Hagerman PJ - Search Results

1

Spastic paraparesis, cerebellar ataxia, and intention tremor: a severe variant of FXTAS?

Jacquemont S, Orrico A, Galli L, Sahota PK, Brunberg JA, Anichini C, Leehey M, Schaeffer S, Hagerman RJ, Hagerman PJ, Tassone F. Jacquemont S, et al. Among authors: hagerman pj, hagerman rj. J Med Genet. 2005 Feb;42(2):e14. doi: 10.1136/jmg.2004.024190. J Med Genet. 2005. PMID: 15689437 Free PMC article. No abstract available.

2

Oral folic acid versus placebo in the treatment of males with the fragile X syndrome.

Hagerman RJ, Jackson AW, Levitas A, Braden M, McBogg P, Kemper M, McGavran L, Berry R, Matus I, Hagerman PJ. Hagerman RJ, et al. Among authors: hagerman pj. Am J Med Genet. 1986 Jan-Feb;23(1-2):241-62. doi: 10.1002/ajmg.1320230119. Am J Med Genet. 1986. PMID: 3513567 Review.

3

The fragile X syndrome: history, diagnosis, and treatment.

Hagerman RJ, McBogg P, Hagerman PJ. Hagerman RJ, et al. Among authors: hagerman pj. J Dev Behav Pediatr. 1983 Jun;4(2):122-30. doi: 10.1097/00004703-198306000-00009. J Dev Behav Pediatr. 1983. PMID: 6348096 Review.

4

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.

5

Clinical involvement and protein expression in individuals with the FMR1 premutation.

Tassone F, Hagerman RJ, Taylor AK, Mills JB, Harris SW, Gane LW, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. Am J Med Genet. 2000 Mar 13;91(2):144-52. doi: 10.1002/(sici)1096-8628(20000313)91:2<144::aid-ajmg14>3.0.co;2-v. Am J Med Genet. 2000. PMID: 10748416

6

Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA.

Tassone F, Hagerman RJ, Loesch DZ, Lachiewicz A, Taylor AK, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. Am J Med Genet. 2000 Sep 18;94(3):232-6. doi: 10.1002/1096-8628(20000918)94:3<232::aid-ajmg9>3.0.co;2-h. Am J Med Genet. 2000. PMID: 10995510

7

A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA.

Tassone F, Hagerman RJ, Taylor AK, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. J Med Genet. 2001 Jul;38(7):453-6. doi: 10.1136/jmg.38.7.453. J Med Genet. 2001. PMID: 11432964 Free PMC article.

8

Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.

Hagerman RJ, Leehey M, Heinrichs W, Tassone F, Wilson R, Hills J, Grigsby J, Gage B, Hagerman PJ. Hagerman RJ, et al. Among authors: hagerman pj. Neurology. 2001 Jul 10;57(1):127-30. doi: 10.1212/wnl.57.1.127. Neurology. 2001. PMID: 11445641

9

Transcription of the FMR1 gene in individuals with fragile X syndrome.

Tassone F, Hagerman RJ, Chamberlain WD, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. Am J Med Genet. 2000 Fall;97(3):195-203. doi: 10.1002/1096-8628(200023)97:3<195::AID-AJMG1037>3.0.CO;2-R. Am J Med Genet. 2000. PMID: 11449488

10

Fragile X syndrome: a model of gene-brain-behavior relationships.

Hagerman RJ, Hagerman PJ. Hagerman RJ, et al. Among authors: hagerman pj. Mol Genet Metab. 2001 Sep-Oct;74(1-2):89-97. doi: 10.1006/mgme.2001.3225. Mol Genet Metab. 2001. PMID: 11592806 Review. No abstract available.

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