Related references
Note: Only part of the references are listed.Fragile X carrier screening and FMR1 allele distribution in the Japanese population
Susumu Otsuka et al.
BRAIN & DEVELOPMENT (2010)
Advances in understanding the molecular basis of FXTAS
Dolores Garcia-Arocena et al.
HUMAN MOLECULAR GENETICS (2010)
Late-onset Huntington disease with intermediate CAG repeats: true or false?
Justus L. Groen et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2010)
Screening for the Presence of FMR1 Premutation Alleles in Women With Parkinsonism
Roberto Cilia et al.
ARCHIVES OF NEUROLOGY (2009)
Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism
D. Z. Loesch et al.
CLINICAL GENETICS (2009)
Parkinsonism in FMR1 premutation carriers may be indistinguishable from Parkinson disease
Deborah A. Hall et al.
PARKINSONISM & RELATED DISORDERS (2009)
Genetic variation of the FMR1 gene among four Mexican populations:: Mestizo, Huichol, Purepecha, and Tarahumara
Patricio Barros-Nunez et al.
AMERICAN JOURNAL OF HUMAN BIOLOGY (2008)
A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile x (FMR1) gene in newborn and high-risk populations
Flora Tassone et al.
JOURNAL OF MOLECULAR DIAGNOSTICS (2008)
FMR1 CGG repeat length predicts motor dysfunction in premutation carriers
M. A. Leehey et al.
NEUROLOGY (2008)
Increased risk of parkinsonism in women who underwent oophorectomy before menopause
W. A. Rocca et al.
NEUROLOGY (2008)
Screen for excess FMR1 premutation alleles among males with Parkinsonism
Jeremy Kraff et al.
ARCHIVES OF NEUROLOGY (2007)
FMR1 Alleles in Parkinson's disease:: Relation to cognitive decline and hallucinations, a longitudinal study
Martin Wilhelm Kurz et al.
JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY (2007)
Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats
Danuta Z. Loesch et al.
JOURNAL OF MEDICAL GENETICS (2007)
Predictive testing for Huntington disease: interpretation and significance of intermediate alleles
A. Semaka et al.
CLINICAL GENETICS (2006)
Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation
B Bodega et al.
HUMAN REPRODUCTION (2006)
An investigation of FRAXA intermediate allele phenotype in a longitudinal sample
S Ennis et al.
ANNALS OF HUMAN GENETICS (2006)
Prevalence of FMR1 repeat expansions in movement disorders - A systematic review
DA Hall et al.
NEUROEPIDEMIOLOGY (2006)
Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB): Report of the Consortium on DLB International Workshop
Ian G. McKeith
JOURNAL OF ALZHEIMERS DISEASE (2006)
FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure
KL Bretherick et al.
HUMAN GENETICS (2005)
Premutations in the FMR1 gene as a modifying factor in Parkin-associated Parkinson's disease?
K Hedrich et al.
MOVEMENT DISORDERS (2005)
Initial diagnoses given to persons with the fragile X associated tremor/ataxia syndrome (FXTAS)
DA Hall et al.
NEUROLOGY (2005)
Association of FMR1 repeat size with ovarian dysfunction
AK Sullivan et al.
HUMAN REPRODUCTION (2005)
Penetrance of the fragile X - Associated tremor/ataxia syndrome in a premutation carrier population
S Jacquemont et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2004)
Risk of Parkinson disease in women - Effect of reproductive characteristics
P Ragonese et al.
NEUROLOGY (2004)
Premutation Alleles associated with Parkinson disease and essential tremor
H Deng et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2004)
Fragile X premutation tremor/ataxia syndrome: Molecular, clinical, and neuroimaging correlates
S Jacquemont et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Cognitive and behavioral performance among FMR1 high-repeat allele carriers surveyed from special education classes
SL Sherman et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
Premutation and intermediate-size FMR1 alleles in 10,572 males from the general population:: Loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles
C Dombrowski et al.
HUMAN MOLECULAR GENETICS (2002)
Hysterectomy, menopause, and estrogen use preceding Parkinson's disease: An exploratory case-control study
MD Benedetti et al.
MOVEMENT DISORDERS (2001)
Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel
H Toledano-Alhadef et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Macular microcirculation characteristics in Parkinson's disease evaluated by OCT-Angiography: a literature review
Evita Evangelia Christou et al.
SEMINARS IN OPHTHALMOLOGY
Share Paper
