Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Tiziana Calarese"'
Autor:
Eva María Olmedo Moreno, Antonella Donato, Tiziana Calarese, Maria Muscolo, Mateo Arias Romero, Tindara Caprì
Publikováno v:
Digibug. Repositorio Institucional de la Universidad de Granada
instname
instname
Italian Dyslexia Association (Messina section); Orientation and Placement Centre -University of Messina (Italy)
Although the number of students with dyslexia enrolled in Italian universities is constantly growing, their presence remains relative
Although the number of students with dyslexia enrolled in Italian universities is constantly growing, their presence remains relative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05c62fe4622e926d00768face91f63ff
https://pubmed.ncbi.nlm.nih.gov/34315192
https://pubmed.ncbi.nlm.nih.gov/34315192
Autor:
Tiziana Calarese, Nicola Vanni, Edoardo Ferlazzo, Sara Gasparini, Pierre Genton, Domenico Italiano, Pasquale Striano, Floriana Fruscione, Federico Zara
Autosomal recessive progressive myoclonus epilepsy due to impaired ceramide synthesis is an extremely rare condition, so far reported in a single family of Algerian origin presenting an unusual, severe form of progressive myoclonus epilepsy character
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcd80d64d59e15029abc47fb10e76196
http://hdl.handle.net/11567/854820
http://hdl.handle.net/11567/854820
Autor:
Irene Aricò, Clemente Cedro, Oliviero Bruni, Placido Bramanti, R. Condurso, Eva Germanò, Antonella Gagliano, Rosalia Silvestri, Giuseppe Vita, Giuseppe Gervasi, Tiziana Calarese, Rosamaria Siracusano
Publikováno v:
Sleep Medicine. 10:1132-1138
To outline specific sleep disturbances in different clinical subsets of Attention Deficit/Hyperactivity Disorder (ADHD) and to confirm, by means of nocturnal video-polysomnography (video-PSG), a variety of sleep disorders in ADHD besides the classica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35644d3c56122db27f8ff6c84d50b0d5
https://doi.org/10.1016/j.sleep.2009.04.003
https://doi.org/10.1016/j.sleep.2009.04.003
Autor:
Virginie Laguitton, Tiziana Calarese, I An, Edoardo Ferlazzo, Domenico Italiano, Pierre Genton, Paolo Di Bella, Placido Bramanti
Publikováno v:
Movement Disorders. 24:1016-1022
We report a family of Algerian origin presenting an unusual, severe form of progressive myoclonus epilepsy characterized by myoclonus, generalized tonic-clonic seizures and moderate to severe cognitive impairment, with probable autosomal recessive in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::803b85eb32b598888f81171734193a3d
https://doi.org/10.1002/mds.22489
https://doi.org/10.1002/mds.22489
Autor:
Pierre Genton, Géraldine Daquin, Paolo Di Bella, Edoardo Ferlazzo, Nathalie Villeneuve, Tiziana Calarese
Publikováno v:
Seizure. 17:735-739
SummaryIctal paresis (IP) is a rare negative motor phenomenon presenting challenging differential diagnostic problems with transient ischemic attacks, post-ictal paralysis, migraine and psychogenic paralysis. Video-EEG undoubtedly represents the esse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d81649b45cdf4f83f44d49183508be3
https://doi.org/10.1016/j.seizure.2008.04.002
https://doi.org/10.1016/j.seizure.2008.04.002
Autor:
Angela Magazù, Rosamaria Siracusano, Gabriele Masi, Clemente Cedro, Chiara Pfanner, Antonella Gagliano, Tiziana Calarese, Stefano Berloffa, Giovanna Ilardo
Tourette's disorder (TD) in children and adolescents is frequently co-morbid with attention-deficit/hyperactivity disorder (ADHD). Dopamine-blockers are the first line treatment for TD, whereas dopamine-agonists, such as stimulants, are the gold-stan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5599173df03f4c33f4bf5b02addc8b5
http://hdl.handle.net/11570/1976421
http://hdl.handle.net/11570/1976421
Publikováno v:
Epilepsybehavior : EB. 19(4)
We describe a unique patient with cerebral calcifications of unknown origin presenting with pharmacoresistant occipital lobe epilepsy and fixation-off sensitivity. Our report further expands the spectrum of seizure disorders associated with fixation-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb82aef1f847e261ae0aecd5bfb09e4c
https://pubmed.ncbi.nlm.nih.gov/21051297
https://pubmed.ncbi.nlm.nih.gov/21051297
Autor:
Edoardo Ferlazzo, Constant Adjien, Maurizio Elia, Placido Bramanti, Renzo Guerrini, Paolo Di Bella, Tiziana Calarese, Pierre Genton, Philippe Gelisse, Pasquale Striano, Arielle Crespel
Publikováno v:
Epilepsia. 50(6)
Lennox-Gastaut syndrome (LGS) is a severe epileptic condition characterized by multiple seizure types including tonic seizures, slow spike-and-wave discharges on electroencephalography (EEG), and cognitive impairment. LGS can occur in apparently heal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52338d63dbf0e46948fa889fec02fced
https://pubmed.ncbi.nlm.nih.gov/19187280
https://pubmed.ncbi.nlm.nih.gov/19187280
Autor:
Addolorata Albachiara, Pierre Genton, Marilena Carbonaro, Adriana Magaudda, Domenico Italiano, Tiziana Calarese, Virgilie Laguitton, Antonietta Coppola, Antonella Gagliano, Nina Fragassi, Placido Bramanti, Edoardo Ferlazzo, Clemente Cedro, Lara Cortese, Pasquale Striano, Edoardo Sessa
The aims of this study were to clarify if patients with Unverricht–Lundborg disease (ULD) have adequate cognitive functioning and to delineate their neuropsychological profile. We evaluated 20 patients with ULD and 20 healthy, matched controls. Mea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::389ddfe25e4795773af089c63ecee91b
http://hdl.handle.net/11567/314921
http://hdl.handle.net/11567/314921
Autor:
Pasquale Striano, Edoardo Sessa, Pierre Genton, Tiziana Calarese, Edoardo Ferlazzo, Komi Assogba, Nathalie Villeneuve, Iliana Pacheva, Ivan Ivanov, Placido Bramanti
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 31(1)
Hypomelanosis of Ito (HI) is a rare neuroectodermal disorder often associated with mental retardation and epilepsy. We report on four new HI patients presenting with heterogeneous seizure manifestations and we review the literature concerning epilept
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d53c5cf7f687bbcf2842db7dd46cc0e
https://pubmed.ncbi.nlm.nih.gov/19902142
https://pubmed.ncbi.nlm.nih.gov/19902142