CINECA IRIS Institutional Research Information System

BATTINI, ROBERTA
 Distribuzione geografica
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Continente #
NA - Nord America 14.129
AS - Asia 10.499
EU - Europa 4.562
SA - Sud America 3.265
AF - Africa 316
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 8
Totale 32.789
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Nazione #
US - Stati Uniti d'America 13.486
SG - Singapore 3.009
BR - Brasile 2.688
CN - Cina 2.644
HK - Hong Kong 2.432
IT - Italia 1.671
VN - Vietnam 1.277
BG - Bulgaria 690
SE - Svezia 636
CA - Canada 512
RU - Federazione Russa 350
DE - Germania 269
TR - Turchia 261
KR - Corea 233
AR - Argentina 224
GB - Regno Unito 188
FI - Finlandia 156
EC - Ecuador 137
IN - India 121
UA - Ucraina 120
ID - Indonesia 118
FR - Francia 104
AT - Austria 96
BD - Bangladesh 94
CI - Costa d'Avorio 76
MX - Messico 73
CO - Colombia 68
ZA - Sudafrica 66
NL - Olanda 56
IQ - Iraq 48
CH - Svizzera 45
PY - Paraguay 44
JP - Giappone 39
VE - Venezuela 36
SN - Senegal 31
CL - Cile 28
MA - Marocco 27
PK - Pakistan 27
PL - Polonia 26
NG - Nigeria 25
SA - Arabia Saudita 25
ES - Italia 24
TN - Tunisia 23
BE - Belgio 22
EG - Egitto 22
UZ - Uzbekistan 18
UY - Uruguay 17
JO - Giordania 16
CZ - Repubblica Ceca 15
PE - Perù 15
IE - Irlanda 13
DZ - Algeria 12
IR - Iran 12
NP - Nepal 12
GR - Grecia 11
LT - Lituania 11
IL - Israele 10
KE - Kenya 10
AE - Emirati Arabi Uniti 9
AU - Australia 9
OM - Oman 9
PA - Panama 9
HN - Honduras 8
HU - Ungheria 8
JM - Giamaica 8
KZ - Kazakistan 8
AL - Albania 7
AZ - Azerbaigian 7
DO - Repubblica Dominicana 7
MY - Malesia 7
TT - Trinidad e Tobago 7
AM - Armenia 6
BN - Brunei Darussalam 6
BO - Bolivia 6
GE - Georgia 6
QA - Qatar 6
RO - Romania 6
SI - Slovenia 6
BH - Bahrain 5
LB - Libano 5
BA - Bosnia-Erzegovina 4
BB - Barbados 4
ET - Etiopia 4
KW - Kuwait 4
PS - Palestinian Territory 4
PT - Portogallo 4
RS - Serbia 4
SY - Repubblica araba siriana 4
BJ - Benin 3
BW - Botswana 3
CR - Costa Rica 3
DK - Danimarca 3
EU - Europa 3
KG - Kirghizistan 3
KH - Cambogia 3
LV - Lettonia 3
MD - Moldavia 3
MN - Mongolia 3
NI - Nicaragua 3
PH - Filippine 3
Totale 32.742
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Città #
Hong Kong 2.424
Ashburn 1.798
Fairfield 1.644
Singapore 1.456
Woodbridge 1.099
Houston 827
Dallas 824
Shanghai 725
Sofia 687
Santa Clara 632
Seattle 602
Beijing 576
Cambridge 551
Wilmington 512
Ottawa 464
Ann Arbor 437
Milan 426
New York 407
Chandler 404
Ho Chi Minh City 380
Hefei 378
Boardman 374
Princeton 361
Lawrence 293
Seoul 226
Medford 212
Hanoi 201
São Paulo 199
Los Angeles 189
Des Moines 186
Istanbul 184
Nanjing 167
Redondo Beach 141
Serra 131
Florence 124
Buffalo 122
Rome 119
Jacksonville 109
Dong Ket 108
Rio de Janeiro 97
San Diego 96
Abidjan 76
Nuremberg 67
Belo Horizonte 66
Brasília 61
Vienna 61
Izmir 53
Munich 53
Nanchang 50
Shenyang 48
Ogden 47
Guayaquil 46
Haiphong 46
Frankfurt am Main 45
Helsinki 45
London 42
Porto Alegre 42
Pisa 41
Quito 41
Curitiba 40
Hebei 40
Marseille 38
Kunming 36
Bern 33
Council Bluffs 33
Dearborn 33
Redwood City 33
Boulder 32
Campinas 32
Changsha 32
Da Nang 32
Chicago 31
Dakar 31
Lappeenranta 31
Tokyo 31
Jiaxing 30
Norwalk 30
Columbus 29
Thái Bình 29
Hyderabad 28
Johannesburg 28
Lancaster 28
Turku 28
Genoa 27
Biên Hòa 26
Goiânia 25
Guangzhou 25
Lagos 25
Dhaka 24
Naples 24
Salvador 24
San Jose 24
Tianjin 24
Bari 23
The Dalles 23
Düsseldorf 21
Jüchen 21
Lucca 21
Recife 21
Jakarta 20
Totale 22.988
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Nome #
Pedagogia speciale della gestione integrata del gruppo classe 306
Aspetti neuropsicologici della distrofia muscolare di Duchenne 210
Prenatal ultrasound and magnetic resonance features in a fetus with Walker-Warburg syndrome. Letters to the editor 204
Psychometric properties of Movement Disorder-Childhood Rating Scale 194
Implicit learning deficit in children with Duchenne muscular dystrophy: Evidence for a cerebellar cognitive impairment? 183
Non-invasive assessment of Neuromuscular Disorders by 7 tesla Magnetic Resonance Imaging and Spectroscopy: Dedicated radio-frequency coil development 173
Responsiveness of the MD-Childhood Rating Scale in dyskinetic cerebral palsy patients undergoing anticholinergic treatment 171
Isolated mild intellectual disability expands the aminoacylase 1 phenotype spectrum 167
Leukoencephalopathy with bilateral anterior temporal lobe cysts: a further case of this new entity 165
The Clinical Impact of Methotrexate-Induced Stroke-Like Neurotoxicity in Paediatric Departments: An Italian Multi-Centre Case-Series 164
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study 164
Focal cortical dysplasia, microcephaly and epilepsy in a boy with 1q21.1-q21.3 duplication 163
Treatment monitoring of brain creatine deficiency syndromes: a 1H and 31P MR spectroscopy study 162
Longitudinal follow up of a boy affected by Pol III-related leukodystrophy: A detailed phenotype description 162
Creatine depletion in a new case with AGAT deficiency: clinical and genetic study in a large pedigree 159
Reading impairment in Duchenne muscular dystrophy: a pilot study to investigate similarities and differences with developmental dyslexia 157
Deletion Extents are not the cause of clinical variability in 22q11.2 deletion syndrome: Does the interaction between DGCR8 and miRNA-CNVs play a major role? 157
Arginine:glycine amidinotransferase (AGAT) deficiency in a newborn: early treatment can prevent phenotypic expression of the disease 157
Diffusion Tractography Biomarkers of Pediatric Cerebellar Hypoplasia/Atrophy: Preliminary Results Using Constrained Spherical Deconvolution 153
Neuropsychological profile and clinical effects of arginine treatment in children with creatine transport deficiency. 149
Ultrafast MR imaging and ultrasonography of fetal brain abnormalities: a comparative study 148
Muscle metabolic alterations assessed by 31-phosphorus magnetic resonance spectroscopy in mild Becker muscular dystrophy 147
A diagnostic dilemma in a family with cystinuria type B resolved by muscle magnetic resonance 146
Bone mineralizatio in survivors of acute lynfoblastic leukemia 145
Movement Disorder-Childhood Rating Scale: A Sensitive Tool to Evaluate Movement Disorders 145
Evaluation and treatment of childhood movement disorders 143
Neurodevelopmental disorders in children with severe to profound sensorineural hearing loss: a clinical study 143
Neurovisual Manifestations in Children with Mild COVID-19: An Association to Remember 142
Gas chromatography/mass spectrometry assay for arginine: glycine-amidinotransferase deficiency 142
Assessment of bone mineral status at phalanges of the hand by morphological analysis of ultrasound graphic trace 141
Assessment of Postural Control in Children with Movement Disorders by Means of a New Technological Tool: A Pilot Study 140
A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation 140
Behavioural and emotional changes during covid-19 lockdown in an italian paediatric population with neurologic and psychiatric disorders 140
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study 138
Unusual clinical and magnetic resonance imaging findings in a family with proteolipid protein gene mutation 136
Gain of function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling 136
Clinical and genetic findings in a series of italian children with pure hereditary spastic paraplegia 135
Fifteen-year follow-up of Italian families affected by arginine glycine amidinotransferase deficiency 134
Brain lactic alkalosis in Aicardi-Goutières Syndrome 133
Kinematic analysis of upper limb in children with movement disorder: Quantitatitative assessment of effectiveness of pharmacological trials. 133
Movement Disorder-Childhood Rating Scale: Reliability and Validity 133
Phenotype and natural history of variant late infantile ceroid-lipofuscinosis 5. 132
Benefits of glucocorticoids in non-ambulant boys/men with Duchenne muscular dystrophy: A multicentric longitudinal study using the Performance of Upper Limb test 131
Parental Practices and Environmental Differences among Infants Living in Upper-Middle and High-Income Countries: A Cross-Sectional Study 130
Proton magnetic resonance spectroscopy (H-1-MRS) of the cerebrum in two young infants with Zellweger syndrome 130
Brain magnetic resonance in the diagnostic evaluation of mitochondrial encephalopathies 130
Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data 130
Androgen receptor blockade does not impair bone mineral density in adolescent females 129
Cyclocreatine treatment ameliorates the cognitive, autistic and epileptic phenotype in a mouse model of Creatine Transporter Deficiency 129
Un'introduzione al PEI 128
Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53 128
Clinical and genetic findings in a series of Italian children with pure hereditary spastic paraplegia. 127
Elevated Serum Creatine Kinase and Small Cerebellum Prompt Diagnosis of Congenital Muscular Dystrophy due to FKRP Mutations. 126
Arginine and glycine stimulate creatine synthesis in creatine transporter 1-deficient lymphoblasts 126
DNA Methylation Biomarkers for Young Children with Idiopathic Autism Spectrum Disorder: A Systematic Review 125
Trehalose Treatment in Zebrafish Model of Lafora Disease 125
Erratum: Variant of Rett syndrome and CDKL5 gene: Clinical and autonomic description of 10 cases (Neuropediatrics (2013) 44 (237-238)) 125
24 month longitudinal data in ambulant boys with duchenne muscular dystrophy 125
Early neurodevelopmental characterization in children with cobalamin C/defect 125
Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome 124
Cognitive, adaptive, and behavioral features in Joubert syndrome 122
Scale for evaluation of movement disorders in the first three years of life 122
Movement Disorders in Children with a Mitochondrial Disease: A Cross-Sectional Survey from the Nationwide Italian Collaborative Network of Mitochondrial Diseases 121
CLINICAL AND MR SPECTROSCOPY FOLLOW-UP OF CT1 DEFICIENT ITALIAN PATIENTS TREATED BY ORAL ARGININE 120
Guanidinoacetate and creatine plus creatinine assessment in physiologic fluids: An effective diagnostic tool for the biochemical diagnosis of arginine : glycine amidinotransferase and guanidinoacetate methyltransferase deficiencies 120
Inborn errors of creatine metabolism and epilepsy. 119
Functional levels and MRI patterns of muscle involvement in upper limbs in Duchenne muscular dystrophy 119
Functional changes in Duchenne muscular dystrophy A 12-month longitudinal cohort study 119
"I have got something positive out of this situation": Psychological benefits of caregiving in relatives of young people with muscular dystrophy 118
Molecular cytogenetic characterization of a new case of patial trisomy 13 (13q11q13.2)Research letter 117
Psychopathological Impact in Patients with History of Rheumatic Fever with or without Sydenham's Chorea: A Multicenter Prospective Study 116
Proton MR spectroscopy of mitochondrial diseases: analysis of brain metabolic abnormalities and their possible diagnostic relevance 116
Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review 116
Movement disorders - Childhood Rating Scale 4-18 revised in children with dyskinetic cerebral palsy 116
Does the assessment of general movements without video observation reliably predict neurological outcome? RID F-1503-2010 115
Variant of Rett syndrome and CDKL5 gene: clinical and autonomic description of 10 cases. 115
Quantitative analysis at 1.5 T muscle MRI in neuromuscular disorderd 115
Inter and intra-rater reliability and minimal detectable difference of movement disorder-childhood rating scale 115
A novel IRF2BPL truncating variant is associated with endolysosomal storage 115
Characterization of Phenotypic Variability in Becker Muscular Dystrophy for Clinical Practice and Towards Trial Readiness: A Two-Years Follow up Study 113
Characterization of seven novel mutations in seven patients with GAMT deficiency 113
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome 113
Children and Young Adults with Epilepsy Exhibit an Interictal Autonomic Dysfunction: A Prospective Exploratory Study 112
Neuropsychological profiles in children with Duchenne muscular dystrophy compared to dyslexic population 112
Efficacy of vigabatrin intervention in a mild phenotypic expression of succinic semialdehyde dehydrogenase deficiency. 112
Mental retardation and verbal dyspraxia in a new patient with de novo creatine transporter (SLC6A8) mutation 112
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy 112
Post-Traumatic Stress Reactions in Caregivers of Children and Adolescents/Young Adults with Severe Diseases: A Systematic Review of Risk and Protective Factors 112
Inter and intra-rater reliability and minimal detectable difference of movement disorder-childhood rating scale 111
Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements 110
Treatment with L-Arginine improves neuropsychological disorders in a child with Creatine transporter defect 110
A Not So Benign Family Pedigree With Hereditary Chorea: A Broader Phenotypic Expression or Additional Picture? 110
Creatine precursors stimulate Cr synthesis in CT1 deficient lymphoblasts 110
Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions 109
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders 109
Expanding CEP290 mutational spectrum in ciliopathies 109
tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia 108
A Retrospective Longitudinal Study in a Cohort of Children With Dyskinetic Cerebral Palsy Treated With Tetrabenazine 108
Four years follow up of ACY1 deficient patient and pedigree study 107
Responsiveness of the Movement Disorder-Childhood Rating Scale in children with movement disorders undergoing oral therapy with tetrabenazine 107
Totale 13.440
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Categoria #
all - tutte 110.508
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 110.508
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021994 0 0 0 0 0 35 162 110 174 93 83 337
2021/20222.762 74 128 50 150 480 451 81 189 106 93 140 820
2022/20231.993 424 238 133 69 206 250 13 119 357 11 160 13
2023/20242.350 174 163 353 135 353 422 85 48 40 38 171 368
2024/20258.916 38 365 55 450 432 707 953 611 941 1.517 1.146 1.701
2025/20268.764 525 1.623 2.070 2.613 932 1.001 0 0 0 0 0 0
Totale 33.479