CNR Institutional Research Information System

PARANO, ENRICO
 Distribuzione geografica
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Continente #
AS - Asia 1.462
NA - Nord America 1.079
EU - Europa 417
SA - Sud America 345
AF - Africa 35
OC - Oceania 5
Totale 3.343
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Nazione #
US - Stati Uniti d'America 1.043
SG - Singapore 695
BR - Brasile 288
CN - Cina 241
VN - Vietnam 178
HK - Hong Kong 165
IT - Italia 127
FR - Francia 121
NL - Olanda 75
IN - India 33
JP - Giappone 29
AR - Argentina 28
KR - Corea 28
GB - Regno Unito 18
BD - Bangladesh 17
ID - Indonesia 16
CA - Canada 15
DE - Germania 12
MX - Messico 11
ZA - Sudafrica 11
RU - Federazione Russa 10
IQ - Iraq 9
TR - Turchia 9
EC - Ecuador 8
FI - Finlandia 8
UA - Ucraina 8
SE - Svezia 6
AU - Australia 5
CL - Cile 5
CO - Colombia 5
IL - Israele 5
KE - Kenya 5
PL - Polonia 5
AT - Austria 4
ES - Italia 4
MA - Marocco 4
PS - Palestinian Territory 4
SA - Arabia Saudita 4
DZ - Algeria 3
EG - Egitto 3
JO - Giordania 3
KW - Kuwait 3
LT - Lituania 3
PK - Pakistan 3
PY - Paraguay 3
SK - Slovacchia (Repubblica Slovacca) 3
TN - Tunisia 3
UY - Uruguay 3
VE - Venezuela 3
AE - Emirati Arabi Uniti 2
BE - Belgio 2
CH - Svizzera 2
DO - Repubblica Dominicana 2
MY - Malesia 2
NP - Nepal 2
OM - Oman 2
PE - Perù 2
PT - Portogallo 2
SV - El Salvador 2
TH - Thailandia 2
UZ - Uzbekistan 2
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
JM - Giamaica 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 3.343
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Città #
Santa Clara 567
Singapore 408
Hong Kong 162
Lauterbourg 85
Ashburn 77
Ho Chi Minh City 68
Hefei 66
Beijing 59
San Jose 59
Dallas 47
Hanoi 39
São Paulo 31
New York 30
Seoul 28
Tokyo 24
Los Angeles 23
Council Bluffs 13
Rio de Janeiro 13
Orem 12
Naples 10
Chennai 9
Da Nang 9
Frankfurt am Main 8
Palermo 8
Brasília 7
Haiphong 7
Buffalo 6
Guarulhos 6
Helsinki 6
Johannesburg 6
Milan 6
Catania 5
Istanbul 5
Nairobi 5
Rome 5
Turin 5
Amsterdam 4
Belo Horizonte 4
Chicago 4
Guangzhou 4
Guayaquil 4
Hyderabad 4
Jacksonville 4
Manchester 4
Minamishinagawa 4
Montreal 4
Porto Alegre 4
Stockholm 4
Bratislava 3
Can Tho 3
Canda 3
Carapicuíba 3
Curitiba 3
Goiânia 3
Joinville 3
Manaus 3
Maracaibo 3
New Delhi 3
Phoenix 3
Piscataway 3
Quito 3
Quảng Ngãi 3
San Antonio 3
Sorocaba 3
São José do Rio Preto 3
São Luís 3
Uberlândia 3
Vila Velha 3
Warsaw 3
Washington 3
Agawam 2
Anaheim 2
Anápolis 2
Aparecida de Goiânia 2
Aracaju 2
Araucária 2
Atlanta 2
Avellino 2
Bengaluru 2
Bergamo 2
Biên Hòa 2
Bologna 2
Brescia 2
Campinas 2
Cardito 2
Caruaru 2
Charlotte 2
Cosmópolis 2
Cuiabá 2
Delhi 2
Depok 2
Dhaka 2
Ercolano 2
Forlì 2
Greensboro 2
Hải Dương 2
Jeddah 2
Juazeiro do Norte 2
Krasnodar 2
Kuwait City 2
Totale 2.098
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Nome #
"Maltrattamenti e Abusi sui Minori: correlazioni cliniche, genetiche ed epigenetiche" 104
Early Life Stress (ELS) Effects on Fetal and Adult Bone Development 71
Severe psychotic symptoms in youth with PANS/PANDAS: case-series 68
Scimitar vein anomaly with multiple cardiac malformations, craniofacial and central nervous system abnormalities in a brother and sister: familial scimitar anomaly or new syndrome? 67
Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review 63
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
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome 53
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures 52
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 50
The Many Faces of Child Abuse: How Clinical, Genetic and Epigenetic Correlates Help Us See the Full Picture 49
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions 49
A girl with palatoschisis, hypodontia, and lower lip pits 47
Child abuse syndrome (CAS): A newly recognized distinct entity 47
Molecular and Neurobiological Imbalance from the Use of Technological Devices During Early Child Development Stages 47
Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability 47
POST TRAUMATIC STRESS DISORDER IN CHILDREN RELATED TO CHILD ABUSE NEW GENETIC AND EPIGENETIC EVIDENCES 44
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 44
A syndrome with coarse face, mental retardation and unusual stereotyped movements 43
Long-term follow-up and novel genotype -phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 43
of 1 Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 42
Febrile infection-related Epilepsy Syndrome (FIRES): a severe encephalopathy with status epilepticus. Literature review and presentation of two new cases 42
Neuropsychological assessment in children with absence epilepsy 41
Low prevalence of neurologic and psychiatric manifestations in children with gluten sensitivity. 40
Chromosome 15q BP4-BP5 Deletion in a Girl with Nocturnal Frontal Lobe Epilepsy, Migraine, Circumscribed Hypertrichosis, and Language Impairment 40
Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review 40
Clinical heterogeneity in familial congenital ptosis: analysis of fourteen cases in one family over five generations 39
ABUSI SUI MINORI: CORRELAZIONI CLINICHE, GENETICHE ED EPIGENETICHE 39
Acute Disseminated Encephalomyelitis: A Long-Term Prospective Study and Meta-Analysis 39
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 38
Neonatal onset of hot water reflex seizures in monozygotic twins subsequently manifesting episodes of alternating hemiplegia. 38
Abusi sui minori: correlazioni cliniche, genetiche ed epigenetiche 37
Child Abuse: clinical and scientific correlates 37
Child abuse and maltratment: clinical, genetic and epigenetic correlates. 36
The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene 36
Progetto Multicentrico ISN, CNR, CATANIA MALATRATTAMENTI E ABUSI SUI MINORI ASPETTI CLINICI, CORRELAZIONI GENETICHE ED EPIGENETICHE 35
Molecular basis of phenotypic heterogeneity in siblings with spinal muscular atrophy 34
Hydranencephaly: cerebral spinal fluid instead of cerebral mantles 34
Epilepsy is not a prominent feature of primary autism 34
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
Identification and analysis of mutations in the Wilson disease gene (ATP7B): Population frequencies, genotype-phenotype correlation, and functional analyses 33
Blepharoptosis in children: our experience at the light of literature 32
Focal neurological deficits in children with beta-thalassemia major 32
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 32
Noninvasive prenatal diagnosis of chromosomal aneuploidies by isolation and analysis of fetal cells from maternal blood 32
PLASMA BETA-ENDORPHIN LEVELS AND NATURAL-KILLER-CELLS IN 2 CASES OF CONGENITAL INDIFFERENCE TO PAIN 32
NRXN1-related disorders, attempt to better define clinical assessment 32
A clinical study of childhood spinal muscular atrophy in Sicily: a review of 75 cases 31
Pediatric autoimmune neuropsychiatry disorder associated with group a streptococcal infection: The role of surgical treatment 30
Bickerstaff's brainstem encephalitis (BBE) in childhood: rapid resolution after intravenous immunoglobulins treatment 30
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene 30
Neonatal peripheral hypotonia: clinical and electromyographic characteristics 30
Aicardi syndrome with multiple tumors: a case report with literature review 30
Anti-brain antibodies in PANDAS versus uncomplicated streptococcal infection 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
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 29
A Systematic Review of Cutaneous Hypopigmentation Disorder Associated with Neurologic Involvement 28
Callosal anomalies with interhemispheric cyst: expanding the phenotype 28
Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: A novel form of CMD 28
Child Abuse: Clinical, Genetic and Epigenetic correlates 28
Congenital muscular dystrophy with syringomyelia 28
Congenital muscular dystrophies: Clinical review and proposed classification 28
HyperCKemia as a biomarker for muscular diseases 28
A new clinical feature associated with familial early-onset of dystonic-guttural tics: An unusual diagnosis of PANDAS 28
Autoimmune neuropsychiatric disorders associated with streptococcal infection: Sydenham chorea, PANDAS, and PANDAS variants. 28
Colobomatous microphthalmia, microcephaly with cerebellar hypoplasia: Association or new syndrome? 27
Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease. 27
Awareness and Recognition: The Importance of the Orthopaedist in Child Abuse 26
Diabetes insipidus in neurobrucellosis 26
Congenital muscular dystrophy: Correlation of muscle biopsy and clinical features 26
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 25
A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions 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
Chronic inflammatory demyelinating polyneuropathy in childhood: clinical and electrophysiological features 24
Fetal nucleated red blood cell counts in peripheral blood of mothers bearing down syndrome fetus 24
Anton-Babinski syndrome in a child with early-stage adrenoleukodystrophy [8] 24
A rare hereditary encephalopathy: Aicardi-Goutières Syndrome | Su una rara encefalopatia ereditaria: La Sindrome di Aicardi-Goutières 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
Myotonic dystrophy in a large Sicilian kinship: a case report 24
Extraordinary intrathecal bone reaction in beta-thalassaemia intermedia 24
Delayed bilateral median nerve injury due to low-tension electric current 24
White matter changes mimicking a leukodystrophy in a patient with Mucopolysaccharidosis: Characterization by MRI 23
Spine and brain malformations in a patient obligate carrier of MTHFR with autism and mental retardation 23
Progetto ISN, CNR: Maltrattamenti e abusi sui minori aspetti clinici e correlazioni scientifiche 23
Reversible palsy of the hypoglossal nerve complicating infectious mononucleosis in a young child 23
Neurological complications in hospitalized patients with pertussis: A 15-year Sicilian experience 23
Headache in childhood: A critical review of 265 patients 23
Seizures are not a predominant feature of primary autism 23
Intrafamilial phenotypic heterogeneity of the Poland complex: A case report 22
Scimitar vein anomaly with multiple cardiac malformations, craniofacial, and central nervous system abnormalities in a brother and sister: Familial scimitar anomaly or new syndrome? 22
A case of extreme brain lesions: Which pathogenetic mechanism? 22
Hemihydranencephaly: Case report and literature review 21
Acute palsy of the recurrent laryngeal nerve complicating Epstein-Barr virus infection 20
Reflex sympathetic dystrophy associated with deep peroneal nerve entrapment 20
A genomewide screen for autism susceptibility loci. 19
Totale 3.367
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Categoria #
all - tutte 11.630
article - articoli 9.991
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 21.621
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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
2025/20261.935 48 103 213 322 383 79 302 125 148 140 72 0
Totale 3.367