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PubPharm (53)
1
Optimizing Care for Autistic Patients in Health Care Settings : A Scoping Review and Call to Action
enthalten in:
Academic pediatrics
| 2024
von
Harris, H.
|
Weissman, L.
|
Friedlaender, E.
| +7
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2
Impairment Types and Combinations Among Adolescents and Young Adults with Disabilities : Colorado 2014-2018
enthalten in:
Academic pediatrics
| 2024
von
Chien, A.
|
Spence, S.
|
Okumura, M.
| +9
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3
Factors Associated With Underutilization of Genetic Testing in Autism Spectrum Disorders
enthalten in:
Pediatric neurology
| 2024
von
Abreu, N.
|
Chiujdea, M.
|
Liu, S.
| +2
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4
Clinical Characteristics of Seizures and Epilepsy in Individuals With Recurrent Deletions and Duplications in the 16p11.2 Region
enthalten in:
Neurology. Genetics
| 2022
von
Moufawad El Achkar, C.
|
Rosen, A.
|
Kessler, S.
| +9
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5
Barriers to Genetic Testing Faced by Pediatric Subspecialists in Autism Spectrum Disorders
enthalten in:
Advances in neurodevelopmental disorders
| 2022
von
Abreu, N.
|
Chiujdea, M.
|
Spence, S.
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6
Barriers to Genetic Testing Faced by Pediatric Subspecialists in Autism Spectrum Disorders
enthalten in:
Advances in neurodevelopmental disorders
| 2022
von
Abreu, N.
|
Chiujdea, M.
|
Spence, S.
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7
Predicting Autism Spectrum Disorder in Very Preterm Infants
enthalten in:
Pediatrics
| 2020
von
Soul, J.
|
Spence, S.
CommentOn: Pediatrics. 2020 Oct;146(4):. - PMID 32900877
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8
Evaluation and Management of the Child With Autism Spectrum Disorder
enthalten in:
Continuum (Minneapolis, Minn.)
| 2018
von
Baumer, N.
|
Spence, S.
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9
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
enthalten in:
Nature neuroscience
| 2017
von
C Yuen, R.
|
Merico, D.
|
Bookman, M.
| +80
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10
16p11.2 deletion and duplication : Characterizing neurologic phenotypes in a large clinically ascertained cohort
enthalten in:
American journal of medical genetics. Part A
| 2016
von
Steinman, K.
|
Spence, S.
|
Ramocki, M.
| +9
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