CNR Institutional Research Information System

PARANO, ENRICO
 Distribuzione geografica
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Continente #
AS - Asia 1.505
NA - Nord America 1.211
EU - Europa 470
SA - Sud America 349
AF - Africa 35
OC - Oceania 5
Totale 3.575
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Nazione #
US - Stati Uniti d'America 1.166
SG - Singapore 697
BR - Brasile 289
CN - Cina 241
VN - Vietnam 178
IT - Italia 175
HK - Hong Kong 166
FR - Francia 121
NL - Olanda 77
BD - Bangladesh 57
IN - India 33
JP - Giappone 29
AR - Argentina 28
KR - Corea 28
CA - Canada 19
GB - Regno Unito 19
ID - Indonesia 16
DE - Germania 12
MX - Messico 11
ZA - Sudafrica 11
RU - Federazione Russa 10
EC - Ecuador 9
IQ - Iraq 9
TR - Turchia 9
FI - Finlandia 8
UA - Ucraina 8
CO - Colombia 6
SE - Svezia 6
AU - Australia 5
CL - Cile 5
ES - Italia 5
IL - Israele 5
KE - Kenya 5
PL - Polonia 5
AT - Austria 4
MA - Marocco 4
PS - Palestinian Territory 4
SA - Arabia Saudita 4
VE - Venezuela 4
DZ - Algeria 3
EG - Egitto 3
JM - Giamaica 3
JO - Giordania 3
KW - Kuwait 3
LT - Lituania 3
PK - Pakistan 3
PY - Paraguay 3
SK - Slovacchia (Repubblica Slovacca) 3
SV - El Salvador 3
TN - Tunisia 3
UY - Uruguay 3
AE - Emirati Arabi Uniti 2
BE - Belgio 2
CH - Svizzera 2
CR - Costa Rica 2
DO - Repubblica Dominicana 2
MY - Malesia 2
NP - Nepal 2
OM - Oman 2
PE - Perù 2
PT - Portogallo 2
TH - Thailandia 2
UZ - Uzbekistan 2
AL - Albania 1
AM - Armenia 1
AO - Angola 1
AZ - Azerbaigian 1
BG - Bulgaria 1
BY - Bielorussia 1
CI - Costa d'Avorio 1
CM - Camerun 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
ET - Etiopia 1
HN - Honduras 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LB - Libano 1
MK - Macedonia 1
MR - Mauritania 1
MW - Malawi 1
NI - Nicaragua 1
PA - Panama 1
PH - Filippine 1
PR - Porto Rico 1
QA - Qatar 1
RO - Romania 1
RS - Serbia 1
SY - Repubblica araba siriana 1
TT - Trinidad e Tobago 1
Totale 3.575
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Città #
Santa Clara 570
Singapore 410
Hong Kong 162
Ashburn 97
Lauterbourg 85
Ho Chi Minh City 68
Hefei 66
San Jose 61
Beijing 59
Dallas 48
Hanoi 39
New York 35
São Paulo 31
Seoul 28
Los Angeles 25
Tokyo 24
Council Bluffs 13
Rio de Janeiro 13
Orem 12
Buffalo 10
Naples 10
Chennai 9
Da Nang 9
Milan 9
Rome 9
Frankfurt am Main 8
Palermo 8
Brasília 7
Chicago 7
Haiphong 7
Verona 7
Catania 6
Guarulhos 6
Helsinki 6
Johannesburg 6
Belo Horizonte 5
Istanbul 5
Nairobi 5
Turin 5
Amsterdam 4
Genoa 4
Guangzhou 4
Guayaquil 4
Hyderabad 4
Jacksonville 4
Manchester 4
Minamishinagawa 4
Montreal 4
Philadelphia 4
Porto Alegre 4
Quito 4
Rockingham 4
Stockholm 4
Washington 4
Arlington Heights 3
Austin 3
Bratislava 3
Brescia 3
Can Tho 3
Canda 3
Carapicuíba 3
Charlotte 3
Curitiba 3
Florence 3
Forlì 3
Goiânia 3
Joinville 3
Manaus 3
Maracaibo 3
New Delhi 3
Padua 3
Phoenix 3
Piscataway 3
Pittsburgh 3
Quảng Ngãi 3
Sacramento 3
San Antonio 3
San Salvador 3
Sorocaba 3
São José do Rio Preto 3
São Luís 3
Toronto 3
Uberlândia 3
Vila Velha 3
Warsaw 3
Agawam 2
Anaheim 2
Anápolis 2
Aparecida de Goiânia 2
Aracaju 2
Araucária 2
Atlanta 2
Avellino 2
Balch Springs 2
Bengaluru 2
Bergamo 2
Biên Hòa 2
Bologna 2
Cambridge 2
Campinas 2
Totale 2.173
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Nome #
"Maltrattamenti e Abusi sui Minori: correlazioni cliniche, genetiche ed epigenetiche" 126
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome 80
Early Life Stress (ELS) Effects on Fetal and Adult Bone Development 76
Scimitar vein anomaly with multiple cardiac malformations, craniofacial and central nervous system abnormalities in a brother and sister: familial scimitar anomaly or new syndrome? 75
Severe psychotic symptoms in youth with PANS/PANDAS: case-series 69
Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review 67
Low prevalence of neurologic and psychiatric manifestations in children with gluten sensitivity. 66
Congenital insensitivity to pain with Anhidrosis (NTRK1 mutation) and early onset renal disease: clinical report on three sibs with a 25-year follow-up in one of them 58
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures 57
Molecular and Neurobiological Imbalance from the Use of Technological Devices During Early Child Development Stages 55
The Many Faces of Child Abuse: How Clinical, Genetic and Epigenetic Correlates Help Us See the Full Picture 54
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions 53
Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability 51
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 50
A girl with palatoschisis, hypodontia, and lower lip pits 49
Child abuse syndrome (CAS): A newly recognized distinct entity 49
Long-term follow-up and novel genotype -phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 47
Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four-member family and an unrelated boy 47
POST TRAUMATIC STRESS DISORDER IN CHILDREN RELATED TO CHILD ABUSE NEW GENETIC AND EPIGENETIC EVIDENCES 45
of 1 Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 45
Febrile infection-related Epilepsy Syndrome (FIRES): a severe encephalopathy with status epilepticus. Literature review and presentation of two new cases 44
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 43
A syndrome with coarse face, mental retardation and unusual stereotyped movements 43
Chromosome 15q BP4-BP5 Deletion in a Girl with Nocturnal Frontal Lobe Epilepsy, Migraine, Circumscribed Hypertrichosis, and Language Impairment 43
Identification and analysis of mutations in the Wilson disease gene (ATP7B): Population frequencies, genotype-phenotype correlation, and functional analyses 42
Neuropsychological assessment in children with absence epilepsy 42
Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review 41
Clinical heterogeneity in familial congenital ptosis: analysis of fourteen cases in one family over five generations 40
ABUSI SUI MINORI: CORRELAZIONI CLINICHE, GENETICHE ED EPIGENETICHE 40
Child Abuse: clinical and scientific correlates 39
Acute Disseminated Encephalomyelitis: A Long-Term Prospective Study and Meta-Analysis 39
Abusi sui minori: correlazioni cliniche, genetiche ed epigenetiche 38
Neonatal onset of hot water reflex seizures in monozygotic twins subsequently manifesting episodes of alternating hemiplegia. 38
The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene 38
Molecular basis of phenotypic heterogeneity in siblings with spinal muscular atrophy 36
Child abuse and maltratment: clinical, genetic and epigenetic correlates. 36
Progetto Multicentrico ISN, CNR, CATANIA MALATRATTAMENTI E ABUSI SUI MINORI ASPETTI CLINICI, CORRELAZIONI GENETICHE ED EPIGENETICHE 36
Hydranencephaly: cerebral spinal fluid instead of cerebral mantles 36
Epilepsy is not a prominent feature of primary autism 35
NRXN1-related disorders, attempt to better define clinical assessment 35
Child Abuse Syndrome (CAS): A Newly Recognized Distinct Entity 34
POST TRAUMATIC STRESS DISORDER IN CHILDREN RELATED TO CHILD ABUSE NEW CLINICAL, GENETIC AND EPIGENETIC EVIDENCES 34
Noninvasive prenatal diagnosis of chromosomal aneuploidies by isolation and analysis of fetal cells from maternal blood 34
Focal neurological deficits in children with beta-thalassemia major 33
Fetal cells in maternal blood: a six-fold increase in women who have undergone amniocentesis and carry a fetus with Down syndrome: a multicenter study 33
A Systematic Review of Cutaneous Hypopigmentation Disorder Associated with Neurologic Involvement 32
Pediatric autoimmune neuropsychiatry disorder associated with group a streptococcal infection: The role of surgical treatment 32
Blepharoptosis in children: our experience at the light of literature 32
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene 32
PLASMA BETA-ENDORPHIN LEVELS AND NATURAL-KILLER-CELLS IN 2 CASES OF CONGENITAL INDIFFERENCE TO PAIN 32
A clinical study of childhood spinal muscular atrophy in Sicily: a review of 75 cases 31
Anti-brain antibodies in PANDAS versus uncomplicated streptococcal infection 31
Congenital muscular dystrophy with syringomyelia 31
Child Abuse: Clinical, Genetic and Epigenetic correlates 30
Bickerstaff's brainstem encephalitis (BBE) in childhood: rapid resolution after intravenous immunoglobulins treatment 30
Neonatal peripheral hypotonia: clinical and electromyographic characteristics 30
A new clinical feature associated with familial early-onset of dystonic-guttural tics: An unusual diagnosis of PANDAS 30
Aicardi syndrome with multiple tumors: a case report with literature review 30
Callosal anomalies with interhemispheric cyst: expanding the phenotype 29
Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: A novel form of CMD 29
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis. 29
Late primary unilateral thalamic hemorrhage in infancy: Report of two cases 29
Electrophysiologic correlates of peripheral nervous system maturation in infancy and childhood 29
HyperCKemia as a biomarker for muscular diseases 29
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 29
Colobomatous microphthalmia, microcephaly with cerebellar hypoplasia: Association or new syndrome? 28
Diabetes insipidus in neurobrucellosis 28
Severe Unilateral Microtia with Aural Atresia, Hair White Patch, Stereotypes in a Young Boy with De novo 16p13.11 Deletion: Reasons for a New Genotype-Phenotype Correlation 28
Congenital muscular dystrophies: Clinical review and proposed classification 28
Autoimmune neuropsychiatric disorders associated with streptococcal infection: Sydenham chorea, PANDAS, and PANDAS variants. 28
Awareness and Recognition: The Importance of the Orthopaedist in Child Abuse 27
Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease. 27
Chronic inflammatory demyelinating polyneuropathy in childhood: clinical and electrophysiological features 26
White matter changes mimicking a leukodystrophy in a patient with Mucopolysaccharidosis: Characterization by MRI 26
Fetal nucleated red blood cell counts in peripheral blood of mothers bearing down syndrome fetus 26
Anton-Babinski syndrome in a child with early-stage adrenoleukodystrophy [8] 26
Congenital muscular dystrophy: Correlation of muscle biopsy and clinical features 26
A rare hereditary encephalopathy: Aicardi-Goutières Syndrome | Su una rara encefalopatia ereditaria: La Sindrome di Aicardi-Goutières 26
Extraordinary intrathecal bone reaction in beta-thalassaemia intermedia 26
Delayed bilateral median nerve injury due to low-tension electric current 26
Reversible palsy of the hypoglossal nerve complicating infectious mononucleosis in a young child 25
A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions 25
Myotonic dystrophy in a large Sicilian kinship: a case report 25
Perrault syndrome: Evidence for progressive nervous system involvement 24
A new clinical feature associated with familial early-onset of dystonic-guttural tics: An unusual diagnosis of PANDAS 24
Spine and brain malformations in a patient obligate carrier of MTHFR with autism and mental retardation 24
Congenital insensitivity to pain with anhidrosis (NTRK1 mutation) and early onset renal disease: Clinical report on three sibs with a 25-year follow-up in one of them 24
Seizures are not a predominant feature of primary autism 24
Intrafamilial phenotypic heterogeneity of the Poland complex: A case report 23
Progetto ISN, CNR: Maltrattamenti e abusi sui minori aspetti clinici e correlazioni scientifiche 23
Neurological complications in hospitalized patients with pertussis: A 15-year Sicilian experience 23
Scimitar vein anomaly with multiple cardiac malformations, craniofacial, and central nervous system abnormalities in a brother and sister: Familial scimitar anomaly or new syndrome? 23
Headache in childhood: A critical review of 265 patients 23
A case of extreme brain lesions: Which pathogenetic mechanism? 23
Reflex sympathetic dystrophy associated with deep peroneal nerve entrapment 22
A genomewide screen for autism susceptibility loci. 22
Hemihydranencephaly: Case report and literature review 21
Acute palsy of the recurrent laryngeal nerve complicating Epstein-Barr virus infection 20
IgG Glycosylation Analysis in Patients with Ring14 Syndrome Unveils Novel Pathomechanisms and New Therapy Perspectives 5
Totale 3.602
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Categoria #
all - tutte 13.597
article - articoli 11.158
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 24.755
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/20242 0 0 0 0 0 0 0 0 0 0 0 2
2024/20251.430 11 5 87 51 551 11 36 18 13 79 312 256
2025/20262.049 48 103 213 322 383 79 302 125 148 140 84 102
2026/2027121 121 0 0 0 0 0 0 0 0 0 0 0
Totale 3.602