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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1998 1
2002 13
2003 4
2004 8
2005 4
2006 3
2007 4
2008 4
2009 11
2010 10
2011 13
2012 12
2013 13
2014 14
2015 15
2016 12
2017 17
2018 8
2019 10
2020 13
2021 15
2022 15
2023 7
2024 4

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201 results

Results by year

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Page 1
Rett syndrome: revised diagnostic criteria and nomenclature.
Neul JL, Kaufmann WE, Glaze DG, Christodoulou J, Clarke AJ, Bahi-Buisson N, Leonard H, Bailey ME, Schanen NC, Zappella M, Renieri A, Huppke P, Percy AK; RettSearch Consortium. Neul JL, et al. Among authors: kaufmann we. Ann Neurol. 2010 Dec;68(6):944-50. doi: 10.1002/ana.22124. Ann Neurol. 2010. PMID: 21154482 Free PMC article.
ABP1-TMK auxin perception for global phosphorylation and auxin canalization.
Friml J, Gallei M, Gelová Z, Johnson A, Mazur E, Monzer A, Rodriguez L, Roosjen M, Verstraeten I, Živanović BD, Zou M, Fiedler L, Giannini C, Grones P, Hrtyan M, Kaufmann WA, Kuhn A, Narasimhan M, Randuch M, Rýdza N, Takahashi K, Tan S, Teplova A, Kinoshita T, Weijers D, Rakusová H. Friml J, et al. Among authors: kaufmann wa. Nature. 2022 Sep;609(7927):575-581. doi: 10.1038/s41586-022-05187-x. Epub 2022 Sep 7. Nature. 2022. PMID: 36071161
Double-blind, randomized, placebo-controlled study of trofinetide in pediatric Rett syndrome.
Glaze DG, Neul JL, Kaufmann WE, Berry-Kravis E, Condon S, Stoms G, Oosterholt S, Della Pasqua O, Glass L, Jones NE, Percy AK; Rett 002 Study Group. Glaze DG, et al. Among authors: kaufmann we. Neurology. 2019 Apr 16;92(16):e1912-e1925. doi: 10.1212/WNL.0000000000007316. Epub 2019 Mar 27. Neurology. 2019. PMID: 30918097 Free PMC article. Clinical Trial.
Severity Assessment in CDKL5 Deficiency Disorder.
Demarest S, Pestana-Knight EM, Olson HE, Downs J, Marsh ED, Kaufmann WE, Partridge CA, Leonard H, Gwadry-Sridhar F, Frame KE, Cross JH, Chin RFM, Parikh S, Panzer A, Weisenberg J, Utley K, Jaksha A, Amin S, Khwaja O, Devinsky O, Neul JL, Percy AK, Benke TA. Demarest S, et al. Among authors: kaufmann we. Pediatr Neurol. 2019 Aug;97:38-42. doi: 10.1016/j.pediatrneurol.2019.03.017. Epub 2019 Mar 27. Pediatr Neurol. 2019. PMID: 31147226 Free PMC article. Review.
Multitier mechanics control stromal adaptations in the swelling lymph node.
Assen FP, Abe J, Hons M, Hauschild R, Shamipour S, Kaufmann WA, Costanzo T, Krens G, Brown M, Ludewig B, Hippenmeyer S, Heisenberg CP, Weninger W, Hannezo E, Luther SA, Stein JV, Sixt M. Assen FP, et al. Among authors: kaufmann wa. Nat Immunol. 2022 Aug;23(8):1246-1255. doi: 10.1038/s41590-022-01257-4. Epub 2022 Jul 11. Nat Immunol. 2022. PMID: 35817845 Free PMC article.
Effects of AFQ056 on language learning in fragile X syndrome.
Berry-Kravis E, Abbeduto L, Hagerman R, Coffey CS, Cudkowicz M, Erickson CA, McDuffie A, Hessl D, Ethridge L, Tassone F, Kaufmann WE, Friedmann K, Bullard L, Hoffmann A, Veenstra-VanderWeele J, Staley K, Klements D, Moshinsky M, Harkey B, Long J, Fedler J, Klingner E, Ecklund D, Costigan M, Huff T, Pearson B; NeuroNEXT FXLEARN Investigators. Berry-Kravis E, et al. Among authors: kaufmann we. J Clin Invest. 2023 Aug 31;134(5):e171723. doi: 10.1172/JCI171723. J Clin Invest. 2023. PMID: 37651202 Free PMC article. Clinical Trial.
Transcriptomic Studies in Mouse Models of Rett Syndrome: A Review.
Sanfeliu A, Kaufmann WE, Gill M, Guasoni P, Tropea D. Sanfeliu A, et al. Among authors: kaufmann we. Neuroscience. 2019 Aug 10;413:183-205. doi: 10.1016/j.neuroscience.2019.06.013. Epub 2019 Jun 21. Neuroscience. 2019. PMID: 31229631 Review.
The behavioral phenotype of FMR1 mutations.
Boyle L, Kaufmann WE. Boyle L, et al. Among authors: kaufmann we. Am J Med Genet C Semin Med Genet. 2010 Nov 15;154C(4):469-76. doi: 10.1002/ajmg.c.30277. Am J Med Genet C Semin Med Genet. 2010. PMID: 20981777 Review.
201 results