R Hagerman
Overview
Explore the profile of R Hagerman including associated specialties, affiliations and a list of published articles.
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Articles
33
Citations
924
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Recent Articles
1.
Dy A, Tassone F, Eldeeb M, Salcedo-Arellano M, Tartaglia N, Hagerman R
Clin Genet
. 2017 Apr;
93(2):216-222.
PMID: 28436599
Background: Individuals with fragile X syndrome (FXS) have both behavioral and medical comorbidities and the latter include obesity in approximately 30% and the Prader-Willi Phenotype (PWP) characterized by severe hyperphagia...
2.
Santa Maria L, Pugin A, Alliende M, Aliaga S, Curotto B, Aravena T, et al.
Clin Genet
. 2013 Sep;
86(4):378-82.
PMID: 24028275
Carriers of an FMR1 premutation allele (55-200 CGG repeats) often develop the neurodegenerative disorders, fragile X-associated tremor/ataxia syndrome (FXTAS). Neurological signs of FXTAS, parkinsonism and rapid onset of cognitive decline...
3.
Au J, Akins R, Berkowitz-Sutherland L, Tang H, Chen Y, Boyd A, et al.
Clin Genet
. 2013 Feb;
84(6):546-51.
PMID: 23373759
FMR1 premutation carriers are common in the general population (1/130-260 females and 1/250-810 males) and can be affected by fragile X-associated tremor ataxia syndrome, fragile X-associated primary ovarian insufficiency, anxiety,...
4.
Berry-Kravis E, Hessl D, Coffey S, Hervey C, Schneider A, Yuhas J, et al.
J Med Genet
. 2009 Jan;
46(4):266-71.
PMID: 19126569
Objective: A pilot open label, single dose trial of fenobam, an mGluR5 antagonist, was conducted to provide an initial evaluation of safety and pharmacokinetics in adult males and females with...
5.
Cornish K, Turk J, Hagerman R
J Intellect Disabil Res
. 2008 May;
52(Pt 6):469-82.
PMID: 18444988
Fragile X syndrome is the world's most common hereditary cause of intellectual disability in men and to a lesser extent in women. The disorder is caused by the silencing of...
6.
Cohen S, Masyn K, Adams J, Hessl D, Rivera S, Tassone F, et al.
Neurology
. 2006 Oct;
67(8):1426-31.
PMID: 17060569
Objectives: To assess changes in regional brain volumes associated with the fragile X-associated tremor/ataxia syndrome (FXTAS) and the molecular correlates of these changes. Methods: We administered molecular, MRI, and neurocognitive...
7.
Cornish K, Turk J, Wilding J, Sudhalter V, Munir F, Kooy F, et al.
J Child Psychol Psychiatry
. 2004 Jul;
45(6):1042-53.
PMID: 15257661
Background: Fragile X syndrome is one of the world's leading hereditary causes of developmental delay in males. The past decade has witnessed an explosion of research that has begun to...
8.
Rogers S, Wehner D, Hagerman R
J Dev Behav Pediatr
. 2002 Jan;
22(6):409-17.
PMID: 11773805
This study was designed to explore the behavioral phenotype of autism in a group of young children with fragile X syndrome (FXS). Twenty-four children with FXS, ages 21 to 48...
9.
Holden J, PERCY M, Allingham-Hawkins D, Brown W, Chiurazzi P, Fisch G, et al.
Am J Med Genet
. 1999 Apr;
83(4):221-36.
PMID: 10208154
No abstract available.
10.