Literature DB >> 11481705

Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17): PPND family. A longitudinal videotape demonstration.

Z K Wszolek1, R H Kardon, E C Wolters, R F Pfeiffer.   

Abstract

Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17), characterized by an autosomal dominant inheritance pattern, has recently been recognized as a distinct entity that can display a confusingly broad clinical phenotype. The pallido-ponto-nigral degeneration (PPND) variant is the prototypical example of the parkinsonism-predominant pattern of FTDP-17. A longitudinal videotape demonstration of the clinical progression of this entity in a single individual, along with brief videotape segments from three additional affected individuals, is presented in order to facilitate recognition of this disorder. Copyright 2001 Movement Disorder Society.

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Year:  2001        PMID: 11481705     DOI: 10.1002/mds.1131

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  3 in total

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Review 2.  Clinical and Neuroimaging Aspects of Familial Frontotemporal Lobar Degeneration Associated with MAPT and GRN Mutations.

Authors:  Bradley F Boeve; Howard Rosen
Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

3.  Rates of lobar atrophy in asymptomatic MAPT mutation carriers.

Authors:  Qin Chen; Bradley F Boeve; Matthew Senjem; Nirubol Tosakulwong; Timothy G Lesnick; Danielle Brushaber; Christina Dheel; Julie Fields; Leah Forsberg; Ralitza Gavrilova; Debra Gearhart; Jonathan Graff-Radford; Neill R Graff-Radford; Clifford R Jack; David T Jones; David S Knopman; Walter K Kremers; Maria Lapid; Rosa Rademakers; Jeremy Syrjanen; Adam L Boxer; Howie Rosen; Zbigniew K Wszolek; Kejal Kantarci
Journal:  Alzheimers Dement (N Y)       Date:  2019-07-30
  3 in total

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