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of 5
pro vyhledávání: '"David Berhanu"'
Autor:
Rafael Correia Barão, David Berhanu, Diogo Bernardo Matos, André Diogo Barata, Rita Sousa, Luís Abegão Pinto
Publikováno v:
Acta Ophthalmologica.
Autor:
Sofia Reimão, Joaquim J. Ferreira, David Berhanu, Carla Guerreiro, Madalena Rosário, Leonor Correia Guedes, Giulia Galati, Rita Moiron Simões
Publikováno v:
E: Imaging.
Background Nigrostriatal dopaminergic neuron degeneration with loss of Substantia Nigra (SN) and Locus Coeruleus (LC) neurons, as well as disruption of iron homeostasis, have been reported in Huntington’s Disease (HD), but literature is still scarc
Autor:
David Berhanu, Carla Guerreiro, João B. L. M. Campos, Francisco Raposo, Tiago Eça, Rita Sousa, Leonel Luis
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Meniere's disease (MD) is a clinical syndrome characterized by recurrent episodes of spontaneous vertigo, unilateral fluctuating sensorineural hearing loss, tinnitus, and aural fullness. Endolymphatic hydrops is recognized as the pathophysiological s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87c3abe0c55304e66aaf16a9851bca4a
Autor:
Rita, Sousa, Francisco, Raposo, Carla, Guerreiro, David, Berhanu, Tiago, Eça, J, Campos, Leonel, Luís
Publikováno v:
Neuroradiology. 63(11)
Ménière's disease (MD) is a clinical syndrome characterized by recurrent episodes of spontaneous vertigo, unilateral fluctuating sensorineural hearing loss, tinnitus, and aural fullness. Endolymphatic hydrops is recognized as the pathophysiological
Autor:
Leah M. Mattiaccio, Kevin M. Antshel, Wendy R. Kates, Frank A. Middleton, Wanda Fremont, David Berhanu
Publikováno v:
Psychiatry Research: Neuroimaging. 259:10-15
Dysfunction of cortical circuitry involving prefrontal cortex, cingulate gyrus and mesial temporal lobe has been implicated in the pathophysiology of psychotic symptoms. 22q11.2 deletion syndrome (22q11DS) is a neurogenetic disorder that comports a 2