Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Iris A. Perez"'
Publikováno v:
ERJ Open Research, Vol 10, Iss 1 (2024)
Externí odkaz:
https://doaj.org/article/9b240170365b4e9b80823fee4c5bf12d
Autor:
Emily S. Gillett, Iris A. Perez
Publikováno v:
Diseases, Vol 4, Iss 3, p 23 (2016)
Prader-Willi syndrome (PWS) is an imprinted genetic disorder conferred by loss of paternal gene expression from chromosome 15q11.2-q13. Individuals with PWS have impairments in ventilatory control and are predisposed toward sleep disordered breathing
Externí odkaz:
https://doaj.org/article/590f3bd1099243f88606ff63c8d852c7
Autor:
Alicia Olivas-Martinez, Beatriz Suarez, Elena Salamanca-Fernandez, Iris Reina-Perez, Andrea Rodriguez-Carrillo, Vicente Mustieles, Nicolás Olea, Carmen Freire, Mariana F. Fernández
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2023)
BackgroundBrain-derived neurotrophic factor (BDNF), a neurotrophic growth factor mainly expressed in the brain, has been proposed as a potential effect biomarker; that is, as a measurable biomarker whose values could be associated with several diseas
Externí odkaz:
https://doaj.org/article/e2b6562d0cfe4e16b6dd3618a2481baf
Publikováno v:
Current Neurology and Neuroscience Reports. 23:25-32
Purpose of Review This paper reviews how sleep is impacted in patients with Prader-Willi syndrome (PWS), focusing on sleep-related breathing disturbances and excessive daytime sleepiness (EDS). Recent Findings Hypothalamic dysfunction may underlie se
Publikováno v:
Paediatric Respiratory Reviews.
Autor:
Gloria Y. Chang, Tate Salazar, Abhishek Karnwal, Sheila S. Kun, Josephine Ellashek, Cathy E. Shin, J. Gordon McComb, Thomas G. Keens, Iris A. Perez
Publikováno v:
Sleep and Breathing. 27:505-510
Autor:
Odeya Kagan, Christina Zhang, Christine McElyea, Thomas G. Keens, Sally L. Davidson Ward, Iris A. Perez
Publikováno v:
Journal of Clinical Sleep Medicine.
Autor:
Laura Lazzarini Wo, Reem Itani, Thomas G. Keens, Araz Marachelian, Jianling Ji, Iris A. Perez
Publikováno v:
Journal of Clinical Sleep Medicine.
Autor:
Ashley Kwon, Madison Lodge, Thomas G. Keens, J. Gordon McComb, Cathy E. Shin, Iris A Perez, Susan Durham
Publikováno v:
J Clin Sleep Med
Congenital central hypoventilation syndrome is a rare genetic disorder affecting ventilatory response to hypercapnia and/or hypoxemia. We describe a case of diaphragm pacing (DP) failure in a 38-year-old woman with congenital central hypoventilation
Autor:
Laura M. Lazzarini, Julie M. Werner, Iris A. Perez, Mitchel Seruya, Leigh Ramos‐Platt, Emmanuelle Tiongson, Thomas G. Keens
Publikováno v:
Pediatric Pulmonology. 57:682-685
Acute flaccid myelitis (AFM) is a rare disease that affects spinal cord gray matter, results in acute flaccid weakness of one or more limbs and predominantly involves the cervical spinal cord, which places patients at higher risk for respiratory fail