These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 21959360)

  • 1. Long-standing prion dementia manifesting as posterior cortical atrophy.
    Depaz R; Haik S; Peoc'h K; Seilhean D; Grabli D; Vicart S; Sarazin M; DeToffol B; Remy C; Fallet-Bianco C; Laplanche JL; Fontaine B; Brandel JP
    Alzheimer Dis Assoc Disord; 2012; 26(3):289-92. PubMed ID: 21959360
    [TBL] [Abstract][Full Text] [Related]  

  • 2. PRNP H187R mutation associated with neuropsychiatric disorders in childhood and dementia.
    Hall DA; Leehey MA; Filley CM; Steinbart E; Montine T; Schellenberg GD; Bosque P; Nixon R; Bird T
    Neurology; 2005 Apr; 64(7):1304-6. PubMed ID: 15824374
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prion disease with a 144 base pair insertion: unusual cerebellar prion protein immunoreactivity.
    Gelpi E; Kovacs GG; Ströbel T; Koperek O; Voigtländer T; Liberski PP; Budka H
    Acta Neuropathol; 2005 Nov; 110(5):513-9. PubMed ID: 16155763
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial spongiform encephalopathy associated with a novel prion protein gene mutation.
    Nitrini R; Rosemberg S; Passos-Bueno MR; da Silva LS; Iughetti P; Papadopoulos M; Carrilho PM; Caramelli P; Albrecht S; Zatz M; LeBlanc A
    Ann Neurol; 1997 Aug; 42(2):138-46. PubMed ID: 9266722
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hypokinesia and presenile dementia in a Dutch family with a novel insertion in the prion protein gene.
    van Gool WA; Hensels GW; Hoogerwaard EM; Wiezer JH; Wesseling P; Bolhuis PA
    Brain; 1995 Dec; 118 ( Pt 6)():1565-71. PubMed ID: 8595485
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dementia associated with a 216 base pair insertion in the prion protein gene. Clinical and neuropathological features.
    Duchen LW; Poulter M; Harding AE
    Brain; 1993 Jun; 116 ( Pt 3)():555-67. PubMed ID: 8513392
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Loss of glycosylation associated with the T183A mutation in human prion disease.
    Grasbon-Frodl E; Lorenz H; Mann U; Nitsch RM; Windl O; Kretzschmar HA
    Acta Neuropathol; 2004 Dec; 108(6):476-84. PubMed ID: 15558291
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Human prion diseases with variant prion protein.
    Kitamoto T; Tateishi J
    Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):391-8. PubMed ID: 7913756
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inherited prion disease with A117V mutation of the prion protein gene: a novel Hungarian family.
    Kovács GG; Ertsey C; Majtényi C; Jelencsik I; László L; Flicker H; Strain L; Szirmai I; Budka H
    J Neurol Neurosurg Psychiatry; 2001 Jun; 70(6):802-5. PubMed ID: 11385020
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A case with a 120 base pair insertional mutation in the prion protein gene: the first case in Japan.
    Beck G; Kawano T; Naba I; Nishimura T; Sawada J; Hazama T
    J Neurol Neurosurg Psychiatry; 2005 May; 76(5):756-7. PubMed ID: 15834045
    [No Abstract]   [Full Text] [Related]  

  • 11. Gerstmann-Sträussler-Scheinker disease with A117V mutation in a second French-Alsatian family.
    Heldt N; Boellaard JW; Brown P; Cervenákova L; Doerr-Schott J; Thomas C; Scherer C; Rohmer F
    Clin Neuropathol; 1998; 17(4):229-34. PubMed ID: 9707339
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Posterior cortical atrophy--a new dementia syndrome or a form of Alzheimer's disease?].
    Pantel J; Schröder J
    Fortschr Neurol Psychiatr; 1996 Dec; 64(12):492-508. PubMed ID: 9053390
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prion disease with octapeptide repeat insertion.
    Vital C; Gray F; Vital A; Ferrer X; Julien J
    Clin Exp Pathol; 1999; 47(3-4):153-9. PubMed ID: 10472735
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Human prion diseases.
    Parchi P; Gambetti P
    Curr Opin Neurol; 1995 Aug; 8(4):286-93. PubMed ID: 7582044
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prion disease causes less severe lesions in human hippocampus than other parts of brain.
    Kaneko M; Sugiyama N; Sasayama D; Yamaoka K; Miyakawa T; Arima K; Tsuchiya K; Hasegawa K; Washizuka S; Hanihara T; Amano N; Yagishita S
    Psychiatry Clin Neurosci; 2008 Jun; 62(3):264-70. PubMed ID: 18588585
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary dysphasic dementia and the Pick-Alzheimer spectrum.
    Morris JC; Cole M; Banker BQ; Wright D
    Ann Neurol; 1984 Oct; 16(4):455-66. PubMed ID: 6497355
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel mutation (G114V) in the prion protein gene in a family with inherited prion disease.
    Rodriguez MM; Peoc'h K; Haïk S; Bouchet C; Vernengo L; Mañana G; Salamano R; Carrasco L; Lenne M; Beaudry P; Launay JM; Laplanche JL
    Neurology; 2005 Apr; 64(8):1455-7. PubMed ID: 15851745
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Inherited prion encephalopathy associated with the novel PRNP H187R mutation: a clinical study.
    Bütefisch CM; Gambetti P; Cervenakova L; Park KY; Hallett M; Goldfarb LG
    Neurology; 2000 Aug; 55(4):517-22. PubMed ID: 10953183
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Early and persistent sensory-psychiatric symptoms in an inherited prion disease with a PrP P105L mutation.
    Shiraishi A; Mizusawa H; Yamada M
    J Neurol; 2002 Dec; 249(12):1740-1. PubMed ID: 12529802
    [No Abstract]   [Full Text] [Related]  

  • 20. Real and imagined clinicopathological limits of "prion dementia".
    Brown P; Kaur P; Sulima MP; Goldfarb LG; Gibbs CJ; Gajdusek DC
    Lancet; 1993 Jan; 341(8838):127-9. PubMed ID: 8093741
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.