scholarly journals Role of interventional radiology in pregnancy complicated by placenta accreta spectrum disorder: systematic review and meta-analysis

2019 ◽  
Vol 53 (6) ◽  
pp. 743-751 ◽  
Author(s):  
F. D'Antonio ◽  
A. Iacovelli ◽  
M. Liberati ◽  
M. Leombroni ◽  
D. Murgano ◽  
...  
Keyword(s):  
Systematic Review ◽  
Interventional Radiology ◽  
Placenta Accreta ◽  
Meta Analysis ◽  
Spectrum Disorder ◽  
Placenta Accreta Spectrum ◽  
In Pregnancy

Role of Interventional Radiology in Pregnancy Complicated by Placenta Accreta Spectrum Disorder

2019 ◽  
Vol 74 (11) ◽  
pp. 641-643
Author(s):  
F. DʼAntonio ◽  
A. Iacovelli ◽  
M. Liberati ◽  
M. Leombroni ◽  
D. Murgano ◽  
...  
Keyword(s):  
Interventional Radiology ◽  
Placenta Accreta ◽  
Spectrum Disorder ◽  
Placenta Accreta Spectrum ◽  
In Pregnancy

scholarly journals A systematic review and meta-analysis of studies on metaphor comprehension in individuals with autism spectrum disorder: Do task properties matter?

2019 ◽  
Vol 40 (6) ◽  
pp. 1421-1454 ◽  
Author(s):  
Tamar Kalandadze ◽  
Valentina Bambini ◽  
Kari-Anne B. Næss
Keyword(s):  
Systematic Review ◽  
Autism Spectrum Disorder ◽  
Syntactic Structure ◽  
Meta Analysis ◽  
Autism Spectrum ◽  
Spectrum Disorder ◽  
Response Format ◽  
Metaphor Comprehension ◽  
The Relationship

AbstractIndividuals with autism spectrum disorder (ASD) often experience difficulty in comprehending metaphors compared to individuals with typical development (TD). However, there is a large variation in the results across studies, possibly related to the properties of the metaphor tasks. This preregistered systematic review and meta-analysis (a) explored the properties of the metaphor tasks used in ASD research, and (b) investigated the group difference between individuals with ASD and TD on metaphor comprehension, as well as the relationship between the task properties and any between-study variation. A systematic search was undertaken in seven relevant databases. Fourteen studies fulfilled our predetermined inclusion criteria. Across tasks, we detected four types of response format and a great variety of metaphors in terms of familiarity, syntactic structure, and linguistic context. Individuals with TD outperformed individuals with ASD on metaphor comprehension (Hedges’ g = −0.63). Verbal explanation response format was utilized in the study showing the largest effect size in the group comparison. However, due to the sparse experimental manipulations, the role of task properties could not be established. Future studies should consider and report task properties to determine their role in metaphor comprehension, and to inform experimental paradigms as well as educational assessment.

scholarly journals Prevalence and main outcomes of placenta accreta spectrum: a systematic review and meta-analysis

2019 ◽  
Vol 221 (3) ◽  
pp. 208-218 ◽  
Author(s):  
Eric Jauniaux ◽  
Catey Bunce ◽  
Lene Grønbeck ◽  
Jens Langhoff-Roos
Keyword(s):  
Systematic Review ◽  
Placenta Accreta ◽  
Meta Analysis ◽  
Placenta Accreta Spectrum

Role of Ultrasound and MRI in Diagnosis of Severe Placenta Accreta Spectrum Disorder: An Intraindividual Assessment With Emphasis on Placental Bulge

2021 ◽  
Author(s):  
Shanigarn Thiravit ◽  
Kimberly Ma ◽  
Inessa Goldman ◽  
Pharuhas Chanprapaph ◽  
Priyanka Jha ◽  
...  
Keyword(s):  
Placenta Accreta ◽  
Spectrum Disorder ◽  
Placenta Accreta Spectrum

scholarly journals VP46.05: Risk factors, histopathology and diagnostic accuracy of posterior placenta accreta spectrum disorders: systematic review and meta‐analysis

2020 ◽  
Vol 56 (S1) ◽  
pp. 269-269
Author(s):  
S. Tinari ◽  
D. Buca ◽  
G. Cali ◽  
I.E. Timor‐Tritsch ◽  
J. Palacios‐Jaraquemada ◽  
...  
Keyword(s):  
Risk Factors ◽  
Systematic Review ◽  
Diagnostic Accuracy ◽  
Placenta Accreta ◽  
Meta Analysis ◽  
Placenta Accreta Spectrum ◽  
Spectrum Disorders

scholarly journals Association of Allelic Variants of the Reelin Gene with Autistic Spectrum Disorder: A Systematic Review and Meta-Analysis of Candidate Gene Association Studies

2020 ◽  
Vol 17 (21) ◽  
pp. 8010
Author(s):  
Ignacio Hernández-García ◽  
Antonio-Javier Chamorro ◽  
Hugo Guillermo Ternavasio-de la Vega ◽  
Cristina Carbonell ◽  
Miguel Marcos ◽  
...  
Keyword(s):  
Systematic Review ◽  
Genetic Variants ◽  
Autistic Spectrum Disorder ◽  
Association Studies ◽  
Meta Analysis ◽  
Spectrum Disorder ◽  
Current Evidence ◽  
Triplet Repeat ◽  
Autistic Spectrum

Autistic spectrum disorder (ASD) is a complex neurodevelopmental disability with a genetic basis, and several studies have suggested a potential role of the reelin gene (RELN) in ASD susceptibility. Accordingly, genetic association studies have explored this potential association, but the results have been controversial thus far. For this reason, we assessed the association of four genetic variants of RELN (the 5′UTR CGG triplet repeat and polymorphisms rs736707, rs362691, and rs2229864) with ASD by means of a systematic review and meta-analysis. We retrieved studies comparing the distribution of the above-mentioned genetic variants between ASD patients and healthy controls. A meta-analysis was conducted using a random effects model, and calculations of the odds ratios (ORs) and confidence intervals (CIs) were performed. A sensitivity analysis and tests to determine the heterogeneity of the results were also performed. Eleven previous studies fulfilled the inclusion criteria and analyzed the association of the above-mentioned genetic variants and ASD. We did not find any significant association between the allele or genotype frequencies of the analyzed polymorphisms and ASD, and large heterogeneity was found for the rs736707 polymorphism. Moreover, no significant differences were found between the 5′UTR triplet repeat and this disorder. In light of current evidence, no single genetic variant within this gene is clearly associated with the development of ASD, and ethnic differences may explain part of the observed heterogeneity. Larger studies among different ethnic groups are needed to establish the role of specific genetic variants within RELN in the etiology of this disorder.

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