Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Roberto, Ebner"'
Publikováno v:
Neuroophthalmology
In this report, we analyse the pre- and post-operative corneal changes observed using in vivo confocal corneal microscopy in a patient with neurotrophic keratitis submitted to a corneal reinnervation surgical procedure. We describe favourable trophic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5b3e5601a80da638151079d28e3329d
https://doi.org/10.1080/01658107.2019.1568508
https://doi.org/10.1080/01658107.2019.1568508
Autor:
Galeno Rojas, Emilia Gatto, Gustavo Da-Prat, Roberto Ebner, María Bres-Bullrich, Victoria Aldinio, Xavier Merchán-del Hierro
Publikováno v:
Tremor and Other Hyperkinetic Movements
Background: Immunological causes of atypical parkinsonisms linked to neuronal specific antibodies have been recently reported. As these are potentially treatable disorders, it is desirable to identify which clinical features may suggest an autoimmune
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81ec61b8a49204f70b37964feccd379c
http://europepmc.org/articles/PMC7394231
http://europepmc.org/articles/PMC7394231
Autor:
Roberto Ebner
Publikováno v:
Neuro-Ophthalmology. 43:289-290
Presence of a fourth nerve palsy and ipsilateral Horner's Syndrome (HS) is an exceptional association. A case of a 54 year-old patient with diplopia due to a fourth nerve palsy and acquired HS on the same is presented along with magnetic resonance im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b90e28eb1f292c0def571e38ea256c8c
https://doi.org/10.1080/01658107.2018.1562475
https://doi.org/10.1080/01658107.2018.1562475
Autor:
Pablo Neumann, Norberto Antongiovanni, Alejandro Fainboim, Isaac Kisinovsky, Hernán Amartino, Gustavo Cabrera, Sergio Carmona, Romina Ceci, Alberto Cicerán, Martín Choua, Griselda Doxastakis, Sonia De Maio, Roberto Ebner, Ana María Escobar, Gustavo Ferrari, Mariano Forrester, Norberto Guelbert, Paula Luna, Cinthia Marchesoni, Francisca Masllorens, Juan Politei, Ricardo Reisin, Diego Ripeau, Paula Rozenfeld, Graciela Serebrinsky, Ana Lía Tarabuso, Juan Trípoli
Publikováno v:
Medicina (Buenos Aires), Vol 73, Iss 5, Pp 482-494 (2013)
La enfermedad de Fabry es un trastorno de almacenamiento lisosomal hereditario ligado al cromosoma X, ocasionado por el déficit de la enzima alfa galactosidasa A. El conocimiento sobre esta patología, y en particular su manejo médico, ha progresad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::9a595ed0c376ec7c105e955b157cc734
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0025-76802013000600020&lng=en&tlng=en
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0025-76802013000600020&lng=en&tlng=en
Publikováno v:
Journal of Neuro-Ophthalmology. 37:e11-e12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a682b7b9c0978ddf915cab5dd740c1ba
https://doi.org/10.1097/wno.0000000000000542
https://doi.org/10.1097/wno.0000000000000542
Publikováno v:
Clinical and Experimental Ophthalmology. 34:689-694
Background: Fabry disease is an X-linked disorder due to a deficiency of α-galactosidase A and leads to the accumulation of globotriaosylceramide (Gb3) in various cells. The detection of Gb3 deposits may help in the diagnosis. To date, no immunofluo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::524e7d79d5ada78ef6d663aeefd4a1e2
https://doi.org/10.1111/j.1442-9071.2006.01318.x
https://doi.org/10.1111/j.1442-9071.2006.01318.x
Publikováno v:
Clinical Genetics. 69:344-348
Fabry disease is an X-linked lysosomal disorder caused by the deficiency of the lysosomal enzyme alpha-galactosidase A (alpha-Gal A). In males, the laboratory diagnosis is based on the demonstration of decreased levels of alpha-Gal A activity, while
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::524fe9690273e99f8c82c9e4e181f65c
https://doi.org/10.1111/j.1399-0004.2006.00594.x
https://doi.org/10.1111/j.1399-0004.2006.00594.x
Publikováno v:
International Ophthalmology. 23:275-278
Purpose: To evaluate if the changes in the peripapillary and papillary retinal nerve fiber layer, in a young girl who presents papillary drusen and ocular hypertension in both eyes. Methods: We studied this case with retinography, Humphrey Visual Fie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e46bd85834866cb0be850ae2e5d1d74
https://doi.org/10.1023/a:1014469608213
https://doi.org/10.1023/a:1014469608213
Autor:
Pablo, Neumann, Norberto, Antongiovanni, Alejandro, Fainboim, Isaac, Kisinovsky, Hernán, Amartino, Gustavo, Cabrera, Sergio, Carmona, Romina, Ceci, Alberto, Cicerán, Martín, Choua, Griselda, Doxastakis, Sonia, De Maio, Roberto, Ebner, Ana María, Escobar, Gustavo, Ferrari, Mariano, Forrester, Norberto, Guelbert, Paula, Luna, Cinthia, Marchesoni, Francisca, Masllorens, Juan, Politei, Ricardo, Reisin, Diego, Ripeau, Paula, Rozenfeld, Graciela, Serebrinsky, Ana Lía, Tarabuso, Juan, Trípoli
Publikováno v:
Medicina. 73(5)
Fabry disease is an X-linked hereditary lysosomal storage disorder caused by deficiency of the enzyme alpha-galactosidase A. Knowledge about this disease, and its medical management, has made remarkable progress in the last decade, including the deve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::749f248ef4a9f5304c8df84d681d87ee
https://pubmed.ncbi.nlm.nih.gov/24152410
https://pubmed.ncbi.nlm.nih.gov/24152410
Autor:
Roberto Ebner
Publikováno v:
Current Opinion in Ophthalmology. 5:27-35
In the reviewed period, articles on peripheral eye movement disorders covered interesting aspects. Localizing value of associated signs, repetitive presentations of palsies, and classical quotations are stressed for the oculomotor nerve. The superior
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72efcc4d139dcac79cf7fdaeb639c815
https://doi.org/10.1097/00055735-199412000-00005
https://doi.org/10.1097/00055735-199412000-00005