Results 111 to 120 of about 3,902,064 (330)
Liderando mejoras de calidad mediante el desarrollo, implementación, y medición de las guías de buenas prácticas de Enfermería / Leading Quality Improvement through Best Practice Guideline Development, Implementation, and Measurement Science / Liderando com melhor qualidade por meio da elaboração, implementação e avaliação de guias de boas práticas na enfermagem
MedUNAB, 2015 Introducción: La búsqueda de prácticas basadas en la evidencia ha estimulado acciones por parte de un número de grupos a nivel mundial para desarrollar herramientas de conocimiento.Irmajean Bajnok, RN., MScN., PhD. , Doris Grinspun, RN., MSN., PhD., LLD (Hon)., O.ONT. , Monique Lloyd, RN., PhD. , Heather McConnell, RN., BScN., MA(Ed). +3 moredoaj Beyond p‐values: Assessing clinical significance in acupuncture research
Advanced Chinese Medicine, EarlyView.Abstract
In acupuncture randomized controlled trials (RCTs), the proper interpretation of results requires a thorough understanding of key statistical concepts such as p‐value, effect size, and the minimal clinically important difference (MCID). This paper explores the relationships among these metrics and their implications for assessing the clinical ...Changzhen Gongwiley +1 more sourceMitochondrial DNA disorders in neuromuscular diseases in diverse populations
Annals of Clinical and Translational Neurology, EarlyView.Abstract
Neuromuscular features are common in mitochondrial DNA (mtDNA) disorders. The genetic architecture of mtDNA disorders in diverse populations is poorly understood. We analysed mtDNA variants from whole‐exome sequencing data in neuromuscular patients from South Africa, Brazil, India, Turkey and Zambia. In 998 individuals, there were two definite Fei Gao, Katherine R Schon, Jana Vandrovcova, Özlem Yayıcı Köken, Sharika Raga, Kireshnee Naidu, Maryke Schoonen, Nimita Rani, Pedro Tomaselli, Dipti Baskar, Musambo Kapapa, Ipek Polat, Lindsay A Wilson, Kumarasamy Thangaraj, Uluç Yiş, Bevinahalli N Nandeesh, David Bearden, Michelle Kvalsund, Franclo Henning, Seena Vengalil, Atchayaram Nalini, Claudia F. R. Sobreira, Wilson Marques, Haluk Topoloğlu, Michael G Hanna, Sireesha Yareeda, Venugopalan Y Vishnu, Francois H van der Westhuizen, Izelle Smuts, Surita Meldau, Jo Wilmshurst, Büşranur Çavdarlı, Jeannine Heckmann, Patrick F Chinnery, Rita Horvath +34 morewiley +1 more sourceA Novel CHMP2B Splicing Variant in Atypical Presentation of Familial Frontotemporal Lobar Degeneration
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT
C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who Sara Rubio‐Guerra, Sara Bernal, David Almenta, Josefina Pérez‐Blanco, Valle Camacho, Isabel Sala, Mª Belén Sánchez‐Saudinós, Jesús García Castro, Judit Selma‐González, Miguel Ángel Santos‐Santos, Álvaro Carbayo, Janina Turon‐Sans, Ricard Rojas‐Garcia, Daniel Alcolea, Juan Fortea, Alberto Lleó, Oriol Dols‐Icardo, Ignacio Illán‐Gala +17 morewiley +1 more sourcePulse Pressure, White Matter Hyperintensities, and Cognition: Mediating Effects Across the Adult Lifespan
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objectives
To investigate whether pulse pressure or mean arterial pressure mediates the relationship between age and white matter hyperintensity load and to examine the mediating effect of white matter hyperintensities on cognition. Methods
Demographic information, blood pressure, current medication lists, and Montreal Cognitive Assessment ...Jade Hannan, Sarah Newman‐Norlund, Natalie Busby, Sarah C. Wilson, Roger Newman‐Norlund, Chris Rorden, Julius Fridriksson, Leonardo Bonilha, Nicholas Riccardi +8 morewiley +1 more source2023 ESC Guidelines for the management of acute coronary syndromes.
European Heart Journal, 2023 R. Byrne, X. Rosselló, J. J. Coughlan, E. Barbato, C. Berry, A. Chieffo, M. Claeys, G. Dan, M. Dweck, M. Galbraith, M. Gilard, L. Hinterbuchner, E. Jankowska, P. Jüni, Takeshi Kimura, V. Kunadian, M. Leósdóttir, R. Lorusso, R. Pedretti, A. Rigopoulos, M. Rubini Giménez, H. Thiele, P. Vranckx, S. Wassmann, N. Wenger, B. Ibáñez, S. Halvorsen, Stefan James, M. Abdelhamid, V. Aboyans, N. Marsan, S. Antoniou, R. Asteggiano, Maria Bäck, D. Capodanno, R. Casado-Arroyo, S. Cassese, J. Čelutkienė, M. Čikeš, J. Collet, G. Ducrocq, V. Falk, L. Fauchier, T. Geisler, Diana A Gorog, L. Holmvang, T. Jaarsma, H. W. Jones, L. Køber, Konstantinos C Koskinas, D. Kotecha, Konstantin A. Krychtiuk, U. Landmesser, G. Lazaros, B. Lewis, B. Lindahl, A. Linhart, M. Løchen, M. Mamas, J. Mcevoy, B. Mihaylova, Richard Mindham, C. Mueller, L. Neubeck, J. Niebauer, J. Nielsen, A. Niessner, V. Paradies, A. Pasquet, Steffen E Petersen, E. Prescott, A. Rakisheva, B. Rocca, Giuseppe M C Rosano, L. Sade, F. Schiele, J. Siller-Matula, C. Sticherling, R. Storey, M. Thielmann, C. Vrints, S. Windecker, R. Wiseth, Adam Witkowski, Mohammed El Amine Bouzid, H. Hayrapetyan, B. Metzler, P. Lancellotti, Mugdim Bajrić, K. Karamfiloff, A. Mitsis, P. Ostadal, Rikke Sørensen, Tamer Elwasify, T. Marandi, Essi Ryödi, Archil Chukhrukidze, J. Mehilli, P. Davlouros, D. Becker, I. Guðmundsdóttir, J. Crowley, Y. Abramowitz, C. Indolfi, Orazbek Sakhov, S. Elezi, M. Beishenkulov, A. Erglis, N. Moussallem, Hisham Benlamin, Olivija Dobilienė, P. Degrell, M. Balbi, A. Grosu, Zouhair Lakhal, Jurrien ten Berg, H. Pejkov, K. Angel, M. de Sousa Almeida, O. Chioncel, L. Bertelli, S. Stojkovic, M. Studencan, P. Radsel, J. Ferreiro, A. Ravn-Fischer, L. Räber, Mohammed Yassin Bani Marjeh, M. Hassine, A. Yıldırır, A. Parkhomenko, A. Banning, E. Arbelo, C. Baigent, M. Borger, S. Buccheri, Borja Ibáñez, X. Rosselló, I. Vaartjes, K. Zeppenfeld +139 moresemanticscholar +1 more sourceFetal Akinesia/Hypokinesia and Arthrogryposis of Neuromuscular Origin: Etiologic Groups, Genetics, and Phenotypic Spectrum
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective
To provide a comprehensive clinical and genetic characterization of individuals with arthrogryposis multiplex congenita (AMC), focusing on the distribution of genetic etiologies across the neuromuscular spectrum and comparing myogenic and neurogenic subtypes. Methods
A total of 105 individuals with AMC were clinically and genetically Florencia Pérez‐Vidarte, Berta Estévez‐Arias, Leslie Matalonga, Delia Yubero, Anna Codina, Carlos Ortez, Julita Medina, Lidia DeSena DeCabo, Laura Carrera‐García, Jesica Expósito‐Escudero, Cristina Jou, Eduardo F. Tizzano, Andres Nascimento, Daniel Natera‐de Benito +13 morewiley +1 more source