Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mateo Alzamora"'
Pulvinar Sign, Stroke and Their Relationship with Fabry Disease: A Systematic Review and Metanalysis
Autor:
Juan Fernando Ortíz, María Belén Solís, Syed Saad Ali, Mahika Khurana, Juan Andrés Moncayo, Nishel Yogesh Kothari, Mateo Alzamora, Ahmed Eissa-Garces, Ghanshyam Patel, Gustavo Andrés Monteros, Meghdeep Sen, Jonathan Quiñonez
Publikováno v:
Neurology International, Vol 14, Iss 2, Pp 497-505 (2022)
Background: Fabry disease (FD) is the second most common lysosomal storage disorder. This disorder affects multiple systems that include the cardiac, renal, and nervous system. The pulvinar sign (PS) is a relatively common sign seen in patients with
Externí odkaz:
https://doaj.org/article/5af32a11546d4d46a49be6adcd5df0da
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
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
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
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
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