Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Paolo Di Bella"'
Autor:
Maurizio Elia, Irene Rutigliano, Michele Sacco, Simona F. Madeo, Malgorzata Wasniewska, Alessandra Li Pomi, Giuliana Trifirò, Paolo Di Bella, Silvana De Lucia, Luigi Vetri, Lorenzo Iughetti, Maurizio Delvecchio
Publikováno v:
Brain Sciences, Vol 11, Iss 8, p 1045 (2021)
Prader–Willi syndrome (PWS) is a rare disease determined by the loss of the paternal copy of the 15q11-q13 region, and it is characterized by hypotonia, hyperphagia, obesity, short stature, hypogonadism, craniofacial dysmorphisms, and cognitive and
Externí odkaz:
https://doaj.org/article/d0ba0dd4177749e89e316604d724781e
Autor:
Manrico Morroni, Daniela Marzioni, Michele Ragno, Paolo Di Bella, Elisabetta Cartechini, Luigi Pianese, Teresa Lorenzi, Mario Castellucci, Marina Scarpelli
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e65482 (2013)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is caused by NOTCH3 gene mutations that result in vascular smooth muscle cell (VSMC) degeneration. Its distinctive feature by electron microscopy (EM
Externí odkaz:
https://doaj.org/article/a4eefdef73ed4e7fb0ef0a2bbb557a60
Autor:
Marina Massei, Paolo Di Bella, Javier Pernas-Álvarez, Michele Turi, Alessandro Leto, Agostino G. Bruzzone
Publikováno v:
Proceedings of the 9th International Workshop on Simulation for Energy, Sustainable Development & Environment (SESDE 2021).
Autor:
Michele Sacco, Simona Filomena Madeo, Irene Rutigliano, Lorenzo Iughetti, Alessandra Li Pomi, Paolo Di Bella, Maurizio Delvecchio, G. Trifirò, Luigi Vetri, Maurizio Elia, Malgorzata Wasniewska, Silvana De Lucia
Publikováno v:
Brain Sciences
Brain Sciences, Vol 11, Iss 1045, p 1045 (2021)
Volume 11
Issue 8
Brain Sciences, Vol 11, Iss 1045, p 1045 (2021)
Volume 11
Issue 8
Prader–Willi syndrome (PWS) is a rare disease determined by the loss of the paternal copy of the 15q11-q13 region, and it is characterized by hypotonia, hyperphagia, obesity, short stature, hypogonadism, craniofacial dysmorphisms, and cognitive and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2865399a051759a0c3b5774418f8b70
https://hdl.handle.net/11380/1251551
https://hdl.handle.net/11380/1251551
Publikováno v:
Multiple Sclerosis and Related Disorders. 37:101373
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
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
Autor:
Giuseppe Anastasi, Daniele Bruschetta, Ludovico Magaudda, Angelo Favaloro, Emanuele Scribano, Demetrio Milardi, Michele Gaeta, Placido Bramanti, Fabio Trimarchi, Paolo Di Bella
Publikováno v:
Journal of Anatomy. 211:399-406
The choice of medical imaging techniques, for the purpose of the present work aimed at studying the anatomy of the knee, derives from the increasing use of images in diagnostics, research and teaching, and the subsequent importance that these methods
Publikováno v:
Neurology. 84(17)
A 60-year-old woman was admitted to our department after a 2-month history of double vision and periorbital pain. Neurologic examination showed a right abducens nerve palsy and neuralgia in the right V1 trigeminal branch. Brain MRI revealed a hyperin