keyword
https://read.qxmd.com/read/38640866/evaluation-of-three-year-neurodevelopmental-outcomes-in-infants-prenatally-exposed-to-substance-use
#21
JOURNAL ARTICLE
Pilar Jarque, Miguel Carmona, Antonia Roca, Bernardino Barcelo, Simona Pichini, Miguel Ángel Elorza, Pilar Sanchis, Yolanda Rendal, Isabel Gomila
INTRODUCTION: Prenatal exposure to substance use is associated with long-term deficits in the neurodevelopment of children. The objective was to investigate the association between cognitive, motor, and language neurodevelopment at three years of age in infants prenatally exposed to substance use. MATERIAL AND METHODS: A prospective matched case-control study was conducted. Biomarkers of fetal exposure were measured in meconium samples. The Bayley Scales of Infant and Toddler Development (BSID-III) were used to calculate neurodevelopment scores...
April 6, 2024: Drug and Alcohol Dependence
https://read.qxmd.com/read/38640516/mental-state-verb-use-in-play-by-preschool-age-children-who-stutter-and-their-mothers
#22
JOURNAL ARTICLE
Stacy A Wagovich, Katie Threlkeld, Lauren Tigner, Julie D Anderson
INTRODUCTION: Preschool-age children use mental state verbs (MSVs; e.g., think, know) to reference thoughts and other cognitive states. In play-based language, MSV use requires conversational flexibility, as speakers shift from discussion of actions happening in the here-and-now to more abstract discussion of mental states. Some evidence suggests that children who stutter (CWS) demonstrate subtle differences in shifting on experimental tasks of cognitive flexibility, differences which may extend to conversational flexibility...
April 16, 2024: Journal of Fluency Disorders
https://read.qxmd.com/read/38639917/-congenital-brain-malformations
#23
REVIEW
Stephanie Spieth, Gabriele Hahn
CLINICAL ISSUE: Malformations of the central nervous system belong to the most common developmental disorders in humans. The clinical presentation of brain malformations is nonspecific including developmental delay, hypotonia, and/or epilepsy. The great heterogeneity concerning etiology, mechanisms of development and morphology is challenging for diagnosis and classification of brain malformations. Thereby recognizing specific malformations is essential for optimal patient management and prognostic evaluation...
April 19, 2024: Radiologie (Heidelb)
https://read.qxmd.com/read/38639319/fructooligosaccharides-intake-during-pregnancy-improves-metabolic-phenotype-of-offspring-in-high-fat-diet-induced-obese-mice
#24
JOURNAL ARTICLE
Junki Miyamoto, Yuna Ando, Akari Nishida, Mayu Yamano, Shunsuke Suzuki, Hiromi Takada, Ikuo Kimura
SCOPE: Obesity and metabolic diseases are closely associated, and individuals who become obese are also prone to type 2 diabetes and cardiovascular disorders. Gut microbiota is mediated by diet and can influence host metabolism and the incidence of metabolic disorders. Recent studies have suggested that improving gut microbiota through a fructooligosaccharide (FOS)-supplemented diet may ameliorate obesity and other metabolic disorders. Although accumulating evidence supports the notion of the developmental origins of health and disease, the underlying mechanisms remain obscure...
April 19, 2024: Molecular Nutrition & Food Research
https://read.qxmd.com/read/38639214/acceptability-of-virtual-psychiatric-consultations-for-routine-follow-ups-post-covid-19-pandemic-for-people-with-intellectual-disabilities-cross-sectional-study
#25
JOURNAL ARTICLE
Samuel Tromans, Sarah Rybczynska-Bunt, Sarah Mitchell, Susan Cummins, David Cox, Jennifer Downing, Paul H Lee, Lucy Teece, Tony Marson, Rohit Shankar
BACKGROUND: After the rapid implementation of digital health services during the COVID-19 pandemic, a paucity of research exists about the suitability of remote consulting in people with intellectual disabilities and their carers, particularly for neuropsychiatric reviews. AIM: This study examines when remote neuropsychiatric routine consulting is suitable for this population. METHOD: A survey was conducted of people with intellectual disabilities and their carers, examining their preference between face-to-face and video consultations for ongoing neuropsychiatric reviews within a rural countywide intellectual disability service in Cornwall, England (population: 538 000)...
April 19, 2024: BJPsych Open
https://read.qxmd.com/read/38638584/prevalence-and-factors-of-sleep-problems-among-japanese-children-a-population-based-study
#26
JOURNAL ARTICLE
Asami Kuki, Ai Terui, Yui Sakamoto, Ayako Osato, Tamaki Mikami, Kazuhiko Nakamura, Manabu Saito
BACKGROUND: High prevalence of sleep problems in not only children with neurodevelopmental disorders (NDS) but also non NDS has been established. However, there are few studies that have looked into population-based and age-specific prevalence of sleep problems of children. Moreover, there are even fewer studies that have investigated the correlation of demographic and lifestyle-related factors affecting sleep problems in children. Considering these, the purpose of this study is to assess the correlation of the prevalence of sleep problems and selected socio-demographic and lifestyle-related factors in 5-year-old Japanese children in population-based study...
2024: Frontiers in Pediatrics
https://read.qxmd.com/read/38638574/il-1%C3%AE-disrupts-the-initiation-of-blood-brain-barrier-development-by-inhibiting-endothelial-wnt-%C3%AE-catenin-signaling
#27
JOURNAL ARTICLE
Audrey R Fetsko, Dylan J Sebo, Lilyana B Budzynski, Alli Scharbarth, Michael R Taylor
During neuroinflammation, the proinflammatory cytokine interleukin-1β (IL-1β) impacts blood-brain barrier (BBB) function by disrupting brain endothelial tight junctions, promoting vascular permeability, and increasing transmigration of immune cells. Here, we examined the effects of Il-1β on the in vivo initiation of BBB development. We generated doxycycline-inducible transgenic zebrafish to secrete Il-1β in the CNS. To validate the utility of our model, we showed Il-1β dose-dependent mortality, recruitment of neutrophils, and expansion of microglia...
May 17, 2024: IScience
https://read.qxmd.com/read/38638543/pearls-of-wisdom-updated-skill-specific-parenting-strategies-in-the-first-6-years
#28
REVIEW
Cara Dosman, Dorrie Koscielnuk, Sheila Gallagher
This article provides knowledge translation on up-to-date parenting strategies (pearls of wisdom). These pearls support the development of specific skills in children from birth through 5 years of age. Paediatricians have indicated that they feel inadequately trained in providing parenting guidance. This article could be used by family physicians, community health nurses, nurse practitioners, and paediatricians as an office reference when providing anticipatory parenting guidance and when there are parent or clinician concerns that relate to various developmental stages...
December 2023: Paediatrics & Child Health
https://read.qxmd.com/read/38638395/empowering-hong-kong-chinese-families-with-autism-a-preliminary-study-of-the-online-hanen-more-than-words-program
#29
JOURNAL ARTICLE
Xin Qi, Qiwei Zhao, Carol K S To
PURPOSE: Parent involvement is crucial for tailored early intervention programs. The Hanen More Than Words (HMTW) program is a parent-implemented language intervention for autistic children. The current study examined the effectiveness of the HMTW program delivered online among Chinese families. METHODS: Using a randomized controlled trial design, 22 Chinese families of autistic children in Hong Kong completed the trial. Baseline and post-intervention assessments were conducted to measure changes in parent-child interaction, parents' use of linguistic facilitation techniques (LFTs), and children's communication skills...
2024: Autism & Developmental Language Impairments
https://read.qxmd.com/read/38638086/grey-matter-alterations-in-generalized-anxiety-disorder-a-voxel-wise-meta-analysis-of-voxel-based-morphometry-studies
#30
REVIEW
Chang-Hsien Ou, Chiu-Shih Cheng, Pei-Ling Lin, Cheng-Lung Lee
OBJECTIVE: Grey matter, a crucial component of the brain, has been found altered in generalized anxiety disorder (GAD) of several voxel-based morphometry studies. The conclusive and consistent grey matter alterations in GAD have not been confirmed. METHOD: Eleven voxel-based morphometry studies of GAD patients were included in the current systematic review and meta-analysis. The linear model of anxiety severity scores was applied to explore the relationship of grey matter alterations and anxiety severity...
April 18, 2024: International Journal of Developmental Neuroscience
https://read.qxmd.com/read/38638074/does-self-compassion-protect-adolescents-with-non-suicidal-self-injury-from-developing-borderline-features-a-two-wave-longitudinal-study
#31
JOURNAL ARTICLE
Diogo Carreiras, Paula Castilho, Marina Cunha
Background: Adolescence is a vulnerable developmental stage for the onset of non-suicidal self-injury (NSSI) and borderline features, which are related psychological phenomena. Self-compassion reflects a sensitivity to own suffering and a motivation to relieve it, consisting of a more positive and beneficial self-to-self relationship. The aim of the present study was to test the effect of self-compassion between borderline features at baseline and six months with a sample of adolescents with a history of NSSI...
April 18, 2024: Journal of Child and Adolescent Mental Health
https://read.qxmd.com/read/38637764/exploring-an-objective-measure-of-overactivity-in-children-with-rare-genetic-syndromes
#32
JOURNAL ARTICLE
Rory O'Sullivan, Stacey Bissell, Georgie Agar, Jayne Spiller, Andrew Surtees, Mary Heald, Emma Clarkson, Aamina Khan, Christopher Oliver, Andrew P Bagshaw, Caroline Richards
BACKGROUND: Overactivity is prevalent in several rare genetic neurodevelopmental syndromes, including Smith-Magenis syndrome, Angelman syndrome, and tuberous sclerosis complex, although has been predominantly assessed using questionnaire techniques. Threats to the precision and validity of questionnaire data may undermine existing insights into this behaviour. Previous research indicates objective measures, namely actigraphy, can effectively differentiate non-overactive children from those with attention-deficit hyperactivity disorder...
April 18, 2024: Journal of Neurodevelopmental Disorders
https://read.qxmd.com/read/38637762/neurobehavioral-outcomes-of-neonatal-asymptomatic-congenital-cytomegalovirus-infection-at-12-months
#33
JOURNAL ARTICLE
Sally M Stoyell, Jed T Elison, Emily Graupmann, Neely C Miller, Jessica Emerick, Elizabeth Ramey, Kristen Sandness, Mark R Schleiss, Erin A Osterholm
BACKGROUND: Congenital cytomegalovirus (cCMV) is the most common congenital viral infection in the United States. Symptomatic infections can cause severe hearing loss and neurological disability, although ~ 90% of cCMV infections are asymptomatic at birth. Despite its prevalence, the long-term neurobehavioral risks of asymptomatic cCMV infections are not fully understood. The objective of this work was to evaluate for potential long-term neurobehavioral sequelae in infants with asymptomatic cCMV...
April 18, 2024: Journal of Neurodevelopmental Disorders
https://read.qxmd.com/read/38637617/genome-wide-association-analyses-identify-95-risk-loci-and-provide-insights-into-the-neurobiology-of-post-traumatic-stress-disorder
#34
JOURNAL ARTICLE
Caroline M Nievergelt, Adam X Maihofer, Elizabeth G Atkinson, Chia-Yen Chen, Karmel W Choi, Jonathan R I Coleman, Nikolaos P Daskalakis, Laramie E Duncan, Renato Polimanti, Cindy Aaronson, Ananda B Amstadter, Soren B Andersen, Ole A Andreassen, Paul A Arbisi, Allison E Ashley-Koch, S Bryn Austin, Esmina Avdibegoviç, Dragan Babić, Silviu-Alin Bacanu, Dewleen G Baker, Anthony Batzler, Jean C Beckham, Sintia Belangero, Corina Benjet, Carisa Bergner, Linda M Bierer, Joanna M Biernacka, Laura J Bierut, Jonathan I Bisson, Marco P Boks, Elizabeth A Bolger, Amber Brandolino, Gerome Breen, Rodrigo Affonseca Bressan, Richard A Bryant, Angela C Bustamante, Jonas Bybjerg-Grauholm, Marie Bækvad-Hansen, Anders D Børglum, Sigrid Børte, Leah Cahn, Joseph R Calabrese, Jose Miguel Caldas-de-Almeida, Chris Chatzinakos, Sheraz Cheema, Sean A P Clouston, Lucía Colodro-Conde, Brandon J Coombes, Carlos S Cruz-Fuentes, Anders M Dale, Shareefa Dalvie, Lea K Davis, Jürgen Deckert, Douglas L Delahanty, Michelle F Dennis, Frank Desarnaud, Christopher P DiPietro, Seth G Disner, Anna R Docherty, Katharina Domschke, Grete Dyb, Alma Džubur Kulenović, Howard J Edenberg, Alexandra Evans, Chiara Fabbri, Negar Fani, Lindsay A Farrer, Adriana Feder, Norah C Feeny, Janine D Flory, David Forbes, Carol E Franz, Sandro Galea, Melanie E Garrett, Bizu Gelaye, Joel Gelernter, Elbert Geuze, Charles F Gillespie, Slavina B Goleva, Scott D Gordon, Aferdita Goçi, Lana Ruvolo Grasser, Camila Guindalini, Magali Haas, Saskia Hagenaars, Michael A Hauser, Andrew C Heath, Sian M J Hemmings, Victor Hesselbrock, Ian B Hickie, Kelleigh Hogan, David Michael Hougaard, Hailiang Huang, Laura M Huckins, Kristian Hveem, Miro Jakovljević, Arash Javanbakht, Gregory D Jenkins, Jessica Johnson, Ian Jones, Tanja Jovanovic, Karen-Inge Karstoft, Milissa L Kaufman, James L Kennedy, Ronald C Kessler, Alaptagin Khan, Nathan A Kimbrel, Anthony P King, Nastassja Koen, Roman Kotov, Henry R Kranzler, Kristi Krebs, William S Kremen, Pei-Fen Kuan, Bruce R Lawford, Lauren A M Lebois, Kelli Lehto, Daniel F Levey, Catrin Lewis, Israel Liberzon, Sarah D Linnstaedt, Mark W Logue, Adriana Lori, Yi Lu, Benjamin J Luft, Michelle K Lupton, Jurjen J Luykx, Iouri Makotkine, Jessica L Maples-Keller, Shelby Marchese, Charles Marmar, Nicholas G Martin, Gabriela A Martínez-Levy, Kerrie McAloney, Alexander McFarlane, Katie A McLaughlin, Samuel A McLean, Sarah E Medland, Divya Mehta, Jacquelyn Meyers, Vasiliki Michopoulos, Elizabeth A Mikita, Lili Milani, William Milberg, Mark W Miller, Rajendra A Morey, Charles Phillip Morris, Ole Mors, Preben Bo Mortensen, Mary S Mufford, Elliot C Nelson, Merete Nordentoft, Sonya B Norman, Nicole R Nugent, Meaghan O'Donnell, Holly K Orcutt, Pedro M Pan, Matthew S Panizzon, Gita A Pathak, Edward S Peters, Alan L Peterson, Matthew Peverill, Robert H Pietrzak, Melissa A Polusny, Bernice Porjesz, Abigail Powers, Xue-Jun Qin, Andrew Ratanatharathorn, Victoria B Risbrough, Andrea L Roberts, Alex O Rothbaum, Barbara O Rothbaum, Peter Roy-Byrne, Kenneth J Ruggiero, Ariane Rung, Heiko Runz, Bart P F Rutten, Stacey Saenz de Viteri, Giovanni Abrahão Salum, Laura Sampson, Sixto E Sanchez, Marcos Santoro, Carina Seah, Soraya Seedat, Julia S Seng, Andrey Shabalin, Christina M Sheerin, Derrick Silove, Alicia K Smith, Jordan W Smoller, Scott R Sponheim, Dan J Stein, Synne Stensland, Jennifer S Stevens, Jennifer A Sumner, Martin H Teicher, Wesley K Thompson, Arun K Tiwari, Edward Trapido, Monica Uddin, Robert J Ursano, Unnur Valdimarsdóttir, Miranda Van Hooff, Eric Vermetten, Christiaan H Vinkers, Joanne Voisey, Yunpeng Wang, Zhewu Wang, Monika Waszczuk, Heike Weber, Frank R Wendt, Thomas Werge, Michelle A Williams, Douglas E Williamson, Bendik S Winsvold, Sherry Winternitz, Christiane Wolf, Erika J Wolf, Yan Xia, Ying Xiong, Rachel Yehuda, Keith A Young, Ross McD Young, Clement C Zai, Gwyneth C Zai, Mark Zervas, Hongyu Zhao, Lori A Zoellner, John-Anker Zwart, Terri deRoon-Cassini, Sanne J H van Rooij, Leigh L van den Heuvel, Murray B Stein, Kerry J Ressler, Karestan C Koenen
Post-traumatic stress disorder (PTSD) genetics are characterized by lower discoverability than most other psychiatric disorders. The contribution to biological understanding from previous genetic studies has thus been limited. We performed a multi-ancestry meta-analysis of genome-wide association studies across 1,222,882 individuals of European ancestry (137,136 cases) and 58,051 admixed individuals with African and Native American ancestry (13,624 cases). We identified 95 genome-wide significant loci (80 new)...
April 18, 2024: Nature Genetics
https://read.qxmd.com/read/38637616/genetic-modifiers-of-rare-variants-in-monogenic-developmental-disorder-loci
#35
JOURNAL ARTICLE
Rebecca Kingdom, Robin N Beaumont, Andrew R Wood, Michael N Weedon, Caroline F Wright
Rare damaging variants in a large number of genes are known to cause monogenic developmental disorders (DDs) and have also been shown to cause milder subclinical phenotypes in population cohorts. Here, we show that carrying multiple (2-5) rare damaging variants across 599 dominant DD genes has an additive adverse effect on numerous cognitive and socioeconomic traits in UK Biobank, which can be partially counterbalanced by a higher educational attainment polygenic score (EA-PGS). Phenotypic deviators from expected EA-PGS could be partly explained by the enrichment or depletion of rare DD variants...
April 18, 2024: Nature Genetics
https://read.qxmd.com/read/38637242/clinical-decisions-in-fetal-neonatal-neurology-ii-gene-environment-expression-over-the-first-1000-days-presenting-as-four-great-neurological-syndromes
#36
REVIEW
Mark S Scher, Sonika Agarwal, Charu Venkatesen
Interdisciplinary fetal-neonatal neurology (FNN) training considers a woman's reproductive and pregnancy health histories when assessing the "four great neonatal neurological syndromes". This maternal-child dyad exemplifies the symptomatic neonatal minority, compared with the silent majority of healthy children who experience preclinical diseases with variable expressions over the first 1000 days. Healthy maternal reports with reassuring fetal surveillance testing preceded signs of fetal distress during parturition...
April 9, 2024: Seminars in Fetal & Neonatal Medicine
https://read.qxmd.com/read/38636773/thrombopoietin-exerts-a-neuroprotective-effect-by-inhibiting-the-suppression-of-neuronal-proliferation-and-axonal-outgrowth-in-intrauterine-growth-restriction-rats
#37
JOURNAL ARTICLE
Satoru Takeshita, Hiroki Kakita, Nami Nakamura, Mari Mori, Kohki Toriuchi, Hiromasa Aoki, Yasumichi Inoue, Hidetoshi Hayashi, Yasumasa Yamada, Mineyoshi Aoyama
Chronic hypoxia in utero causes intrauterine growth restriction (IUGR) of the fetus. IUGR infants are known to be at higher risk for neurodevelopmental disorders, but the mechanism is unclear. In this study, we analyzed the structure of the cerebral cortex using IUGR model rats generated through a reduced uterine perfusion pressure operation. IUGR rats exhibited thinner cerebral white matter and enlarged lateral ventricles compared with control rats. Expression of neuron cell markers, Satb2, microtubule-associated protein (MAP)-2, α-tubulin, and nestin was reduced in IUGR rats, indicating that neurons were diminished at various developmental stages in IUGR rats, from neural stem cells to mature neurons...
April 16, 2024: Experimental Neurology
https://read.qxmd.com/read/38636560/aging-as-a-loss-of-morphostatic-information-a-developmental-bioelectricity-perspective
#38
REVIEW
Léo Pio-Lopez, Michael Levin
Maintaining order at the tissue level is crucial throughout the lifespan, as failure can lead to cancer and an accumulation of molecular and cellular disorders. Perhaps, the most consistent and pervasive result of these failures is aging, which is characterized by the progressive loss of function and decline in the ability to maintain anatomical homeostasis and reproduce. This leads to organ malfunction, diseases, and ultimately death. The traditional understanding of aging is that it is caused by the accumulation of molecular and cellular damage...
April 16, 2024: Ageing Research Reviews
https://read.qxmd.com/read/38636559/towards-prolonging-ovarian-reproductive-life-insights-into-trace-elements-homeostasis
#39
REVIEW
Weicheng Tang, Xiaoran Zhu, Ying Chen, Shuhong Yang, Chuqing Wu, Dan Chen, Liru Xue, Yican Guo, Yun Dai, Simin Wei, Mingfu Wu, Meng Wu, Shixuan Wang
Ovarian aging is marked by a reduction in the quantity and quality of ovarian follicles, leading to a decline in female fertility and ovarian endocrine function. While the biological characteristics of ovarian aging are well-established, the exact mechanisms underlying this process remain elusive. Recent studies underscore the vital role of trace elements (TEs) in maintaining ovarian function. Imbalances in TEs can lead to ovarian aging, characterized by reduced enzyme activity, hormonal imbalances, ovulatory disorders, and decreased fertility...
April 16, 2024: Ageing Research Reviews
https://read.qxmd.com/read/38636517/identification-of-signaling-pathways-that-specify-a-subset-of-migrating-enteric-neural-crest-cells-at-the-wavefront-in-mouse-embryos
#40
JOURNAL ARTICLE
Bingyan Zhou, Chenzhao Feng, Song Sun, Xuyong Chen, Didi Zhuansun, Di Wang, Xiaosi Yu, Xinyao Meng, Jun Xiao, Luyao Wu, Jing Wang, Jing Wang, Ke Chen, Zejian Li, Jingyi You, Handan Mao, Shimin Yang, Jiaxin Zhang, Chunlei Jiao, Zhi Li, Donghai Yu, Xiaojuan Wu, Tianqi Zhu, Jixin Yang, Lei Xiang, Jiazhe Liu, Tailiang Chai, Juan Shen, Chuan-Xi Mao, Juncheng Hu, Xingjie Hao, Bo Xiong, Shan Zheng, Zhihua Liu, Jiexiong Feng
During enteric nervous system (ENS) development, pioneering wavefront enteric neural crest cells (ENCCs) initiate gut colonization. However, the molecular mechanisms guiding their specification and niche interaction are not fully understood. We used single-cell RNA sequencing and spatial transcriptomics to map the spatiotemporal dynamics and molecular landscape of wavefront ENCCs in mouse embryos. Our analysis shows a progressive decline in wavefront ENCC potency during migration and identifies transcription factors governing their specification and differentiation...
April 15, 2024: Developmental Cell
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