CNR Institutional Research Information System

PARANO, ENRICO
 Distribuzione geografica
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Continente #
AS - Asia 1.543
NA - Nord America 1.503
EU - Europa 531
SA - Sud America 377
AF - Africa 38
Continente sconosciuto - Info sul continente non disponibili 27
OC - Oceania 6
Totale 4.025
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Nazione #
US - Stati Uniti d'America 1.443
SG - Singapore 698
BR - Brasile 297
CN - Cina 243
IT - Italia 227
VN - Vietnam 186
HK - Hong Kong 167
FR - Francia 123
NL - Olanda 79
BD - Bangladesh 65
IN - India 33
AR - Argentina 31
JP - Giappone 29
KR - Corea 28
CA - Canada 25
ID - Indonesia 24
GB - Regno Unito 22
CO - Colombia 16
DE - Germania 12
TR - Turchia 12
EC - Ecuador 11
MX - Messico 11
ZA - Sudafrica 11
RU - Federazione Russa 10
IQ - Iraq 9
VE - Venezuela 9
FI - Finlandia 8
UA - Ucraina 8
AT - Austria 6
SE - Svezia 6
AU - Australia 5
CL - Cile 5
CR - Costa Rica 5
ES - Italia 5
IL - Israele 5
JM - Giamaica 5
KE - Kenya 5
PH - Filippine 5
PL - Polonia 5
MA - Marocco 4
PS - Palestinian Territory 4
SA - Arabia Saudita 4
TH - Thailandia 4
DZ - Algeria 3
EG - Egitto 3
HN - Honduras 3
JO - Giordania 3
KW - Kuwait 3
LT - Lituania 3
MY - Malesia 3
PK - Pakistan 3
PY - Paraguay 3
SK - Slovacchia (Repubblica Slovacca) 3
SV - El Salvador 3
TN - Tunisia 3
TT - Trinidad e Tobago 3
UY - Uruguay 3
AE - Emirati Arabi Uniti 2
BE - Belgio 2
CH - Svizzera 2
DO - Repubblica Dominicana 2
NP - Nepal 2
OM - Oman 2
PE - Perù 2
PT - Portogallo 2
SC - Seychelles 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
FJ - Figi 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LB - Libano 1
MK - Macedonia 1
MR - Mauritania 1
MU - Mauritius 1
MW - Malawi 1
NI - Nicaragua 1
PA - Panama 1
PR - Porto Rico 1
QA - Qatar 1
RO - Romania 1
RS - Serbia 1
SY - Repubblica araba siriana 1
Totale 3.998
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Città #
Santa Clara 572
Singapore 411
Hong Kong 162
Ashburn 115
San Jose 103
Lauterbourg 85
Ho Chi Minh City 70
Hefei 66
Beijing 61
Dallas 50
Hanoi 40
New York 36
Los Angeles 32
São Paulo 31
Seoul 28
Tokyo 24
Council Bluffs 17
Milan 16
Naples 14
Phoenix 13
Rio de Janeiro 13
Orem 12
Rome 12
Buffalo 11
Catania 10
Chicago 10
Da Nang 10
Chennai 9
Atlanta 8
Brasília 8
Frankfurt am Main 8
Palermo 8
Guarulhos 7
Haiphong 7
Verona 7
Helsinki 6
Houston 6
Istanbul 6
Jacksonville 6
Johannesburg 6
Belo Horizonte 5
Genoa 5
Manchester 5
Nairobi 5
Philadelphia 5
Quito 5
Turin 5
Washington 5
Amsterdam 4
Bogotá 4
Bologna 4
Brooklyn 4
Columbia 4
Denver 4
Florence 4
Guangzhou 4
Guayaquil 4
Hyderabad 4
Las Vegas 4
Louisville 4
Minamishinagawa 4
Montreal 4
Orlando 4
Pittsburgh 4
Porto Alegre 4
Richmond 4
Rockingham 4
San Antonio 4
San José 4
Stockholm 4
The Bronx 4
Toronto 4
Arlington Heights 3
Austin 3
Birmingham 3
Bratislava 3
Brescia 3
Can Tho 3
Canda 3
Carapicuíba 3
Charlotte 3
Curitiba 3
Dhaka 3
Figino 3
Forlì 3
Goiânia 3
Joinville 3
La Plata 3
Manaus 3
Maracaibo 3
Miami 3
Milwaukee 3
New Delhi 3
Padua 3
Piscataway 3
Quảng Ngãi 3
Sacramento 3
San Pedro Sula 3
San Salvador 3
Sorocaba 3
Totale 2.336
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Nome #
"Maltrattamenti e Abusi sui Minori: correlazioni cliniche, genetiche ed epigenetiche" 136
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome 88
Early Life Stress (ELS) Effects on Fetal and Adult Bone Development 82
Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review 81
Scimitar vein anomaly with multiple cardiac malformations, craniofacial and central nervous system abnormalities in a brother and sister: familial scimitar anomaly or new syndrome? 80
Severe psychotic symptoms in youth with PANS/PANDAS: case-series 73
Low prevalence of neurologic and psychiatric manifestations in children with gluten sensitivity. 71
Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability 69
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 63
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures 61
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions 60
Molecular and Neurobiological Imbalance from the Use of Technological Devices During Early Child Development Stages 58
The Many Faces of Child Abuse: How Clinical, Genetic and Epigenetic Correlates Help Us See the Full Picture 56
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 56
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 54
Long-term follow-up and novel genotype -phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 53
Febrile infection-related Epilepsy Syndrome (FIRES): a severe encephalopathy with status epilepticus. Literature review and presentation of two new cases 52
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 51
Identification and analysis of mutations in the Wilson disease gene (ATP7B): Population frequencies, genotype-phenotype correlation, and functional analyses 51
Child abuse syndrome (CAS): A newly recognized distinct entity 51
of 1 Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 51
A girl with palatoschisis, hypodontia, and lower lip pits 50
Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review 50
A syndrome with coarse face, mental retardation and unusual stereotyped movements 49
POST TRAUMATIC STRESS DISORDER IN CHILDREN RELATED TO CHILD ABUSE NEW GENETIC AND EPIGENETIC EVIDENCES 47
Chromosome 15q BP4-BP5 Deletion in a Girl with Nocturnal Frontal Lobe Epilepsy, Migraine, Circumscribed Hypertrichosis, and Language Impairment 47
Clinical heterogeneity in familial congenital ptosis: analysis of fourteen cases in one family over five generations 46
ABUSI SUI MINORI: CORRELAZIONI CLINICHE, GENETICHE ED EPIGENETICHE 46
Neuropsychological assessment in children with absence epilepsy 46
The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene 45
Abusi sui minori: correlazioni cliniche, genetiche ed epigenetiche 44
Acute Disseminated Encephalomyelitis: A Long-Term Prospective Study and Meta-Analysis 44
Molecular basis of phenotypic heterogeneity in siblings with spinal muscular atrophy 41
Child Abuse: clinical and scientific correlates 41
Focal neurological deficits in children with beta-thalassemia major 41
Neonatal onset of hot water reflex seizures in monozygotic twins subsequently manifesting episodes of alternating hemiplegia. 40
Progetto Multicentrico ISN, CNR, CATANIA MALATRATTAMENTI E ABUSI SUI MINORI ASPETTI CLINICI, CORRELAZIONI GENETICHE ED EPIGENETICHE 40
Hydranencephaly: cerebral spinal fluid instead of cerebral mantles 40
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene 40
Child abuse and maltratment: clinical, genetic and epigenetic correlates. 39
Epilepsy is not a prominent feature of primary autism 37
Pediatric autoimmune neuropsychiatry disorder associated with group a streptococcal infection: The role of surgical treatment 36
Blepharoptosis in children: our experience at the light of literature 36
POST TRAUMATIC STRESS DISORDER IN CHILDREN RELATED TO CHILD ABUSE NEW CLINICAL, GENETIC AND EPIGENETIC EVIDENCES 36
Noninvasive prenatal diagnosis of chromosomal aneuploidies by isolation and analysis of fetal cells from maternal blood 36
NRXN1-related disorders, attempt to better define clinical assessment 36
A Systematic Review of Cutaneous Hypopigmentation Disorder Associated with Neurologic Involvement 35
Child Abuse Syndrome (CAS): A Newly Recognized Distinct Entity 35
Neonatal peripheral hypotonia: clinical and electromyographic characteristics 35
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 35
A clinical study of childhood spinal muscular atrophy in Sicily: a review of 75 cases 34
Awareness and Recognition: The Importance of the Orthopaedist in Child Abuse 34
Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: A novel form of CMD 34
Anti-brain antibodies in PANDAS versus uncomplicated streptococcal infection 34
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 34
A genomewide screen for autism susceptibility loci. 34
Child Abuse: Clinical, Genetic and Epigenetic correlates 33
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis. 33
Late primary unilateral thalamic hemorrhage in infancy: Report of two cases 33
HyperCKemia as a biomarker for muscular diseases 33
PLASMA BETA-ENDORPHIN LEVELS AND NATURAL-KILLER-CELLS IN 2 CASES OF CONGENITAL INDIFFERENCE TO PAIN 33
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 33
Bickerstaff's brainstem encephalitis (BBE) in childhood: rapid resolution after intravenous immunoglobulins treatment 32
Congenital muscular dystrophy with syringomyelia 32
A new clinical feature associated with familial early-onset of dystonic-guttural tics: An unusual diagnosis of PANDAS 32
Aicardi syndrome with multiple tumors: a case report with literature review 32
Colobomatous microphthalmia, microcephaly with cerebellar hypoplasia: Association or new syndrome? 31
Diabetes insipidus in neurobrucellosis 31
Electrophysiologic correlates of peripheral nervous system maturation in infancy and childhood 31
Delayed bilateral median nerve injury due to low-tension electric current 31
White matter changes mimicking a leukodystrophy in a patient with Mucopolysaccharidosis: Characterization by MRI 30
Callosal anomalies with interhemispheric cyst: expanding the phenotype 30
Fetal nucleated red blood cell counts in peripheral blood of mothers bearing down syndrome fetus 30
Anton-Babinski syndrome in a child with early-stage adrenoleukodystrophy [8] 30
Congenital muscular dystrophies: Clinical review and proposed classification 30
Reversible palsy of the hypoglossal nerve complicating infectious mononucleosis in a young child 30
A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions 30
Myotonic dystrophy in a large Sicilian kinship: a case report 29
Autoimmune neuropsychiatric disorders associated with streptococcal infection: Sydenham chorea, PANDAS, and PANDAS variants. 29
Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease. 29
Chronic inflammatory demyelinating polyneuropathy in childhood: clinical and electrophysiological features 28
A rare hereditary encephalopathy: Aicardi-Goutières Syndrome | Su una rara encefalopatia ereditaria: La Sindrome di Aicardi-Goutières 28
Neurological complications in hospitalized patients with pertussis: A 15-year Sicilian experience 28
Extraordinary intrathecal bone reaction in beta-thalassaemia intermedia 28
Intrafamilial phenotypic heterogeneity of the Poland complex: A case report 27
Congenital muscular dystrophy: Correlation of muscle biopsy and clinical features 27
Headache in childhood: A critical review of 265 patients 27
A case of extreme brain lesions: Which pathogenetic mechanism? 27
Perrault syndrome: Evidence for progressive nervous system involvement 26
A new clinical feature associated with familial early-onset of dystonic-guttural tics: An unusual diagnosis of PANDAS 26
Spine and brain malformations in a patient obligate carrier of MTHFR with autism and mental retardation 26
Scimitar vein anomaly with multiple cardiac malformations, craniofacial, and central nervous system abnormalities in a brother and sister: Familial scimitar anomaly or new syndrome? 26
Seizures are not a predominant feature of primary autism 26
Progetto ISN, CNR: Maltrattamenti e abusi sui minori aspetti clinici e correlazioni scientifiche 25
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 25
Hemihydranencephaly: Case report and literature review 25
Reflex sympathetic dystrophy associated with deep peroneal nerve entrapment 24
Acute palsy of the recurrent laryngeal nerve complicating Epstein-Barr virus infection 21
IgG Glycosylation Analysis in Patients with Ring14 Syndrome Unveils Novel Pathomechanisms and New Therapy Perspectives 14
Totale 4.025
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Categoria #
all - tutte 15.305
article - articoli 12.719
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 28.024
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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
2026/2027544 153 122 269 0 0 0 0 0 0 0 0 0
Totale 4.025