IRIS
BATTISTI, CARLA
 Distribuzione geografica
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Continente #
NA - Nord America 314
EU - Europa 165
AS - Asia 23
AF - Africa 6
SA - Sud America 3
OC - Oceania 2
Totale 513
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Nazione #
US - Stati Uniti d'America 304
IT - Italia 68
IE - Irlanda 39
DE - Germania 18
VN - Vietnam 16
FR - Francia 14
CA - Canada 10
GB - Regno Unito 10
SE - Svezia 6
ZA - Sudafrica 6
JP - Giappone 5
CZ - Repubblica Ceca 3
DK - Danimarca 3
CL - Cile 2
AE - Emirati Arabi Uniti 1
AU - Australia 1
BE - Belgio 1
BR - Brasile 1
CH - Svizzera 1
CN - Cina 1
FI - Finlandia 1
NZ - Nuova Zelanda 1
RO - Romania 1
Totale 513
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Città #
Siena 41
Dublin 37
Fairfield 36
Ashburn 29
Seattle 28
Cambridge 23
Woodbridge 23
Buffalo 21
Santa Cruz 18
Dong Ket 15
Essen 12
Ottawa 9
Ann Arbor 8
Southend 8
Wilmington 7
Chicago 6
Houston 6
Rome 6
Stockholm 6
Clearwater 5
Las Vegas 5
Los Angeles 5
Muizenberg 5
Taku 4
Boardman 3
Milan 3
New York 3
Provo 3
San Diego 3
San Francisco 3
Florence 2
Grosseto 2
Jacksonville 2
Lake Forest 2
Phoenix 2
Auckland 1
Austin 1
Bagno a Ripoli 1
Bari 1
Castellaneta 1
Dallas 1
Durban 1
Easton 1
Falls Church 1
Hanoi 1
Helsinki 1
Henderson 1
Henrico 1
Jersey City 1
Jona 1
Mainz 1
Messina 1
Muncie 1
Munich 1
Mérignac 1
Naples 1
Padova 1
Paris 1
Ponta Grossa 1
Portland 1
Salem 1
Santa Maria a Monte 1
Scranton 1
Sesto Fiorentino 1
Shanghai 1
Sindelfingen 1
Toronto 1
Toulouse 1
University Park 1
Totale 425
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Nome #
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study, file e0feeaa7-ee5e-44d2-e053-6605fe0a8db0 133
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study, file e0feeaa7-ee64-44d2-e053-6605fe0a8db0 133
Next-generation sequencing approach to hyperCKemia: A 2-year cohort study, file e0feeaa8-a0b3-44d2-e053-6605fe0a8db0 84
Functional and Brain Activation Changes Following Specialized Upper-Limb Exercise in Parkinson's Disease, file e0feeaa9-28ce-44d2-e053-6605fe0a8db0 46
Analysis of opa1 isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 gene, file e0feeaa6-6d23-44d2-e053-6605fe0a8db0 36
Neurophthalmologic and Orthoptic Ambulatory Assessments Reveal Ocular and Visual Changes in Patients With Early Alzheimer and Parkinson's Disease, file e0feeaa9-8b63-44d2-e053-6605fe0a8db0 31
Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease, file e0feeaab-c246-44d2-e053-6605fe0a8db0 23
Electrodiagnosis in cranial botulism, file e0feeaa5-b75a-44d2-e053-6605fe0a8db0 9
Diagnosis, treatment, and follow-up of patients with cerebral amyloid angiopathy-related inflammation, file 55ca6824-1767-4678-a0c5-a6f1aee1b747 7
FOLR1 Gene Variation With Adult-Onset Cerebral Folate Deficiency and Stable Clinical and MRI Features up to 2 Years, file 8392baf0-e744-48fc-8c25-78016b4c811d 5
Oxidative stress-induced apoptosis in peripheral blood lymphocytes from patients with POLG-related disorders, file e0feeaa6-2eb9-44d2-e053-6605fe0a8db0 4
A case report of FAVA syndrome in a young woman carrying a mutation in the PIK3CA gene, file c1ecfb0a-5ed4-423b-85b6-190e9ede2505 3
Apoptosis and Oxidative Stress in Neurodegenerative Diseases., file e0feeaa5-030e-44d2-e053-6605fe0a8db0 3
Evaluation of brain apoptosis in a CADASIL postmortem case, file e0feeaa4-c1ed-44d2-e053-6605fe0a8db0 2
Oxidative stress-induced apoptosis in two patients with Alagille syndrome., file e0feeaa4-f37b-44d2-e053-6605fe0a8db0 2
Electron-dense lamellated inclusions in 2 siblings with Kufor-Rakeb syndrome., file e0feeaa4-fdf2-44d2-e053-6605fe0a8db0 2
Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease., file e0feeaa4-e282-44d2-e053-6605fe0a8db0 1
Autonomic dysfunction in mental retardation and spastic paraparesis with MECP2 mutation., file e0feeaa4-ed53-44d2-e053-6605fe0a8db0 1
Cerebrolysin administration reduces oxidative-stress induced apoptosis in limphocytes from healthy subjects, file e0feeaa4-f215-44d2-e053-6605fe0a8db0 1
C9ORF72 gene expansion in a patient with intellectual disability and psychiatric disease, file e0feeaa6-2847-44d2-e053-6605fe0a8db0 1
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients, file e0feeaaa-6321-44d2-e053-6605fe0a8db0 1
Prevalence and impact of COVID-19 in Parkinson’s disease: evidence from a multi-center survey in Tuscany region, file e0feeaaa-7ea5-44d2-e053-6605fe0a8db0 1
Totale 529
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Categoria #
all - tutte 5.916
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 5.916
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201930 0 0 0 0 0 0 0 0 0 9 12 9
2019/202077 9 5 3 8 7 4 5 7 12 5 8 4
2020/2021110 5 7 4 4 4 13 5 16 4 17 14 17
2021/2022101 7 10 3 3 4 2 6 7 1 8 38 12
2022/2023120 2 6 27 10 16 15 10 17 1 8 4 4
2023/202477 6 1 6 6 7 16 23 5 3 4 0 0
Totale 529