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Page 1
Tophaceous gout of the nose in a male FMR1 premutation carrier.
Tang SJ, Giri S, Pahlavan N, Han SH, Santos ER, Espinal G, Aishworiya R, Schneider A, Hessl D, Rivera SM, Hagerman RJ. Tang SJ, et al. Among authors: hessl d. Clin Case Rep. 2022 Nov 27;10(11):e6586. doi: 10.1002/ccr3.6586. eCollection 2022 Nov. Clin Case Rep. 2022. PMID: 36447664 Free PMC article.
Progression of tremor and ataxia in male carriers of the FMR1 premutation.
Leehey MA, Berry-Kravis E, Min SJ, Hall DA, Rice CD, Zhang L, Grigsby J, Greco CM, Reynolds A, Lara R, Cogswell J, Jacquemont S, Hessl DR, Tassone F, Hagerman R, Hagerman PJ. Leehey MA, et al. Among authors: hessl dr. Mov Disord. 2007 Jan 15;22(2):203-6. doi: 10.1002/mds.21252. Mov Disord. 2007. PMID: 17133502
Recommendations from multi-disciplinary focus groups on cascade testing and genetic counseling for fragile X-associated disorders.
McConkie-Rosell A, Abrams L, Finucane B, Cronister A, Gane LW, Coffey SM, Sherman S, Nelson LM, Berry-Kravis E, Hessl D, Chiu S, Street N, Vatave A, Hagerman RJ. McConkie-Rosell A, et al. Among authors: hessl d. J Genet Couns. 2007 Oct;16(5):593-606. doi: 10.1007/s10897-007-9099-y. Epub 2007 May 12. J Genet Couns. 2007. PMID: 17497108
Advances in the treatment of fragile X syndrome.
Hagerman RJ, Berry-Kravis E, Kaufmann WE, Ono MY, Tartaglia N, Lachiewicz A, Kronk R, Delahunty C, Hessl D, Visootsak J, Picker J, Gane L, Tranfaglia M. Hagerman RJ, et al. Among authors: hessl d. Pediatrics. 2009 Jan;123(1):378-90. doi: 10.1542/peds.2008-0317. Pediatrics. 2009. PMID: 19117905 Free PMC article. Review.
161 results