CINECA IRIS Institutional Research Information System

BATTINI, ROBERTA
 Distribuzione geografica
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Continente #
NA - Nord America 16.163
AS - Asia 12.125
EU - Europa 5.548
SA - Sud America 3.436
AF - Africa 398
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 8
Totale 37.689
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Nazione #
US - Stati Uniti d'America 15.419
SG - Singapore 3.436
CN - Cina 2.978
BR - Brasile 2.768
HK - Hong Kong 2.439
IT - Italia 2.105
VN - Vietnam 1.620
BG - Bulgaria 690
SE - Svezia 642
CA - Canada 566
FR - Francia 425
RU - Federazione Russa 363
DE - Germania 302
TR - Turchia 288
AR - Argentina 255
KR - Corea 233
GB - Regno Unito 219
FI - Finlandia 216
JP - Giappone 207
IN - India 193
BD - Bangladesh 146
EC - Ecuador 144
ID - Indonesia 129
UA - Ucraina 127
AT - Austria 96
CO - Colombia 83
ZA - Sudafrica 82
MX - Messico 81
CI - Costa d'Avorio 79
IQ - Iraq 79
NL - Olanda 79
VE - Venezuela 57
CH - Svizzera 50
PK - Pakistan 50
PY - Paraguay 49
SA - Arabia Saudita 49
MA - Marocco 41
ES - Italia 40
CL - Cile 35
PL - Polonia 34
TN - Tunisia 32
PH - Filippine 31
SN - Senegal 31
UZ - Uzbekistan 30
NG - Nigeria 27
EG - Egitto 24
BE - Belgio 23
JO - Giordania 22
JM - Giamaica 21
KE - Kenya 20
UY - Uruguay 19
DZ - Algeria 17
IE - Irlanda 17
NP - Nepal 17
PE - Perù 16
CZ - Repubblica Ceca 15
KZ - Kazakistan 14
MY - Malesia 14
GR - Grecia 13
AE - Emirati Arabi Uniti 12
AZ - Azerbaigian 12
IL - Israele 12
IR - Iran 12
LT - Lituania 11
ET - Etiopia 10
PA - Panama 10
SI - Slovenia 10
AL - Albania 9
AU - Australia 9
BB - Barbados 9
CR - Costa Rica 9
DO - Repubblica Dominicana 9
HN - Honduras 9
HU - Ungheria 9
LB - Libano 9
OM - Oman 9
TH - Thailandia 9
TT - Trinidad e Tobago 9
BO - Bolivia 8
QA - Qatar 8
RO - Romania 8
SY - Repubblica araba siriana 8
AM - Armenia 7
BH - Bahrain 7
BN - Brunei Darussalam 7
GE - Georgia 7
PS - Palestinian Territory 7
AO - Angola 6
BA - Bosnia-Erzegovina 6
KW - Kuwait 6
KG - Kirghizistan 5
MD - Moldavia 5
MN - Mongolia 5
PT - Portogallo 5
RS - Serbia 5
LV - Lettonia 4
LY - Libia 4
NI - Nicaragua 4
BJ - Benin 3
BW - Botswana 3
Totale 37.613
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Città #
Hong Kong 2.424
Ashburn 2.028
Singapore 1.831
Fairfield 1.637
Woodbridge 1.093
Dallas 865
Houston 833
Shanghai 723
Sofia 685
Santa Clara 641
San Jose 627
Seattle 602
Beijing 585
Cambridge 552
Wilmington 508
Ho Chi Minh City 473
Milan 463
Ottawa 463
New York 444
Ann Arbor 436
Chandler 400
Hefei 378
Boardman 374
Princeton 360
Lauterbourg 292
Lawrence 292
Hanoi 289
Council Bluffs 281
Los Angeles 239
Seoul 226
Medford 211
São Paulo 211
Tokyo 200
Istanbul 194
Des Moines 188
Nanjing 170
Redondo Beach 140
Rome 139
Serra 134
Florence 131
Buffalo 127
Jacksonville 114
Dong Ket 107
Helsinki 105
Rio de Janeiro 100
San Diego 99
Abidjan 79
Naples 73
Frankfurt am Main 69
Nuremberg 68
Belo Horizonte 65
Haiphong 65
Brasília 62
Vienna 61
Pisa 56
Izmir 53
Munich 53
Da Nang 52
London 51
Nanchang 51
Guayaquil 48
Shenyang 48
Ogden 47
Bari 45
Chicago 45
Porto Alegre 45
Columbus 43
Quito 42
Hebei 40
Curitiba 39
Marseille 38
Kunming 37
Genoa 36
Changsha 35
Dearborn 35
Johannesburg 35
Bern 33
Campinas 33
Redwood City 33
Boulder 32
Dhaka 32
Thái Bình 32
Atlanta 31
Biên Hòa 31
Dakar 31
Hyderabad 31
Jiaxing 31
Baghdad 30
Lappeenranta 30
Norwalk 30
Orem 30
Guangzhou 29
Lancaster 29
Turin 29
Turku 28
Montreal 27
Brooklyn 26
Goiânia 25
Lagos 25
Salvador 24
Totale 25.642
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Nome #
Pedagogia speciale della gestione integrata del gruppo classe 529
Creatine depletion in a new case with AGAT deficiency: clinical and genetic study in a large pedigree 385
Aspetti neuropsicologici della distrofia muscolare di Duchenne 243
Prenatal ultrasound and magnetic resonance features in a fetus with Walker-Warburg syndrome. Letters to the editor 234
Psychometric properties of Movement Disorder-Childhood Rating Scale 217
Cyclocreatine treatment ameliorates the cognitive, autistic and epileptic phenotype in a mouse model of Creatine Transporter Deficiency 211
Non-invasive assessment of Neuromuscular Disorders by 7 tesla Magnetic Resonance Imaging and Spectroscopy: Dedicated radio-frequency coil development 207
Implicit learning deficit in children with Duchenne muscular dystrophy: Evidence for a cerebellar cognitive impairment? 202
The Clinical Impact of Methotrexate-Induced Stroke-Like Neurotoxicity in Paediatric Departments: An Italian Multi-Centre Case-Series 194
Assessment of Postural Control in Children with Movement Disorders by Means of a New Technological Tool: A Pilot Study 192
DNA Methylation Biomarkers for Young Children with Idiopathic Autism Spectrum Disorder: A Systematic Review 190
Un'introduzione al PEI 190
Responsiveness of the MD-Childhood Rating Scale in dyskinetic cerebral palsy patients undergoing anticholinergic treatment 186
Isolated mild intellectual disability expands the aminoacylase 1 phenotype spectrum 182
Focal cortical dysplasia, microcephaly and epilepsy in a boy with 1q21.1-q21.3 duplication 179
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study 179
Behavioural and emotional changes during covid-19 lockdown in an italian paediatric population with neurologic and psychiatric disorders 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? 174
Reading impairment in Duchenne muscular dystrophy: a pilot study to investigate similarities and differences with developmental dyslexia 173
Neurovisual Manifestations in Children with Mild COVID-19: An Association to Remember 172
Leukoencephalopathy with bilateral anterior temporal lobe cysts: a further case of this new entity 172
Treatment monitoring of brain creatine deficiency syndromes: a 1H and 31P MR spectroscopy study 171
Longitudinal follow up of a boy affected by Pol III-related leukodystrophy: A detailed phenotype description 171
Trehalose Treatment in Zebrafish Model of Lafora Disease 160
Diffusion Tractography Biomarkers of Pediatric Cerebellar Hypoplasia/Atrophy: Preliminary Results Using Constrained Spherical Deconvolution 160
Ultrafast MR imaging and ultrasonography of fetal brain abnormalities: a comparative study 159
Neuropsychological profile and clinical effects of arginine treatment in children with creatine transport deficiency. 158
Bone mineralizatio in survivors of acute lynfoblastic leukemia 157
Parental Practices and Environmental Differences among Infants Living in Upper-Middle and High-Income Countries: A Cross-Sectional Study 155
Neurodevelopmental disorders in children with severe to profound sensorineural hearing loss: a clinical study 153
Evaluation and treatment of childhood movement disorders 152
Movement Disorder-Childhood Rating Scale: A Sensitive Tool to Evaluate Movement Disorders 152
Muscle metabolic alterations assessed by 31-phosphorus magnetic resonance spectroscopy in mild Becker muscular dystrophy 152
Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome 152
Assessment of bone mineral status at phalanges of the hand by morphological analysis of ultrasound graphic trace 151
A diagnostic dilemma in a family with cystinuria type B resolved by muscle magnetic resonance 151
Clinical and genetic findings in a series of italian children with pure hereditary spastic paraplegia 150
A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation 150
Characterization of Phenotypic Variability in Becker Muscular Dystrophy for Clinical Practice and Towards Trial Readiness: A Two-Years Follow up Study 149
Gas chromatography/mass spectrometry assay for arginine: glycine-amidinotransferase deficiency 149
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study 148
Unusual clinical and magnetic resonance imaging findings in a family with proteolipid protein gene mutation 147
Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data 146
Gain of function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling 144
Movement Disorder-Childhood Rating Scale: Reliability and Validity 144
Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53 144
Post-Traumatic Stress Reactions in Caregivers of Children and Adolescents/Young Adults with Severe Diseases: A Systematic Review of Risk and Protective Factors 144
Psychopathological Impact in Patients with History of Rheumatic Fever with or without Sydenham's Chorea: A Multicenter Prospective Study 143
Brain lactic alkalosis in Aicardi-Goutières Syndrome 143
Kinematic analysis of upper limb in children with movement disorder: Quantitatitative assessment of effectiveness of pharmacological trials. 143
Fifteen-year follow-up of Italian families affected by arginine glycine amidinotransferase deficiency 142
Androgen receptor blockade does not impair bone mineral density in adolescent females 141
Benefits of glucocorticoids in non-ambulant boys/men with Duchenne muscular dystrophy: A multicentric longitudinal study using the Performance of Upper Limb test 141
Arginine and glycine stimulate creatine synthesis in creatine transporter 1-deficient lymphoblasts 141
Enhancing DLG2 Implications in Neuropsychiatric Disorders: Analysis of a Cohort of Eight Patients with 11q14.1 Imbalances 137
Brain magnetic resonance in the diagnostic evaluation of mitochondrial encephalopathies 137
Erratum: Variant of Rett syndrome and CDKL5 gene: Clinical and autonomic description of 10 cases (Neuropediatrics (2013) 44 (237-238)) 136
Phenotype and natural history of variant late infantile ceroid-lipofuscinosis 5. 136
Movement Disorders in Children with a Mitochondrial Disease: A Cross-Sectional Survey from the Nationwide Italian Collaborative Network of Mitochondrial Diseases 136
A Retrospective Longitudinal Study in a Cohort of Children With Dyskinetic Cerebral Palsy Treated With Tetrabenazine 135
Children and Young Adults with Epilepsy Exhibit an Interictal Autonomic Dysfunction: A Prospective Exploratory Study 134
Clinical and genetic findings in a series of Italian children with pure hereditary spastic paraplegia. 134
Scale for evaluation of movement disorders in the first three years of life 134
Association between Reported Sleep Disorders and Behavioral Issues in Children with Myotonic Dystrophy Type 1—Results from a Retrospective Analysis in Italy 133
Proton magnetic resonance spectroscopy (H-1-MRS) of the cerebrum in two young infants with Zellweger syndrome 133
Elevated Serum Creatine Kinase and Small Cerebellum Prompt Diagnosis of Congenital Muscular Dystrophy due to FKRP Mutations. 133
24 month longitudinal data in ambulant boys with duchenne muscular dystrophy 133
Early neurodevelopmental characterization in children with cobalamin C/defect 133
Cognitive, adaptive, and behavioral features in Joubert syndrome 131
Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review 131
Responsiveness of the Movement Disorder-Childhood Rating Scale in children with movement disorders undergoing oral therapy with tetrabenazine 130
Functional changes in Duchenne muscular dystrophy A 12-month longitudinal cohort study 130
A Potential Biomarker of Brain Activity in Autism Spectrum Disorders: A Pilot fNIRS Study in Female Preschoolers 129
Proton MR spectroscopy of mitochondrial diseases: analysis of brain metabolic abnormalities and their possible diagnostic relevance 129
CLINICAL AND MR SPECTROSCOPY FOLLOW-UP OF CT1 DEFICIENT ITALIAN PATIENTS TREATED BY ORAL ARGININE 128
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 128
Functional levels and MRI patterns of muscle involvement in upper limbs in Duchenne muscular dystrophy 128
Creatine precursors stimulate Cr synthesis in CT1 deficient lymphoblasts 128
Inborn errors of creatine metabolism and epilepsy. 127
Quantitative analysis at 1.5 T muscle MRI in neuromuscular disorderd 127
"I have got something positive out of this situation": Psychological benefits of caregiving in relatives of young people with muscular dystrophy 127
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome 127
Expanding Phenotype of Poirier-Bienvenu Syndrome: New Evidence from an Italian Multicentrical Cohort of Patients 125
Congenital Myopathy as a Phenotypic Expression of CACNA1S Gene Mutation: Case Report and Systematic Review of the Literature 124
Does the assessment of general movements without video observation reliably predict neurological outcome? RID F-1503-2010 124
A novel IRF2BPL truncating variant is associated with endolysosomal storage 124
Movement disorders - Childhood Rating Scale 4-18 revised in children with dyskinetic cerebral palsy 124
Neuropsychological profiles in children with Duchenne muscular dystrophy compared to dyslexic population 123
Variant of Rett syndrome and CDKL5 gene: clinical and autonomic description of 10 cases. 123
Molecular cytogenetic characterization of a new case of patial trisomy 13 (13q11q13.2)Research letter 122
Inter and intra-rater reliability and minimal detectable difference of movement disorder-childhood rating scale 122
Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements 122
A Not So Benign Family Pedigree With Hereditary Chorea: A Broader Phenotypic Expression or Additional Picture? 122
tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia 121
Characterization of seven novel mutations in seven patients with GAMT deficiency 121
Four years follow up of ACY1 deficient patient and pedigree study 120
Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions 120
Treatment with L-Arginine improves neuropsychological disorders in a child with Creatine transporter defect 120
Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1 120
Expanding CEP290 mutational spectrum in ciliopathies 120
Totale 15.430
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Categoria #
all - tutte 124.672
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 124.672
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.752 74 128 50 147 478 450 81 188 106 93 140 817
2022/20231.978 422 234 132 69 204 247 13 119 356 11 158 13
2023/20242.348 174 163 353 135 352 422 85 48 40 38 171 367
2024/20258.832 38 364 55 443 412 692 944 608 934 1.513 1.142 1.687
2025/202613.765 518 1.614 2.063 2.598 920 996 1.369 756 975 889 743 324
2026/202786 86 0 0 0 0 0 0 0 0 0 0 0
Totale 38.412