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Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2021 | 3 |
2022 | 2 |
2023 | 0 |
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Page 1
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thorberg o[au]
(3 results)?
A disease-causing variant in HNRNPH2 inherited from an unaffected mother with skewed X-inactivation.
Am J Med Genet A. 2022 Feb;188(2):668-671. doi: 10.1002/ajmg.a.62549. Epub 2021 Oct 31.
Am J Med Genet A. 2022.
PMID: 34719854
No abstract available.
Convolutional neural network-aided tuber segmentation in tuberous sclerosis complex patients correlates with electroencephalogram.
Park DK, Kim W, Thornburg OS, McBrian DK, McKhann GM, Feldstein NA, Maddocks AB, Gonzalez E, Shen MY, Akman C, Provenzano FA.
Park DK, et al. Among authors: thornburg os.
Epilepsia. 2022 Jun;63(6):1530-1541. doi: 10.1111/epi.17227. Epub 2022 Mar 31.
Epilepsia. 2022.
PMID: 35301716
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Cross-sectional, quantitative analysis of motor function in females with HNRNPH2-related disorder.
Salazar R, Beenders S, LaMarca NM, Thornburg O, Rubin-Thompson L, Snow A, Goldman S, Chung WK, Bain JM.
Salazar R, et al. Among authors: thornburg o.
Res Dev Disabil. 2021 Dec;119:104110. doi: 10.1016/j.ridd.2021.104110. Epub 2021 Nov 16.
Res Dev Disabil. 2021.
PMID: 34794115
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Detailed Clinical and Psychological Phenotype of the X-linked HNRNPH2-Related Neurodevelopmental Disorder.
Bain JM, Thornburg O, Pan C, Rome-Martin D, Boyle L, Fan X, Devinsky O, Frye R, Hamp S, Keator CG, LaMarca NM, Maddocks ABR, Madruga-Garrido M, Niederhoffer KY, Novara F, Peron A, Poole-Di Salvo E, Salazar R, Skinner SA, Soares G, Goldman S, Chung WK.
Bain JM, et al. Among authors: thornburg o.
Neurol Genet. 2021 Jan 29;7(1):e551. doi: 10.1212/NXG.0000000000000551. eCollection 2021 Feb.
Neurol Genet. 2021.
PMID: 33728377
Free PMC article.
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