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Did you mean westerman r (278 results)?
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy.
Fehlings DL, Zarrei M, Engchuan W, Sondheimer N, Thiruvahindrapuram B, MacDonald JR, Higginbotham EJ, Thapa R, Behlim T, Aimola S, Switzer L, Ng P, Wei J, Danthi PS, Pellecchia G, Lamoureux S, Ho K, Pereira SL, de Rijke J, Sung WWL, Mowjoodi A, Howe JL, Nalpathamkalam T, Manshaei R, Ghaffari S, Whitney J, Patel RV, Hamdan O, Shaath R, Trost B, Knights S, Samdup D, McCormick A, Hunt C, Kirton A, Kawamura A, Mesterman R, Gorter JW, Dlamini N, Merico D, Hilali M, Hirschfeld K, Grover K, Bautista NX, Han K, Marshall CR, Yuen RKC, Subbarao P, Azad MB, Turvey SE, Mandhane P, Moraes TJ, Simons E, Maxwell G, Shevell M, Costain G, Michaud JL, Hamdan FF, Gauthier J, Uguen K, Stavropoulos DJ, Wintle RF, Oskoui M, Scherer SW. Fehlings DL, et al. Among authors: mesterman r. Nat Genet. 2024 Apr;56(4):585-594. doi: 10.1038/s41588-024-01686-x. Epub 2024 Mar 29. Nat Genet. 2024. PMID: 38553553
Definition and classification of hyperkinetic movements in childhood.
Sanger TD, Chen D, Fehlings DL, Hallett M, Lang AE, Mink JW, Singer HS, Alter K, Ben-Pazi H, Butler EE, Chen R, Collins A, Dayanidhi S, Forssberg H, Fowler E, Gilbert DL, Gorman SL, Gormley ME Jr, Jinnah HA, Kornblau B, Krosschell KJ, Lehman RK, MacKinnon C, Malanga CJ, Mesterman R, Michaels MB, Pearson TS, Rose J, Russman BS, Sternad D, Swoboda KJ, Valero-Cuevas F. Sanger TD, et al. Among authors: mesterman r. Mov Disord. 2010 Aug 15;25(11):1538-49. doi: 10.1002/mds.23088. Mov Disord. 2010. PMID: 20589866 Free PMC article. Review.
The Pediatric Autism Research Cohort (PARC) Study: protocol for a patient-oriented prospective study examining trajectories of functioning in children with autism.
Kata A, McPhee PG, Chen YJ, Zwaigenbaum L, Singal D, Roncadin C, Bennett T, Carter M, Di Rezze B, Drmic I, Duku E, Fournier S, Frei J, Gentles SJ, Georgiades K, Hanlon-Dearman A, Hoult L, Kelley E, Koller J, de Camargo OK, Lai J, Mahoney B, Mesterman R, Ng O, Robertson S, Rosenbaum P, Salt M, Zubairi MS, Georgiades S. Kata A, et al. Among authors: mesterman r. BMJ Open. 2024 Apr 29;14(4):e083045. doi: 10.1136/bmjopen-2023-083045. BMJ Open. 2024. PMID: 38684247 Free PMC article.
Answering the call: co-designing a global trials network for cerebral palsy.
Novak I, Fahey M, Dan B, Craig S, Griffin A, Gross P, Justiniano MD, Webb A, Namara MM, Nielsen JB, Snelling T, Ritterband-Rosenbaum A, Shrader MW; CP Global Clinical Trials Network. Novak I, et al. Lancet Reg Health Eur. 2024 Jul 26;44:101015. doi: 10.1016/j.lanepe.2024.101015. eCollection 2024 Sep. Lancet Reg Health Eur. 2024. PMID: 39444706 Free PMC article. No abstract available.
Missense variants in the N-terminal domain of the A isoform of FHF2/FGF13 cause an X-linked developmental and epileptic encephalopathy.
Fry AE, Marra C, Derrick AV, Pickrell WO, Higgins AT, Te Water Naude J, McClatchey MA, Davies SJ, Metcalfe KA, Tan HJ, Mohanraj R, Avula S, Williams D, Brady LI, Mesterman R, Tarnopolsky MA, Zhang Y, Yang Y, Wang X; Genomics England Research Consortium; Rees MI, Goldfarb M, Chung SK. Fry AE, et al. Among authors: mesterman r. Am J Hum Genet. 2021 Jan 7;108(1):176-185. doi: 10.1016/j.ajhg.2020.10.017. Epub 2020 Nov 26. Am J Hum Genet. 2021. PMID: 33245860 Free PMC article.
An Infant With Persistent Failure to Thrive.
Shethwala S, Mesterman R, Kam A. Shethwala S, et al. Among authors: mesterman r. Clin Pediatr (Phila). 2016 Jan;55(1):93-6. doi: 10.1177/0009922815584222. Epub 2015 Apr 29. Clin Pediatr (Phila). 2016. PMID: 25926670 No abstract available.
33 results