Features 37
Spontaneous MRI improvement and absence of cerebral calcification in Aicardi-Goutières syndrome: Diagnostic and disease-monitoring implications 33
Placental features of fetal vascular malperfusion and infant neurodevelopmental outcomes at 2 years of age in severe fetal growth restriction 31
Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C 29
Totale 757
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Categoria #
all - tutte 3.323
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 3.323
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202038 12 11 0 0 0 0 0 1 1 8 5 0
2020/202140 0 1 0 5 1 5 0 8 11 5 2 2
2021/2022119 2 1 3 2 6 13 3 4 7 7 16 55
2022/2023396 36 38 4 42 38 31 0 22 170 4 9 2
2023/2024148 17 31 11 12 11 40 3 10 0 9 4 0
Totale 757