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Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome.
Baker EK, Arpone M, Vera SA, Bretherton L, Ure A, Kraan CM, Bui M, Ling L, Francis D, Hunter MF, Elliott J, Rogers C, Field MJ, Cohen J, Maria LS, Faundes V, Curotto B, Morales P, Trigo C, Salas I, Alliende AM, Amor DJ, Godler DE. Baker EK, et al. Among authors: ure a. J Neurodev Disord. 2019 Dec 26;11(1):41. doi: 10.1186/s11689-019-9288-7. J Neurodev Disord. 2019. PMID: 31878865 Free PMC article.
FMR1 mRNA from full mutation alleles is associated with ABC-CFX scores in males with fragile X syndrome.
Baker EK, Arpone M, Kraan C, Bui M, Rogers C, Field M, Bretherton L, Ling L, Ure A, Cohen J, Hunter MF, Santa María L, Faundes V, Curotto B, Morales P, Trigo C, Salas I, Alliende A, Amor DJ, Godler DE. Baker EK, et al. Among authors: ure a. Sci Rep. 2020 Jul 16;10(1):11701. doi: 10.1038/s41598-020-68465-6. Sci Rep. 2020. PMID: 32678152 Free PMC article.
Autism: One or many spectrums?
Ure A, Rose V, Bernie C, Williams K. Ure A, et al. J Paediatr Child Health. 2018 Oct;54(10):1068-1072. doi: 10.1111/jpc.14176. J Paediatr Child Health. 2018. PMID: 30294997
Delineating the autistic phenotype in children with neurofibromatosis type 1.
Chisholm AK, Haebich KM, Pride NA, Walsh KS, Lami F, Ure A, Maloof T, Brignell A, Rouel M, Granader Y, Maier A, Barton B, Darke H, Dabscheck G, Anderson VA, Williams K, North KN, Payne JM. Chisholm AK, et al. Among authors: ure a. Mol Autism. 2022 Jan 4;13(1):3. doi: 10.1186/s13229-021-00481-3. Mol Autism. 2022. PMID: 34983638 Free PMC article.
77 results