Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Rosario Maria S. Riel-Romero"'
Autor:
Rachel Triay, Prabandh Buchhanolla, Alexas Gaudet, Victoria Winter, Alexandra Gaudet, Mehdi Faraji, Eduardo Gonzalez-Toledo, Harish Siddaiah, Hugo H. Cuellar-Saenz, Steven Bailey, Vijayakumar Javalkar, Rosario Maria S. Riel-Romero, Roger E. Kelley, Felicity N. E. Gavins, Junaid Ansari
Publikováno v:
Biomedicines, Vol 10, Iss 2, p 435 (2022)
(1) Background: COVID-19 infection is responsible for the ongoing pandemic and acute cerebrovascular disease (CVD) has been observed in COVID-19 patients. (2) Methods: We conducted a retrospective, observational study of hospitalized adult patients a
Externí odkaz:
https://doaj.org/article/da9ca4d8571541258716d9b4752a79f6
Publikováno v:
Cureus.
Autor:
Piyush Kalakoti, Hai Sun, Vikas Mishra, Kanika Sharma, Anil Nanda, Christina Notarianni, Miriam Henry, Rosario Maria S. Riel-Romero
Publikováno v:
Clinical Neurology and Neurosurgery. 158:82-89
Objectives Prior to enactment of the Affordable Care Act(ACA), several reports demonstrated remarkable racial disparities in access to surgical care for epileptic patients. Implementation of ACA provided healthcare access to 7–16 million uninsured
Autor:
Phillip L. Pearl, Saurabh R. Sinha, Janna Cheek, Rosario Maria S. Riel-Romero, Daniel San-Juan, Olga Selioutski, Lucy Sullivan, John D. Kuratani, Frank W. Drislane, Tammy N. Tsuchida, Mark M. Stecker
Publikováno v:
Journal of Clinical Neurophysiology. 33:320-323
This revision to the EEG Guidelines is an update incorporating the current electroencephalography technology and practice. It was previously published as Guideline 2. Similar to the prior guideline, it delineates the aspects of Guideline 1 that shoul
Autor:
Arun Asha Kalra, Eduardo Gonzalez-Toledo, Sujithra Velayuthan, Senthilkumar Sankararaman, Rosario Maria S. Riel-Romero
Publikováno v:
Journal of Pediatric Neurology. 10:301-308
Herpes simplex virus (HSV) type 1 frequently causes fulminant encephalitis and it is the most common etiological agent for sporadic encephalitis in the developed world. We report a case of HSV encephalitis in a 7-month-old infant with bilateral thala
Publikováno v:
Journal of Neurosciences in Rural Practice, Vol 05, Pp S097-S099 (2014)
Journal of Neurosciences in Rural Practice
Journal of Neurosciences in Rural Practice
Sir, Deletions in the Forkhead-box P2(FOXP2) gene are characteristically associated with language impairment. We report a 3-year-old girl with global developmental delay who had a deletion in the long arm of chromosome 7 involving the FOXP2 gene. She
Publikováno v:
Pediatric Neurology. 47:451-454
A brain abscess is uncommon but potentially lethal. Common predisposing risk factors include congenital cyanotic heart disease, immunocompromised status, and the presence of septic foci. We describe a left frontal brain abscess accompanied by fever,
Autor:
James B. Pinskton, Christina Ledbetter, Peimin Zhu, John E. Shaughnessy, Nestor Dela Cruz, Piyush Kalakoti, Kanika Sharma, Hai Sun, Rosario Maria S. Riel-Romero, Anil Nanda, Rimal H. Dossani, Christina Notarianni, Eduardo Gonzalez-Toledo, Alireza Minagar
Publikováno v:
World neurosurgery. 93
Background Psammoma bodies (PBs) are whorled, laminated hyaline spherules containing calcium deposits. Intracranially, the presence of PBs is associated with variants of meningioma and pituitary lesions, as well as aging choroid plexus. Limited infor
Publikováno v:
Pediatric Neurology. 32:53-55
This report describes a male neonate with unusual neuroradiologic findings at birth. The patient's subsequent clinical course and the evolution of his findings on serial magnetic resonance imaging and magnetic resonance venograms are consistent with
Publikováno v:
Journal of child neurology. 26(1)
Lymphocytic hypophysitis, an autoimmune mediated chronic inflammation of the pituitary gland, is uncommon in children.1 The usual presentation is with symptoms secondary to pressure from the enlargement of the gland itself and or impairment of pituit