Results 31 to 40 of about 467 (143)

Low Serum Tryptophan Levels as an Indicator of Global Cognitive Performance in Nondemented Women over 50 Years of Age

Oxidative Medicine and Cellular Longevity, Volume 2018, Issue 1, 2018., 2018
Aging is a physiological decline process. The number of older adults is growing around the world; therefore, the incidence of cognitive impairment, dementia, and other diseases related to aging increases. The main cellular factors that converge in the aging process are mitochondrial dysfunction, antioxidant impairment, inflammation, and immune response
L. A. Ramos-Chávez, G. Roldán-Roldán, B. García-Juárez, D. González-Esquivel, G. Pérez de la Cruz, B. Pineda, D. Ramírez-Ortega, I. García Muñoz, B. Jiménez Herrera, C. Ríos, S. Gómez-Manzo, J. Marcial-Quino, L. Sánchez Chapul, P. Carrillo Mora, V. Pérez de la Cruz, Simona M. Monti   +15 more
wiley   +1 more source

Tratamientos respiratorios en la enfermedad neuromuscular

Anales de Pediatría, 2014
In a previous article, a review was presented of the respiratory pathophysiology of the patient with neuromuscular disease, as well as their clinical evaluation and the major complications causing pulmonary deterioration. This article presents the respiratory treatments required to preserve lung function in neuromuscular disease as long as possible, as
Martínez Carrasco C, Cols Roig M, Salcedo Posadas A, Sardon Prado O, Asensio de la Cruz O, Torrent Vernetta A   +5 more
openaire   +2 more sources

Relevancia del síndrome piramidal en la esclerosis lateral amiotrófica

Neurología, 2018
Resumen: Introducción: Los signos piramidales (hiperreflexia, espasticidad, signo de Babinski) son fundamentales para el diagnóstico de esclerosis lateral amiotrófica (ELA).
N. Álvarez, L. Díez, C. Avellaneda, M. Serra, M.Á. Rubio   +4 more
doaj   +1 more source

FISIOPATOLOGÍA DE LAS ENFERMEDADES PULMONARES RESTRICTIVAS

Neumología Pediátrica, 2023
Las enfermedades restrictivas comprenden un grupo heterogéneo de trastornos que se caracterizan por una alteración en la distensibilidad pulmonar, generada por enfermedades del parénquima o intersticio pulmonar o por problemas extrapulmonares ...
Mónica Saavedra Bentjerodt
doaj   +1 more source

Descifrando el papel pronóstico de la inmunoglobulina G sérica en el síndrome de Guillain-Barré durante el tratamiento con inmunoglobulina intravenosa

Gaceta Médica de México
Antecedentes: El síndrome de Guillain-Barré (SGB) se asocia a una frecuencia de 20 % de discapacidad a largo plazo. Este estudio examina la fisiopatología del SGB y el papel de la inmunoglobulina (Ig) intravenosa.
Javier A. Galnares-Olalde, Juan C. López-Hernández, Verónica Domínguez-Tobón, Edwin S. Vargas-Cañas   +3 more
doaj   +1 more source

Validación de Neuromyotype: un teclado inteligente para la evaluación de pacientes con atrofia muscular espinal 5q

Neurología
Resumen: Introducción: La atrofia muscular espinal 5q (AME) es una enfermedad genética neurodegenerativa que afecta a las motoneuronas alfa produciendo debilidad progresiva.
P. Lizandra Cortés, D. Poveda Verdú, A. Albert Férriz, N.C. Ñungo-Garzón, M.C. Domine, T. Sevilla-Mantecón, I. Pitarch-Castellano, J.F. Vázquez-Costa   +7 more
doaj   +1 more source

Relevance of the pyramidal syndrome in amyotrophic lateral sclerosis

Neurología (English Edition), 2018
Introduction: Pyramidal signs (hyperreflexia, spasticity, Babinski sign) are essential for the diagnosis of amyotrophic lateral sclerosis (ALS). However, these signs are not always present at onset and may vary over time, besides which their role in ...
N. Álvarez, L. Díez, C. Avellaneda, M. Serra, M.Á. Rubio   +4 more
doaj   +1 more source

Validation of Neuromyotype: a smart keyboard for the evaluation of spinal muscular atrophy patients

Neurología (English Edition)
Introduction: Spinal muscular atrophy 5q (SMA) is a genetic neurodegenerative disease that affects alpha motor neurons producing progressive weakness. New outcome measures are currently required to accurately characterise the disease progression and the ...
P. Lizandra Cortés, D. Poveda Verdú, A. Albert Férriz, N.C. Ñungo-Garzón, M.C. Domine, T. Sevilla-Mantecón, I. Pitarch-Castellano, J.F. Vázquez-Costa   +7 more
doaj   +1 more source

Differential gene expression of ABCG2, SLC22A12, IL-1β, and ALPK1 in peripheral blood leukocytes of primary gout patients with hyperuricemia and their comorbidities: a case–control study

European Journal of Medical Research, 2022
Background The ABCG2, SLC22A12, and ALPK1 genes have been strongly associated with dysfunction of urate metabolism in patients with gout, but it is unknown how these transporters are expressed in patients with acute or chronic gout.
Paniagua-Díaz Natsuko, Sanchez-Chapul Laura, Clavijo-Cornejo Denise, Ventura-Ríos Lucio, Aguilar-Salinas Carlos, Sanchez-Muñoz Fausto, López-Macay Ambar   +6 more
doaj   +1 more source

Clinical Outcomes and Rehabilitation Requirements in Guillain–Barré Syndrome: An 18‐Year Experience From a Neurological Center in Argentina

Acta Neurologica Scandinavica, Volume 2026, Issue 1, 2026.
Background and Objectives Guillain–Barré syndrome is the most common cause of acute acquired neuromuscular paralysis worldwide and is frequently associated with significant disability requiring rehabilitation. However, data on rehabilitation requirements and their clinical predictors remain limited, particularly in low‐ and middle‐income countries.
José M. Pastor Rueda, Lucas Alessandro, Agustín Puebla, Ricardo Kirchner, Christian Gath, Fabio Barroso, Ankit Dhoundiyal   +6 more
wiley   +1 more source