Zobrazeno 1 - 10
of 45
pro vyhledávání: '"E. Olaya"'
Autor:
Yousef AlMutawa, Diana E. Olaya, Gao S. Huang, Marta Kaminska, Josephine Pressacco, Jonathan Spicer, Oren Steinmetz
Publikováno v:
EJVES Vascular Forum, Vol 60, Iss , Pp 8-11 (2023)
Introduction: Lobar torsion is a rare, challenging diagnosis that requires a high index of suspicion and prompt investigation and management. Detection and urgent fixation or lung resection are critical to avoid catastrophic sequelae of lung necrosis
Externí odkaz:
https://doaj.org/article/cd099d4d7c454ad5a2cfa2b29a4a6ce6
Autor:
Sara E. Mole, Angela Schulz, Eben Badoe, Samuel F. Berkovic, Emily C. de Los Reyes, Simon Dulz, Paul Gissen, Norberto Guelbert, Charles M. Lourenco, Heather L. Mason, Jonathan W. Mink, Noreen Murphy, Miriam Nickel, Joffre E. Olaya, Maurizio Scarpa, Ingrid E. Scheffer, Alessandro Simonati, Nicola Specchio, Ina Von Löbbecke, Raymond Y. Wang, Ruth E. Williams
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-19 (2021)
Abstract Background CLN2 disease (Neuronal Ceroid Lipofuscinosis Type 2) is an ultra-rare, neurodegenerative lysosomal storage disease, caused by an enzyme deficiency of tripeptidyl peptidase 1 (TPP1). Lack of disease awareness and the non-specificit
Externí odkaz:
https://doaj.org/article/dca030d850824609987aa2702f2ac2b3
Autor:
Kavyakantha Remakanthakurup Sindhu, Duy Ngo, Hernando Ombao, Joffre E Olaya, Daniel W Shrey, Beth A Lopour
Publikováno v:
Journal of Neural Engineering. 20:026002
Objective. Intracranial electroencephalogram (iEEG) plays a critical role in the treatment of neurological diseases, such as epilepsy and Parkinson’s disease, as well as the development of neural prostheses and brain computer interfaces. While elec
Autor:
Joseph B. Cantey, Cynthia C. Correa, Daniel D. Dugi, Erin Huff, Jorge E. Olaya, Rachael Farner
Publikováno v:
Pediatrics
BACKGROUND AND OBJECTIVES Antibiotic overuse is associated with adverse neonatal outcomes. Many medically underserved centers lack pediatric antibiotic stewardship program (ASP) support. Telestewardship may mitigate this disparity. Authors of this st
Autor:
Kavyakantha Remakanthakurup Sindhu, Duy Ngo, Hernando Ombao, Joffre E. Olaya, Daniel W. Shrey, Beth A. Lopour
Intracranial EEG (iEEG) plays a critical role in the treatment of neurological diseases, such as epilepsy and Parkinson’s disease, as well as the development of neural prostheses and brain computer interfaces. While electrode geometries vary widely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f74a5d6bdee234cf36bbebbd4acb265d
https://doi.org/10.1101/2022.01.05.475164
https://doi.org/10.1101/2022.01.05.475164
Autor:
Ruth Williams, Norberto Guelbert, Maurizio Scarpa, Samuel F. Berkovic, Raymond Y. Wang, Noreen Murphy, Nicola Specchio, Simon Dulz, Paul Gissen, Joffre E Olaya, Emily de los Reyes, Jonathan W. Mink, Ingrid E. Scheffer, Alessandro Simonati, Sara E. Mole, Angela Schulz, Miriam Nickel, Eben Badoe, Ina von Löbbecke, Heather L Mason, Charles Marques Lourenço
Publikováno v:
Orphanet journal of rare diseases, vol 16, iss 1
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-19 (2021)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-19 (2021)
Orphanet Journal of Rare Diseases
Background CLN2 disease (Neuronal Ceroid Lipofuscinosis Type 2) is an ultra-rare, neurodegenerative lysosomal storage disease, caused by an enzyme deficiency of tripeptidyl peptidase 1 (TPP1). Lack of disease awareness and the non-specificity of pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d908a653f3465b251f513b2d8297451f
https://hdl.handle.net/11577/3486195
https://hdl.handle.net/11577/3486195
Autor:
Mole, Sara E., Schulz, Angela, Eben Badoe, Berkovic, Samuel F., De Los Reyes, Emily C., Dulz, Simon, Gissen, Paul, Guelbert, Norberto, Lourenco, Charles M., Mason, Heather L., Mink, Jonathan W., Murphy, Noreen, Nickel, Miriam, Joffre E. Olaya, Scarpa, Maurizio, Scheffer, Ingrid E., Simonati, Alessandro, Specchio, Nicola, Von Löbbecke, Ina, Wang, Raymond Y., Williams, Ruth E.
Additional file 2: Poster. Methodology to develop guidelines for the management of patients with CLN2 disease.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c927f48ddfeefa5b67a7e4cd8645b6a
Autor:
Mole, Sara E., Schulz, Angela, Eben Badoe, Berkovic, Samuel F., De Los Reyes, Emily C., Dulz, Simon, Gissen, Paul, Guelbert, Norberto, Lourenco, Charles M., Mason, Heather L., Mink, Jonathan W., Murphy, Noreen, Nickel, Miriam, Joffre E. Olaya, Scarpa, Maurizio, Scheffer, Ingrid E., Simonati, Alessandro, Specchio, Nicola, Von Löbbecke, Ina, Wang, Raymond Y., Williams, Ruth E.
Additional file 1: Appendices. Appendices 1–9.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::042c85438a58bf51ecbdc7ab38fba8f3
Autor:
Tuan Dao, Aaron Goldberg, Jody Pathare, Clay Hoerig, Chenue Abongwa, William G Loudon, Joffre E Olaya, Ashley Plant-Fox, Ali Nael Amzajerdi
Publikováno v:
Neuro-Oncology
Background Ewing sarcoma (EWS) is a rare type of pediatric bone and soft tissue tumor that accounts for approximately 1% of all pediatric malignancies. It most commonly occurs in the long bones or axial skeleton, and rarely includes extraosseous site
Publikováno v:
Dominio de las Ciencias, Vol 4, Iss 3 Especial, Pp 771-779 (2017)
El uso de un fármaco sin haber sido prescrito por un médico, puede provocar daños multisistémicos en diferentes órganos del cuerpo humano, (riñones, hígado, estómago, sistema nervioso) con esta realidad abordo el tema con el objetivo de dar a