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Results: 1-25 |
Results: 25
Fragile X syndrome: A model of gene-brain-behavior relationships
Authors: Hagerman, RJ Hagerman, PJ
Citation: Rj. Hagerman et Pj. Hagerman, Fragile X syndrome: A model of gene-brain-behavior relationships, MOL GEN MET, 74(1-2), 2001, pp. 89-97
Auditory evoked magnetic fields in adults with fragile X syndrome
Authors: Rojas, DC Benkers, TL Rogers, SJ Teale, PD Reite, ML Hagerman, RJ
Citation: Dc. Rojas et al., Auditory evoked magnetic fields in adults with fragile X syndrome, NEUROREPORT, 12(11), 2001, pp. 2573-2576
Profile of cognitive functioning in women with the fragile X mutation
Authors: Bennetto, L Pennington, BF Porter, D Taylor, AK Hagerman, RJ
Citation: L. Bennetto et al., Profile of cognitive functioning in women with the fragile X mutation, NEUROPSYCHL, 15(2), 2001, pp. 290-299
Discourse processing in women with fragile X syndrome: Evidence for a deficit establishing coherence
Authors: Simon, JA Keenan, JM Pennington, BF Taylor, AK Hagerman, RJ
Citation: Ja. Simon et al., Discourse processing in women with fragile X syndrome: Evidence for a deficit establishing coherence, COGN NEUROP, 18(1), 2001, pp. 1-18
Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X
Authors: Hagerman, RJ Leehey, M Heinrichs, W Tassone, F Wilson, R Hills, J Grigsby, J Gage, B Hagerman, PJ
Citation: Rj. Hagerman et al., Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X, NEUROLOGY, 57(1), 2001, pp. 127-130
A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA
Authors: Tassone, F Hagerman, RJ Taylor, AK Hagerman, PJ
Citation: F. Tassone et al., A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA, J MED GENET, 38(7), 2001, pp. 453-456
Sensory modulation dysfunction in children with attention-deficit-hyperactivity disorder
Authors: Mangeot, SD Miller, LJ McIntosh, DN McGrath-Clarke, J Simon, J Hagerman, RJ Goldson, E
Citation: Sd. Mangeot et al., Sensory modulation dysfunction in children with attention-deficit-hyperactivity disorder, DEVELOP MED, 43(6), 2001, pp. 399-406
Transcription of the FMR1 gene in individuals with fragile X syndrome
Authors: Tassone, F Hagerman, RJ Chamberlain, WD Hagerman, PJ
Citation: F. Tassone et al., Transcription of the FMR1 gene in individuals with fragile X syndrome, AM J MED G, 97(3), 2000, pp. 195-203
Melatonin profiles and sleep characteristics in boys with fragile X syndrome: A preliminary study
Authors: Gould, EL Loesch, DZ Martin, MJ Hagerman, RJ Armstrong, SM Huggins, RM
Citation: El. Gould et al., Melatonin profiles and sleep characteristics in boys with fragile X syndrome: A preliminary study, AM J MED G, 95(4), 2000, pp. 307-315
Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA
Authors: Tassone, F Hagerman, RJ Loesch, DZ Lachiewicz, A Taylor, AK Hagerman, PJ
Citation: F. Tassone et al., Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA, AM J MED G, 94(3), 2000, pp. 232-236
Clinical involvement and protein expression in individuals with the FMR1 premutation
Authors: Tassone, F Hagerman, RJ Taylor, AK Mills, JB Harris, SW Gane, LW Hagerman, PJ
Citation: F. Tassone et al., Clinical involvement and protein expression in individuals with the FMR1 premutation, AM J MED G, 91(2), 2000, pp. 144-152
Elevated levels of FMR1 mRNA in carrier males: A new mechanism of involvement in the fragile-X syndrome
Authors: Tassone, F Hagerman, RJ Taylor, AK Gane, LW Godfrey, TE Hagerman, PJ
Citation: F. Tassone et al., Elevated levels of FMR1 mRNA in carrier males: A new mechanism of involvement in the fragile-X syndrome, AM J HU GEN, 66(1), 2000, pp. 6-15
Psychopharmacological interventions in fragile X syndrome, fetal alcohol syndrome, Prader-Willi syndrome, Angelman syndrome, Smith-Magenis syndrome, and velocardiofacial syndrome
Authors: Hagerman, RJ
Citation: Rj. Hagerman, Psychopharmacological interventions in fragile X syndrome, fetal alcohol syndrome, Prader-Willi syndrome, Angelman syndrome, Smith-Magenis syndrome, and velocardiofacial syndrome, MENT RET D, 5(4), 1999, pp. 305-313
Fragile X syndrome: new developments
Authors: Harris, SW Hagerman, RJ
Citation: Sw. Harris et Rj. Hagerman, Fragile X syndrome: new developments, CUR OPIN P, 12(5), 1999, pp. 573-578
Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development
Authors: 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
Citation: Dl. Freedenberg et al., Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development, AM J MED G, 85(3), 1999, pp. 197-201
Tissue heterogeneity of the FMR1 mutation in a high-functioning male with fragile X syndrome
Authors: Taylor, AK Tassone, F Dyer, PN Hersch, SM Harris, JB Greenough, WT Hagerman, RJ
Citation: Ak. Taylor et al., Tissue heterogeneity of the FMR1 mutation in a high-functioning male with fragile X syndrome, AM J MED G, 84(3), 1999, pp. 233-239
Strong similarities of the FMR1 mutation in multiple tissues: Postmortem studies of a male with a full mutation and a male carrier of a premutation
Authors: Tassone, F Hagerman, RJ Gane, LW Taylor, AK
Citation: F. Tassone et al., Strong similarities of the FMR1 mutation in multiple tissues: Postmortem studies of a male with a full mutation and a male carrier of a premutation, AM J MED G, 84(3), 1999, pp. 240-244
FMRP expression as a potential prognostic indicator in fragile X syndrome
Authors: Tassone, F Hagerman, RJ Ikle, DN Dyer, PN Lampe, M Willemsen, R Oostra, BA Taylor, AK
Citation: F. Tassone et al., FMRP expression as a potential prognostic indicator in fragile X syndrome, AM J MED G, 84(3), 1999, pp. 250-261
Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: A preliminary report
Authors: Miller, LJ McIntosh, DN McGrath, J Shyu, V Lampe, M Taylor, AK Tassone, F Neitzel, K Stackhouse, T Hagerman, RJ
Citation: Lj. Miller et al., Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: A preliminary report, AM J MED G, 83(4), 1999, pp. 268-279
Fragile X syndrome and selective mutism
Authors: Hagerman, RJ Hills, J Scharfenaker, S Lewis, H
Citation: Rj. Hagerman et al., Fragile X syndrome and selective mutism, AM J MED G, 83(4), 1999, pp. 313-317
Compound heterozygous female with fragile X syndrome
Authors: Linden, MG Tassone, F Gane, LW Hills, JL Hagerman, RJ Taylor, AK
Citation: Mg. Linden et al., Compound heterozygous female with fragile X syndrome, AM J MED G, 83(4), 1999, pp. 318-321
Epilepsy and EEG findings in males with fragile X syndrome
Authors: Musumeci, SA Hagerman, RJ Ferri, R Bosco, P Dalla Bernardina, B Tassinari, CA De Sarro, GB Elia, M
Citation: Sa. Musumeci et al., Epilepsy and EEG findings in males with fragile X syndrome, EPILEPSIA, 40(8), 1999, pp. 1092-1099
Sensory-modulation disruption, electrodermal responses, and functional behaviors
Authors: McIntosh, DN Miller, LJ Shyu, V Hagerman, RJ
Citation: Dn. Mcintosh et al., Sensory-modulation disruption, electrodermal responses, and functional behaviors, DEVELOP MED, 41(9), 1999, pp. 608-615
Clinical and molecular aspects of fragile X syndrome
Authors: Hagerman, RJ
Citation: Rj. Hagerman, Clinical and molecular aspects of fragile X syndrome, DEV COGN NE, 1999, pp. 27-42
Fragile X syndrome
Authors: Hagerman, RJ Lampe, ME
Citation: Rj. Hagerman et Me. Lampe, Fragile X syndrome, HANDBOOK OF NEURODEVELOPMENTAL AND GENETIC DISORDERS IN CHILDREN, 1999, pp. 298-316
Risultati: 1-25 |