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 *

198 related articles for article (PubMed ID: 30922590)

  • 1. Jules Sottas (1866-1945) forgotten despite the eponym: "Dejerine-Sottas syndrome".
    Walusinski O
    Rev Neurol (Paris); 2019 May; 175(5):283-290. PubMed ID: 30922590
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Alfred Vulpian and Jean-Martin Charcot in each other's shadow? From Castor and Pollux at La Salpêtrière to neurology forever.
    Bogousslavsky J; Walusinski O; Moulin T
    Eur Neurol; 2011; 65(4):215-22. PubMed ID: 21422760
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Jules Dejerine and the peripheral nervous system.
    Mathis S; Vallat JM
    Neurology; 2017 Aug; 89(6):611-615. PubMed ID: 28784633
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Jules Joseph Déjerine versus Pierre Marie.
    Paciaroni M; Bogousslavsky J
    Front Neurol Neurosci; 2011; 29():162-169. PubMed ID: 20938154
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Jules Joseph Dejerine: an outstanding neurologist and Charcot's enemy.
    Kondo GK; Schramm CC; Novaes MRR; Teive HAG
    Arq Neuropsiquiatr; 2018 May; 76(5):352-354. PubMed ID: 29898083
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dejerine-Sottas disease (progressive hypertrophic polyneuropathy).
    Pearce JM
    Eur Neurol; 2006; 55(2):115-7. PubMed ID: 16645280
    [No Abstract]   [Full Text] [Related]  

  • 7. [Charcot and his legacy to medicine].
    Camacho Aguilera JF
    Gac Med Mex; 2012; 148(3):321-6. PubMed ID: 22820369
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Aphasia: debates].
    Roch Lecours A
    Rev Neurol (Paris); 1999 Oct; 155(10):833-47. PubMed ID: 10546298
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Jules Tinel (1879-1952): Beyond the eponym, the man and his forgotten neurological contributions.
    Walusinski O
    Rev Neurol (Paris); 2017 Jun; 173(6):364-373. PubMed ID: 28377088
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Augusta Marie Déjerine-Klumpke: much more than just Déjerine's wife.
    Nogueira EAG; Carvalho VM; Queiroz MV; Rosa GR; Fragoso YD
    Arq Neuropsiquiatr; 2018 Feb; 76(2):117-119. PubMed ID: 29489967
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Édouard Brissaud, Fulgence Raymond and the succession of Charcot.
    Tatu L
    Front Neurol Neurosci; 2011; 29():52-60. PubMed ID: 20938146
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Adolphe Gubler (1821-1879) or Parisian neurology outside La Salpêtrière in the age of Jean-Martin Charcot.
    Walusinski O
    Rev Neurol (Paris); 2019 Apr; 175(4):207-216. PubMed ID: 30922591
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene.
    Roa BB; Dyck PJ; Marks HG; Chance PF; Lupski JR
    Nat Genet; 1993 Nov; 5(3):269-73. PubMed ID: 8275092
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Duels of Pierre Marie and Jules Dejerine.
    Teive H; Ferreira MG; Camargo CHF; Munhoz RP; Walusinski O
    Eur Neurol; 2020; 83(3):345-350. PubMed ID: 32690851
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Joseph Jumentié (1879-1928), a forgotten neurologist.
    Walusinski O
    Rev Neurol (Paris); 2018; 174(1-2):4-12. PubMed ID: 28673659
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chapter 40: history of neurology in France.
    Clarac F; Boller F
    Handb Clin Neurol; 2010; 95():629-56. PubMed ID: 19892143
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel homozygous mutation of the myelin Po gene producing Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III).
    Ikegami T; Nicholson G; Ikeda H; Ishida A; Johnston H; Wise G; Ouvrier R; Hayasaka K
    Biochem Biophys Res Commun; 1996 May; 222(1):107-10. PubMed ID: 8630052
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dejerine-Sottas disease: a case report.
    Marinho JL; Alonso Nieto JL; Calore EE
    Sao Paulo Med J; 2003 Sep; 121(5):207-9. PubMed ID: 14666293
    [TBL] [Abstract][Full Text] [Related]  

  • 19. De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III).
    Hayasaka K; Himoro M; Sawaishi Y; Nanao K; Takahashi T; Takada G; Nicholson GA; Ouvrier RA; Tachi N
    Nat Genet; 1993 Nov; 5(3):266-8. PubMed ID: 7506095
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Marcel Proust's lifelong tour of the Parisian Neurological Intelligentsia: from Brissaud and Dejerine to Sollier and Babinski.
    Bogousslavsky J
    Eur Neurol; 2007; 57(3):129-36. PubMed ID: 17213718
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.