BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 15798438)

  • 1. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephaloapthy (CADASIL): a hereditary cerebrovascular disease, which can be diagnosed by skin biopsy electron microscopy.
    Ishiko A; Shimizu A; Nagata E; Ohta K; Tanaka M
    Am J Dermatopathol; 2005 Apr; 27(2):131-4. PubMed ID: 15798438
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Notch3 ectodomain is a major component of granular osmiophilic material (GOM) in CADASIL.
    Ishiko A; Shimizu A; Nagata E; Takahashi K; Tabira T; Suzuki N
    Acta Neuropathol; 2006 Sep; 112(3):333-9. PubMed ID: 16871402
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. Electron microscopy analysis of skin biopsies in CADASIL disease.
    Cotrutz CE; Indrei A; Bădescu L; Dacălu C; Neamţu M; Dumitrescu GF; Stefanache F; Petreuş T
    Rom J Morphol Embryol; 2010; 51(3):455-7. PubMed ID: 20809020
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients.
    Tikka S; Mykkänen K; Ruchoux MM; Bergholm R; Junna M; Pöyhönen M; Yki-Järvinen H; Joutel A; Viitanen M; Baumann M; Kalimo H
    Brain; 2009 Apr; 132(Pt 4):933-9. PubMed ID: 19174371
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Vasculopathic changes of CADASIL can be focal in skin biopsies.
    Schultz A; Santoianni R; Hewan-Lowe K
    Ultrastruct Pathol; 1999; 23(4):241-7. PubMed ID: 10503743
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): diagnostic skin biopsy changes determined by electron microscopy.
    Walsh JS; Perniciaro C; Meschia JF
    J Am Acad Dermatol; 2000 Dec; 43(6):1125-7. PubMed ID: 11100036
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. [A case of CADASIL without characteristic anterior temporal pole lesion diagnosed by skin biopsy].
    Konno T; Umeda M; Umeda Y; Nozaki H; Oyake M; Fujita N
    Rinsho Shinkeigaku; 2011 Oct; 51(10):770-3. PubMed ID: 22019870
    [TBL] [Abstract][Full Text] [Related]  

  • 10. CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): a neurovascular disease diagnosed by ultrastructural examination of the skin.
    Kanitakis J; Thobois S; Claudy A; Broussolle E
    J Cutan Pathol; 2002 Sep; 29(8):498-501. PubMed ID: 12207744
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Skin and sural nerve biopsies: ultrastructural findings in the first genetically confirmed cases of CADASIL in Serbia.
    Lackovic V; Bajcetic M; Lackovic M; Novakovic I; Labudović Borović M; Pavlovic A; Zidverc-Trajkovic J; Dzolic E; Rovcanin B; Sternic N; Kostic V
    Ultrastruct Pathol; 2012 Oct; 36(5):325-35. PubMed ID: 23025651
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Nephroangiosclerosis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: is NOTCH3 mutation the common culprit?
    Guerrot D; François A; Boffa JJ; Boulos N; Hanoy M; Legallicier B; Triquenot-Bagan A; Guyant-Marechal L; Laquerriere A; Freguin-Bouilland C; Ronco P; Godin M
    Am J Kidney Dis; 2008 Aug; 52(2):340-5. PubMed ID: 18572291
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Renal involvement in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): report of a case with a six-year follow-up.
    Ragno M; Trojano L; Pianese L; Boni MV; Silvestri S; Mambelli V; Lorenzi T; Scarpelli M; Morroni M
    Histol Histopathol; 2012 Oct; 27(10):1307-14. PubMed ID: 22936449
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Nuclear abnormalities in vascular myocytes in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    Dziewulska D; Nycz E; Rajczewska-Oleszkiewicz C; Bojakowski J; Sulejczak D
    Neuropathology; 2018 Dec; 38(6):601-608. PubMed ID: 30402942
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CADASIL disease, an inherited slowly progressive vascular dementia: case report with radiologic and electron microscopic findings.
    Shuja S; Lindquist J; Lee KP; Silliman S; Makary R
    J Stroke Cerebrovasc Dis; 2009; 18(6):491-3. PubMed ID: 19900654
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Differential diagnosis of a vascular leukoencephalopathy within a CADASIL family: use of skin biopsy electron microscopy study and direct genotypic screening.
    Furby A; Vahedi K; Force M; Larrouy S; Ruchoux MM; Joutel A; Tournier-Lasserve E
    J Neurol; 1998 Nov; 245(11):734-40. PubMed ID: 9808243
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CADASIL Presenting as Acute Bilateral Multiple Subcortical Infarcts without a Characteristic Temporal Pole or Any External Capsule Lesions.
    Ando T; Goto Y; Mano K; Ueda A; Ando Y; Mizuta I; Mizuno T
    Intern Med; 2016; 55(19):2873-2876. PubMed ID: 27725551
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [CADASIL].
    Uchino M
    Brain Nerve; 2008 Nov; 60(11):1224-34. PubMed ID: 19069156
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Ruchoux MM; Guerouaou D; Vandenhaute B; Pruvo JP; Vermersch P; Leys D
    Acta Neuropathol; 1995; 89(6):500-12. PubMed ID: 7676806
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: two novel mutations in the NOTCH3 gene in Chinese.
    Lee YC; Yang AH; Liu HC; Wong WJ; Lu YC; Chang MH; Soong BW
    J Neurol Sci; 2006 Jul; 246(1-2):111-5. PubMed ID: 16580020
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.