CNR Institutional Research Information System

PARANO, ENRICO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
AS - Asia 68
NA - Nord America 28
EU - Europa 7
Totale 103
Salva come PNG Salva come JPEG
Nazione #
SG - Singapore 66
US - Stati Uniti d'America 28
IT - Italia 6
CN - Cina 2
AT - Austria 1
Totale 103
Salva come PNG Salva come JPEG
Città #
Singapore 54
Santa Clara 8
Santa Croce sull'Arno 2
Forest City 1
Messina 1
Rome 1
Vienna 1
Totale 68
Salva come PNG Salva come JPEG
Nome #
Early Life Stress (ELS) Effects on Fetal and Adult Bone Development 7
A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions 5
"Maltrattamenti e Abusi sui Minori: correlazioni cliniche, genetiche ed epigenetiche" 3
POST TRAUMATIC STRESS DISORDER IN CHILDREN RELATED TO CHILD ABUSE NEW GENETIC AND EPIGENETIC EVIDENCES 3
Child abuse and maltratment: clinical, genetic and epigenetic correlates. 3
Neuropsychological assessment in children with absence epilepsy 3
Scimitar vein anomaly with multiple cardiac malformations, craniofacial and central nervous system abnormalities in a brother and sister: familial scimitar anomaly or new syndrome? 2
Abusi sui minori: correlazioni cliniche, genetiche ed epigenetiche 2
Early Life Stress (ELS) Effects on Fetal and Adult Bone Development 2
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome 2
Neonatal onset of hot water reflex seizures in monozygotic twins subsequently manifesting episodes of alternating hemiplegia. 2
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 2
Colobomatous microphthalmia, microcephaly with cerebellar hypoplasia: Association or new syndrome? 2
Hydranencephaly: cerebral spinal fluid instead of cerebral mantles 2
ABUSI SUI MINORI: CORRELAZIONI CLINICHE, GENETICHE ED EPIGENETICHE 2
Chromosome 15q BP4-BP5 Deletion in a Girl with Nocturnal Frontal Lobe Epilepsy, Migraine, Circumscribed Hypertrichosis, and Language Impairment 2
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 2
of 1 Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 2
Febrile infection-related Epilepsy Syndrome (FIRES): a severe encephalopathy with status epilepticus. Literature review and presentation of two new cases 2
Child Abuse Syndrome (CAS): A Newly Recognized Distinct Entity 2
Reversible palsy of the hypoglossal nerve complicating infectious mononucleosis in a young child 2
Neurological complications in hospitalized patients with pertussis: A 15-year Sicilian experience 2
Scimitar vein anomaly with multiple cardiac malformations, craniofacial, and central nervous system abnormalities in a brother and sister: Familial scimitar anomaly or new syndrome? 2
POST TRAUMATIC STRESS DISORDER IN CHILDREN RELATED TO CHILD ABUSE NEW CLINICAL, GENETIC AND EPIGENETIC EVIDENCES 2
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 1
Severe psychotic symptoms in youth with PANS/PANDAS: case-series 1
A girl with palatoschisis, hypodontia, and lower lip pits 1
Clinical heterogeneity in familial congenital ptosis: analysis of fourteen cases in one family over five generations 1
Low prevalence of neurologic and psychiatric manifestations in children with gluten sensitivity. 1
Molecular basis of phenotypic heterogeneity in siblings with spinal muscular atrophy 1
A clinical study of childhood spinal muscular atrophy in Sicily: a review of 75 cases 1
A new clinical feature associated with familial early-onset of dystonic-guttural tics: An unusual diagnosis of PANDAS 1
Child Abuse: clinical and scientific correlates 1
Pediatric autoimmune neuropsychiatry disorder associated with group a streptococcal infection: The role of surgical treatment 1
Child abuse syndrome (CAS): A newly recognized distinct entity 1
Reflex sympathetic dystrophy associated with deep peroneal nerve entrapment 1
Awareness and Recognition: The Importance of the Orthopaedist in Child Abuse 1
Focal neurological deficits in children with beta-thalassemia major 1
White matter changes mimicking a leukodystrophy in a patient with Mucopolysaccharidosis: Characterization by MRI 1
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions 1
Callosal anomalies with interhemispheric cyst: expanding the phenotype 1
Long-term follow-up and novel genotype -phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 1
Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: A novel form of CMD 1
Anti-brain antibodies in PANDAS versus uncomplicated streptococcal infection 1
Child Abuse: Clinical, Genetic and Epigenetic correlates 1
Spine and brain malformations in a patient obligate carrier of MTHFR with autism and mental retardation 1
Fetal nucleated red blood cell counts in peripheral blood of mothers bearing down syndrome fetus 1
Diabetes insipidus in neurobrucellosis 1
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis. 1
Progetto ISN, CNR: Maltrattamenti e abusi sui minori aspetti clinici e correlazioni scientifiche 1
Bickerstaff's brainstem encephalitis (BBE) in childhood: rapid resolution after intravenous immunoglobulins treatment 1
Anton-Babinski syndrome in a child with early-stage adrenoleukodystrophy [8] 1
A rare hereditary encephalopathy: Aicardi-Goutières Syndrome | Su una rara encefalopatia ereditaria: La Sindrome di Aicardi-Goutières 1
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene 1
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 1
Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review 1
Epilepsy is not a prominent feature of primary autism 1
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures 1
Neonatal peripheral hypotonia: clinical and electromyographic characteristics 1
Acute Disseminated Encephalomyelitis: A Long-Term Prospective Study and Meta-Analysis 1
Myotonic dystrophy in a large Sicilian kinship: a case report 1
Headache in childhood: A critical review of 265 patients 1
Autoimmune neuropsychiatric disorders associated with streptococcal infection: Sydenham chorea, PANDAS, and PANDAS variants. 1
Noninvasive prenatal diagnosis of chromosomal aneuploidies by isolation and analysis of fetal cells from maternal blood 1
PLASMA BETA-ENDORPHIN LEVELS AND NATURAL-KILLER-CELLS IN 2 CASES OF CONGENITAL INDIFFERENCE TO PAIN 1
Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease. 1
Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability 1
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 1
Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review 1
A genomewide screen for autism susceptibility loci. 1
The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene 1
Totale 107
Salva come PNG Salva come JPEG
Categoria #
all - tutte 1.265
article - articoli 1.126
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.391
Salva come PNG Salva come JPEG


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
2024/2025105 11 5 89 0 0 0 0 0 0 0 0 0
Totale 107