BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 37598468)

  • 1. NOTCH3 C201R variant causes cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) that can be confused with early-onset Alzheimer's disease.
    Korvatska O; Bucks SA; Yoda RA; Nolan A; Dorschner MO; Tsuang D; Jayadev S; Raskind WH; Bird TD
    J Neurol Sci; 2023 Sep; 452():120763. PubMed ID: 37598468
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A Novel Heterozygous Variant in Exon 19 of NOTCH3 in a Saudi Family with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.
    Algahtani H; Shirah B; Alharbi SY; Al-Qahtani MH; Abdulkareem AA; Naseer MI
    J Stroke Cerebrovasc Dis; 2020 Jul; 29(7):104832. PubMed ID: 32414585
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    Mönkäre S; Kuuluvainen L; Schleutker J; Myllykangas L; Pöyhönen M
    Acta Neurol Scand; 2022 Nov; 146(5):643-651. PubMed ID: 36086804
    [TBL] [Abstract][Full Text] [Related]  

  • 4.
    Cho BPH; Nannoni S; Harshfield EL; Tozer D; Gräf S; Bell S; Markus HS
    J Neurol Neurosurg Psychiatry; 2021 Jul; 92(7):694-701. PubMed ID: 33712516
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Family Members With a Pathogenic
    Hack RJ; Gravesteijn G; Cerfontaine MN; Hegeman IM; Mulder AA; Lesnik Oberstein SAJ; Rutten JW
    Stroke; 2022 Jun; 53(6):1964-1974. PubMed ID: 35300531
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The role of NOTCH3 variants in Alzheimer's disease and subcortical vascular dementia in the Chinese population.
    Guo L; Jiao B; Liao X; Xiao X; Zhang W; Yuan Z; Liu X; Zhou L; Wang X; Zhu Y; Yang Q; Wang J; Tang B; Shen L
    CNS Neurosci Ther; 2021 Aug; 27(8):930-940. PubMed ID: 33942994
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel and Recurring NOTCH3 Mutations in Two Chinese Patients with CADASIL.
    Chen X; Deng S; Xu H; Hou D; Hu P; Yang Y; Wen J; Deng H; Yuan L
    Neurodegener Dis; 2019; 19(1):35-42. PubMed ID: 31212292
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel heterozygous NOTCH3 pathogenic variant found in two Chinese patients with CADASIL.
    Li S; Chen Y; Shan H; Ma F; Shi M; Xue J
    J Clin Neurosci; 2017 Dec; 46():85-89. PubMed ID: 28867359
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy with a Novel NOTCH3 Cys323Trp Mutation Presenting Border-Zone Infarcts: A Case Report and Literature Review.
    Tojima M; Saito S; Yamamoto Y; Mizuno T; Ihara M; Fukuda H
    J Stroke Cerebrovasc Dis; 2016 Aug; 25(8):e128-30. PubMed ID: 27241575
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Non-convulsive status epilepticus as the initial manifestation in a family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    González F; Bala M; Saucedo M; Bandeo L; Pacio G; Chertcoff A; De Francesco L; León Cejas L; Pacha MS; Uribe Roca C; Martínez O; Fernández Pardal M; Reisin R; Bonardo P
    Neurologia (Engl Ed); 2023 Mar; 38(2):82-86. PubMed ID: 36402400
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A case of CADASIL caused by NOTCH3 c.512_605delinsA heterozygous mutation.
    Liu J; Zhang Q; Wang Q; Luan S; Dong X; Cao H; Tao D; Dong H; Ji X
    J Clin Lab Anal; 2021 Nov; 35(11):e24027. PubMed ID: 34558736
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Global Cardiovascular Risk Profile and Cerebrovascular Abnormalities in Presymptomatic Individuals with CADASIL or Autosomal Dominant Alzheimer's Disease.
    Schoemaker D; Velilla-Jimenez L; Zuluaga Y; Baena A; Ospina C; Bocanegra Y; Alvarez S; Ochoa-Escudero M; Guzmán-Vélez E; Martinez J; Lopera F; Arboleda-Velasquez JF; Quiroz YT
    J Alzheimers Dis; 2021; 82(2):841-853. PubMed ID: 34092645
    [TBL] [Abstract][Full Text] [Related]  

  • 13.
    Lee YC; Chung CP; Chang MH; Wang SJ; Liao YC
    Neurology; 2020 Jan; 94(1):e87-e96. PubMed ID: 31792094
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL family.
    Abou Al-Shaar H; Qadi N; Al-Hamed MH; Meyer BF; Bohlega S
    J Neurol Sci; 2016 Aug; 367():239-43. PubMed ID: 27423596
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cerebral Microbleed Burdens in Specific Brain Regions Are Associated With Disease Severity of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy.
    Chung CP; Chen JW; Chang FC; Li WC; Lee YC; Chen LF; Liao YC
    J Am Heart Assoc; 2020 Jul; 9(13):e016233. PubMed ID: 32552418
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Broad phenotype of cysteine-altering
    Rutten JW; Hack RJ; Duering M; Gravesteijn G; Dauwerse JG; Overzier M; van den Akker EB; Slagboom E; Holstege H; Nho K; Saykin A; Dichgans M; Malik R; Lesnik Oberstein SAJ
    Neurology; 2020 Sep; 95(13):e1835-e1843. PubMed ID: 32732295
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) associated with a novel C82R mutation in the NOTCH3 gene.
    Zea-Sevilla MA; Bermejo-Velasco P; Serrano-Heranz R; Calero M
    J Alzheimers Dis; 2015; 43(2):363-7. PubMed ID: 25096610
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Recognition of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) in Two Oligosymptomatic Sisters with Low CADASIL Scale Scores and a Venous Dysplasia: Report of a Novel Greek Family.
    Paraskevas GP; Constantinides VC; Yapijakis C; Kararizou E; Kapaki EN; Bougea A
    J Stroke Cerebrovasc Dis; 2018 Sep; 27(9):e191-e195. PubMed ID: 29706439
    [TBL] [Abstract][Full Text] [Related]  

  • 19. NOTCH3 Gene Mutation in a Chilean Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Family.
    Gallardo A; Latapiat V; Rivera A; Fonseca B; Roldan A; Sandoval P; Sánchez C; Matamala JM
    J Stroke Cerebrovasc Dis; 2020 Feb; 29(2):104530. PubMed ID: 31813735
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Associated With a Novel In-Frame Mutation in the NOTCH3 Gene in a Japanese Patient.
    Takeshi Y; Suda S; Shimoyama T; Aoki J; Suzuki K; Okubo S; Mizuta I; Mizuno T; Kimura K
    J Stroke Cerebrovasc Dis; 2020 Jan; 29(1):104482. PubMed ID: 31699577
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.