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Page 1
Introduction.
Sherr EH. Sherr EH. Semin Pediatr Neurol. 2009 Sep;16(3):99-100. doi: 10.1016/j.spen.2009.07.004. Semin Pediatr Neurol. 2009. PMID: 19778706 No abstract available.
Evidence report: Genetic and metabolic testing on children with global developmental delay: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.
Michelson DJ, Shevell MI, Sherr EH, Moeschler JB, Gropman AL, Ashwal S. Michelson DJ, et al. Among authors: sherr eh. Neurology. 2011 Oct 25;77(17):1629-35. doi: 10.1212/WNL.0b013e3182345896. Epub 2011 Sep 28. Neurology. 2011. PMID: 21956720 Review.
Clinical Reasoning: An encephalopathic 3-day-old infant.
Gelfand AA, Sznewajs A, Glass HC, Jelin AC, Sherr EH. Gelfand AA, et al. Among authors: sherr eh. Neurology. 2011 Jul 5;77(1):e1-5. doi: 10.1212/WNL.0b013e3182231407. Neurology. 2011. PMID: 21727263 Free PMC article. No abstract available.
NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects.
Lu W, Quintero-Rivera F, Fan Y, Alkuraya FS, Donovan DJ, Xi Q, Turbe-Doan A, Li QG, Campbell CG, Shanske AL, Sherr EH, Ahmad A, Peters R, Rilliet B, Parvex P, Bassuk AG, Harris DJ, Ferguson H, Kelly C, Walsh CA, Gronostajski RM, Devriendt K, Higgins A, Ligon AH, Quade BJ, Morton CC, Gusella JF, Maas RL. Lu W, et al. Among authors: sherr eh. PLoS Genet. 2007 May 25;3(5):e80. doi: 10.1371/journal.pgen.0030080. PLoS Genet. 2007. PMID: 17530927 Free PMC article.
160 results