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 *

304 related articles for article (PubMed ID: 28782182)

  • 21. A novel heterozygous HTRA1 mutation is associated with autosomal dominant hereditary cerebral small vessel disease.
    Zhuo ZL; Cong L; Zhang J; Zhao XT
    Mol Genet Genomic Med; 2020 Jun; 8(6):e1111. PubMed ID: 32239807
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Cerebral small vessel disease caused by a novel heterozygous mutation in HTRA1.
    Thaler FS; Catak C; Einhäupl M; Müller S; Seelos K; Wollenweber FA; Kümpfel T
    J Neurol Sci; 2018 May; 388():19-21. PubMed ID: 29627020
    [No Abstract]   [Full Text] [Related]  

  • 23. A Chinese CARASIL Patient Caused by Novel Compound Heterozygous Mutations in HTRA1.
    Xie F; Zhang LS
    J Stroke Cerebrovasc Dis; 2018 Oct; 27(10):2840-2842. PubMed ID: 30068478
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prevalence of CADASIL and Fabry Disease in a Cohort of MRI Defined Younger Onset Lacunar Stroke.
    Kilarski LL; Rutten-Jacobs LC; Bevan S; Baker R; Hassan A; Hughes DA; Markus HS;
    PLoS One; 2015; 10(8):e0136352. PubMed ID: 26305465
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A Case of Leukoencephalopathy and Small Vessels Disease Caused by a Novel HTRA1 Homozygous Mutation.
    Gündüz T; Demirkol Y; Doğan Ö; Demir S; Akçakaya NH
    J Stroke Cerebrovasc Dis; 2019 Nov; 28(11):104354. PubMed ID: 31494012
    [TBL] [Abstract][Full Text] [Related]  

  • 26. One Disease with two Faces: Semidominant Inheritance of a Novel HTRA1 Mutation in a Consanguineous Family.
    Bekircan-Kurt CE; Çetinkaya A; Gocmen R; Koşukcu C; Soylemezoglu F; Arsava EM; Tuncer A; Erdem-Ozdamar S; Akarsu NA; Topcuoglu MA
    J Stroke Cerebrovasc Dis; 2021 Sep; 30(9):105997. PubMed ID: 34303089
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel heterozygous HTRA1 mutation in an Asian family with CADASIL-like disease.
    Cao H; Liu J; Tian W; Ji X; Wang Q; Luan S; Dong X; Dong H
    J Clin Lab Anal; 2022 Feb; 36(2):e24174. PubMed ID: 34951056
    [TBL] [Abstract][Full Text] [Related]  

  • 28. CARASIL - A Review of Patients from India.
    Khandelwal D; Mathur V; Vyas A; Ghunawat J; Bagaria AK
    Neurol India; 2021; 69(5):1359-1362. PubMed ID: 34747813
    [TBL] [Abstract][Full Text] [Related]  

  • 29.
    Uemura M; Nozaki H; Kato T; Koyama A; Sakai N; Ando S; Kanazawa M; Hishikawa N; Nishimoto Y; Polavarapu K; Nalini A; Hanazono A; Kuzume D; Shindo A; El-Ghanem M; Abe A; Sato A; Yoshida M; Ikeuchi T; Mizuta I; Mizuno T; Onodera O
    Front Neurol; 2020; 11():545. PubMed ID: 32719647
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Molecular mechanism and therapeutic strategy for cerebral small vessel disease].
    Hara K
    Rinsho Shinkeigaku; 2010 Nov; 50(11):852-4. PubMed ID: 21921470
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A novel mutation of the high-temperature requirement A serine peptidase 1 (HTRA1) gene in a Chinese family with cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL).
    Chen Y; He Z; Meng S; Li L; Yang H; Zhang X
    J Int Med Res; 2013 Oct; 41(5):1445-55. PubMed ID: 23963851
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients.
    Pantoni L; Pescini F; Nannucci S; Sarti C; Bianchi S; Dotti MT; Federico A; Inzitari D
    Neurology; 2010 Jan; 74(1):57-63. PubMed ID: 20038773
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Whole-exome sequencing of Finnish patients with vascular cognitive impairment.
    Mönkäre S; Kuuluvainen L; Kun-Rodrigues C; Carmona S; Schleutker J; Bras J; Pöyhönen M; Guerreiro R; Myllykangas L
    Eur J Hum Genet; 2021 Apr; 29(4):663-671. PubMed ID: 33268848
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease.
    Schmidt H; Zeginigg M; Wiltgen M; Freudenberger P; Petrovic K; Cavalieri M; Gider P; Enzinger C; Fornage M; Debette S; Rotter JI; Ikram MA; Launer LJ; Schmidt R;
    Brain; 2011 Nov; 134(Pt 11):3384-97. PubMed ID: 22006983
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Association of
    Cerfontaine MN; Hack RJ; Gesierich B; Duering M; Witjes-Ané MW; Rodríguez-Girondo M; Gravesteijn G; Rutten J; Lesnik Oberstein SAJ
    Neurology; 2024 May; 102(10):e209310. PubMed ID: 38713890
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Association of Vascular Risk Factors and Genetic Factors With Penetrance of Variants Causing Monogenic Stroke.
    Cho BPH; Harshfield EL; Al-Thani M; Tozer DJ; Bell S; Markus HS
    JAMA Neurol; 2022 Dec; 79(12):1303-1311. PubMed ID: 36300346
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Hereditary cerebral small vessel disease: Assessment of a HTRA1 variant using protein stability predictors and 3D modelling.
    Hidalgo Mayoral I; Martínez-Salio A; Llamas-Velasco S; Gómez-Majón I; Arteche-López A; Quesada-Espinosa JF; Palma Milla C; Lezana Rosales JM; Pérez de la Fuente R; Juárez Rufián A; Sierra Tomillo O; Sánchez Calvín MT; Gómez Rodríguez MJ; Ramos Gómez P; Villarejo-Galende A; Díaz-Guzmán J; Ortega-Casarrubios MÁ; Calleja-Castaño P; Moreno-García M
    Eur J Med Genet; 2022 Aug; 65(8):104539. PubMed ID: 35705147
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Distinct molecular mechanisms of HTRA1 mutants in manifesting heterozygotes with CARASIL.
    Nozaki H; Kato T; Nihonmatsu M; Saito Y; Mizuta I; Noda T; Koike R; Miyazaki K; Kaito M; Ito S; Makino M; Koyama A; Shiga A; Uemura M; Sekine Y; Murakami A; Moritani S; Hara K; Yokoseki A; Kuwano R; Endo N; Momotsu T; Yoshida M; Nishizawa M; Mizuno T; Onodera O
    Neurology; 2016 May; 86(21):1964-74. PubMed ID: 27164673
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Systematic Review of Cerebral Phenotypes Associated With Monogenic Cerebral Small-Vessel Disease.
    Whittaker E; Thrippleton S; Chong LYW; Collins VG; Ferguson AC; Henshall DE; Lancastle E; Wilkinson T; Wilson B; Wilson K; Sudlow C; Wardlaw J; Rannikmäe K
    J Am Heart Assoc; 2022 Jun; 11(12):e025629. PubMed ID: 35699195
    [TBL] [Abstract][Full Text] [Related]  

  • 40. High frequency of
    Uemura M; Hatano Y; Nozaki H; Ando S; Kondo H; Hanazono A; Iwanaga A; Murota H; Osakada Y; Osaki M; Kanazawa M; Kanai M; Shibata Y; Saika R; Miyatake T; Aizawa H; Ikeuchi T; Tomimoto H; Mizuta I; Mizuno T; Ishihara T; Onodera O
    J Neurol Neurosurg Psychiatry; 2023 Jan; 94(1):74-81. PubMed ID: 36261288
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.