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 *

170 related articles for article (PubMed ID: 28747762)

  • 21. 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]  

  • 22. Myelin protein zero (MPZ) gene mutations in nonduplication type 1 Charcot-Marie-Tooth disease.
    Roa BB; Warner LE; Garcia CA; Russo D; Lovelace R; Chance PF; Lupski JR
    Hum Mutat; 1996; 7(1):36-45. PubMed ID: 8664899
    [TBL] [Abstract][Full Text] [Related]  

  • 23. New vistas on the pathomechanism of Charcot-Marie-Tooth and related peripheral neuropathies.
    Müller HW
    Ann N Y Acad Sci; 1999 Sep; 883():152-9. PubMed ID: 10586241
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients.
    Mersiyanova IV; Ismailov SM; Polyakov AV; Dadali EL; Fedotov VP; Nelis E; Löfgren A; Timmerman V; van Broeckhoven C; Evgrafov OV
    Hum Mutat; 2000; 15(4):340-7. PubMed ID: 10737979
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Dynamics of the Peripheral Membrane Protein P2 from Human Myelin Measured by Neutron Scattering--A Comparison between Wild-Type Protein and a Hinge Mutant.
    Laulumaa S; Nieminen T; Lehtimäki M; Aggarwal S; Simons M; Koza MM; Vattulainen I; Kursula P; Natali F
    PLoS One; 2015; 10(6):e0128954. PubMed ID: 26068118
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Myelin protein zero gene mutations in Taiwanese patients with Charcot-Marie-Tooth disease type 1.
    Lee YC; Soong BW; Lin KP; Lee HY; Wu ZA; Kao KP
    J Neurol Sci; 2004 Apr; 219(1-2):95-100. PubMed ID: 15050444
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B.
    Latour P; Blanquet F; Nelis E; Bonnebouche C; Chapon F; Diraison P; Ollagnon E; Dautigny A; Pham-Dinh D; Chazot G
    Hum Mutat; 1995; 6(1):50-4. PubMed ID: 7550231
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Conformational Stability and Pathogenic Misfolding of the Integral Membrane Protein PMP22.
    Schlebach JP; Narayan M; Alford C; Mittendorf KF; Carter BD; Li J; Sanders CR
    J Am Chem Soc; 2015 Jul; 137(27):8758-68. PubMed ID: 26102530
    [TBL] [Abstract][Full Text] [Related]  

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

  • 31. Mutations in the Myelin Protein Zero result in a spectrum of Charcot-Marie-Tooth phenotypes.
    Kochański A
    Acta Myol; 2004 May; 23(1):6-9. PubMed ID: 15298082
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Unraveling the etiology of myelin disorders: the P2 case in Charcot-Marie-Tooth disease.
    Pusterla J; Montich GG; Oliveira RG
    FEBS J; 2021 Dec; 288(23):6677-6679. PubMed ID: 34327848
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Screening for
    Zhao X; Jiang MM; Yan YZ; Liu L; Xie YZ; Li XB; Hu ZM; Zi XH; Xia K; Tang BS; Zhang RX
    Chin Med J (Engl); 2018 Jan; 131(2):151-155. PubMed ID: 29336362
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [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]  

  • 35. Clinical and electrophysiological features in Charcot-Marie-Tooth disease with mutations in the NEFL gene.
    Miltenberger-Miltenyi G; Janecke AR; Wanschitz JV; Timmerman V; Windpassinger C; Auer-Grumbach M; Löscher WN
    Arch Neurol; 2007 Jul; 64(7):966-70. PubMed ID: 17620486
    [TBL] [Abstract][Full Text] [Related]  

  • 36. New mutation of the myelin P0 gene in a pedigree of Charcot-Marie-Tooth neuropathy 1.
    Himoro M; Yoshikawa H; Matsui T; Mitsui Y; Takahashi M; Kaido M; Nishimura T; Sawaishi Y; Takada G; Hayasaka K
    Biochem Mol Biol Int; 1993 Sep; 31(1):169-73. PubMed ID: 7505151
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Axonal Charcot-Marie-Tooth disease patient-derived motor neurons demonstrate disease-specific phenotypes including abnormal electrophysiological properties.
    Saporta MA; Dang V; Volfson D; Zou B; Xie XS; Adebola A; Liem RK; Shy M; Dimos JT
    Exp Neurol; 2015 Jan; 263():190-9. PubMed ID: 25448007
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mutation testing in Charcot-Marie-Tooth neuropathy.
    Nicholson GA
    Ann N Y Acad Sci; 1999 Sep; 883():383-8. PubMed ID: 10586262
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease and related neuropathies.
    Silander K; Meretoja P; Juvonen V; Ignatius J; Pihko H; Saarinen A; Wallden T; Herrgård E; Aula P; Savontaus ML
    Hum Mutat; 1998; 12(1):59-68. PubMed ID: 9633821
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Missense mutations in the SH3TC2 protein causing Charcot-Marie-Tooth disease type 4C affect its localization in the plasma membrane and endocytic pathway.
    Lupo V; Galindo MI; Martínez-Rubio D; Sevilla T; Vílchez JJ; Palau F; Espinós C
    Hum Mol Genet; 2009 Dec; 18(23):4603-14. PubMed ID: 19744956
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.