Hagerman RJ - Search Results

1

Cognitive, anxiety and mood disorders in the fragile X-associated tremor/ataxia syndrome.

Bourgeois JA, Cogswell JB, Hessl D, Zhang L, Ono MY, Tassone F, Farzin F, Brunberg JA, Grigsby J, Hagerman RJ. Bourgeois JA, et al. Among authors: hagerman rj. Gen Hosp Psychiatry. 2007 Jul-Aug;29(4):349-56. doi: 10.1016/j.genhosppsych.2007.03.003. Gen Hosp Psychiatry. 2007. PMID: 17591512 Free PMC article.

2

Verbal learning and memory among heterozygous fragile X females.

Grigsby J, Kemper MB, Hagerman RJ. Grigsby J, et al. Among authors: hagerman rj. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):111-5. doi: 10.1002/ajmg.1320430116. Am J Med Genet. 1992. PMID: 1605177

3

Neuropsychological dysfunction among affected heterozygous fragile X females.

Grigsby JP, Kemper MB, Hagerman RJ, Myers CS. Grigsby JP, et al. Among authors: hagerman rj. Am J Med Genet. 1990 Jan;35(1):28-35. doi: 10.1002/ajmg.1320350107. Am J Med Genet. 1990. PMID: 1689106

4

Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: a preliminary report.

Miller LJ, McIntosh DN, McGrath J, Shyu V, Lampe M, Taylor AK, Tassone F, Neitzel K, Stackhouse T, Hagerman RJ. Miller LJ, et al. Among authors: hagerman rj. Am J Med Genet. 1999 Apr 2;83(4):268-79. Am J Med Genet. 1999. PMID: 10208160

5

Compound heterozygous female with fragile X syndrome.

Linden MG, Tassone F, Gane LW, Hills JL, Hagerman RJ, Taylor AK. Linden MG, et al. Among authors: hagerman rj. Am J Med Genet. 1999 Apr 2;83(4):318-21. Am J Med Genet. 1999. PMID: 10208169

6

Tissue heterogeneity of the FMR1 mutation in a high-functioning male with fragile X syndrome.

Taylor AK, Tassone F, Dyer PN, Hersch SM, Harris JB, Greenough WT, Hagerman RJ. Taylor AK, et al. Among authors: hagerman rj. Am J Med Genet. 1999 May 28;84(3):233-9. Am J Med Genet. 1999. PMID: 10331599

7

Tassone F, Hagerman RJ, Gane LW, Taylor AK. Tassone F, et al. Among authors: hagerman rj. Am J Med Genet. 1999 May 28;84(3):240-4. Am J Med Genet. 1999. PMID: 10331600

8

FMRP expression as a potential prognostic indicator in fragile X syndrome.

Tassone F, Hagerman RJ, Iklé DN, Dyer PN, Lampe M, Willemsen R, Oostra BA, Taylor AK. Tassone F, et al. Among authors: hagerman rj. Am J Med Genet. 1999 May 28;84(3):250-61. Am J Med Genet. 1999. PMID: 10331602

9

Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development.

Freedenberg DL, Gane LW, Richards CS, Lampe M, Hills J, O'Connor R, Manchester D, Taylor A, Tassone F, Hulseberg D, Hagerman RJ, Patil SR. Freedenberg DL, et al. Among authors: hagerman rj. Am J Med Genet. 1999 Jul 30;85(3):197-201. doi: 10.1002/(sici)1096-8628(19990730)85:3<197::aid-ajmg1>3.0.co;2-o. Am J Med Genet. 1999. PMID: 10398226

10

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

Tassone F, Hagerman RJ, Taylor AK, Gane LW, Godfrey TE, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. Am J Hum Genet. 2000 Jan;66(1):6-15. doi: 10.1086/302720. Am J Hum Genet. 2000. PMID: 10631132 Free PMC article.

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