Results 31 to 40 of about 2,200,980 (154)

Valoración de importancia de la inteligencia artificial en educación médica en académicos del departamento de ciencias médicas de la Universidad de Antofagasta: un estudio descriptivo

ARS Medica
Introducción: En los últimos 25 años se han producido avances significativos en el ámbito de la inteligencia artificial (IA), la que ha cobrado relevancia en los últimos años, especialmente después de la pandemia por COVID – 19 para apoyar el desarrollo
Alberto Torres-Belma, Juan Fernández-Gallardo, Daniela Apablaza-Venegas, Loreto García-Rosas, Claudia Álvarez-Iguaín   +4 more
doaj   +1 more source

Exposure to Gestational Intermittent Hypoxia Does Not Impair the Metabolic Function or Accelerate the Biological Ageing Process of Offspring of Either Sex

Journal of Sleep Research, Volume 35, Issue 3, June 2026.
ABSTRACT Obstructive sleep apnea (OSA), marked by intermittent hypoxia, is associated with obesity, type 2 diabetes and metabolic associated fatty liver disease. In pregnancy, it remains underdiagnosed despite links to gestational diabetes, hypertension, and foetal growth restriction.
Esther Valverde‐Perez, Margarida B. Almeida, Joana F. Sacramento, Elena Olea, Jesus Prieto‐Lloret, Asuncion Rocher, Silvia V. Conde   +6 more
wiley   +1 more source

Biografía de Pablo Picasso [PDF]

, 2011
Biografía del artista plástico Pablo PicassoSociedad de Educación Médica de La ...
Sociedad de Educación Médica de La Plata
core  

Informed Consent as a Human Right in the Inter‐American Human Rights System (IAHRS)

Developing World Bioethics, Volume 26, Issue 1, Page 11-16, March 2026.
ABSTRACT Informed consent is presented as a fundamental right and principle in modern medical practice. It involves obtaining permission from a patient before any medical procedure, treatment, or research protocol. Although not explicitly recognized as a standalone right in international human rights instruments, informed consent in healthcare is ...
Diana Rocío Bernal‐Camargo, Ana Isabel Gómez–Córdoba   +1 more
wiley   +1 more source

Missense Variants in the Second Transmembrane Domain of TMEM17 Disrupt Its Stability and Function and Lead to a Wide Phenotypic Spectrum of Ciliopathies

Clinical Genetics, Volume 109, Issue 2, Page 305-315, February 2026.
Missense variants in TMEM17 disrupt its localization and function at the ciliary transition zone, leading to a wide range of ciliopathy phenotypes, from OFD6 and Joubert syndromes to Meckel syndrome. ABSTRACT Ciliopathies are rare genetic disorders characterized by significant genetic and phenotypic variability.
Lucile Boutaud, Chunmei Li, Candice Moncler, Laure Verlin, Meriem Garfa‐Traoré, Nicolas Bourgon, Dhruvin Akbari, Jeanne Porée, Valentina Serpieri, Marine Panza, Lynda Haddad, Patrick Nitschké, Jacqueline Aziza, Cristina Matt, Enza Maria Valente, Patricia Gargallo, Charlotte Dubucs, Tania Attié‐Bitach, Michel R. Leroux, Sophie Thomas   +19 more
wiley   +1 more source

Impacto del proceso de enseñanza endoscópica en la detección de adenomas colónicos

Revista de Gastroenterología de México, 2014
Antecedentes: El impacto que el proceso de entrenamiento endoscópico ejerce sobre la calidad de la colonoscopia en un medio hispanoamericano es escasa. Objetivo: Determinar el efecto del entrenamiento en la técnica de colonoscopia sobre la detección de ...
J.S. Lasa, R. Moore, A.D. Peralta, G. Dima, I. Zubiaurre, M. Arguello, M. Senderovsky, L. Moretti, A. Avagnina, L. Soifer   +9 more
doaj   +1 more source

Encefalitis autoinmune seronegativa asociada a síndrome de Sjögren primario

Revista Argentina de Reumatología, 2023
La encefalitis autoinmune es un trastorno inmunomediado que compromete distintos territorios del parénquima cerebral, involucrando frecuentemente la materia gris profunda o la corteza, con o sin compromiso de la materia blanca, meninges o médula espinal.
Carlos Alfonso González Gómez, María Laura de la Torre, Cecilia Nora Pisoni   +2 more
doaj   +1 more source

Structural and functional dissection of the WH2/DAD motif of INF2, a formin linked to human inherited degenerative disorders

The FEBS Journal, Volume 293, Issue 3, Page 825-841, February 2026.
The INF2 WH2/DAD domain, composed of hydrophobic and basic regions, forms a single α‐helix in solution. The hydrophobic segment is essential for INF2 function, as its deletion disrupts actin dynamics and causes nuclear abnormalities, like those seen in pathogenic INF2 DID variants. In contrast, natural INF2 WH2/DAD variants found in patients with renal
Leticia Labat‐de‐Hoz, Laura Fernández‐Martín, Paula Morales, Isabel Correas, María Ángeles Jiménez, Miguel Angel Alonso   +5 more
wiley   +1 more source

A Computational Study of the NMR Chemical Shifts of Polynitropyrazoles

Magnetic Resonance in Chemistry, Volume 64, Issue 1, Page 97-113, January 2026.
The 1H, 13C, 15N, and 17O chemical shifts of 91 nitro‐1H‐pyrazoles at GIAO/B3LYP/6‐311++G(d,p) level. The calculated chemical shifts were compared with available experimental data using an empirical equation that relates absolute shieldings to chemical shifts.
Arturo Alcorta, Rosa M. Claramunt, José Elguero, Ibon Alkorta   +3 more
wiley   +1 more source

Los polimorfismos de ITPA no predicen un riesgo adicional más allá de TPMT y NUDT15 para citopenia inducida por tiopurina en la enfermedad inflamatoria intestinal

Revista de Gastroenterología de México
Resumen: Introducción y objetivos: La leucopenia relacionada con tiopurina está asociada con polimorfismos en la tiopurina metiltransferasa (TPMT, por sus siglas en inglés) y con el gen NUDT15. Sin embargo, estos polimorfismos explican solo una fracción
A. Jena, N. Grover, P. Bhatia, M. Singh, D. Lad, K.K. Prasad, H. Singh, U. Dutta, V. Sharma   +8 more
doaj   +1 more source