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Results 1 - 10 of 14 for Frontotemporal disorders
  1. Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (IBMPFD) is a condition that can affect the muscles, bones, and brain.The first symptom of IBMPFD is often muscle weakness (myopathy), ...
  2. ... sclerosis 7 Frontotemporal dementia National Organization for Rare Disorders (NORD) FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 7; FTDALS7 ...
  3. ... Tdp43 inclusions Frontotemporal dementia National Organization for Rare Disorders (NORD) FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED PubMed ...
  4. ... body myopathy with early-onset Paget disease and frontotemporal dementia (IBMPFD). This rare disease causes muscle weakness (myopathy) and can also include ...
  5. ... Wilhelmsen-Lynch disease Genetic Testing Registry: Frontotemporal dementia Frontotemporal dementia National Organization for Rare Disorders (NORD) ClinicalTrials.gov FRONTOTEMPORAL DEMENTIA; FTD PubMed Boeve ...
  6. ... DCTN1 gene mutation is associated with a brain disorder called frontotemporal dementia (FTD) without the features of amyotrophic lateral sclerosis (ALS). This disorder occurs in mid- to late adulthood and is ...
  7. ... G, Gennarelli M, Padovani A. TARDBP mutations in frontotemporal lobar degeneration: frequency, clinical features, and disease course. Rejuvenation Res. 2010 Oct;13(5):509- ...
  8. ... impaired function of lysosomes. Unlike in GRN-related frontotemporal lobar degeneration (described below), people with CLN11 disease do not appear to have build up of ...
  9. ... throughout the brain is characteristic of CHMP2B-related frontotemporal dementia. Many of the features of this disease result from neuronal death in regions near the ...
  10. ... history of ALS or a related condition called frontotemporal dementia (FTD), which is a progressive brain disorder that affects personality, behavior, and language. The signs ...
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