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 *

257 related articles for article (PubMed ID: 15714997)

  • 21. CADASIL syndrome in a large Turkish kindred caused by the R90C mutation in the Notch3 receptor.
    Utku U; Celik Y; Uyguner O; Yüksel-Apak M; Wollnik B
    Eur J Neurol; 2002 Jan; 9(1):23-8. PubMed ID: 11784372
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [A new Spanish family with CADASIL associated with 346C>T mutation of NOTCH3 gene].
    Avila A; Bello J; Maho P; Gómez MI
    Neurologia; 2007 Sep; 22(7):484-7. PubMed ID: 17853970
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Arg133Cys mutation of Notch3 in two unrelated Japanese families with CADASIL.
    Uyama E; Tokunaga M; Suenaga A; Kotorii S; Kamimura K; Takahashi K; Tabira T; Uchino M
    Intern Med; 2000 Sep; 39(9):732-7. PubMed ID: 10969905
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Sporadic vascular dementia as clinical presentation of a new missense mutation within exon 7 of NOTCH3 gene.
    Pradotto L; Azan G; Doriguzzi C; Valentini C; Mauro A
    J Neurol Sci; 2008 Aug; 271(1-2):207-10. PubMed ID: 18499132
    [TBL] [Abstract][Full Text] [Related]  

  • 25. CADASIL with a novel NOTCH3 mutation (Cys478Tyr).
    Ozaki K; Irioka T; Ishikawa K; Mizusawa H
    J Stroke Cerebrovasc Dis; 2015 Mar; 24(3):e61-2. PubMed ID: 25595846
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Functional analysis of a recurrent missense mutation in Notch3 in CADASIL.
    Haritunians T; Chow T; De Lange RP; Nichols JT; Ghavimi D; Dorrani N; St Clair DM; Weinmaster G; Schanen C
    J Neurol Neurosurg Psychiatry; 2005 Sep; 76(9):1242-8. PubMed ID: 16107360
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hypomorphic NOTCH3 alleles do not cause CADASIL in humans.
    Rutten JW; Boon EM; Liem MK; Dauwerse JG; Pont MJ; Vollebregt E; Maat-Kievit AJ; Ginjaar HB; Lakeman P; van Duinen SG; Terwindt GM; Lesnik Oberstein SA
    Hum Mutat; 2013 Nov; 34(11):1486-9. PubMed ID: 24000151
    [TBL] [Abstract][Full Text] [Related]  

  • 28. CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy): an Australian perspective.
    Chuah TL; Tan KM; Flanagan S; Hyland V; Sullivan AA; Henderson R; MacMillan J; Lander C
    J Clin Neurosci; 2001 Sep; 8(5):404-6. PubMed ID: 11535004
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Renal involvement in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    Kusaba T; Hatta T; Kimura T; Sonomura K; Tanda S; Kishimoto N; Kameyama H; Okigaki M; Mori Y; Ishigami N; Mizuno T; Nakagawa M; Matsubara H
    Clin Nephrol; 2007 Mar; 67(3):182-7. PubMed ID: 17390743
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Cerebral autosomal dominant arteriolopathy with subcortical infarcts and leucoencephalopathy].
    Bruls E; Moonen G; Sadzot B
    Rev Med Liege; 2007 Jan; 62(1):36-43. PubMed ID: 17343128
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A pathogenic mutation on exon 21 of the NOTCH3 gene causing CADASIL in an octogenarian paucisymptomatic patient.
    Pescini F; Bianchi S; Salvadori E; Poggesi A; Dotti MT; Federico A; Inzitari D; Pantoni L
    J Neurol Sci; 2008 Apr; 267(1-2):170-3. PubMed ID: 18022198
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A novel CADASIL-causing mutation in a stroke patient.
    Vikelis M; Papatriantafyllou J; Karageorgiou CE
    Swiss Med Wkly; 2007 Jun; 137(21-22):323-5. PubMed ID: 17629811
    [TBL] [Abstract][Full Text] [Related]  

  • 33. An unusual case of elderly-onset cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with multiple cerebrovascular risk factors.
    Watanabe M; Adachi Y; Jackson M; Yamamoto-Watanabe Y; Wakasaya Y; Shirahama I; Takamura A; Matsubara E; Kawarabayashi T; Shoji M
    J Stroke Cerebrovasc Dis; 2012 Feb; 21(2):143-5. PubMed ID: 20851625
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Myocardial infarction in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    Lesnik Oberstein SA; Jukema JW; Van Duinen SG; Macfarlane PW; van Houwelingen HC; Breuning MH; Ferrari MD; Haan J
    Medicine (Baltimore); 2003 Jul; 82(4):251-6. PubMed ID: 12861102
    [TBL] [Abstract][Full Text] [Related]  

  • 35. CADASIL can mimic multiple sclerosis.
    Phillips CD; Zuckerman SJ;
    J La State Med Soc; 2010; 162(3):174. PubMed ID: 20666172
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel Notch3 Gly89Cys mutation in a Serbian CADASIL family.
    Pavlovic AM; Dobricic V; Semnic R; Lackovic V; Novakovic I; Bajcetic M; Sternic N
    Acta Neurol Belg; 2013 Sep; 113(3):299-302. PubMed ID: 23319290
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mutations of the notch3 gene in non-caucasian patients with suspected CADASIL syndrome.
    Kotorii S; Takahashi K; Kamimura K; Nishio T; Arima K; Yamada H; Uyama E; Uchino M; Suenaga A; Matsumoto M; Kuchel G; Rouleau GA; Tabira T
    Dement Geriatr Cogn Disord; 2001; 12(3):185-93. PubMed ID: 11244211
    [TBL] [Abstract][Full Text] [Related]  

  • 38. CADASIL: a common form of hereditary arteriopathy causing brain infarcts and dementia.
    Kalimo H; Ruchoux MM; Viitanen M; Kalaria RN
    Brain Pathol; 2002 Jul; 12(3):371-84. PubMed ID: 12146805
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [A case of CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and lekoencephalopathy) with Notch 3 (Arg169Cys) mutation and typical granular osmiophilic materials in peripheral small arteries].
    Kotani N; Hara H; Fujimura H; Miyashita T; Miyaguchi K; Tabira T
    Rinsho Shinkeigaku; 2004; 44(4-5):274-9. PubMed ID: 15287509
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation.
    Tuominen S; Juvonen V; Amberla K; Jolma T; Rinne JO; Tuisku S; Kurki T; Marttila R; Pöyhönen M; Savontaus ML; Viitanen M; Kalimo H
    Stroke; 2001 Aug; 32(8):1767-74. PubMed ID: 11486103
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.