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 *

166 related articles for article (PubMed ID: 38744461)

  • 1. Highlighting the past and future of inherited peripheral neuropathies.
    Zuchner S
    J Neurol Neurosurg Psychiatry; 2024 May; ():. PubMed ID: 38744461
    [No Abstract]   [Full Text] [Related]  

  • 2. [Molecular genetics of inherited neuropathies].
    Takashima H
    Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease). Molecular-genetic aspects].
    Hertz MJ; Jensen AD; Brandt CA; Bisgård C
    Ugeskr Laeger; 1995 Jun; 157(25):3613-8. PubMed ID: 7652980
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Targeting the colony stimulating factor 1 receptor alleviates two forms of Charcot-Marie-Tooth disease in mice.
    Klein D; Patzkó Á; Schreiber D; van Hauwermeiren A; Baier M; Groh J; West BL; Martini R
    Brain; 2015 Nov; 138(Pt 11):3193-205. PubMed ID: 26297559
    [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. The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood.
    Ouvrier RA; McLeod JG; Conchin TE
    Brain; 1987 Feb; 110 ( Pt 1)():121-48. PubMed ID: 3467805
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A practical approach to the genetic neuropathies.
    Rossor AM; Evans MR; Reilly MM
    Pract Neurol; 2015 Jun; 15(3):187-98. PubMed ID: 25898997
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Charcot-Marie-Tooth disease and other inherited neuropathies.
    Saporta MA
    Continuum (Minneap Minn); 2014 Oct; 20(5 Peripheral Nervous System Disorders):1208-25. PubMed ID: 25299278
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Beware next-generation sequencing gene panels as the first-line genetic test in Charcot-Marie-Tooth disease.
    Record CJ; Pipis M; Poh R; Polke JM; Reilly MM
    J Neurol Neurosurg Psychiatry; 2023 Apr; 94(4):327-328. PubMed ID: 36376020
    [No Abstract]   [Full Text] [Related]  

  • 10. Charcot-Marie-Tooth disease type 2 associated with mutation of the myelin protein zero gene.
    Marrosu MG; Vaccargiu S; Marrosu G; Vannelli A; Cianchetti C; Muntoni F
    Neurology; 1998 May; 50(5):1397-401. PubMed ID: 9595994
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Axonal Charcot-Marie-Tooth Disease: from Common Pathogenic Mechanisms to Emerging Treatment Opportunities.
    McCray BA; Scherer SS
    Neurotherapeutics; 2021 Oct; 18(4):2269-2285. PubMed ID: 34606075
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Canine inherited motor and sensory neuropathies: an updated classification in 22 breeds and comparison to Charcot-Marie-Tooth disease.
    Granger N
    Vet J; 2011 Jun; 188(3):274-85. PubMed ID: 20638305
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary motor-sensory neuropathies. Charcot-Marie-Tooth syndrome.
    Bird TD
    Neurol Clin; 1989 Feb; 7(1):9-23. PubMed ID: 2646524
    [TBL] [Abstract][Full Text] [Related]  

  • 14. From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myelin proteins.
    Harding AE
    Brain; 1995 Jun; 118 ( Pt 3)():809-18. PubMed ID: 7541290
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical features and molecular genetics of hereditary peripheral neuropathies.
    Kuhlenbäumer G; Young P; Hünermund G; Ringelstein B; Stögbauer F
    J Neurol; 2002 Dec; 249(12):1629-50. PubMed ID: 12529785
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Progress in clinical neurosciences: Charcot-Marie-Tooth disease and related inherited peripheral neuropathies.
    Benstead TJ; Grant IA
    Can J Neurol Sci; 2001 Aug; 28(3):199-214. PubMed ID: 11513338
    [TBL] [Abstract][Full Text] [Related]  

  • 17. High diagnostic yield with algorithmic molecular approach on hereditary neuropathies.
    Ceylan GG; Habiloğlu E; Çavdarlı B; Tuncez E; Bilen S; Köken ÖY; Gündüz CNS
    Rev Assoc Med Bras (1992); 2023; 69(2):233-239. PubMed ID: 36790232
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The importance of quantitative electron microscopy in studying hypertrophic neuropathies. A comparison between a case of Déjérine Sottas disease (HMSN III) and a case of the hypertrophic form of Charcot-Marie-Tooth disease (HMSN I).
    Tredici G; Petruccioli-Pizzini MG; Gergely A; Coletti A
    Int J Tissue React; 1984; 6(3):267-74. PubMed ID: 6090332
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene.
    Sanmaneechai O; Feely S; Scherer SS; Herrmann DN; Burns J; Muntoni F; Li J; Siskind CE; Day JW; Laura M; Sumner CJ; Lloyd TE; Ramchandren S; Shy RR; Grider T; Bacon C; Finkel RS; Yum SW; Moroni I; Piscosquito G; Pareyson D; Reilly MM; Shy ME;
    Brain; 2015 Nov; 138(Pt 11):3180-92. PubMed ID: 26310628
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Overlapping molecular pathological themes link Charcot-Marie-Tooth neuropathies and hereditary spastic paraplegias.
    Timmerman V; Clowes VE; Reid E
    Exp Neurol; 2013 Aug; 246():14-25. PubMed ID: 22285450
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.