http://www.cnr.it/ontology/cnr/individuo/unitaDiPersonaleInterno/MATRICOLA5731
ENRICO PARANO
- Type
- Label
- ENRICO PARANO (literal)
- ENRICO PARANO (literal)
- Subject
- Persona in rapporto
- Autore CNR di
- Delayed bilateral median nerve injury due to low-tension electric current (Articolo in rivista) (Prodotto della ricerca)
- Congenital muscular dystrophies: Clinical review and proposed classification (Articolo in rivista) (Prodotto della ricerca)
- Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Spine and brain malformations in a patient obligate carrier of MTHFR with autism and mental retardation (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Hydranencephaly: cerebral spinal fluid instead of cerebral mantles (Articolo in rivista) (Prodotto della ricerca)
- Bickerstaff's brainstem encephalitis (BBE) in childhood: rapid resolution after intravenous immunoglobulins treatment (Articolo in rivista) (Prodotto della ricerca)
- A new clinical feature associated with familial early-onset of dystonic-guttural tics: An unusual diagnosis of PANDAS (Articolo in rivista) (Prodotto della ricerca)
- Congenital muscular dystrophy with syringomyelia (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Aicardi syndrome with multiple tumors: a case report with literature review (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Intrafamilial phenotypic heterogeneity of the Poland complex: A case report (Articolo in rivista) (Prodotto della ricerca)
- Congenital muscular dystrophy: Correlation of muscle biopsy and clinical features (Articolo in rivista) (Prodotto della ricerca)
- A clinical study of childhood spinal muscular atrophy in Sicily: a review of 75 cases (Articolo in rivista) (Prodotto della ricerca)
- Electrophysiologic correlates of peripheral nervous system maturation in infancy and childhood (Articolo in rivista) (Prodotto della ricerca)
- The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene (Articolo in rivista) (Prodotto della ricerca)
- Chronic inflammatory demyelinating polyneuropathy in childhood: clinical and electrophysiological features (Articolo in rivista) (Prodotto della ricerca)
- PLASMA BETA-ENDORPHIN LEVELS AND NATURAL-KILLER-CELLS IN 2 CASES OF CONGENITAL INDIFFERENCE TO PAIN (Articolo in rivista) (Prodotto della ricerca)
- Mapping, cloning and genetic characterization of the region containing the Wilson disease gene (Articolo in rivista) (Prodotto della ricerca)
- Neonatal peripheral hypotonia: clinical and electromyographic characteristics (Articolo in rivista) (Prodotto della ricerca)
- Extraordinary intrathecal bone reaction in beta-thalassaemia intermedia (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Anti-brain antibodies in PANDAS versus uncomplicated streptococcal infection (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A genomewide screen for autism susceptibility loci. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Scimitar vein anomaly with multiple cardiac malformations, craniofacial and central nervous system abnormalities in a brother and sister: familial scimitar anomaly or new syndrome? (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Blepharoptosis in children: our experience at the light of literature (Articolo in rivista) (Prodotto della ricerca)
- 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 (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Pediatric autoimmune neuropsychiatry disorder associated with group a streptococcal infection: The role of surgical treatment (Articolo in rivista) (Prodotto della ricerca)
- Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease. (Articolo in rivista) (Prodotto della ricerca)
- Anton-Babinski syndrome in a child with early-stage adrenoleukodystrophy [8] (Articolo in rivista) (Prodotto della ricerca)
- A syndrome with coarse face, mental retardation and unusual stereotyped movements (Articolo in rivista) (Prodotto della ricerca)
- Clinical heterogeneity in familial congenital ptosis: analysis of fourteen cases in one family over five generations (Articolo in rivista) (Prodotto della ricerca)
- Acute Disseminated Encephalomyelitis: A Long-Term Prospective Study and Meta-Analysis (Articolo in rivista) (Prodotto della ricerca)
- Fetal nucleated red blood cell counts in peripheral blood of mothers bearing down syndrome fetus (Articolo in rivista) (Prodotto della ricerca)
- White matter changes mimicking a leukodystrophy in a patient with Mucopolysaccharidosis: Characterization by MRI (Articolo in rivista) (Prodotto della ricerca)
- Noninvasive prenatal diagnosis of chromosomal aneuploidies by isolation and analysis of fetal cells from maternal blood (Articolo in rivista) (Prodotto della ricerca)
- Colobomatous microphthalmia, microcephaly with cerebellar hypoplasia: Association or new syndrome? (Articolo in rivista) (Prodotto della ricerca)
- Neuropsychological assessment in children with absence epilepsy (Articolo in rivista) (Prodotto della ricerca)
- Reversible palsy of the hypoglossal nerve complicating infectious mononucleosis in a young child (Articolo in rivista) (Prodotto della ricerca)
- Focal neurological deficits in children with beta-thalassemia major (Articolo in rivista) (Prodotto della ricerca)
- Autoimmune neuropsychiatric disorders associated with streptococcal infection: Sydenham chorea, PANDAS, and PANDAS variants. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Low prevalence of neurologic and psychiatric manifestations in children with gluten sensitivity. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Epilepsy is not a prominent feature of primary autism (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- 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 (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Callosal anomalies with interhemispheric cyst: expanding the phenotype (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- HyperCKemia as a biomarker for muscular diseases (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Neonatal onset of hot water reflex seizures in monozygotic twins subsequently manifesting episodes of alternating hemiplegia. (Articolo in rivista) (Prodotto della ricerca)
- Myotonic dystrophy in a large Sicilian kinship: a case report (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A girl with palatoschisis, hypodontia, and lower lip pits (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A rare hereditary encephalopathy: Aicardi-Goutières Syndrome | Su una rara encefalopatia ereditaria: La Sindrome di Aicardi-Goutières (Articolo in rivista) (Prodotto della ricerca)
- Headache in childhood: A critical review of 265 patients (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A case of extreme brain lesions: Which pathogenetic mechanism? (Articolo in rivista) (Prodotto della ricerca)
- Diabetes insipidus in neurobrucellosis (Articolo in rivista) (Prodotto della ricerca)
- Perrault syndrome: Evidence for progressive nervous system involvement (Articolo in rivista) (Prodotto della ricerca)
- Reflex sympathetic dystrophy associated with deep peroneal nerve entrapment (Articolo in rivista) (Prodotto della ricerca)
- Hemihydranencephaly: Case report and literature review (Articolo in rivista) (Prodotto della ricerca)
- Molecular basis of phenotypic heterogeneity in siblings with spinal muscular atrophy (Articolo in rivista) (Prodotto della ricerca)
- Acute palsy of the recurrent laryngeal nerve complicating Epstein-Barr virus infection (Articolo in rivista) (Prodotto della ricerca)
- Neurological complications in hospitalized patients with pertussis: A 15-year Sicilian experience (Articolo in rivista) (Prodotto della ricerca)
- A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions (Articolo in rivista) (Prodotto della ricerca)
- Identification and analysis of mutations in the Wilson disease gene (ATP7B): Population frequencies, genotype-phenotype correlation, and functional analyses (Articolo in rivista) (Prodotto della ricerca)
- Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: A novel form of CMD (Articolo in rivista) (Prodotto della ricerca)
- Coautore
- Nome
- Cognome
- Afferisce a
- Ha pubblicazioni con
- Http://www.cnr.it/ontology/persone.owl#argomentoDiRicercaSimile
Incoming links:
- Http://www.cnr.it/ontology/persone.owl#argomentoDiRicercaSimile
- Ha afferente
- Coautore
- Ha pubblicazioni con
- Rapporto con persona
- Autore CNR
- 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 (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Callosal anomalies with interhemispheric cyst: expanding the phenotype (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Autoimmune neuropsychiatric disorders associated with streptococcal infection: Sydenham chorea, PANDAS, and PANDAS variants. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Neonatal onset of hot water reflex seizures in monozygotic twins subsequently manifesting episodes of alternating hemiplegia. (Articolo in rivista) (Prodotto della ricerca)
- Clinical heterogeneity in familial congenital ptosis: analysis of fourteen cases in one family over five generations (Articolo in rivista) (Prodotto della ricerca)
- Low prevalence of neurologic and psychiatric manifestations in children with gluten sensitivity. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- HyperCKemia as a biomarker for muscular diseases (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Scimitar vein anomaly with multiple cardiac malformations, craniofacial and central nervous system abnormalities in a brother and sister: familial scimitar anomaly or new syndrome? (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A genomewide screen for autism susceptibility loci. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Anti-brain antibodies in PANDAS versus uncomplicated streptococcal infection (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease. (Articolo in rivista) (Prodotto della ricerca)
- A syndrome with coarse face, mental retardation and unusual stereotyped movements (Articolo in rivista) (Prodotto della ricerca)
- Blepharoptosis in children: our experience at the light of literature (Articolo in rivista) (Prodotto della ricerca)
- Acute Disseminated Encephalomyelitis: A Long-Term Prospective Study and Meta-Analysis (Articolo in rivista) (Prodotto della ricerca)
- 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 (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Epilepsy is not a prominent feature of primary autism (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Headache in childhood: A critical review of 265 patients (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Perrault syndrome: Evidence for progressive nervous system involvement (Articolo in rivista) (Prodotto della ricerca)
- A case of extreme brain lesions: Which pathogenetic mechanism? (Articolo in rivista) (Prodotto della ricerca)
- Hemihydranencephaly: Case report and literature review (Articolo in rivista) (Prodotto della ricerca)
- Identification and analysis of mutations in the Wilson disease gene (ATP7B): Population frequencies, genotype-phenotype correlation, and functional analyses (Articolo in rivista) (Prodotto della ricerca)
- A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions (Articolo in rivista) (Prodotto della ricerca)
- Spine and brain malformations in a patient obligate carrier of MTHFR with autism and mental retardation (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Aicardi syndrome with multiple tumors: a case report with literature review (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Congenital muscular dystrophy with syringomyelia (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Congenital muscular dystrophy: Correlation of muscle biopsy and clinical features (Articolo in rivista) (Prodotto della ricerca)
- A clinical study of childhood spinal muscular atrophy in Sicily: a review of 75 cases (Articolo in rivista) (Prodotto della ricerca)
- The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene (Articolo in rivista) (Prodotto della ricerca)
- Electrophysiologic correlates of peripheral nervous system maturation in infancy and childhood (Articolo in rivista) (Prodotto della ricerca)
- PLASMA BETA-ENDORPHIN LEVELS AND NATURAL-KILLER-CELLS IN 2 CASES OF CONGENITAL INDIFFERENCE TO PAIN (Articolo in rivista) (Prodotto della ricerca)
- Chronic inflammatory demyelinating polyneuropathy in childhood: clinical and electrophysiological features (Articolo in rivista) (Prodotto della ricerca)
- Mapping, cloning and genetic characterization of the region containing the Wilson disease gene (Articolo in rivista) (Prodotto della ricerca)
- Pediatric autoimmune neuropsychiatry disorder associated with group a streptococcal infection: The role of surgical treatment (Articolo in rivista) (Prodotto della ricerca)
- Anton-Babinski syndrome in a child with early-stage adrenoleukodystrophy [8] (Articolo in rivista) (Prodotto della ricerca)
- White matter changes mimicking a leukodystrophy in a patient with Mucopolysaccharidosis: Characterization by MRI (Articolo in rivista) (Prodotto della ricerca)
- Fetal nucleated red blood cell counts in peripheral blood of mothers bearing down syndrome fetus (Articolo in rivista) (Prodotto della ricerca)
- Noninvasive prenatal diagnosis of chromosomal aneuploidies by isolation and analysis of fetal cells from maternal blood (Articolo in rivista) (Prodotto della ricerca)
- Neuropsychological assessment in children with absence epilepsy (Articolo in rivista) (Prodotto della ricerca)
- Colobomatous microphthalmia, microcephaly with cerebellar hypoplasia: Association or new syndrome? (Articolo in rivista) (Prodotto della ricerca)
- Focal neurological deficits in children with beta-thalassemia major (Articolo in rivista) (Prodotto della ricerca)
- Reversible palsy of the hypoglossal nerve complicating infectious mononucleosis in a young child (Articolo in rivista) (Prodotto della ricerca)
- Myotonic dystrophy in a large Sicilian kinship: a case report (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A girl with palatoschisis, hypodontia, and lower lip pits (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A rare hereditary encephalopathy: Aicardi-Goutières Syndrome | Su una rara encefalopatia ereditaria: La Sindrome di Aicardi-Goutières (Articolo in rivista) (Prodotto della ricerca)
- Diabetes insipidus in neurobrucellosis (Articolo in rivista) (Prodotto della ricerca)
- Reflex sympathetic dystrophy associated with deep peroneal nerve entrapment (Articolo in rivista) (Prodotto della ricerca)
- Molecular basis of phenotypic heterogeneity in siblings with spinal muscular atrophy (Articolo in rivista) (Prodotto della ricerca)
- Neurological complications in hospitalized patients with pertussis: A 15-year Sicilian experience (Articolo in rivista) (Prodotto della ricerca)
- Acute palsy of the recurrent laryngeal nerve complicating Epstein-Barr virus infection (Articolo in rivista) (Prodotto della ricerca)
- Delayed bilateral median nerve injury due to low-tension electric current (Articolo in rivista) (Prodotto della ricerca)
- Congenital muscular dystrophies: Clinical review and proposed classification (Articolo in rivista) (Prodotto della ricerca)
- Hydranencephaly: cerebral spinal fluid instead of cerebral mantles (Articolo in rivista) (Prodotto della ricerca)
- Bickerstaff's brainstem encephalitis (BBE) in childhood: rapid resolution after intravenous immunoglobulins treatment (Articolo in rivista) (Prodotto della ricerca)
- A new clinical feature associated with familial early-onset of dystonic-guttural tics: An unusual diagnosis of PANDAS (Articolo in rivista) (Prodotto della ricerca)
- Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: A novel form of CMD (Articolo in rivista) (Prodotto della ricerca)
- Intrafamilial phenotypic heterogeneity of the Poland complex: A case report (Articolo in rivista) (Prodotto della ricerca)
- Neonatal peripheral hypotonia: clinical and electromyographic characteristics (Articolo in rivista) (Prodotto della ricerca)
- Extraordinary intrathecal bone reaction in beta-thalassaemia intermedia (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Http://www.w3.org/2004/02/skos/core#isSubjectOf