Výsledky vyhledávání - "R R Trifiletti"

Epilepsy is not a Prominent Feature of Primary Autism

Autor: Piero Pavone, R. R. Trifiletti, Enrico Parano, Martino Ruggieri, Agata Fiumara, Gemma Incorpora

Publikováno v: Neuropediatrics 35 (2004): 207–210.
info:cnr-pdr/source/autori:Pavone P; Incorpora, G; Flumara, A ; Parano, E; Trifiletti, RR; Ruggieri, M ./titolo:Epilepsy is not a prominent feature of primary autism/doi:/rivista:Neuropediatrics/anno:2004/pagina_da:207/pagina_a:210/intervallo_pagine:207–210/volume:35

The authors report on a series of 72 patients (57 male, 15 female; aged from 4 to 21 years) affected by autism with the aim of evaluate their experience regarding the prevalence of seizure and/or epilepsy. Patients were divided into two groups: the f

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::715ca09562029778cdf16e8d68057df0
https://doi.org/10.1055/s-2004-821079

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Metabolic Disorders Presenting with Behavioral Symptoms in the Schoolaged Child

Autor: A M Packard, R R Trifiletti

Publikováno v: Child and Adolescent Psychiatric Clinics of North America. 8:791-806

This article presents some principles useful in identifying children with neuropsychiatric symptoms who prove to have metabolic disease. In general, any organic condition that produces cortical dysfunction could present with psychiatric symptomatolog

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::339edfd7ead487b8fdcb70a979ef1faa
https://doi.org/10.1016/s1056-4993(18)30154-8

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Immune Mechanisms in Pediatric Neuropsychiatric Disorders: Tourette’s Syndrome, OCD, and PANDAS

Autor: R R Trifiletti, A M Packard

Publikováno v: Child and Adolescent Psychiatric Clinics of North America. 8:767-775

The authors have reviewed recent data supporting the presence of immune abnormalities in several neuropsychiatric disorders (TS, OCD, and PANDAS). Several groups agree that there is a subset of patients with TS and OCD (perhaps about 10%) for whom th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bd8bb657dead0b9c79932e73dab7745c
https://doi.org/10.1016/s1056-4993(18)30152-4

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Focal Neurological Deficits in Children with β-Thalassemia Major

Autor: Gemma Incorpora, F Di Gregorio, Maria Antonietta Romeo, Piero Pavone, E Parano, R. R. Trifiletti

Publikováno v: Scopus-Elsevier
Europe PubMed Central

The hematologic disorder beta-thalassemia major is relatively common in Southern Italy. Stroke is a well described, though infrequently reported, complication of this disorder. We now report our experience regarding 300 children with beta-thalassemia

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a1f85b452cc96f4ee0b46980bf93db3
https://doi.org/10.1055/s-2007-973457

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Molecular basis of phenotypic heterogeneity in siblings with spinal muscular atrophy

Autor: R. R. Trifiletti, Lorenzo Pavone, Enrico Parano, Raffaele Falsaperla, Ching Wang

Publikováno v: Annals of Neurology. 40:247-251

We report on a family with childhood-onset spinal muscular atrophy with intrafamilial phenotypic variation. Typical of a large majority of such patients, both the child with spinal muscular atrophy type I and the child with type II were missing both

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39b34065bfb02904468d018c17e0ed24
https://doi.org/10.1002/ana.410400219

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Aicardi syndrome with multiple tumors: a case report with literature review

Autor: Agata Polizzi, R. R. Trifiletti, Maria Donatella Cocuzza, Elizabeth A. Bolan, Enrico Parano, Gemma Incorpora

Publikováno v: Brain & development (Tokyo, 1979) 17 (1995): 283–285. doi:10.1016/0387-7604(95)00045-D
info:cnr-pdr/source/autori:Trifiletti R.R.; Incorpora G.; Polizzi A.; Cocuzza M.D.; Bolan E.A.; Parano E./titolo:Aicardi syndrome with multiple tumors: a case report with literature review/doi:10.1016%2F0387-7604(95)00045-D/rivista:Brain & development (Tokyo, 1979)/anno:1995/pagina_da:283/pagina_a:285/intervallo_pagine:283–285/volume:17

A 5-year-old girl with Aicardi syndrome, choroid plexus papilloma and multiple gastric hyperplastic polyps is reported. Gastric polyposis is unusual in the pediatric age group and has not previously been reported in a patient with Aicardi syndrome. A

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d96940a9143f6a66c23bafa9d436177c
https://doi.org/10.1016/0387-7604(95)00045-d

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Neuropsychological assessment in children with absence epilepsy

Autor: Gemma Incorpora, Rio Bianchini, Piero Pavone, A. Pavone, R. R. Trifiletti, Enrico Parano

Publikováno v: Neurology 56 (2001): 1047–1051.
info:cnr-pdr/source/autori:Pavone, Piero; Bianchini, Rio; Trífiletti, Rosario Rich; Incorpora, Gemma G.; Pavone, Antonino; Parano, Enrico/titolo:Neuropsychological assessment in children with absence epilepsy/doi:/rivista:Neurology/anno:2001/pagina_da:1047/pagina_a:1051/intervallo_pagine:1047–1051/volume:56
Scopus-Elsevier

Objective: To define cognitive deficits in children with absence epilepsy. Background: Cognitive deficits have often been reported in children with epilepsy, but have rarely been characterized in patients with a specific epileptic syndrome. Methods:

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edd950480cca174cb8c146622c28b4a2
https://pubmed.ncbi.nlm.nih.gov/11723307

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Fetal nucleated red blood cell counts in peripheral blood of mothers bearing down syndrome fetus

Autor: Piero Pavone, Agata Grillo, R. R. Trifiletti, Haruo Takabayashi, Enrico Parano, Ernesto Falcidia

Publikováno v: Neuropediatrics 32 (2001): 147–149. doi:10.1055/s-2001-16612
info:cnr-pdr/source/autori:Parano, Enrico; Falcidia, Ernesto; Grillo, Agata; Takabayashi, Haruo; Trífiletti, Rosario Rich; Pavone, Piero/titolo:Fetal nucleated red blood cell counts in peripheral blood of mothers bearing down syndrome fetus/doi:10.1055%2Fs-2001-16612/rivista:Neuropediatrics/anno:2001/pagina_da:147/pagina_a:149/intervallo_pagine:147–149/volume:32

Currently, prenatal detection of Down syndrome and other most common aneuploidies relies on invasive procedures such as amniocentesis and villocentesis, and on non-invasive screening tests such as second trimester maternal serum screening (Triple tes

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3a6b87004297c8382f0da74b798a09b
https://publications.cnr.it/doc/303505

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Colobomatous microphthalmia, microcephaly with cerebellar hypoplasia: association or new syndrome?

Autor: P, Pavone, E, Parano, A, Polizzi, R R, Trifiletti

Publikováno v: American journal of medical genetics. 92(4)

We report on a 3.5-year-old girl with microcephaly, microphthalmia, coloboma of the iris, mild developmental delay, and other minor anomalies. Neuroimaging showed marked cerebellar and vermian hypoplasia. This condition has not been described previou

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https://pubmed.ncbi.nlm.nih.gov/10842296

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Metabolic disorders presenting with behavioral symptoms in the school-aged child

Autor: R R, Trifiletti, A M, Packard

Publikováno v: Child and adolescent psychiatric clinics of North America. 8(4)

This article presented some principles useful in identifying children with neuropsychiatric symptoms who will prove to have metabolic disease. In general, any organic condition that produces cortical dysfunction could present with psychiatric symptom

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d63f079774e11259c00467c630010855
https://pubmed.ncbi.nlm.nih.gov/10553204

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