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 *

277 related articles for article (PubMed ID: 36625892)

  • 21. Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease.
    Verdura E; Hervé D; Scharrer E; Amador Mdel M; Guyant-Maréchal L; Philippi A; Corlobé A; Bergametti F; Gazal S; Prieto-Morin C; Beaufort N; Le Bail B; Viakhireva I; Dichgans M; Chabriat H; Haffner C; Tournier-Lasserve E
    Brain; 2015 Aug; 138(Pt 8):2347-58. PubMed ID: 26063658
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Two Unique Mutations in HTRA1-Related Cerebral Small Vessel Disease in North America and Africa and Literature Review.
    Shang T; Pinho M; Ray D; Khera A
    J Stroke Cerebrovasc Dis; 2021 Nov; 30(11):106029. PubMed ID: 34461444
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease.
    Di Donato I; Bianchi S; Gallus GN; Cerase A; Taglia I; Pescini F; Nannucci S; Battisti C; Inzitari D; Pantoni L; Zini A; Federico A; Dotti MT
    CNS Neurosci Ther; 2017 Sep; 23(9):759-765. PubMed ID: 28782182
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Cerebral Small Vessel Disease Related to a Heterozygous Nonsense Mutation in HTRA1.
    Ohta K; Ozawa T; Fujinaka H; Goto K; Nakajima T
    Intern Med; 2020 May; 59(10):1309-1313. PubMed ID: 32101834
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Histopathologic features of an autopsied patient with cerebral small vessel disease and a heterozygous HTRA1 mutation.
    Ito J; Nozaki H; Toyoshima Y; Abe T; Sato A; Hashidate H; Igarashi S; Onodera O; Takahashi H; Kakita A
    Neuropathology; 2018 May; ():. PubMed ID: 29797751
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CARASIL)].
    Uemura M; Nozaki H; Onodera O
    Brain Nerve; 2017 Jan; 69(1):25-33. PubMed ID: 28126975
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A human induced pluripotent stem cell model from a patient with hereditary cerebral small vessel disease carrying a heterozygous R302Q mutation in HTRA1.
    Qian E; Uemura M; Kobayashi H; Nakamura S; Ozawa F; Yoshimatsu S; Ishikawa M; Onodera O; Morimoto S; Okano H
    Inflamm Regen; 2023 Apr; 43(1):23. PubMed ID: 37009886
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Heterozygous HTRA1 missense mutation in CADASIL-like family disease.
    Wu X; Li C; Mao J; Li L; Liu Y; Hou Y
    Braz J Med Biol Res; 2018 Mar; 51(5):e6632. PubMed ID: 29561953
    [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. Blood-brain barrier leakage is more widespread in patients with cerebral small vessel disease.
    Zhang CE; Wong SM; van de Haar HJ; Staals J; Jansen JF; Jeukens CR; Hofman PA; van Oostenbrugge RJ; Backes WH
    Neurology; 2017 Jan; 88(5):426-432. PubMed ID: 28031395
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Identified novel heterozygous
    Chen MJ; Zhang Y; Luo WJ; Dong HL; Wei Q; Zhang J; Ruan QQ; Ni W; Li HF
    Front Genet; 2022; 13():909131. PubMed ID: 36035189
    [No Abstract]   [Full Text] [Related]  

  • 32. Blood-brain barrier leakage in relation to white matter hyperintensity volume and cognition in small vessel disease and normal aging.
    Zhang CE; Wong SM; Uiterwijk R; Backes WH; Jansen JFA; Jeukens CRLPN; van Oostenbrugge RJ; Staals J
    Brain Imaging Behav; 2019 Apr; 13(2):389-395. PubMed ID: 29572621
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Characterization of Heterozygous
    Lee YC; Chung CP; Chao NC; Fuh JL; Chang FC; Soong BW; Liao YC
    Stroke; 2018 Jul; 49(7):1593-1601. PubMed ID: 29895533
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Clinicoradiographic and genetic features of cerebral small vessel disease indicate variability in mode of inheritance for monoallelic HTRA1 variants.
    Muthusamy K; Ferrer A; Klee EW; Wierenga KJ; Gavrilova RH
    Mol Genet Genomic Med; 2021 Oct; 9(10):e1799. PubMed ID: 34510819
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Increased extracellular fluid is associated with white matter fiber degeneration in CADASIL: in vivo evidence from diffusion magnetic resonance imaging.
    Yu X; Yin X; Hong H; Wang S; Jiaerken Y; Zhang F; Pasternak O; Zhang R; Yang L; Lou M; Zhang M; Huang P
    Fluids Barriers CNS; 2021 Jun; 18(1):29. PubMed ID: 34193191
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): from discovery to gene identification.
    Fukutake T
    J Stroke Cerebrovasc Dis; 2011; 20(2):85-93. PubMed ID: 21215656
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Case report: Two unique nonsense mutations in
    Chen W; Wang Y; Huang S; Yang X; Shen L; Wu D
    Front Neurol; 2022; 13():1069453. PubMed ID: 36619910
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 14.