BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 23487805)

  • 1. Rare neurological diseases: a practical approach to management.
    Dani KA; Murray LJ; Razvi S
    Pract Neurol; 2013 Aug; 13(4):219-27. PubMed ID: 23487805
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rare neurological diseases: a united approach is needed.
    The Lancet Neurology
    Lancet Neurol; 2011 Feb; 10(2):109. PubMed ID: 21256450
    [No Abstract]   [Full Text] [Related]  

  • 3. Rare neurological diseases: a Pandora's box for neurology (an European and Italian perspective).
    Federico A
    Rev Neurol (Paris); 2013 Feb; 169 Suppl 1():S12-7. PubMed ID: 23452765
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rare treatable neurologic diseases.
    Lorincz MT; Fink JK
    Semin Neurol; 2012 Nov; 32(5):489-90. PubMed ID: 23677655
    [No Abstract]   [Full Text] [Related]  

  • 5. Headache meets neurology and psychiatry: a framework for diagnosis.
    Haddad N; McMinn B; Hartley L
    Arch Dis Child Educ Pract Ed; 2016 Aug; 101(4):200-5. PubMed ID: 27225011
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Awareness of rare and genetic neurological diseases among italian neurologist. A national survey.
    Mancuso M; Filosto M; Lamperti C; Musumeci O; Santorelli FM; Servidei S; Valente EM; Zeviani M; Mancardi G; Tedeschi G; Federico A
    Neurol Sci; 2020 Jun; 41(6):1567-1570. PubMed ID: 31989346
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Multiomics tools for the diagnosis and treatment of rare neurological disease.
    Crowther LM; Poms M; Plecko B
    J Inherit Metab Dis; 2018 May; 41(3):425-434. PubMed ID: 29536202
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Have centers of rare neurological diseases changed their practices and management of the hereditary cerebellar ataxias?].
    Tranchant C
    Rev Neurol (Paris); 2013 Feb; 169 Suppl 1():S23-7. PubMed ID: 23452767
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Orphanet and its consortium: where to find expert-validated information on rare diseases].
    Maiella S; Rath A; Angin C; Mousson F; Kremp O
    Rev Neurol (Paris); 2013 Feb; 169 Suppl 1():S3-8. PubMed ID: 23452769
    [TBL] [Abstract][Full Text] [Related]  

  • 10. European Academy of Neurology guidance for developing and reporting clinical practice guidelines on rare neurological diseases.
    Aleksovska K; Kobulashvili T; Costa J; Zimmermann G; Ritchie K; Reinhard C; Vignatelli L; Fanciulli A; Damian M; Pavlakova L; Burgunder JM; Kopishinskaya S; Rakusa M; Kovacs N; Erdogan FF; Linton LR; Copetti M; Lamperti C; Servidei S; Evangelista T; Ayme S; Pareyson D; Sellner J; Krarup C; de Visser M; van den Bergh P; Toscano A; Graessner H; Berger T; Bassetti C; Vidailhet M; Trinka E; Deuschl G; Federico A; Leone MA
    Eur J Neurol; 2022 Jun; 29(6):1571-1586. PubMed ID: 35318776
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Functional neurological symptoms.
    Stone J
    J R Coll Physicians Edinb; 2011 Mar; 41(1):38-41; quiz 42. PubMed ID: 21365066
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Child-to-adult transition: a survey of current practices within the European Reference Network for Rare Neurological Diseases (ERN-RND).
    Nanetti L; Kearney M; Boesch S; Stovickova L; Ortigoza-Escobar JD; Macaya A; Gomez-Andres D; Roze E; Molnar MJ; Wolf NI; Darling A; Vasco G; Bertini E; Indelicato E; Neubauer D; Haack TB; Sagi JC; Danti FR; Sival D; Zanni G; Kolk A; Boespflug-Tanguy O; Schols L; van de Warrenburg B; Vidailhet M; Willemsen MA; Buizer AI; Orzes E; Ripp S; Reinhard C; Moroni I; Mariotti C;
    Neurol Sci; 2024 Mar; 45(3):1007-1016. PubMed ID: 37853291
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Rare diseases, definitions and epidemiology].
    Donnart A; Viollet V; Roinet-Tournay M
    Soins Pediatr Pueric; 2013; (274):14-6. PubMed ID: 24228328
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Management of children with neurological disorders.
    Aminoff MJ; Boller F; Swaab DF
    Handb Clin Neurol; 2013; 111():vii. PubMed ID: 23622231
    [No Abstract]   [Full Text] [Related]  

  • 15. Polish activity within Orphanet Europe--state of art of database and services.
    Jezela-Stanek A; Karczmarewicz D; Chrzanowska KH; Krajewska-Walasek M
    Dev Period Med; 2015; 19(4):536-41. PubMed ID: 26982769
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Management options for rare diseases in children and adolescents in Georgia (experience of the country with transitional economy).
    Pagava K; Abesadze G; Uberi N; Korinteli I; Paghava I; Kvezereli-Kopadze M; Parulava T; Korinteli M; Kiseliova T
    Georgian Med News; 2011 Apr; (193):8-11. PubMed ID: 21617265
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Periprocedural antithrombotic management for lumbar puncture: Association of British Neurologists clinical guideline.
    Dodd KC; Emsley HCA; Desborough MJR; Chhetri SK
    Pract Neurol; 2018 Dec; 18(6):436-446. PubMed ID: 30154234
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Role and actions of the orphan rare diseases reference center for central hypersomnias in France].
    Vecchierini MF; Léger D; Arnufl I; Dauvilliers Y
    Rev Neurol (Paris); 2013 Feb; 169 Suppl 1():S56-62. PubMed ID: 23452773
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Positive signs of functional weakness.
    Tremolizzo L; Susani E; Riva MA; Cesana G; Ferrarese C; Appollonio I
    J Neurol Sci; 2014 May; 340(1-2):13-8. PubMed ID: 24656598
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Rare diseases, a public health issue].
    Donnart A; Viollet V; Roinet-Tournay M
    Soins Pediatr Pueric; 2013; (274):17-9. PubMed ID: 24228329
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.