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 *

192 related articles for article (PubMed ID: 26227883)

  • 1. Absence of Dystrophin Related Protein-2 disrupts Cajal bands in a patient with Charcot-Marie-Tooth disease.
    Brennan KM; Bai Y; Pisciotta C; Wang S; Feely SM; Hoegger M; Gutmann L; Moore SA; Gonzalez M; Sherman DL; Brophy PJ; Züchner S; Shy ME
    Neuromuscul Disord; 2015 Oct; 25(10):786-93. PubMed ID: 26227883
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Expanding the Clinical Spectrum of
    Sivera R; Pelayo-Negro AL; Jericó I; Domínguez-González C; Horga A; Rodriguez De Rivera FJ; Gallardo E; Tembl JI; Bermejo-Guerrero L; Pagola Lorz MI; Azorín I; Cordoba M; Fenollar-Cortés MDM; Millet E; Vilchez JJ; Espinós C; Apellániz-Ruiz M; Sevilla T
    Neurology; 2024 Apr; 102(7):e209174. PubMed ID: 38513194
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A murine model of Charcot-Marie-Tooth disease 4F reveals a role for the C-terminus of periaxin in the formation and stabilization of Cajal bands.
    Sherman DL; Brophy PJ
    Wellcome Open Res; 2018; 3():20. PubMed ID: 29623298
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Specific disruption of a schwann cell dystrophin-related protein complex in a demyelinating neuropathy.
    Sherman DL; Fabrizi C; Gillespie CS; Brophy PJ
    Neuron; 2001 Jun; 30(3):677-87. PubMed ID: 11430802
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Drp2 and periaxin form Cajal bands with dystroglycan but have distinct roles in Schwann cell growth.
    Sherman DL; Wu LM; Grove M; Gillespie CS; Brophy PJ
    J Neurosci; 2012 Jul; 32(27):9419-28. PubMed ID: 22764250
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review.
    Berciano J; García A; Gallardo E; Peeters K; Pelayo-Negro AL; Álvarez-Paradelo S; Gazulla J; Martínez-Tames M; Infante J; Jordanova A
    J Neurol; 2017 Aug; 264(8):1655-1677. PubMed ID: 28364294
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy.
    Claeys KG; Züchner S; Kennerson M; Berciano J; Garcia A; Verhoeven K; Storey E; Merory JR; Bienfait HM; Lammens M; Nelis E; Baets J; De Vriendt E; Berneman ZN; De Veuster I; Vance JM; Nicholson G; Timmerman V; De Jonghe P
    Brain; 2009 Jul; 132(Pt 7):1741-52. PubMed ID: 19502294
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Shortened internodal length of dermal myelinated nerve fibres in Charcot-Marie-Tooth disease type 1A.
    Saporta MA; Katona I; Lewis RA; Masse S; Shy ME; Li J
    Brain; 2009 Dec; 132(Pt 12):3263-73. PubMed ID: 19923170
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Myelinated fibers in Charcot-Marie-Tooth disease type 1B with Arg98His mutation of Po protein.
    Ohnishi A; Yamamoto T; Yamamori S; Sudo K; Fukushima Y; Ikeda M
    J Neurol Sci; 1999 Dec; 171(2):97-109. PubMed ID: 10581375
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Myelin abnormality in Charcot-Marie-Tooth type 4J recapitulates features of acquired demyelination.
    Hu B; McCollum M; Ravi V; Arpag S; Moiseev D; Castoro R; Mobley B; Burnette B; Siskind C; Day J; Yawn R; Feely S; Li Y; Yan Q; Shy M; Li J
    Ann Neurol; 2018 Apr; 83(4):756-770. PubMed ID: 29518270
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pathomechanisms of mutant proteins in Charcot-Marie-Tooth disease.
    Niemann A; Berger P; Suter U
    Neuromolecular Med; 2006; 8(1-2):217-42. PubMed ID: 16775378
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Clinicopathological features in two families with MARS-related Charcot-Marie-Tooth disease.
    Ma Z; Lv H; Zhang H; Wang H; Li J; Yu M; Zhu Y; Huang D; Meng L; Yuan Y
    Neuropathology; 2022 Dec; 42(6):505-511. PubMed ID: 35723632
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Charcot-Marie-Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genes.
    Street VA; Meekins G; Lipe HP; Seltzer WK; Carter GT; Kraft GH; Bird TD
    Neuromuscul Disord; 2002 Oct; 12(7-8):643-50. PubMed ID: 12207932
    [TBL] [Abstract][Full Text] [Related]  

  • 17. X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic study.
    Birouk N; LeGuern E; Maisonobe T; Rouger H; Gouider R; Tardieu S; Gugenheim M; Routon MC; Léger JM; Agid Y; Brice A; Bouche P
    Neurology; 1998 Apr; 50(4):1074-82. PubMed ID: 9566397
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Remodeling of motor nerve terminals in demyelinating axons of periaxin-null mice.
    Court FA; Brophy PJ; Ribchester RR
    Glia; 2008 Mar; 56(4):471-9. PubMed ID: 18205176
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease.
    Guilbot A; Williams A; Ravisé N; Verny C; Brice A; Sherman DL; Brophy PJ; LeGuern E; Delague V; Bareil C; Mégarbané A; Claustres M
    Hum Mol Genet; 2001 Feb; 10(4):415-21. PubMed ID: 11157804
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: a 20-year study.
    Bird TD; Kraft GH; Lipe HP; Kenney KL; Sumi SM
    Ann Neurol; 1997 Apr; 41(4):463-9. PubMed ID: 9124803
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.