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 *

203 related articles for article (PubMed ID: 12721871)

  • 1. [CADASIL: a case with clinical, radiological, histological and genetic diagnoses].
    Posada IJ; García-Morales I; Martínez MA; Hoenicka J; Bermejo F
    Neurologia; 2003 May; 18(4):229-33. PubMed ID: 12721871
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [From gene to disease; from Notch3 to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].
    Oberstein SA; Bakker E; Ferrari MD; Haan J
    Ned Tijdschr Geneeskd; 2001 Feb; 145(8):359-60. PubMed ID: 11257815
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. An Italian case of CADASIL with mutation CGC-TCG in codon 1006, exon 19 Notch3 gene.
    Guidetti D; Casali B; Mazzei RL; Cenacchi G; De Berti G; Zuccoli G; Nicoli D; Conforti FL; Sprovieri T; Pasquinelli G; Brini M
    Neurol Sci; 2004 Feb; 24(6):401-6. PubMed ID: 14767686
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Rufa A; De Stefano N; Dotti MT; Bianchi S; Sicurelli F; Stromillo ML; D'Aniello B; Federico A
    Arch Neurol; 2004 Apr; 61(4):577-80. PubMed ID: 15096408
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Ruchoux MM; Domenga V; Brulin P; Maciazek J; Limol S; Tournier-Lasserve E; Joutel A
    Am J Pathol; 2003 Jan; 162(1):329-42. PubMed ID: 12507916
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Japanese CADASIL case with limited dementia who had the Notch 3 R141C mutation].
    Ishibashi K; Murata T; Miki Y; Hara M; Mori H
    No To Shinkei; 2005 May; 57(5):415-8. PubMed ID: 15981641
    [TBL] [Abstract][Full Text] [Related]  

  • 9. CADASIL: a monogenic condition causing stroke and subcortical vascular dementia.
    Dichgans M
    Cerebrovasc Dis; 2002; 13 Suppl 2():37-41. PubMed ID: 11901241
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Incipient CADASIL.
    Lesnik Oberstein SA; van den Boom R; Middelkoop HA; Ferrari MD; Knaap YM; van Houwelingen HC; Breuning MH; van Buchem MA; Haan J
    Arch Neurol; 2003 May; 60(5):707-12. PubMed ID: 12756134
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: phenotypic and mutational spectrum.
    Dichgans M
    J Neurol Sci; 2002 Nov; 203-204():77-80. PubMed ID: 12417361
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [NOTCH3 gene mutations in four Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].
    Wang ZX; Lu H; Zhang Y; Bu DF; Niu XY; Zhang Z; Huang YN; Yuan Y
    Zhonghua Yi Xue Za Zhi; 2004 Jul; 84(14):1175-80. PubMed ID: 15387979
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel mutation (C67Y)in the NOTCH3 gene in a Korean CADASIL patient.
    Moon SY; Kim HY; Seok JI; Kwon JC; Ki CS; Kim JW; Suh YL; Na DL
    J Korean Med Sci; 2003 Feb; 18(1):141-4. PubMed ID: 12589106
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].
    Ueda M; Nakaguma R; Ando Y
    Rinsho Byori; 2009 Mar; 57(3):242-51. PubMed ID: 19363995
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    Lesnik Oberstein SA; Haan J
    Panminerva Med; 2004 Dec; 46(4):265-76. PubMed ID: 15876982
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Migraine with aura and white matter abnormalities: Notch3 mutation.
    Ceroni M; Poloni TE; Tonietti S; Fabozzi D; Uggetti C; Frediani F; Simonetti F; Malaspina A; Alimonti D; Celano M; Ferrari M; Carrera P
    Neurology; 2000 May; 54(9):1869-71. PubMed ID: 10802804
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. An animal model for the molecular genetics of CADASIL. (Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy).
    Fryxell KJ; Soderlund M; Jordan TV
    Stroke; 2001 Jan; 32(1):6-11. PubMed ID: 11136906
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The spectrum of mutations for CADASIL diagnosis.
    Federico A; Bianchi S; Dotti MT
    Neurol Sci; 2005 Jun; 26(2):117-24. PubMed ID: 15995828
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.