CINECA IRIS Institutional Research Information System

BATTINI, ROBERTA
 Distribuzione geografica
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Continente #
NA - Nord America 19.075
AS - Asia 12.208
EU - Europa 5.670
SA - Sud America 3.497
Continente sconosciuto - Info sul continente non disponibili 734
AF - Africa 401
OC - Oceania 11
Totale 41.596
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Nazione #
US - Stati Uniti d'America 18.267
SG - Singapore 3.460
CN - Cina 2.995
BR - Brasile 2.818
HK - Hong Kong 2.451
IT - Italia 2.172
VN - Vietnam 1.626
BG - Bulgaria 693
SE - Svezia 678
CA - Canada 606
FR - Francia 426
RU - Federazione Russa 365
DE - Germania 302
TR - Turchia 291
AR - Argentina 258
KR - Corea 233
GB - Regno Unito 222
FI - Finlandia 217
JP - Giappone 208
IN - India 197
BD - Bangladesh 151
EC - Ecuador 145
ID - Indonesia 132
UA - Ucraina 127
AT - Austria 96
CO - Colombia 85
NL - Olanda 85
ZA - Sudafrica 84
MX - Messico 82
CI - Costa d'Avorio 79
IQ - Iraq 79
VE - Venezuela 60
PK - Pakistan 51
CH - Svizzera 50
PY - Paraguay 50
SA - Arabia Saudita 50
ES - Italia 41
MA - Marocco 41
CL - Cile 36
PL - Polonia 34
TN - Tunisia 32
PH - Filippine 31
SN - Senegal 31
UZ - Uzbekistan 30
JM - Giamaica 29
NG - Nigeria 27
EG - Egitto 24
JO - Giordania 24
BE - Belgio 23
KE - Kenya 20
UY - Uruguay 19
CR - Costa Rica 18
NP - Nepal 18
DZ - Algeria 17
IE - Irlanda 17
PE - Perù 16
CZ - Repubblica Ceca 15
MY - Malesia 15
KZ - Kazakistan 14
AE - Emirati Arabi Uniti 13
GR - Grecia 13
AZ - Azerbaigian 12
IL - Israele 12
IR - Iran 12
LT - Lituania 12
HN - Honduras 11
DO - Repubblica Dominicana 10
ET - Etiopia 10
OM - Oman 10
PA - Panama 10
SI - Slovenia 10
TT - Trinidad e Tobago 10
AL - Albania 9
AU - Australia 9
BB - Barbados 9
HU - Ungheria 9
LB - Libano 9
TH - Thailandia 9
BO - Bolivia 8
QA - Qatar 8
RO - Romania 8
SY - Repubblica araba siriana 8
AM - Armenia 7
BA - Bosnia-Erzegovina 7
BH - Bahrain 7
BN - Brunei Darussalam 7
GE - Georgia 7
PS - Palestinian Territory 7
AO - Angola 6
KW - Kuwait 6
KG - Kirghizistan 5
MD - Moldavia 5
MN - Mongolia 5
PT - Portogallo 5
RS - Serbia 5
GT - Guatemala 4
LV - Lettonia 4
LY - Libia 4
NI - Nicaragua 4
BJ - Benin 3
Totale 40.792
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Città #
Hong Kong 2.436
Ashburn 2.180
Singapore 1.840
Fairfield 1.644
Woodbridge 1.100
Dallas 881
Houston 843
Shanghai 728
Sofia 688
Santa Clara 670
San Jose 652
Seattle 607
Beijing 589
Council Bluffs 586
Cambridge 556
Wilmington 514
Milan 480
Ho Chi Minh City 474
Ottawa 465
New York 463
Ann Arbor 437
Chandler 406
Hefei 378
Boardman 376
Princeton 361
Lauterbourg 293
Lawrence 293
Hanoi 289
Los Angeles 275
São Paulo 232
Seoul 226
Medford 212
Tokyo 200
Istanbul 196
Des Moines 190
Nanjing 171
Rome 147
Buffalo 142
Redondo Beach 141
Florence 134
Serra 134
Jacksonville 116
Dong Ket 108
Helsinki 106
San Diego 101
Rio de Janeiro 100
Abidjan 79
Atlanta 77
Naples 74
Frankfurt am Main 69
Nuremberg 68
Belo Horizonte 65
Haiphong 65
Brasília 62
Vienna 61
Pisa 56
Da Nang 53
Izmir 53
London 53
Munich 53
Nanchang 51
Guayaquil 48
Shenyang 48
Chicago 47
Ogden 47
Columbus 46
Bari 45
Porto Alegre 45
Quito 42
Curitiba 41
Montreal 41
Genoa 40
Hebei 40
Marseille 38
Kunming 37
Changsha 35
Dearborn 35
Johannesburg 35
Campinas 34
Bern 33
Dhaka 33
Redwood City 33
Boulder 32
Orem 32
Thái Bình 32
Biên Hòa 31
Dakar 31
Hyderabad 31
Jiaxing 31
Turin 31
Baghdad 30
Lappeenranta 30
Norwalk 30
Phoenix 30
Toronto 30
Brooklyn 29
Guangzhou 29
Lancaster 29
San Francisco 28
Turku 28
Totale 26.486
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Nome #
Pedagogia speciale della gestione integrata del gruppo classe 541
Epilepsy expands the phenotype of L‐arginine:glycine amidinotransferase deficiency 419
Creatine depletion in a new case with AGAT deficiency: clinical and genetic study in a large pedigree 386
Aspetti neuropsicologici della distrofia muscolare di Duchenne 248
Prenatal ultrasound and magnetic resonance features in a fetus with Walker-Warburg syndrome. Letters to the editor 238
Cyclocreatine treatment ameliorates the cognitive, autistic and epileptic phenotype in a mouse model of Creatine Transporter Deficiency 220
Psychometric properties of Movement Disorder-Childhood Rating Scale 219
Non-invasive assessment of Neuromuscular Disorders by 7 tesla Magnetic Resonance Imaging and Spectroscopy: Dedicated radio-frequency coil development 210
Looking for “fNIRS Signature” in Autism Spectrum: A Systematic Review Starting From Preschoolers 204
Implicit learning deficit in children with Duchenne muscular dystrophy: Evidence for a cerebellar cognitive impairment? 203
DNA Methylation Biomarkers for Young Children with Idiopathic Autism Spectrum Disorder: A Systematic Review 198
The Clinical Impact of Methotrexate-Induced Stroke-Like Neurotoxicity in Paediatric Departments: An Italian Multi-Centre Case-Series 197
Un'introduzione al PEI 194
Assessment of Postural Control in Children with Movement Disorders by Means of a New Technological Tool: A Pilot Study 194
The Italian Angelman Syndrome Registry (IReAS): a tool for standardized data collection and genotype-phenotype analysis 189
Individuation of predictive parameters of posterior cranial fossa decompression in pediatric patients with Chiari I malformation and autism spectrum disorder 189
Responsiveness of the MD-Childhood Rating Scale in dyskinetic cerebral palsy patients undergoing anticholinergic treatment 187
Age at onset and gene variants predict lifespan and disease duration in childhood neuronal ceroid lipofuscinoses 187
fNIRS as a biomarker for X-linked neurodevelopmental disorders: leveraging visual processing to assess brain function? 184
Isolated mild intellectual disability expands the aminoacylase 1 phenotype spectrum 184
Muscle Imaging Approaches in Marinesco–Sjögren Syndrome: A Systematic Review and Two New Clinical Reports 184
Focal cortical dysplasia, microcephaly and epilepsy in a boy with 1q21.1-q21.3 duplication 183
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study 181
Reading impairment in Duchenne muscular dystrophy: a pilot study to investigate similarities and differences with developmental dyslexia 178
Clinical-genetic features of the TBCE-related spectrum disorders: A focus on the childhood-onset neurodegenerative phenotype 177
Behavioural and emotional changes during covid-19 lockdown in an italian paediatric population with neurologic and psychiatric disorders 177
Leukoencephalopathy with bilateral anterior temporal lobe cysts: a further case of this new entity 175
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? 175
Potential impact of early pharmacological treatment on gene therapy outcomes in AADC deficiency 174
Dynamic electro‐clinical features in Guanidinoacetate N‐methyltransferase deficiency: A familial case series 174
Neurovisual Manifestations in Children with Mild COVID-19: An Association to Remember 174
Longitudinal follow up of a boy affected by Pol III-related leukodystrophy: A detailed phenotype description 173
Arginine:glycine amidinotransferase (AGAT) deficiency in a newborn: early treatment can prevent phenotypic expression of the disease 173
Treatment monitoring of brain creatine deficiency syndromes: a 1H and 31P MR spectroscopy study 172
Trehalose Treatment in Zebrafish Model of Lafora Disease 167
Ultrafast MR imaging and ultrasonography of fetal brain abnormalities: a comparative study 163
Diffusion Tractography Biomarkers of Pediatric Cerebellar Hypoplasia/Atrophy: Preliminary Results Using Constrained Spherical Deconvolution 162
Bone mineralizatio in survivors of acute lynfoblastic leukemia 159
Neuropsychological profile and clinical effects of arginine treatment in children with creatine transport deficiency. 159
Parental Practices and Environmental Differences among Infants Living in Upper-Middle and High-Income Countries: A Cross-Sectional Study 158
A diagnostic dilemma in a family with cystinuria type B resolved by muscle magnetic resonance 156
Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data 156
Evaluation and treatment of childhood movement disorders 155
Movement Disorder-Childhood Rating Scale: A Sensitive Tool to Evaluate Movement Disorders 155
Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome 155
Muscle metabolic alterations assessed by 31-phosphorus magnetic resonance spectroscopy in mild Becker muscular dystrophy 154
Clinical and genetic findings in a series of italian children with pure hereditary spastic paraplegia 153
Neurodevelopmental disorders in children with severe to profound sensorineural hearing loss: a clinical study 153
Assessment of bone mineral status at phalanges of the hand by morphological analysis of ultrasound graphic trace 153
A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation 153
Gas chromatography/mass spectrometry assay for arginine: glycine-amidinotransferase deficiency 152
Characterization of Phenotypic Variability in Becker Muscular Dystrophy for Clinical Practice and Towards Trial Readiness: A Two-Years Follow up Study 151
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study 151
Post-Traumatic Stress Reactions in Caregivers of Children and Adolescents/Young Adults with Severe Diseases: A Systematic Review of Risk and Protective Factors 151
Unusual clinical and magnetic resonance imaging findings in a family with proteolipid protein gene mutation 149
Gain of function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling 148
Movement Disorder-Childhood Rating Scale: Reliability and Validity 148
Natural history of KBG syndrome in a large European cohort 147
Fifteen-year follow-up of Italian families affected by arginine glycine amidinotransferase deficiency 146
Arginine and glycine stimulate creatine synthesis in creatine transporter 1-deficient lymphoblasts 145
Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53 145
Brain lactic alkalosis in Aicardi-Goutières Syndrome 144
Kinematic analysis of upper limb in children with movement disorder: Quantitatitative assessment of effectiveness of pharmacological trials. 144
Benefits of glucocorticoids in non-ambulant boys/men with Duchenne muscular dystrophy: A multicentric longitudinal study using the Performance of Upper Limb test 144
Psychopathological Impact in Patients with History of Rheumatic Fever with or without Sydenham's Chorea: A Multicenter Prospective Study 143
Erratum: Variant of Rett syndrome and CDKL5 gene: Clinical and autonomic description of 10 cases (Neuropediatrics (2013) 44 (237-238)) 142
Androgen receptor blockade does not impair bone mineral density in adolescent females 142
Brain magnetic resonance in the diagnostic evaluation of mitochondrial encephalopathies 140
A Retrospective Longitudinal Study in a Cohort of Children With Dyskinetic Cerebral Palsy Treated With Tetrabenazine 140
Children and Young Adults with Epilepsy Exhibit an Interictal Autonomic Dysfunction: A Prospective Exploratory Study 138
A Potential Biomarker of Brain Activity in Autism Spectrum Disorders: A Pilot fNIRS Study in Female Preschoolers 138
Movement Disorders in Children with a Mitochondrial Disease: A Cross-Sectional Survey from the Nationwide Italian Collaborative Network of Mitochondrial Diseases 138
Enhancing DLG2 Implications in Neuropsychiatric Disorders: Analysis of a Cohort of Eight Patients with 11q14.1 Imbalances 137
Association between Reported Sleep Disorders and Behavioral Issues in Children with Myotonic Dystrophy Type 1—Results from a Retrospective Analysis in Italy 137
Clinical and genetic findings in a series of Italian children with pure hereditary spastic paraplegia. 137
Scale for evaluation of movement disorders in the first three years of life 137
Phenotype and natural history of variant late infantile ceroid-lipofuscinosis 5. 137
Elevated Serum Creatine Kinase and Small Cerebellum Prompt Diagnosis of Congenital Muscular Dystrophy due to FKRP Mutations. 136
Early neurodevelopmental characterization in children with cobalamin C/defect 136
Proton magnetic resonance spectroscopy (H-1-MRS) of the cerebrum in two young infants with Zellweger syndrome 135
24 month longitudinal data in ambulant boys with duchenne muscular dystrophy 135
Cognitive, adaptive, and behavioral features in Joubert syndrome 134
Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review 133
Expanding Phenotype of Poirier-Bienvenu Syndrome: New Evidence from an Italian Multicentrical Cohort of Patients 132
Proton MR spectroscopy of mitochondrial diseases: analysis of brain metabolic abnormalities and their possible diagnostic relevance 132
Responsiveness of the Movement Disorder-Childhood Rating Scale in children with movement disorders undergoing oral therapy with tetrabenazine 132
Functional changes in Duchenne muscular dystrophy A 12-month longitudinal cohort study 132
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 130
Functional levels and MRI patterns of muscle involvement in upper limbs in Duchenne muscular dystrophy 130
Creatine precursors stimulate Cr synthesis in CT1 deficient lymphoblasts 130
CLINICAL AND MR SPECTROSCOPY FOLLOW-UP OF CT1 DEFICIENT ITALIAN PATIENTS TREATED BY ORAL ARGININE 129
Quantitative analysis at 1.5 T muscle MRI in neuromuscular disorderd 129
Inborn errors of creatine metabolism and epilepsy. 128
"I have got something positive out of this situation": Psychological benefits of caregiving in relatives of young people with muscular dystrophy 128
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome 128
Does the assessment of general movements without video observation reliably predict neurological outcome? RID F-1503-2010 127
Movement disorders - Childhood Rating Scale 4-18 revised in children with dyskinetic cerebral palsy 127
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy 126
A novel IRF2BPL truncating variant is associated with endolysosomal storage 126
Congenital Myopathy as a Phenotypic Expression of CACNA1S Gene Mutation: Case Report and Systematic Review of the Literature 125
Totale 16.643
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Categoria #
all - tutte 132.396
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 132.396
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.688 0 128 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
2024/20258.890 38 365 55 450 429 705 950 610 939 1.516 1.143 1.690
2025/202613.806 520 1.617 2.069 2.611 922 999 1.370 758 978 894 744 324
2026/20273.101 536 2.565 0 0 0 0 0 0 0 0 0 0
Totale 41.596