BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 37064943)

  • 1. Contactin-Associated Protein-Like 2-Related Peripheral Nerve Hyperexcitability Associated With Charcot-Marie-Tooth Type 4F.
    Ferrara JM; Wiid M; Burke S
    Neurohospitalist; 2023 Apr; 13(2):164-168. PubMed ID: 37064943
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A Case Report on Charcot-Marie-Tooth Disease with a Novel Periaxin Gene Mutation.
    Datta S; Kataria S; Govindarajan R
    Cureus; 2019 Jul; 11(7):e5111. PubMed ID: 31523542
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel Compound Heterozygous Nonsense PRX Mutations in a Korean Dejerine-Sottas Neuropathy Family.
    Choi YJ; Hyun YS; Nam SH; Koo H; Hong YB; Chung KW; Choi BO
    J Clin Neurol; 2015 Jan; 11(1):92-6. PubMed ID: 25628743
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic epidemiology of Charcot-Marie-Tooth disease.
    Braathen GJ
    Acta Neurol Scand Suppl; 2012; (193):iv-22. PubMed ID: 23106488
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene.
    Taioli F; Cabrini I; Cavallaro T; Acler M; Fabrizi GM
    Brain; 2011 Feb; 134(Pt 2):608-17. PubMed ID: 21252112
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pathological evidence of demyelination in the recurrent laryngeal, phrenic, and oculomotor nerves in Charcot-Marie-Tooth disease 4F.
    Maeda K; Yamamoto Y; Ohuchi M; Sakashita T; Shiohara M; Namura T; Shintaku M; Matsuura E; Takashima H
    eNeurologicalSci; 2021 Dec; 25():100358. PubMed ID: 34993357
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Neuropathology of the spinal nerve roots, spinal cord, and brain in the first autopsied case of Charcot-Marie-Tooth disease 4F with a D651N mutation in the periaxin gene.
    Shintaku M; Maeda K; Shiohara M; Namura T; Kushima R
    Neuropathology; 2021 Aug; 41(4):281-287. PubMed ID: 34002422
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies.
    Chance PF; Fischbeck KH
    Hum Mol Genet; 1994; 3 Spec No():1503-7. PubMed ID: 7849745
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Correlation between the histopathologic, genotypic, and phenotypic features of hereditary peripheral neuropathies in childhood.
    Ouvrier R
    J Child Neurol; 1996 Mar; 11(2):133-46. PubMed ID: 8881991
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The spatiotemporal matching pattern of Ezrin/Periaxin involved in myoblast differentiation and fusion and Charcot-Marie-Tooth disease-associated muscle atrophy.
    Zhang RN; Bao X; Liu Y; Wang Y; Li XY; Tan G; Mbadhi MN; Xu W; Yang Q; Yao LY; Chen L; Zhao XY; Hu CQ; Zhang JX; Zheng HT; Wu Y; Li S; Chen SJ; Chen SY; Lv J; Shi LL; Tang JM
    J Transl Med; 2023 Mar; 21(1):173. PubMed ID: 36870952
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Late-onset Charcot-Marie-Tooth disease 4F caused by periaxin gene mutation.
    Tokunaga S; Hashiguchi A; Yoshimura A; Maeda K; Suzuki T; Haruki H; Nakamura T; Okamoto Y; Takashima H
    Neurogenetics; 2012 Nov; 13(4):359-65. PubMed ID: 22847150
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A 71-nucleotide deletion in the periaxin gene in an Italian patient with late-onset slowly progressive demyelinating Charcot-Marie-Tooth disease.
    Citrigno L; Zoccolella S; Lastella P; Simone IL; Muglia M
    Eur J Neurol; 2020 Oct; 27(10):2109-2110. PubMed ID: 32460404
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Systematic review of the clinical spectrum of CASPR2 antibody syndrome.
    Boyko M; Au KLK; Casault C; de Robles P; Pfeffer G
    J Neurol; 2020 Apr; 267(4):1137-1146. PubMed ID: 31912210
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Inherited neuropathies: Charcot-Marie-Tooth disease and related disorders.
    Chance PF; Lupski JR
    Baillieres Clin Neurol; 1994 Aug; 3(2):373-85. PubMed ID: 7952853
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The function of the Periaxin gene during nerve repair in a model of CMT4F.
    Williams AC; Brophy PJ
    J Anat; 2002 Apr; 200(4):323-30. PubMed ID: 12090399
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Inherited peripheral neuropathy.
    Keller MP; Chance PF
    Semin Neurol; 1999; 19(4):353-62. PubMed ID: 10716658
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel mutation in the periaxin gene causal to Charcot-Marie-Tooth disease type 4F.
    Chen YH; Zhang H; Meng LB; Tang XY; Gong T; Yin J
    J Int Med Res; 2020 Feb; 48(2):300060519862064. PubMed ID: 31426691
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Molecular basis of Charcot-Marie-Tooth neuropathy].
    Hayasaka K
    Nihon Rinsho; 1996 Aug; 54(8):2243-51. PubMed ID: 8810804
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations in the MORC2 gene cause axonal Charcot-Marie-Tooth disease.
    Sevilla T; Lupo V; Martínez-Rubio D; Sancho P; Sivera R; Chumillas MJ; García-Romero M; Pascual-Pascual SI; Muelas N; Dopazo J; Vílchez JJ; Palau F; Espinós C
    Brain; 2016 Jan; 139(Pt 1):62-72. PubMed ID: 26497905
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.