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In-depth investigations of adolescents and adults with holoprosencephaly identify unique characteristics.
Weiss K, Kruszka P, Guillen Sacoto MJ, Addissie YA, Hadley DW, Hadsall CK, Stokes B, Hu P, Roessler E, Solomon B, Wiggs E, Thurm A, Hufnagel RB, Zein WM, Hahn JS, Stashinko E, Levey E, Baldwin D, Clegg NJ, Delgado MR, Muenke M. Weiss K, et al. Among authors: wiggs e. Genet Med. 2018 Jan;20(1):14-23. doi: 10.1038/gim.2017.68. Epub 2017 Jun 22. Genet Med. 2018. PMID: 28640243 Free PMC article.
The neuropsychological phenotype of Chediak-Higashi disease.
Shirazi TN, Snow J, Ham L, Raglan GB, Wiggs EA, Summers AC, Toro C, Introne WJ. Shirazi TN, et al. Among authors: wiggs ea. Orphanet J Rare Dis. 2019 May 6;14(1):101. doi: 10.1186/s13023-019-1049-x. Orphanet J Rare Dis. 2019. PMID: 31060595 Free PMC article.
Executive Function and Adaptive Behavior in Muenke Syndrome.
Yarnell CM, Addissie YA, Hadley DW, Guillen Sacoto MJ, Agochukwu NB, Hart RA, Wiggs EA, Platte P, Paelecke Y, Collmann H, Schweitzer T, Kruszka P, Muenke M. Yarnell CM, et al. J Pediatr. 2015 Aug;167(2):428-34. doi: 10.1016/j.jpeds.2015.04.080. Epub 2015 May 28. J Pediatr. 2015. PMID: 26028288 Free PMC article.
Disease progression in C9orf72 mutation carriers.
Floeter MK, Traynor BJ, Farren J, Braun LE, Tierney M, Wiggs EA, Wu T. Floeter MK, et al. Among authors: wiggs ea. Neurology. 2017 Jul 18;89(3):234-241. doi: 10.1212/WNL.0000000000004115. Epub 2017 Jun 14. Neurology. 2017. PMID: 28615433 Free PMC article.
74 results