Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jennifer M Argudo"'
Autor:
Juan Fernando Ortiz, Jennifer M. Argudo, Mario Yépez, Juan Andrés Moncayo, Hyder Tamton, Alex S. Aguirre, Ghanshyam Patel, Meghdeep Sen, Ayushi Mistry, Ray Yuen, Ahmed Eissa-Garces, Diego Ojeda, Samir Ruxmohan
Publikováno v:
Clocks & Sleep, Vol 4, Iss 2, Pp 287-299 (2022)
Kleine–Levin syndrome (KLS) is characterized by episodes of hypersomnia. Additionally, these patients can present with hyperphagia, hypersexuality, abnormal behavior, and cognitive dysfunction. Functional neuroimaging studies such as fMRI-BOLD, Pos
Externí odkaz:
https://doaj.org/article/b45a9f04302f414989c9dbdeae823180
Autor:
Iván Nicolas Ayala, Syed Aziz, Jennifer M. Argudo, Mario Yepez, Mikaela Camacho, Diego Ojeda, Alex S. Aguirre, Sebastian Oña, Andres F. Andrade, Ananya Vasudhar, Juan A. Moncayo, Gashaw Hassen, Juan Fernando Ortiz, Willian Tambo
Publikováno v:
Brain Sciences, Vol 12, Iss 8, p 1040 (2022)
Ataxia is a constellation of symptoms that involves a lack of coordination, imbalance, and difficulty walking. Hereditary ataxia occurs when a person is born with defective genes, and this degenerative disorder may progress for several years. There i
Externí odkaz:
https://doaj.org/article/04eb660813544b4bab04083eeaf17eb0
Autor:
Jennifer M Argudo, Olga M Astudillo Moncayo, Walter Insuasti, Gabriela Garofalo, Alex S Aguirre, Sebastian Encalada, Jose Villamarin, Sebastian Oña, Maria Gabriela Tenemaza, Ahmed Eissa-Garcés, Sakina Matcheswalla, Juan Fernando Ortiz
Publikováno v:
Cureus.
Autor:
Juan A Moncayo, Maite N Vargas, Isabel Castillo, Pablo V Granda, Andrea M Duque, Jennifer M Argudo, Sakina Matcheswalla, Guillermo E Lopez Dominguez, Gustavo Monteros, Andres F Andrade, Diego Ojeda, Mario Yepez
Publikováno v:
Cureus. 14(7)
Protocadherin 19 (PCDH19) syndrome is inherited as an X-linked pattern and affects mainly females. This syndrome is caused by a mutation in the PCDH19 gene encoding for the protocadherin protein. It is characterized by refractory seizures during febr
Understanding Protein Protocadherin-19 (PCDH19) Syndrome: A Literature Review of the Pathophysiology
Autor:
Juan A Moncayo, Ivan N Ayala, Jennifer M Argudo, Alex S Aguirre, Jashank Parwani, Ana Pachano, Diego Ojeda, Steven Cordova, Maria Gracia Mora, Christiany M Tapia, Juan Fernando Ortiz
Publikováno v:
Cureus.
PCDH19 syndrome is a monogenic epilepsy related to the protein protocadherin-19 (PCDH19) gene, which encodes for a protein important for brain development. The protein also seems to regulate gamma-aminobutyric acid type A receptors (GABA(A)(R)). The