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 *

89 related articles for article (PubMed ID: 25562086)

  • 1. Author response.
    Echaniz-Laguna A; Latour P
    Neurology; 2014 Nov; 83(21):1991. PubMed ID: 25562086
    [No Abstract]   [Full Text] [Related]  

  • 2. Phenotypic spectrum and incidence of TRPV4 mutations in patients with inherited axonal neuropathy.
    Sullivan JM; Landouré G; Gaudet R; Sumner CJ
    Neurology; 2014 Nov; 83(21):1991. PubMed ID: 25404646
    [No Abstract]   [Full Text] [Related]  

  • 3. Phenotypic spectrum and incidence of TRPV4 mutations in patients with inherited axonal neuropathy.
    Echaniz-Laguna A; Dubourg O; Carlier P; Carlier RY; Sabouraud P; Péréon Y; Chapon F; Thauvin-Robinet C; Laforêt P; Eymard B; Latour P; Stojkovic T
    Neurology; 2014 May; 82(21):1919-26. PubMed ID: 24789864
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Disease mechanisms in inherited neuropathies.
    Suter U; Scherer SS
    Nat Rev Neurosci; 2003 Sep; 4(9):714-26. PubMed ID: 12951564
    [No Abstract]   [Full Text] [Related]  

  • 5. Lymphocyte TRPV 1-4 gene expression and MIF blood levels in a young girl clinically diagnosed with HSAN IV.
    Bachiocco V; Bergamaschi R; Spinsanti G; Lima M; Romagnoli R; Sorda G; Aloisi AM
    Clin J Pain; 2011 Sep; 27(7):631-4. PubMed ID: 21436684
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary sensory neuropathies.
    Thomas PK
    Brain Pathol; 1993 Apr; 3(2):157-63. PubMed ID: 8293177
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation in FAM134B causing severe hereditary sensory neuropathy.
    Murphy SM; Davidson GL; Brandner S; Houlden H; Reilly MM
    J Neurol Neurosurg Psychiatry; 2012 Jan; 83(1):119-20. PubMed ID: 21115472
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3.
    Kornak U; Mademan I; Schinke M; Voigt M; Krawitz P; Hecht J; Barvencik F; Schinke T; Gießelmann S; Beil FT; Pou-Serradell A; Vílchez JJ; Beetz C; Deconinck T; Timmerman V; Kaether C; De Jonghe P; Hübner CA; Gal A; Amling M; Mundlos S; Baets J; Kurth I
    Brain; 2014 Mar; 137(Pt 3):683-92. PubMed ID: 24459106
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Indifference rather than insensitivity to pain.
    Klein CJ; Sinnreich M; Dyck PJ
    Ann Neurol; 2003 Mar; 53(3):417-8; author reply 418-9. PubMed ID: 12601714
    [No Abstract]   [Full Text] [Related]  

  • 10. [A familial case with hereditary pressure-sensitive neuropathy, with "tomacula"--the first case in Japan].
    Minauchi Y; Kohka M; Igata A; Ohkatsu Y
    Rinsho Shinkeigaku; 1982 Oct; 22(10):918-25. PubMed ID: 6963557
    [No Abstract]   [Full Text] [Related]  

  • 11. Charcot-Marie-Tooth disease (hereditary motor sensory neuropathies) and hereditary sensory and autonomic neuropathies.
    Bertorini T; Narayanaswami P; Rashed H
    Neurologist; 2004 Nov; 10(6):327-37. PubMed ID: 15518599
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Case of hereditary sensory neuropathy with atypical clinical course].
    Sawicka E; Czyzewski K; Drac H
    Neurol Neurochir Pol; 1979; 13(5):541-8. PubMed ID: 293503
    [TBL] [Abstract][Full Text] [Related]  

  • 13. No mutation in the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with hereditary sensory and autonomic neuropathy type V.
    Toscano E; Simonati A; Indo Y; Andria G
    Ann Neurol; 2002 Aug; 52(2):224-7. PubMed ID: 12210794
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Late-onset hereditary sensory neuropathy type I due to SPTLC1 mutation: autopsy findings.
    Lindahl AJ; Lhatoo SD; Campbell MJ; Nicholson G; Love S
    Clin Neurol Neurosurg; 2006 Dec; 108(8):780-3. PubMed ID: 16271825
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Early-onset severe hereditary sensory and autonomic neuropathy type 1 with S331F SPTLC1 mutation.
    Suh BC; Hong YB; Nakhro K; Nam SH; Chung KW; Choi BO
    Mol Med Rep; 2014 Feb; 9(2):481-6. PubMed ID: 24247255
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Three patients in a Chinese family with hereditary sensory neuropathy mimicking leprosy.
    Shen J; Zhang G; Yang R; Hu T; Zhou M
    Lepr Rev; 2008 Dec; 79(4):441-6. PubMed ID: 19274992
    [No Abstract]   [Full Text] [Related]  

  • 17. Hereditary neuropathies in childhood: morphologic hallmarks and pathophysiologic mechanisms.
    Gabreëls-Festin A
    J Child Neurol; 1999 Jan; 14(1):52-3. PubMed ID: 10223855
    [No Abstract]   [Full Text] [Related]  

  • 18. Disease mechanisms in hereditary sensory and autonomic neuropathies.
    Verpoorten N; De Jonghe P; Timmerman V
    Neurobiol Dis; 2006 Feb; 21(2):247-55. PubMed ID: 16183296
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Oral manifestations, dental management, and a rare homozygous mutation of the PRDM12 gene in a boy with hereditary sensory and autonomic neuropathy type VIII: a case report and review of the literature.
    Elhennawy K; Reda S; Finke C; Graul-Neumann L; Jost-Brinkmann PG; Bartzela T
    J Med Case Rep; 2017 Aug; 11(1):233. PubMed ID: 28807049
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hereditary perforating ulcers of the foot: "hereditary sensory radicular neuropathy".
    Shahriaree H; Kotcamp WW; Sheikh S; Sajadi K
    Clin Orthop Relat Res; 1979 May; (140):189-93. PubMed ID: 289445
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.