Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ivan Mateo Alzamora"'
Autor:
Juan Fernando Ortiz, Claudio Cruz, Amrapali Patel, Mahika Khurana, Ahmed Eissa-Garcés, Ivan Mateo Alzamora, Taras Halan, Abbas Altamimi, Samir Ruxmohan, Urvish K. Patel
Publikováno v:
Brain Sciences, Vol 11, Iss 6, p 805 (2021)
Stroke is a leading cause of death and disability, and novel treatments need to be found, particularly drugs with neuroprotective and restorative effects. Lately, there has been an increased interest in the relationship between opioids and ischemic s
Externí odkaz:
https://doaj.org/article/5c660a3855ec4d20bc7dcc8a9856da02
Autor:
Adam Atoot, Paul W Millhouse, Victor D. Cuenca, Domenica Herrera-Bucheli, Ivan Mateo Alzamora, Jashank Parwani, Ahmed Eissa-Garcés, Wilson Cueva, Juan Fernando Ortiz, Mahika Khurana, Abbas Altamimi, Gashaw Hassen
Publikováno v:
Cureus
Fabry disease (FD) is an X-linked disorder involving multiple organs. Stroke is a serious and frequent complication of FD. Cryptogenic stroke is a common presentation of FD, especially in the young population. The etiology of cryptogenic stroke is hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ca8210caa7ecae2cd808bb8650f7a20
http://europepmc.org/articles/PMC8654093
http://europepmc.org/articles/PMC8654093
Autor:
Jessica Hidalgo, Samir Ruxmohan, Amrapali Patel, Ivan Mateo Alzamora, Juan Fernando Ortiz, Mahika Khurana
Publikováno v:
Cureus
Megacephaly polymicrogyria, polydactyly, hydrocephalus (MPPH) is an extremely rare condition caused by a defect in the AKT3, CCND2, or PIKR2 genes. Although the prevalence of the syndrome is very low, there is a significant clinical and radiological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cfffe1c5d5afaea42bc044b4fb7fb4a
https://doi.org/10.7759/cureus.16132
https://doi.org/10.7759/cureus.16132
Autor:
Urvish K Patel, Claudio Cruz, Amrapali Patel, Samir Ruxmohan, Taras Halan, Ahmed Eissa-Garcés, Abbas Altamimi, Ivan Mateo Alzamora, Juan Fernando Ortiz, Mahika Khurana
Publikováno v:
Brain Sciences
Brain Sciences, Vol 11, Iss 805, p 805 (2021)
Brain Sciences, Vol 11, Iss 805, p 805 (2021)
Stroke is a leading cause of death and disability, and novel treatments need to be found, particularly drugs with neuroprotective and restorative effects. Lately, there has been an increased interest in the relationship between opioids and ischemic s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::290fbe138eb25bb768de49e3fcf66991
http://europepmc.org/articles/PMC8233760
http://europepmc.org/articles/PMC8233760
Publikováno v:
Cureus
Griscelli syndrome (GS) is a rare syndrome characterized by hypopigmentation, immunodeficiency, and neurological features. The genes Ras-related protein (RAB27A) and Myosin-Va (MYO5A) are involved in this condition's pathogenesis. We present a GS typ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c10a16df9e0af1ba53ea2b28da438430
http://europepmc.org/articles/PMC8109045
http://europepmc.org/articles/PMC8109045