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Page 1
CERT1 mutations perturb human development by disrupting sphingolipid homeostasis.
Gehin C, Lone MA, Lee W, Capolupo L, Ho S, Adeyemi AM, Gerkes EH, Stegmann AP, López-Martín E, Bermejo-Sánchez E, Martínez-Delgado B, Zweier C, Kraus C, Popp B, Strehlow V, Gräfe D, Knerr I, Jones ER, Zamuner S, Abriata LA, Kunnathully V, Moeller BE, Vocat A, Rommelaere S, Bocquete JP, Ruchti E, Limoni G, Van Campenhoudt M, Bourgeat S, Henklein P, Gilissen C, van Bon BW, Pfundt R, Willemsen MH, Schieving JH, Leonardi E, Soli F, Murgia A, Guo H, Zhang Q, Xia K, Fagerberg CR, Beier CP, Larsen MJ, Valenzuela I, Fernández-Álvarez P, Xiong S, Śmigiel R, López-González V, Armengol L, Morleo M, Selicorni A, Torella A, Blyth M, Cooper NS, Wilson V, Oegema R, Herenger Y, Garde A, Bruel AL, Tran Mau-Them F, Maddocks AB, Bain JM, Bhat MA, Costain G, Kannu P, Marwaha A, Champaigne NL, Friez MJ, Richardson EB, Gowda VK, Srinivasan VM, Gupta Y, Lim TY, Sanna-Cherchi S, Lemaitre B, Yamaji T, Hanada K, Burke JE, Jakšić AM, McCabe BD, De Los Rios P, Hornemann T, D'Angelo G, Gennarino VA. Gehin C, et al. Among authors: maddocks ab. J Clin Invest. 2023 May 15;133(10):e165019. doi: 10.1172/JCI165019. J Clin Invest. 2023. PMID: 36976648 Free PMC article.
Approach to New-Onset Psychosis in Pediatrics: A Review of Current Practice and an Interdisciplinary Consensus-Driven Clinical Pathway at a Single-Center Institution.
Jonokuchi AJ, Fenster DB, McCann TA, Gangopadhyay M, Giordano M, Maddocks AB, Ekladios M, Turek CM, Mroczkowski MM, Jamal N, Vargas WS. Jonokuchi AJ, et al. Among authors: maddocks ab. J Child Neurol. 2023 Mar;38(3-4):216-222. doi: 10.1177/08830738231156804. Epub 2023 Feb 21. J Child Neurol. 2023. PMID: 37165651 Review.
Understanding Bilateral Skull Fractures in Infancy: A Retrospective Multicenter Case Review.
O'Hara MA, Valvano TJ, Kashyap M, Daly JC, Bachim AN, Care MM, Egge MK, Kondis JS, Lenane AM, Maddocks ABR, Metz JB, Nielsen AK, Reeder KN, Ruda MT, Segal R, Sugarman JM, Weeks K, Oral R. O'Hara MA, et al. Among authors: maddocks abr. Pediatr Emerg Care. 2023 May 1;39(5):329-334. doi: 10.1097/PEC.0000000000002704. Epub 2022 Apr 13. Pediatr Emerg Care. 2023. PMID: 35413039
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: maddocks abr. 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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