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1.
Race, ethnicity, and ancestry reporting in genetic counseling research: A focused mapping review and synthesis.
J Genet Couns
; 2024 Feb 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-38362950
2.
Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome.
Am J Med Genet A
; 191(2): 357-369, 2023 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-36349505
3.
Concussion Knowledge and Self-Reported Behaviors in Youth Rugby Players and Their Coaches: A Population-Wide Cross-Sectional Survey.
Clin J Sport Med
; 33(5): 541-551, 2023 09 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-37185576
4.
Missed intracranial injuries are rare in emergency departments using the PECARN head injury decision rules.
Childs Nerv Syst
; 37(1): 55-62, 2021 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32424442
5.
Cognitive, behavioral, and social functioning in children and adults with Dravet syndrome.
Epilepsy Behav
; 112: 107319, 2020 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-32858363
6.
External validation of the DIVA and DIVA3 clinical predictive rules to identify difficult intravenous access in paediatric patients.
Emerg Med J
; 37(12): 762-767, 2020 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-33082150
7.
DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome.
Int J Mol Sci
; 21(20)2020 Oct 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-33086711
8.
Accuracy of NEXUS II head injury decision rule in children: a prospective PREDICT cohort study.
Emerg Med J
; 36(1): 4-11, 2019 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-30127072
9.
Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing.
Int J Mol Sci
; 20(16)2019 Aug 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-31405222
10.
Penetrating head injuries in children presenting to the emergency department in Australia and New Zealand: A PREDICT prospective study.
J Paediatr Child Health
; 54(8): 861-865, 2018 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-29579354
11.
Partially methylated alleles, microdeletion, and tissue mosaicism in a fragile X male with tremor and ataxia at 30 years of age: A case report.
Am J Med Genet A
; 170(12): 3327-3332, 2016 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-27696642
12.
Emotion recognition from facial expressions: a normative study of the Ekman 60-Faces Test in the Italian population.
Neurol Sci
; 35(7): 1015-21, 2014 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-24442557
13.
Effectiveness of a Novel Tablet Application in Reducing Guideline Deviations During Pediatric Cardiac Arrest: A Randomized Clinical Trial.
JAMA Netw Open
; 6(8): e2327272, 2023 08 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-37535352
14.
The impact of cognitive aids on resuscitation performance in in-hospital cardiac arrest scenarios: a systematic review and meta-analysis.
Intern Emerg Med
; 17(7): 2143-2158, 2022 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-36031672
15.
Agreement between parents' and clinical researchers' ratings of behavioral problems in children with fragile X syndrome and chromosome 15 imprinting disorders.
Res Dev Disabil
; 131: 104338, 2022 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-36179574
16.
PediAppRREST: effectiveness of an interactive cognitive support tablet app in reducing deviations from guidelines in the management of paediatric cardiac arrest: protocol for a simulation-based randomised controlled trial.
BMJ Open
; 11(7): e047208, 2021 07 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-34321297
17.
Development and Usability of a Novel Interactive Tablet App (PediAppRREST) to Support the Management of Pediatric Cardiac Arrest: Pilot High-Fidelity Simulation-Based Study.
JMIR Mhealth Uhealth
; 8(10): e19070, 2020 10 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32788142
18.
FMR1 mRNA from full mutation alleles is associated with ABC-CFX scores in males with fragile X syndrome.
Sci Rep
; 10(1): 11701, 2020 07 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-32678152
19.
Clinical and Molecular Differences between 4-Year-Old Monozygous Male Twins Mosaic for Normal, Premutation and Fragile X Full Mutation Alleles.
Genes (Basel)
; 10(4)2019 04 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-30959842
20.
Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome.
J Neurodev Disord
; 11(1): 41, 2019 12 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-31878865