about
Anti-brain antibodies in PANDAS versus uncomplicated streptococcal infectionMolecular basis of phenotypic heterogeneity in siblings with spinal muscular atrophyA new clinical feature associated with familial early-onset of dystonic-guttural tics: An unusual diagnosis of PANDASA multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions.TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa.Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analysesHydranencephaly: cerebral spinal fluid instead of cerebral mantlesLife-threatening neurological syndrome in Down's syndrome.HyperCKemia as a biomarker for muscular diseases.Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis.A clinical study of childhood spinal muscular atrophy in Sicily: a review of 75 cases.Pediatric autoimmune neuropsychiatric disorder associated with group a streptococcal infection: the role of surgical treatment.Bickerstaff's brainstem encephalitis (BBE) in childhood: rapid resolution after intravenous immunoglobulins treatment.Recurrent peripheral neuropathy in a girl with celiac disease.[Post-influenza viral myositis: report of a case]Blepharoptosis in children: our experience at the light of literature.New trends in cesarean section.Anton-Babinski syndrome in a child with early-stage adrenoleukodystrophy.A syndrome with coarse face, mental retardation and unusual stereotyped movements*.Callosal anomalies with interhemispheric cyst: expanding the phenotype.Epilepsy is not a prominent feature of primary autism.Peripheral lymphocyte subsets and other immune aspects in Rett syndrome.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.Syndactyly type 1 with cataracts and mental retardation.Neuropsychological assessment in children with absence epilepsy.Delayed bilateral median nerve injury due to low-tension electric current.Intrafamilial phenotypic heterogeneity of the Poland complex: a case reportNeonatal onset of hot water reflex seizures in monozygotic twins subsequently manifesting episodes of alternating hemiplegiaClinical Heterogeneity in Familial Congenital Ptosis: Analysis of Fourteen Cases in One Family Over Five GenerationsPerrault syndrome: Evidence for progressive nervous system involvementScimitar vein anomaly with multiple cardiac malformations, craniofacial, and central nervous system abnormalities in a brother and sister: Familial scimitar anomaly or new syndrome?Clinical heterogeneity in eyelid myoclonia, with absences, and epilepsyNoninvasive prenatal diagnosis of chromosomal aneuploidies by isolation and analysis of fetal cells from maternal bloodFetal Nucleated Red Blood Cell Counts in Peripheral Blood of Mothers Bearing Down Syndrome FetusArthrogryposis Multiplex Congenita and Pituitary Ectopia. A Case ReportTuberous breast deformity in an adolescent girl with Hurler-Scheie syndromeDiabetes insipidus in neurobrucellosisVein of Galen malformation and infantile spasmsReversible palsy of the hypoglossal nerve complicating infectious mononucleosis in a young childNeurological complications in hospitalized patients with pertussis: a 15-year Sicilian experience
P50
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P50
description
researcher, ORCID id # 0000-0002-0713-7339
@en
wetenschapper
@nl
name
ENRICO PARANO
@ast
ENRICO PARANO
@en
ENRICO PARANO
@es
ENRICO PARANO
@nl
type
label
ENRICO PARANO
@ast
ENRICO PARANO
@en
ENRICO PARANO
@es
ENRICO PARANO
@nl
prefLabel
ENRICO PARANO
@ast
ENRICO PARANO
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ENRICO PARANO
@es
ENRICO PARANO
@nl
P106
P21
P31
P496
0000-0002-0713-7339