Zobrazeno 1 - 10
of 64
pro vyhledávání: '"trisomy 21 (Down syndrome)"'
Autor:
Alessandro De Falco, Antonella Gambale, Michele Pinelli, Teresa Suero, Luigia De Falco, Achille Iolascon, Stefania Martone
Publikováno v:
Cells, Vol 13, Iss 13, p 1078 (2024)
Chromosomal rearrangements can interfere with the disjunction and segregation of other chromosome pairs not involved in the rearrangements, promoting the occurrence of numerical abnormalities in resulting gametes and predisposition to trisomy in offs
Externí odkaz:
https://doaj.org/article/87232c82875143928fa7b37d57e3ee19
Autor:
Frontiers Production Office
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Externí odkaz:
https://doaj.org/article/ceb2affda9ea4179ade252f00a713703
Autor:
Michele Polfuss, Linda G. Bandini, Michele N. Ravelli, Zijian Huang, Andrea Moosreiner, Dale A. Schoeller, Chiang-Ching Huang, Dan Ding, Cristen Berry, Emma Marston, Azeem Hussain, Timothy C. Shriver, Kathleen J. Sawin
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundThe consequences of obesity are ominous, yet healthcare professionals are not adequately preventing or treating obesity in youth with Down syndrome (DS). Total daily energy expenditure (TDEE) is the energy expended in 24 h through physical
Externí odkaz:
https://doaj.org/article/f408a87acfd447d9936de7a8bb350f58
Autor:
Ester Miyuki Nakamura-Palacios, Aldren Thomazini Falçoni Júnior, Gabriela Lolli Tanese, Ana Carla Estellita Vogeley, Aravind Kumar Namasivayam
Publikováno v:
Brain Sciences, Vol 14, Iss 1, p 58 (2024)
Apraxia of speech is a persistent speech motor disorder that affects speech intelligibility. Studies on speech motor disorders with transcranial Direct Current Stimulation (tDCS) have been mostly directed toward examining post-stroke aphasia. Only a
Externí odkaz:
https://doaj.org/article/09ff0e1e61314ef3a1643044845fe7e3
Autor:
Elisa Fucà, Flavia Cirillo, Laura Celestini, Paolo Alfieri, Diletta Valentini, Floriana Costanzo, Stefano Vicari
Publikováno v:
Frontiers in Psychiatry, Vol 13 (2023)
IntroductionChildren and adolescents with intellectual disability (ID) exhibit higher rates of oppositional defiant disorder (ODD) than typically developing (TD) peers. However, studies focusing on the investigation of ODD prevalence in youth with Do
Externí odkaz:
https://doaj.org/article/f9f049bd34f14efcaa9e636aa5cff2ee
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2023)
BackgroundChildren with Trisomy 21 (T21) are at an increased risk of sleep-disordered breathing (SDB), which can impact daily functioning and cause other health complications. Accordingly, it is imperative to diagnose and treat SDB in this population
Externí odkaz:
https://doaj.org/article/57ddf849ffab4dbdad4ad688da95b4a6
Akademický článek
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Autor:
Elisa Fucà, Floriana Costanzo, Luciana Ursumando, Laura Celestini, Vittorio Scoppola, Silvia Mancini, Diletta Valentini, Alberto Villani, Stefano Vicari
Publikováno v:
Frontiers in Psychology, Vol 13 (2022)
Sleep is a major concern, especially in people with Down Syndrome (DS). Beyond Obstructive Sleep Apnea, a number of other sleep difficulties have been reported in children with DS, such as delayed sleep onset, night-time awakenings, and early morning
Externí odkaz:
https://doaj.org/article/90306ad90daa46ccaee8f2f870746bbd
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2022)
This review will address the place of innovative, non-chemotherapy, non-CAR-T targeted therapies in the treatment of Acute Lymphoblastic Leukaemia (ALL), focusing on their use in the hematopoietic stem cell transplant (HSCT) context. The focus will b
Externí odkaz:
https://doaj.org/article/0be02365426940169892e8f4f849f7f9
Autor:
Francesca Antonaros, Margherita Pitocco, Domenico Abete, Beatrice Vione, Allison Piovesan, Lorenza Vitale, Pierluigi Strippoli, Maria Caracausi, Maria Chiara Pelleri
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Down syndrome (DS) is caused by trisomy of chromosome 21 and it is the most common genetic cause of intellectual disability (ID) in humans. Subjects with DS show a typical phenotype marked by facial dysmorphisms and ID. Partial trisomy 21 (PT21) is a
Externí odkaz:
https://doaj.org/article/6f441a97b5eb4ee096425029ecf7df5b