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Cyanosis in a Previously Well Child.
Bhat MA, Plunk MR, Basel DG, Hanson SJ. Bhat MA, et al. Among authors: basel dg. Pediatr Rev. 2021 Nov;42(11):619-624. doi: 10.1542/pir.2020-002055. Pediatr Rev. 2021. PMID: 34725222 No abstract available.
Pseudoarthrosis of the Ulna in Neurofibromatosis Type I.
McCoy G, Joyce J, Basel D, Siegel DH. McCoy G, et al. J Pediatr. 2016 Oct;177:330. doi: 10.1016/j.jpeds.2016.06.054. Epub 2016 Jul 22. J Pediatr. 2016. PMID: 27453377 No abstract available.
Adaptive behavior in young children with neurofibromatosis type 1.
Klein-Tasman BP, Colon AM, Brei N, van der Fluit F, Casnar CL, Janke KM, Basel D, Siegel DH, Walker JA. Klein-Tasman BP, et al. Int J Pediatr. 2013;2013:690432. doi: 10.1155/2013/690432. Epub 2013 Nov 19. Int J Pediatr. 2013. PMID: 24348581 Free PMC article.
Molecular mechanics and dynamic simulations of well-known Kabuki syndrome-associated KDM6A variants reveal putative mechanisms of dysfunction.
Chi YI, Stodola TJ, De Assuncao TM, Leverence EN, Tripathi S, Dsouza NR, Mathison AJ, Basel DG, Volkman BF, Smith BC, Lomberk G, Zimmermann MT, Urrutia R. Chi YI, et al. Among authors: basel dg. Orphanet J Rare Dis. 2021 Feb 5;16(1):66. doi: 10.1186/s13023-021-01692-w. Orphanet J Rare Dis. 2021. PMID: 33546721 Free PMC article.
Liver failure and x-linked immunodeficiency type 47.
Gumm AJ, Basel DG, Thakrar P, Suchi M, Telega G. Gumm AJ, et al. Among authors: basel dg. Pediatr Transplant. 2020 Dec;24(8):e13808. doi: 10.1111/petr.13808. Epub 2020 Aug 13. Pediatr Transplant. 2020. PMID: 32790950
Association of Piebaldism, multiple café-au-lait macules, and intertriginous freckling: clinical evidence of a common pathway between KIT and sprouty-related, ena/vasodilator-stimulated phosphoprotein homology-1 domain containing protein 1 (SPRED1).
Chiu YE, Dugan S, Basel D, Siegel DH. Chiu YE, et al. Pediatr Dermatol. 2013 May-Jun;30(3):379-82. doi: 10.1111/j.1525-1470.2012.01858.x. Epub 2012 Sep 28. Pediatr Dermatol. 2013. PMID: 23016555 Free PMC article.
70 results