Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Carlos Burneo-Rosales"'
Publikováno v:
IDCases, Vol 17, Iss , Pp - (2019)
Acute transverse myelitis is a rare inflammatory demyelinating disorder characterized by relatively acute onset of motor, sensory, and autonomic dysfunction. Mycobacterium tuberculosis is a very rare cause of transverse myelitis. We present a patient
Externí odkaz:
https://doaj.org/article/4770b98232d0480a964c9ae836257cb7
Autor:
Alberto Ortega-Rosales, Yomara Quizhpe-Ocampo, María Montalvo-Flores, Carlos Burneo-Rosales, Gilda Romero-Ulloa
Publikováno v:
IDCases, Vol 18, Iss , Pp - (2019)
Fusarium keratomycosis is a destructive eye infection that is difficult to treat and produces a poor outcome, which can affect healthy patients. Keratomycoses are rare and can be underdiagnosed, thus, direct microscopic examination and culture are es
Externí odkaz:
https://doaj.org/article/22f8b3d456c9451c9c636e36b19cafae
Autor:
Carlos Burneo-Rosales, Alberto Ortega-Rosales, Gilda Romero-Ulloa, María Montalvo-Flores, Yomara Quizhpe-Ocampo
Publikováno v:
IDCases, Vol 18, Iss, Pp-(2019)
IDCases
IDCases
Fusarium keratomycosis is a destructive eye infection that is difficult to treat and produces a poor outcome, which can affect healthy patients. Keratomycoses are rare and can be underdiagnosed, thus, direct microscopic examination and culture are es
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8528fc000d94513bb4c3239728c7f3f
http://www.sciencedirect.com/science/article/pii/S2214250919302288
http://www.sciencedirect.com/science/article/pii/S2214250919302288
Publikováno v:
F1000Research. 8:755
Introduction: Lysosomal storage disorders are a rare group of diseases with genetic origin in which Gaucher Disease (GD) stands out as the most frequent. GD type 1 is the most common form of this condition, and patients with this pathology present wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e205d1f4e69d8a32da67c8d0ca9f4dd1
https://doi.org/10.12688/f1000research.18802.2
https://doi.org/10.12688/f1000research.18802.2