Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Raymond Ferri"'
Autor:
Marcio Sotero De Menezes, Nadja Kadom, William McClintock, William D. Gaillard, Phillip L. Pearl, Elizabeth Molloy-Wells, L. G. Vezina, Raymond Ferri, Elizabeth Gilles, Joan A. Conry, Nancy Elling, Russell P. Saneto, Robert McCarter, Ari Heffron, Stacey Trzcinski, Howard P. Goodkin
Publikováno v:
Epilepsia. 50:184-194
Summary Purpose: Investigate whether patients on vigabatrin demonstrated new-onset and reversible T2-weighted magnetic resonance imaging (MRI) abnormalities. Methods: MRI of patients treated during vigabatrin therapy was reviewed, following detection
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab715cd6690d1033e33f9f3f74192d0d
https://doi.org/10.1111/j.1528-1167.2008.01728.x
https://doi.org/10.1111/j.1528-1167.2008.01728.x
Autor:
Christine R. Kaneski, David F. Moore, Roscoe O. Brady, Gheona Altarescu, Mark T. Gladwin, Raymond Ferri, Kinuko Suzuki, Peter Herscovitch, Meg Pease-Fye, Raphael Schiffmann, Leland T.C. Scott
Publikováno v:
Circulation. 104:1506-1512
Background Fabry disease is an X-linked lysosomal deficiency of α-galactosidase A that results in cellular accumulation of galacto-conjugates such as globotriosylceramide, particularly in blood vessels. It is associated with early-onset stroke and k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d09b81c719f6e6a735d08a12b5bb9acf
https://doi.org/10.1161/hc3801.096352
https://doi.org/10.1161/hc3801.096352
Autor:
Phillip L, Pearl, Louis G, Vezina, Russell P, Saneto, Robert, McCarter, Elizabeth, Molloy-Wells, Ari, Heffron, Stacey, Trzcinski, William M, McClintock, Joan A, Conry, Nancy J, Elling, Howard P, Goodkin, Marcio Sotero, de Menezes, Raymond, Ferri, Elizabeth, Gilles, Nadja, Kadom, William D, Gaillard
Publikováno v:
Epilepsia. 50(2)
Investigate whether patients on vigabatrin demonstrated new-onset and reversible T(2)-weighted magnetic resonance imaging (MRI) abnormalities.MRI of patients treated during vigabatrin therapy was reviewed, following detection of new basal ganglia, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c52abfd8759b3d21fdb2bf7d7e19c688
https://pubmed.ncbi.nlm.nih.gov/18783433
https://pubmed.ncbi.nlm.nih.gov/18783433
Autor:
Gheona Altarescu, David F. Moore, Andrew E. Arai, Raymond Ferri, Gustavo A. Charria-Ortiz, Neal Jeffries, Geoffrey S. F. Ling, Raphael Schiffmann, Roscoe O. Brady, Thais Weibel, K. P. Frei
Publikováno v:
Stroke. 33(2)
Background and Purpose — Fabry disease is an X-linked inherited disorder resulting from a deficiency of α-galactosidase A. Cerebrovascular disease in Fabry disease includes small-vessel disease and larger-vessel ectasia in a predominantly posterio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f197acbb28a16b884e9985da0a72c11f
https://pubmed.ncbi.nlm.nih.gov/11823664
https://pubmed.ncbi.nlm.nih.gov/11823664