Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Daniela, Laino"'
Autor:
Susanna Esposito, Daniela Laino, Renato D’Alonzo, Annalisa Mencarelli, Lorenza Di Genova, Antonella Fattorusso, Alberto Argentiero, Elisabetta Mencaroni
Publikováno v:
Journal of Translational Medicine, Vol 17, Iss 1, Pp 1-8 (2019)
Abstract Background There are no guidelines concerning the best approach to improving sleep, but it has been shown that it can benefit the affected children and their entire families. The aim of this review is to analyse the efficacy and safety of me
Externí odkaz:
https://doaj.org/article/2a71d05abfd7451ea7a5fa12d31373ed
Autor:
Renato D’Alonzo, Elisabetta Mencaroni, Lorenza Di Genova, Daniela Laino, Nicola Principi, Susanna Esposito
Publikováno v:
Frontiers in Microbiology, Vol 9 (2018)
Mycoplasma pneumoniae is mainly recognized as a respiratory pathogen, although it is associated with the development of several extra-respiratory conditions in up to 25% of the cases. Diseases affecting the nervous system, both the peripheral (PNS) a
Externí odkaz:
https://doaj.org/article/2c0042dc8bb54c1cb0f29f4046a6df4f
Autor:
Annalisa Mencarelli, Daniela Laino, Lorenza Di Genova, Antonella Fattorusso, Elisabetta Mencaroni, Susanna Esposito, Alberto Argentiero, Renato D'Alonzo
Publikováno v:
Journal of Translational Medicine, Vol 17, Iss 1, Pp 1-8 (2019)
Journal of Translational Medicine
Journal of Translational Medicine
Background There are no guidelines concerning the best approach to improving sleep, but it has been shown that it can benefit the affected children and their entire families. The aim of this review is to analyse the efficacy and safety of melatonin i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::704b96005c3eaaaf98a8a23edd44b35c
http://link.springer.com/article/10.1186/s12967-019-1835-1
http://link.springer.com/article/10.1186/s12967-019-1835-1
Autor:
Gian Luigi Marseglia, Thomas Foiadelli, Maria Valentina Spartà, Lucio Lobefalo, Vincenzo Salpietro, Alberto Verrotti, Salvatore Savasta, Daniela Laino
Publikováno v:
European Journal of Pediatrics. 174:697-701
Stickler syndrome is a genetically heterogeneous collagenopathy characterized by auditory, ocular, musculoskeletal, and orofacial abnormalities. Stickler syndrome type 1 typically presents ophthalmologic involvement and is due to heterozygous defects
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50fbb1cbfa92310f7104633c5f90b6b7
https://doi.org/10.1007/s00431-015-2514-8
https://doi.org/10.1007/s00431-015-2514-8
Publikováno v:
International Journal of Environmental Research and Public Health, Vol 15, Iss 10, p 2232 (2018)
International Journal of Environmental Research and Public Health
International Journal of Environmental Research and Public Health
Febrile seizures (FS), events associated with a fever in the absence of an intracranial infection, hypoglycaemia, or an acute electrolyte imbalance, occur in children between six months and six years of age. FS are the most common type of convulsions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ded9e314e9177a588c9c6a9601ae2166
https://doi.org/10.3390/ijerph15102232
https://doi.org/10.3390/ijerph15102232
Autor:
Ve E. Rinaldi, Giangennaro Coppola, M. Rauchenzauner, Salvatore Savasta, Renata Rizzo, Pasquale Parisi, L. Giordano, Francesca Ragona, Lucia Margari, R. Gaggero, G.L. Marseglia, Pasquale Striano, Giuseppe Capovilla, G. Di Gennaro, Daniela Laino, Vincenzo Belcastro, Alberto Spalice, Maria Esposito, Salvatore Grosso, Francesca Felicia Operto, Nelia Zamponi, Piero Pavone, S. Siliquini, Raffaella Cusmai, Agnese Suppiej, Alberto Verrotti, Irene Toldo, Sara Matricardi, Caterina Cerminara
Background and purpose: Our aim was to describe the clinical and electrical features and the long-term evolution of childhood occipital epilepsy of Gastaut (COE-G) in a cohort of patients and to compare long-term prognosis between patients with and w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04ad0e73462c2249ec3ab503d83836a5
http://hdl.handle.net/11591/368833
http://hdl.handle.net/11591/368833
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 105(9)
Aim: Although there have been frequent clinical reports about sleep disturbances in children with learning disabilities, no data are available about the prevalence of sleep disturbances in children with developmental dyslexia (DD). This study evaluat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be1ab898e439f2825f31e930643cd33b
https://pubmed.ncbi.nlm.nih.gov/27514003
https://pubmed.ncbi.nlm.nih.gov/27514003
Autor:
Alberto, Verrotti, Raffaella, Cusmai, Daniela, Laino, Marco, Carotenuto, Maria, Esposito, Raffaele, Falsaperla, Lucia, Margari, Renata, Rizzo, Salvatore, Savasta, Salvatore, Grosso, Pasquale, Striano, Vincenzo, Belcastro, Emilio, Franzoni, Paolo, Curatolo, Lucio, Giordano, Elena, Freri, Sara, Matricardi, Dario, Pruna, Irene, Toldo, Elisabetta, Tozzi, Lucio, Lobefalo, Francesca, Operto, Emma, Altobelli, Francesco, Chiarelli, Alberto, Spalice
Prader–Willi syndrome is a multisystemic genetic disorder that can be associated with epilepsy. There is insufficient information concerning the clinical and electroencephalographic characteristics of epilepsy and the long-term outcome of these pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::780ae345f93035b6524bea14f8068fb1
http://hdl.handle.net/20.500.11769/49465
http://hdl.handle.net/20.500.11769/49465
Publikováno v:
Molecular & Cellular Epilepsy.
Despite several studies there are still some issues concerning the correct diagnosis of epilepsy that should be distinguished from many other critical symptoms and diseases. Moreover, the assessment of a specific epileptic syndrome can have some degr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61d85eacd7be7ca838282029ae03b5a6
https://doi.org/10.14800/mce.165
https://doi.org/10.14800/mce.165
Publikováno v:
World journal of pediatrics : WJP. 10(2)
Epilepsy associated with Prader-Willi syndrome (PWS) represents an early and important complication, often not clearly reported and described in the literature. Consequently, there are controversial data about the clinical characteristics of epilepsy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95e84c60f4f0be73def365e59c3d42d6
https://pubmed.ncbi.nlm.nih.gov/24801229
https://pubmed.ncbi.nlm.nih.gov/24801229