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1.
Atypical vocal quality in women with the FMR1 premutation: an indicator of impaired sensorimotor control.
Exp Brain Res
; 241(8): 1975-1987, 2023 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-37347418
2.
Verbal inhibition declines among older women with high FMR1 premutation expansions: A prospective study.
Brain Cogn
; 159: 105851, 2022 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-35279590
3.
Response Inhibition Deficits in Women with the FMR1 Premutation are Associated with Age and Fall Risk.
Brain Cogn
; 148: 105675, 2021 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-33387817
4.
Family as a Context for Child Development: Mothers with the FMR1 Premutation and Their Children with Fragile X Syndrome.
Semin Speech Lang
; 42(4): 277-286, 2021 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-34311480
5.
Inhibition deficits are modulated by age and CGG repeat length in carriers of the FMR1 premutation allele who are mothers of children with fragile X syndrome.
Brain Cogn
; 139: 105511, 2020 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-31887710
6.
A novel eye-tracking paradigm for indexing social avoidance-related behavior in fragile X syndrome.
Am J Med Genet B Neuropsychiatr Genet
; 183(1): 5-16, 2020 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-31418535
7.
Cortisol profiles differentiated in adolescents and young adult males with fragile X syndrome versus autism spectrum disorder.
Dev Psychobiol
; 60(1): 78-89, 2018 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-29171019
8.
Biobehavioral composite of social aspects of anxiety in young adults with fragile X syndrome contrasted to autism spectrum disorder.
Am J Med Genet B Neuropsychiatr Genet
; 177(7): 665-675, 2018 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-30307687
9.
Phonological awareness and reading in boys with fragile X syndrome.
J Child Psychol Psychiatry
; 56(1): 30-9, 2015 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-24889646
10.
Social Communication Delay in an Unbiased Sample of Preschoolers With the FMR1 Premutation.
J Speech Lang Hear Res
; : 1-17, 2024 Jun 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-38889222
11.
Predictors, Parental Views, and Concordance Across Diagnostic Sources of Autism in Male Youth with Fragile X Syndrome: Clinical Best Estimate and Community Diagnoses.
Res Child Adolesc Psychopathol
; 51(7): 989-1004, 2023 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-36867382
12.
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.
Cells
; 12(18)2023 09 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-37759552
13.
Defining genetically meaningful language and personality traits in relatives of individuals with fragile X syndrome and relatives of individuals with autism.
Am J Med Genet B Neuropsychiatr Genet
; 159B(6): 660-8, 2012 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-22693142
14.
Maternal Pragmatic Language Difficulties in the FMR1 Premutation and the Broad Autism Phenotype: Associations with Individual and Family Outcomes.
J Autism Dev Disord
; 52(2): 835-851, 2022 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-33813684
15.
Attention/Deficit Hyperactivity Disorder in Adolescent and Young Adult Males With Fragile X Syndrome.
Am J Intellect Dev Disabil
; 127(3): 213-230, 2022 05 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35443049
16.
Family history of FXTAS is associated with age-related cognitive-linguistic decline among mothers with the FMR1 premutation.
J Neurodev Disord
; 14(1): 7, 2022 01 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-35026985
17.
Daily Living Skills in Adolescent and Young Adult Males With Fragile X Syndrome.
Am J Intellect Dev Disabil
; 127(1): 64-83, 2022 01 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-34979036
18.
Cluttering in the Speech of Young Men With Fragile X Syndrome.
J Speech Lang Hear Res
; 65(3): 954-969, 2022 03 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-35196138
19.
Low normal FMR1 genotype in older adult women: Psychological well-being and motor function.
Arch Gerontol Geriatr
; 103: 104789, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35981426
20.
The FMR1 Premutation Phenotype and Mother-Youth Synchrony in Fragile X Syndrome.
Am J Intellect Dev Disabil
; 126(6): 443-459, 2021 11 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-34700350