Zobrazeno 1 - 10
of 232
pro vyhledávání: '"E, Parano"'
Autor:
Roberto Caraballo, R Falsaperla, Xena Giada Pappalardo, E Parano, Andrea D. Praticò, Piero Pavone
Background Atypical Benign Partial Epilepsy (ABPE), recognized also as pseudo-Lennox syndrome, is an uncommon form of epilepsy characterized by generalized minor seizures such as atonic, absences, or myoclonic seizures, and electroencephalographic pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed27dfed208e086c72b21b7dd7b8cbbc
https://doi.org/10.21203/rs.3.rs-315555/v1
https://doi.org/10.21203/rs.3.rs-315555/v1
Autor:
Chiara Battaglia, Francesco Nicita, Lucia Iozzi, Giovanna Vitaliti, R Falsaperla, E Parano, Alberto Spalice, Piero Pavone, Sung Yoon Cho, Dong Kyu Jin, Salvatore Savasta, Andreana Zecchini, Vincenzo Belcastro, Alberto Verrotti
Publikováno v:
Neuropsychiatry.
Pediatric Autoimmune Neuropsychiatric Disorder associated with Streptococcal Infection (PANDAS) is characterized with main clinical features including obsessive-compulsive disorders and tics, acute-onset in prepubertal age, relapsing-remitting course
Akademický článek
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Publikováno v:
1st International Congress on Advances Pediatrics-New frontiers in neurological surgery, neonatology, nutrition, broncopneumoallergology, gastroenterology and skin diseases, Conrnell university-Uris auditorium Weill Medical College (New York), USA, 3-6 Dicembre 2016
info:cnr-pdr/source/autori:E. Parano; X. G. Pappalardo; P. Pavone; M. Ruggieri; S. Cavallaro/congresso_nome:1st International Congress on Advances Pediatrics-New frontiers in neurological surgery, neonatology, nutrition, broncopneumoallergology, gastroenterology and skin diseases/congresso_luogo:Conrnell university-Uris auditorium Weill Medical College (New York), USA/congresso_data:3-6 Dicembre 2016/anno:2015/pagina_da:/pagina_a:/intervallo_pagine
info:cnr-pdr/source/autori:E. Parano; X. G. Pappalardo; P. Pavone; M. Ruggieri; S. Cavallaro/congresso_nome:1st International Congress on Advances Pediatrics-New frontiers in neurological surgery, neonatology, nutrition, broncopneumoallergology, gastroenterology and skin diseases/congresso_luogo:Conrnell university-Uris auditorium Weill Medical College (New York), USA/congresso_data:3-6 Dicembre 2016/anno:2015/pagina_da:/pagina_a:/intervallo_pagine
In children or adolescents who experiences severe traumatic events, including situations where someone's life (themselves and/or parents' lives) is threatened, or when major injuries occur (e.g., victims or witnesses of physical/sexual abuse), or vic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::fe7f8279f1acb9c2445225d7b95acd8c
http://www.cnr.it/prodotto/i/356283
http://www.cnr.it/prodotto/i/356283
Publikováno v:
Neuropediatrics (2005).
info:cnr-pdr/source/autori:Barone R, Lempereur L, Anastasi M, Parano E, Pavone P./titolo: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/doi:/rivista:Neuropediatrics/anno:2005/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Barone R, Lempereur L, Anastasi M, Parano E, Pavone P./titolo: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/doi:/rivista:Neuropediatrics/anno:2005/pagina_da:/pagina_a:/intervallo_pagine:/volume
Congenital insensitivity to pain with anhidrosis (CIPA) is an autosomal recessive disorder caused by mutations in the neurotrophic tyrosine receptor kinase 1 (NTRK1) gene which encodes the receptor for nerve growth factor (NGF). We report the clinica
Akademický článek
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Akademický článek
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Autor:
Gemma Incorpora, F Di Gregorio, Maria Antonietta Romeo, Piero Pavone, E Parano, R. R. Trifiletti
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
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
Akademický článek
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Publikováno v:
Clinical neurology and neurosurgery (Dutch-Flem. ed.) 102 (2000): 163–165. doi:10.1016/S0303-8467(00)00089-5
info:cnr-pdr/source/autori:Trífiletti, Rosario Rich; Restivo, Domenico Antonio Ntonio; Pavone, Piero; Giuffrida, Salvatore A M; Parano, Enrico/titolo:Diabetes insipidus in neurobrucellosis/doi:10.1016%2FS0303-8467(00)00089-5/rivista:Clinical neurology and neurosurgery (Dutch-Flem. ed.)/anno:2000/pagina_da:163/pagina_a:165/intervallo_pagine:163–165/volume:102
info:cnr-pdr/source/autori:Trífiletti, Rosario Rich; Restivo, Domenico Antonio Ntonio; Pavone, Piero; Giuffrida, Salvatore A M; Parano, Enrico/titolo:Diabetes insipidus in neurobrucellosis/doi:10.1016%2FS0303-8467(00)00089-5/rivista:Clinical neurology and neurosurgery (Dutch-Flem. ed.)/anno:2000/pagina_da:163/pagina_a:165/intervallo_pagine:163–165/volume:102
Brucellosis is an infection due to Brucella species and is characterized by acute febrile illness, chilly sensations, sweats, weakness, generalized malaise, body aches and headache. The involvement of the nervous system is rare. A few cases have been