CINECA IRIS Institutional Research Information System

BATTINI, ROBERTA
 Distribuzione geografica
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Continente #
NA - Nord America 15.549
AS - Asia 12.167
EU - Europa 5.413
SA - Sud America 3.466
AF - Africa 399
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 8
Totale 37.013
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Nazione #
US - Stati Uniti d'America 14.840
SG - Singapore 3.454
CN - Cina 2.981
BR - Brasile 2.798
HK - Hong Kong 2.445
IT - Italia 1.988
VN - Vietnam 1.624
BG - Bulgaria 693
SE - Svezia 646
CA - Canada 543
FR - Francia 425
RU - Federazione Russa 364
DE - Germania 301
TR - Turchia 290
AR - Argentina 256
KR - Corea 233
FI - Finlandia 217
GB - Regno Unito 212
JP - Giappone 208
IN - India 193
BD - Bangladesh 145
EC - Ecuador 144
ID - Indonesia 130
UA - Ucraina 127
AT - Austria 96
ZA - Sudafrica 83
CO - Colombia 81
MX - Messico 80
CI - Costa d'Avorio 79
IQ - Iraq 79
NL - Olanda 69
VE - Venezuela 58
PK - Pakistan 51
CH - Svizzera 50
PY - Paraguay 50
SA - Arabia Saudita 50
MA - Marocco 41
ES - Italia 35
CL - Cile 34
PL - Polonia 32
TN - Tunisia 32
PH - Filippine 31
SN - Senegal 31
UZ - Uzbekistan 30
NG - Nigeria 27
EG - Egitto 24
JO - Giordania 24
BE - Belgio 23
KE - Kenya 20
JM - Giamaica 19
UY - Uruguay 19
NP - Nepal 18
DZ - Algeria 17
IE - Irlanda 16
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 11
DO - Repubblica Dominicana 10
ET - Etiopia 10
OM - Oman 10
PA - Panama 10
SI - Slovenia 10
AL - Albania 9
AU - Australia 9
HU - Ungheria 9
LB - Libano 9
TH - Thailandia 9
BO - Bolivia 8
CR - Costa Rica 8
HN - Honduras 8
QA - Qatar 8
RO - Romania 8
SY - Repubblica araba siriana 8
AM - Armenia 7
BB - Barbados 7
BH - Bahrain 7
BN - Brunei Darussalam 7
GE - Georgia 7
PS - Palestinian Territory 7
TT - Trinidad e Tobago 7
AO - Angola 6
BA - Bosnia-Erzegovina 6
KW - Kuwait 6
KG - Kirghizistan 5
MD - Moldavia 5
MN - Mongolia 5
PT - Portogallo 5
LV - Lettonia 4
LY - Libia 4
NI - Nicaragua 4
RS - Serbia 4
BJ - Benin 3
BW - Botswana 3
Totale 36.941
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Città #
Hong Kong 2.430
Ashburn 1.927
Singapore 1.834
Fairfield 1.644
Woodbridge 1.099
Dallas 830
Houston 828
Shanghai 725
Sofia 688
Santa Clara 636
Seattle 607
San Jose 593
Beijing 585
Cambridge 555
Wilmington 512
Ho Chi Minh City 474
Ottawa 464
Ann Arbor 437
Milan 434
New York 418
Chandler 405
Hefei 378
Boardman 373
Princeton 361
Lauterbourg 293
Lawrence 293
Hanoi 289
Seoul 226
Los Angeles 216
São Paulo 214
Medford 212
Tokyo 200
Istanbul 196
Des Moines 189
Council Bluffs 177
Nanjing 171
Redondo Beach 141
Serra 134
Rome 132
Florence 128
Buffalo 125
Jacksonville 113
Dong Ket 108
Helsinki 106
Rio de Janeiro 100
San Diego 100
Abidjan 79
Frankfurt am Main 69
Nuremberg 68
Belo Horizonte 65
Haiphong 65
Naples 65
Brasília 62
Vienna 61
Pisa 56
Izmir 53
Munich 53
Da Nang 52
Nanchang 51
Guayaquil 48
Shenyang 48
Ogden 47
Bari 45
Porto Alegre 45
London 44
Quito 42
Curitiba 41
Hebei 40
Chicago 38
Marseille 38
Kunming 37
Columbus 36
Genoa 36
Changsha 35
Johannesburg 35
Campinas 34
Dearborn 34
Bern 33
Redwood City 33
Boulder 32
Dhaka 32
Thái Bình 32
Biên Hòa 31
Dakar 31
Hyderabad 31
Jiaxing 31
Baghdad 30
Lappeenranta 30
Norwalk 30
Guangzhou 29
Lancaster 28
Turku 28
Goiânia 26
Atlanta 25
Lagos 25
Salvador 24
Tashkent 24
The Dalles 24
Tianjin 24
Turin 24
Totale 25.279
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Nome #
Pedagogia speciale della gestione integrata del gruppo classe 503
Prenatal ultrasound and magnetic resonance features in a fetus with Walker-Warburg syndrome. Letters to the editor 231
Aspetti neuropsicologici della distrofia muscolare di Duchenne 227
Psychometric properties of Movement Disorder-Childhood Rating Scale 215
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 191
DNA Methylation Biomarkers for Young Children with Idiopathic Autism Spectrum Disorder: A Systematic Review 189
Responsiveness of the MD-Childhood Rating Scale in dyskinetic cerebral palsy patients undergoing anticholinergic treatment 184
Isolated mild intellectual disability expands the aminoacylase 1 phenotype spectrum 181
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
Assessment of Postural Control in Children with Movement Disorders by Means of a New Technological Tool: A Pilot Study 175
Leukoencephalopathy with bilateral anterior temporal lobe cysts: a further case of this new entity 171
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? 171
Treatment monitoring of brain creatine deficiency syndromes: a 1H and 31P MR spectroscopy study 170
Reading impairment in Duchenne muscular dystrophy: a pilot study to investigate similarities and differences with developmental dyslexia 170
Longitudinal follow up of a boy affected by Pol III-related leukodystrophy: A detailed phenotype description 170
Behavioural and emotional changes during covid-19 lockdown in an italian paediatric population with neurologic and psychiatric disorders 170
Arginine:glycine amidinotransferase (AGAT) deficiency in a newborn: early treatment can prevent phenotypic expression of the disease 169
Creatine depletion in a new case with AGAT deficiency: clinical and genetic study in a large pedigree 168
Un'introduzione al PEI 165
Neurovisual Manifestations in Children with Mild COVID-19: An Association to Remember 161
Trehalose Treatment in Zebrafish Model of Lafora Disease 160
Diffusion Tractography Biomarkers of Pediatric Cerebellar Hypoplasia/Atrophy: Preliminary Results Using Constrained Spherical Deconvolution 159
Ultrafast MR imaging and ultrasonography of fetal brain abnormalities: a comparative study 158
Neuropsychological profile and clinical effects of arginine treatment in children with creatine transport deficiency. 157
Bone mineralizatio in survivors of acute lynfoblastic leukemia 156
Parental Practices and Environmental Differences among Infants Living in Upper-Middle and High-Income Countries: A Cross-Sectional Study 152
Evaluation and treatment of childhood movement disorders 152
Neurodevelopmental disorders in children with severe to profound sensorineural hearing loss: a clinical study 152
Muscle metabolic alterations assessed by 31-phosphorus magnetic resonance spectroscopy in mild Becker muscular dystrophy 152
Assessment of bone mineral status at phalanges of the hand by morphological analysis of ultrasound graphic trace 151
Movement Disorder-Childhood Rating Scale: A Sensitive Tool to Evaluate Movement Disorders 151
Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome 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
Gas chromatography/mass spectrometry assay for arginine: glycine-amidinotransferase deficiency 147
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study 146
Cyclocreatine treatment ameliorates the cognitive, autistic and epileptic phenotype in a mouse model of Creatine Transporter Deficiency 146
Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data 145
Unusual clinical and magnetic resonance imaging findings in a family with proteolipid protein gene mutation 144
Gain of function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling 144
Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53 144
Kinematic analysis of upper limb in children with movement disorder: Quantitatitative assessment of effectiveness of pharmacological trials. 143
Movement Disorder-Childhood Rating Scale: Reliability and Validity 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
Post-Traumatic Stress Reactions in Caregivers of Children and Adolescents/Young Adults with Severe Diseases: A Systematic Review of Risk and Protective Factors 141
Brain lactic alkalosis in Aicardi-Goutières Syndrome 140
Benefits of glucocorticoids in non-ambulant boys/men with Duchenne muscular dystrophy: A multicentric longitudinal study using the Performance of Upper Limb test 140
Arginine and glycine stimulate creatine synthesis in creatine transporter 1-deficient lymphoblasts 140
Characterization of Phenotypic Variability in Becker Muscular Dystrophy for Clinical Practice and Towards Trial Readiness: A Two-Years Follow up Study 139
Brain magnetic resonance in the diagnostic evaluation of mitochondrial encephalopathies 137
Psychopathological Impact in Patients with History of Rheumatic Fever with or without Sydenham's Chorea: A Multicenter Prospective Study 136
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
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
Enhancing DLG2 Implications in Neuropsychiatric Disorders: Analysis of a Cohort of Eight Patients with 11q14.1 Imbalances 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
Scale for evaluation of movement disorders in the first three years of life 133
A Retrospective Longitudinal Study in a Cohort of Children With Dyskinetic Cerebral Palsy Treated With Tetrabenazine 133
24 month longitudinal data in ambulant boys with duchenne muscular dystrophy 132
Association between Reported Sleep Disorders and Behavioral Issues in Children with Myotonic Dystrophy Type 1—Results from a Retrospective Analysis in Italy 131
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
Early neurodevelopmental characterization in children with cobalamin C/defect 130
Functional changes in Duchenne muscular dystrophy A 12-month longitudinal cohort study 129
CLINICAL AND MR SPECTROSCOPY FOLLOW-UP OF CT1 DEFICIENT ITALIAN PATIENTS TREATED BY ORAL ARGININE 128
Functional levels and MRI patterns of muscle involvement in upper limbs in Duchenne muscular dystrophy 128
A Potential Biomarker of Brain Activity in Autism Spectrum Disorders: A Pilot fNIRS Study in Female Preschoolers 127
Responsiveness of the Movement Disorder-Childhood Rating Scale in children with movement disorders undergoing oral therapy with tetrabenazine 127
Creatine precursors stimulate Cr synthesis in CT1 deficient lymphoblasts 127
Proton MR spectroscopy of mitochondrial diseases: analysis of brain metabolic abnormalities and their possible diagnostic relevance 126
Quantitative analysis at 1.5 T muscle MRI in neuromuscular disorderd 126
"I have got something positive out of this situation": Psychological benefits of caregiving in relatives of young people with muscular dystrophy 126
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 126
Inborn errors of creatine metabolism and epilepsy. 125
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome 125
Expanding Phenotype of Poirier-Bienvenu Syndrome: New Evidence from an Italian Multicentrical Cohort of Patients 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
Does the assessment of general movements without video observation reliably predict neurological outcome? RID F-1503-2010 123
Congenital Myopathy as a Phenotypic Expression of CACNA1S Gene Mutation: Case Report and Systematic Review of the Literature 122
Neuropsychological profiles in children with Duchenne muscular dystrophy compared to dyslexic population 122
Variant of Rett syndrome and CDKL5 gene: clinical and autonomic description of 10 cases. 122
Inter and intra-rater reliability and minimal detectable difference of movement disorder-childhood rating scale 122
Molecular cytogenetic characterization of a new case of patial trisomy 13 (13q11q13.2)Research letter 121
tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia 121
Characterization of seven novel mutations in seven patients with GAMT deficiency 121
A Not So Benign Family Pedigree With Hereditary Chorea: A Broader Phenotypic Expression or Additional Picture? 121
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
Four years follow up of ACY1 deficient patient and pedigree study 119
Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements 119
Inter and intra-rater reliability and minimal detectable difference of movement disorder-childhood rating scale 119
Totale 14.988
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Categoria #
all - tutte 120.164
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 120.164
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021420 0 0 0 0 0 0 0 0 0 0 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
2024/20258.890 38 365 55 450 429 705 950 610 939 1.516 1.143 1.690
2025/202613.023 520 1.617 2.069 2.611 922 999 1.370 758 978 894 285 0
Totale 37.712