Validation of a Paralimbic-Related Subcortical Brain Dysmaturation MRI Score in Infants with Congenital Heart Disease.

Autor: Reynolds, William T., Votava-Smith, Jodie K., Gabriel, George, Lee, Vincent K., Rajagopalan, Vidya, Wu, Yijen, Liu, Xiaoqin, Yagi, Hisato, Slabicki, Ruby, Gibbs, Brian, Tran, Nhu N., Weisert, Molly, Cabral, Laura, Subramanian, Subramanian, Wallace, Julia, del Castillo, Sylvia, Baust, Tracy, Weinberg, Jacqueline G., Lorenzi Quigley, Lauren, Gaesser, Jenna

Publikováno v: Journal of Clinical Medicine; Oct2024, Vol. 13 Issue 19, p5772, 34p

16 - Neurology

Autor: Safier, Robert A., Cleves-Bayon, Catalina, Gaesser, Jenna

Publikováno v: In Zitelli and Davis’ Atlas of Pediatric Physical Diagnosis Edition: Eighth Edition. 2023:562-592

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Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency (Genetics in Medicine, (2021), 23, 9, (1705-1714), 10.1038/s41436-021-01194-x)

Autor: Wortmann, Saskia B., Ziętkiewicz, Szymon, Guerrero-Castillo, Sergio, Feichtinger, René G., Wagner, Matias, Russell, Jacqui, Ellaway, Carolyn, Mróz, Dagmara, Wyszkowski, Hubert, Weis, Denisa, Hannibal, Iris, von Stülpnagel, Celina, Cabrera-Orefice, Alfredo, Lichter-Konecki, Uta, Gaesser, Jenna, Windreich, Randy, Myers, Kasiani C., Lorsbach, Robert, Dale, Russell C., Gersting, Søren, Prada, Carlos E., Christodoulou, John, Wolf, Nicole I., Venselaar, Hanka, Mayr, Johannes A., Wevers, Ron A.

Publikováno v: Genetics in Medicine, 23(9). Lippincott Williams and Wilkins
Wortmann, S B, Ziętkiewicz, S, Guerrero-Castillo, S, Feichtinger, R G, Wagner, M, Russell, J, Ellaway, C, Mróz, D, Wyszkowski, H, Weis, D, Hannibal, I, von Stülpnagel, C, Cabrera-Orefice, A, Lichter-Konecki, U, Gaesser, J, Windreich, R, Myers, K C, Lorsbach, R, Dale, R C, Gersting, S, Prada, C E, Christodoulou, J, Wolf, N I, Venselaar, H, Mayr, J A & Wevers, R A 2021, ' Correction to : Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency (Genetics in Medicine, (2021), 23, 9, (1705-1714), 10.1038/s41436-021-01194-x) ', Genetics in Medicine, vol. 23, no. 9, pp. 1789 . https://doi.org/10.1038/s41436-021-01280-0

Unfortunately the funding information was not given. Funding is as follows: This work was funded by the ERA PerMed project PerMiM (Austrian Science Fund FWF, I4704-B) to S.B.W. This study was supported by a “Sonata Bis 5” grant of the National Sc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7604daffb7dc71b596b79e782c1f40dd
https://research.vumc.nl/en/publications/26ef6ee5-7c81-49b0-bc79-4ba302df7fe2

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