Citations 9

Can Clinical Features Predict Tau Pathology in Patients with Behavioral Variant Frontotemporal Dementia (bvFTD)? (P05.101)

Neurology | December 7, 2023 | Volume: 80 | Issue: 7_supplement | Pages: No page available

10.1212/wnl.80.7_supplement.p05.101

Brain amyloidosis ascertainment from cognitive, imaging, and peripheral blood protein measures

Neurology | January 22, 2015 | Volume: 84 | Issue: 7 | Pages: 729-737

10.1212/wnl.0000000000001231 | PMID 25609767

C9ORF72 repeat expansions in cases with previously identified pathogenic mutations

Neurology | September 12, 2013 | Volume: 81 | Issue: 15 | Pages: 1332-1341

10.1212/wnl.0b013e3182a8250c | PMID 24027057

Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases

Neurology | July 27, 2012 | Volume: 79 | Issue: 9 | Pages: 878-882

10.1212/wnl.0b013e3182661d14 | PMID 22843265

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

Neurology | May 14, 2012 | Volume: 56 | Issue: 12 | Pages: 1702-1706

10.1212/wnl.56.12.1702 | PMID 11425937

P4‐166: Determinants of survival in autopsy‐confirmed patients with behavioral variant frontotemporal dementia (bvFTD): Second Report of the international bvFTD criteria consortium (FTDC)

Alzheimer's & Dementia | August 1, 2011 | Volume: 7 | Issue: 4S_Part_22 | Pages: No page available

10.1016/j.jalz.2011.05.2188

TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers

Neurology | December 22, 2010 | Volume: 76 | Issue: 5 | Pages: 467-474

10.1212/wnl.0b013e31820a0e3b | PMID 21178100

A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly

Proceedings of the National Academy of Sciences | April 19, 2010 | Volume: 107 | Issue: 18 | Pages: 8404-8409

10.1073/pnas.0910878107 | PMID 20404173

A recently identified variant within the fat mass and obesity-associated ( FTO ) gene is carried by 46% of Western Europeans and is associated with an ~1.2 kg higher weight, on average, in adults and an ~1 cm greater waist circumference. With >1 billion overweight and 300 million obese persons worldwide, it is crucial to understand the implications of carrying this very common allele for the health of our aging population. FTO is highly expressed in the brain and elevated body mass index (BMI) is associated with brain atrophy, but it is unknown how the obesity-associated risk allele affects human brain structure. We therefore generated 3D maps of regional brain volume differences in 206 healthy elderly subjects scanned with MRI and genotyped as part of the Alzheimer's Disease Neuroimaging Initiative. We found a pattern of systematic brain volume deficits in carriers of the obesity-associated risk allele versus noncarriers. Relative to structure volumes in the mean template, FTO risk allele carriers versus noncarriers had an average brain volume difference of ~8% in the frontal lobes and 12% in the occipital lobes—these regions also showed significant volume deficits in subjects with higher BMI. These brain differences were not attributable to differences in cholesterol levels, hypertension, or the volume of white matter hyperintensities; which were not detectably higher in FTO risk allele carriers versus noncarriers. These brain maps reveal that a commonly carried susceptibility allele for obesity is associated with structural brain atrophy, with implications for the health of the elderly.
A 74-year-old woman with progressive right-hand tremor and inability to use her right side

Neurology | October 26, 2009 | Volume: 73 | Issue: 17 | Pages: 1399-1405

10.1212/wnl.0b013e3181bd80fe | PMID 19858463