CINECA IRIS Institutional Research Information System

BATTINI, ROBERTA
 Distribuzione geografica
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Continente #
NA - Nord America 14.434
AS - Asia 10.594
EU - Europa 4.598
SA - Sud America 3.266
AF - Africa 319
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 8
Totale 33.229
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Nazione #
US - Stati Uniti d'America 13.790
SG - Singapore 3.087
BR - Brasile 2.688
CN - Cina 2.653
HK - Hong Kong 2.432
IT - Italia 1.684
VN - Vietnam 1.280
BG - Bulgaria 690
SE - Svezia 636
CA - Canada 512
RU - Federazione Russa 351
DE - Germania 271
TR - Turchia 261
KR - Corea 233
AR - Argentina 224
GB - Regno Unito 188
FI - Finlandia 167
EC - Ecuador 138
IN - India 123
UA - Ucraina 120
ID - Indonesia 119
FR - Francia 111
AT - Austria 96
BD - Bangladesh 94
CI - Costa d'Avorio 76
MX - Messico 74
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 28
PK - Pakistan 27
PL - Polonia 26
SA - Arabia Saudita 26
NG - Nigeria 25
ES - Italia 24
TN - Tunisia 24
BE - Belgio 22
EG - Egitto 22
UZ - Uzbekistan 18
UY - Uruguay 17
JO - Giordania 16
CZ - Repubblica Ceca 15
PE - Perù 15
IE - Irlanda 14
DZ - Algeria 12
IR - Iran 12
NP - Nepal 12
GR - Grecia 11
KE - Kenya 11
LT - Lituania 11
IL - Israele 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
BA - Bosnia-Erzegovina 5
BH - Bahrain 5
LB - Libano 5
BB - Barbados 4
ET - Etiopia 4
KG - Kirghizistan 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
KH - Cambogia 3
LV - Lettonia 3
MD - Moldavia 3
MN - Mongolia 3
NI - Nicaragua 3
PH - Filippine 3
Totale 33.182
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Città #
Hong Kong 2.424
Ashburn 1.815
Fairfield 1.644
Singapore 1.527
Woodbridge 1.099
Houston 827
Dallas 824
Shanghai 725
Sofia 687
Santa Clara 633
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
San Jose 284
Seoul 226
Medford 212
Hanoi 203
São Paulo 199
Los Angeles 191
Des Moines 186
Istanbul 184
Nanjing 167
Redondo Beach 141
Serra 131
Florence 125
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
Helsinki 56
Izmir 53
Munich 53
Nanchang 50
Shenyang 48
Haiphong 47
Ogden 47
Frankfurt am Main 46
Guayaquil 46
London 42
Porto Alegre 42
Quito 42
Pisa 41
Curitiba 40
Hebei 40
Marseille 38
Kunming 36
Council Bluffs 35
Bern 33
Chicago 33
Dearborn 33
Redwood City 33
Boulder 32
Campinas 32
Changsha 32
Da Nang 32
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
Naples 26
Goiânia 25
Guangzhou 25
Lagos 25
Dhaka 24
Salvador 24
Tianjin 24
Bari 23
The Dalles 23
Düsseldorf 21
Jüchen 21
Lucca 21
Recife 21
Jakarta 20
Totale 23.362
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Nome #
Pedagogia speciale della gestione integrata del gruppo classe 313
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 208
Psychometric properties of Movement Disorder-Childhood Rating Scale 198
Implicit learning deficit in children with Duchenne muscular dystrophy: Evidence for a cerebellar cognitive impairment? 185
Non-invasive assessment of Neuromuscular Disorders by 7 tesla Magnetic Resonance Imaging and Spectroscopy: Dedicated radio-frequency coil development 176
Responsiveness of the MD-Childhood Rating Scale in dyskinetic cerebral palsy patients undergoing anticholinergic treatment 175
The Clinical Impact of Methotrexate-Induced Stroke-Like Neurotoxicity in Paediatric Departments: An Italian Multi-Centre Case-Series 170
Isolated mild intellectual disability expands the aminoacylase 1 phenotype spectrum 170
Focal cortical dysplasia, microcephaly and epilepsy in a boy with 1q21.1-q21.3 duplication 169
Leukoencephalopathy with bilateral anterior temporal lobe cysts: a further case of this new entity 166
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study 164
Treatment monitoring of brain creatine deficiency syndromes: a 1H and 31P MR spectroscopy study 163
Longitudinal follow up of a boy affected by Pol III-related leukodystrophy: A detailed phenotype description 162
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? 161
Creatine depletion in a new case with AGAT deficiency: clinical and genetic study in a large pedigree 160
Reading impairment in Duchenne muscular dystrophy: a pilot study to investigate similarities and differences with developmental dyslexia 158
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. 150
Bone mineralizatio in survivors of acute lynfoblastic leukemia 149
Ultrafast MR imaging and ultrasonography of fetal brain abnormalities: a comparative study 149
Neurovisual Manifestations in Children with Mild COVID-19: An Association to Remember 148
Assessment of Postural Control in Children with Movement Disorders by Means of a New Technological Tool: A Pilot Study 147
Evaluation and treatment of childhood movement disorders 147
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 147
Movement Disorder-Childhood Rating Scale: A Sensitive Tool to Evaluate Movement Disorders 146
Neurodevelopmental disorders in children with severe to profound sensorineural hearing loss: a clinical study 144
Assessment of bone mineral status at phalanges of the hand by morphological analysis of ultrasound graphic trace 144
Gas chromatography/mass spectrometry assay for arginine: glycine-amidinotransferase deficiency 142
Behavioural and emotional changes during covid-19 lockdown in an italian paediatric population with neurologic and psychiatric disorders 141
A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation 140
Unusual clinical and magnetic resonance imaging findings in a family with proteolipid protein gene mutation 139
Clinical and genetic findings in a series of italian children with pure hereditary spastic paraplegia 138
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study 138
Brain lactic alkalosis in Aicardi-Goutières Syndrome 136
Fifteen-year follow-up of Italian families affected by arginine glycine amidinotransferase deficiency 136
Gain of function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling 136
Un'introduzione al PEI 134
Parental Practices and Environmental Differences among Infants Living in Upper-Middle and High-Income Countries: A Cross-Sectional Study 134
Trehalose Treatment in Zebrafish Model of Lafora Disease 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
Proton magnetic resonance spectroscopy (H-1-MRS) of the cerebrum in two young infants with Zellweger syndrome 131
Benefits of glucocorticoids in non-ambulant boys/men with Duchenne muscular dystrophy: A multicentric longitudinal study using the Performance of Upper Limb test 131
Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data 131
Brain magnetic resonance in the diagnostic evaluation of mitochondrial encephalopathies 130
DNA Methylation Biomarkers for Young Children with Idiopathic Autism Spectrum Disorder: A Systematic Review 129
Elevated Serum Creatine Kinase and Small Cerebellum Prompt Diagnosis of Congenital Muscular Dystrophy due to FKRP Mutations. 129
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
Clinical and genetic findings in a series of Italian children with pure hereditary spastic paraplegia. 128
Erratum: Variant of Rett syndrome and CDKL5 gene: Clinical and autonomic description of 10 cases (Neuropediatrics (2013) 44 (237-238)) 128
Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53 128
Arginine and glycine stimulate creatine synthesis in creatine transporter 1-deficient lymphoblasts 127
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
Movement Disorders in Children with a Mitochondrial Disease: A Cross-Sectional Survey from the Nationwide Italian Collaborative Network of Mitochondrial Diseases 124
Cognitive, adaptive, and behavioral features in Joubert syndrome 123
Psychopathological Impact in Patients with History of Rheumatic Fever with or without Sydenham's Chorea: A Multicenter Prospective Study 122
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 122
Scale for evaluation of movement disorders in the first three years of life 122
CLINICAL AND MR SPECTROSCOPY FOLLOW-UP OF CT1 DEFICIENT ITALIAN PATIENTS TREATED BY ORAL ARGININE 121
Functional levels and MRI patterns of muscle involvement in upper limbs in Duchenne muscular dystrophy 121
Inborn errors of creatine metabolism and epilepsy. 120
"I have got something positive out of this situation": Psychological benefits of caregiving in relatives of young people with muscular dystrophy 120
Characterization of Phenotypic Variability in Becker Muscular Dystrophy for Clinical Practice and Towards Trial Readiness: A Two-Years Follow up Study 119
Functional changes in Duchenne muscular dystrophy A 12-month longitudinal cohort study 119
Proton MR spectroscopy of mitochondrial diseases: analysis of brain metabolic abnormalities and their possible diagnostic relevance 118
Does the assessment of general movements without video observation reliably predict neurological outcome? RID F-1503-2010 118
Molecular cytogenetic characterization of a new case of patial trisomy 13 (13q11q13.2)Research letter 118
Variant of Rett syndrome and CDKL5 gene: clinical and autonomic description of 10 cases. 118
Movement disorders - Childhood Rating Scale 4-18 revised in children with dyskinetic cerebral palsy 117
Neuropsychological profiles in children with Duchenne muscular dystrophy compared to dyslexic population 116
Inter and intra-rater reliability and minimal detectable difference of movement disorder-childhood rating scale 116
Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review 116
Quantitative analysis at 1.5 T muscle MRI in neuromuscular disorderd 115
A novel IRF2BPL truncating variant is associated with endolysosomal storage 115
Children and Young Adults with Epilepsy Exhibit an Interictal Autonomic Dysfunction: A Prospective Exploratory Study 113
Characterization of seven novel mutations in seven patients with GAMT deficiency 113
A Not So Benign Family Pedigree With Hereditary Chorea: A Broader Phenotypic Expression or Additional Picture? 113
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome 113
Efficacy of vigabatrin intervention in a mild phenotypic expression of succinic semialdehyde dehydrogenase deficiency. 112
Responsiveness of the Movement Disorder-Childhood Rating Scale in children with movement disorders undergoing oral therapy with tetrabenazine 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
A Retrospective Longitudinal Study in a Cohort of Children With Dyskinetic Cerebral Palsy Treated With Tetrabenazine 112
Enhancing DLG2 Implications in Neuropsychiatric Disorders: Analysis of a Cohort of Eight Patients with 11q14.1 Imbalances 111
Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements 111
Inter and intra-rater reliability and minimal detectable difference of movement disorder-childhood rating scale 111
Creatine precursors stimulate Cr synthesis in CT1 deficient lymphoblasts 111
Expanding CEP290 mutational spectrum in ciliopathies 111
Four years follow up of ACY1 deficient patient and pedigree study 110
Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions 110
Treatment with L-Arginine improves neuropsychological disorders in a child with Creatine transporter defect 110
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders 109
Totale 13.623
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Categoria #
all - tutte 111.889
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 111.889
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021959 0 0 0 0 0 0 162 110 174 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
2025/20269.209 525 1.623 2.070 2.613 932 1.002 444 0 0 0 0 0
Totale 33.924