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 *

168 related articles for article (PubMed ID: 14287596)

  • 1. [CLINICAL AND CYTOGENETIC FINDINGS ON A FAMILIAL STRAIN OF NEURAL PROGRESSIVE MUSCULAR ATROPHY OF THE CHARCOT-MARIE TYPE].
    IMBERCIADORI E
    Riv Neurobiol; 1964; 10():509-14. PubMed ID: 14287596
    [No Abstract]   [Full Text] [Related]  

  • 2. [A FAMILY OF PROGRESSIVE NEUROPATHIC MUSCULAR ATROPHY (CHARCOT-MARIE-TOOTH TYPE)].
    ANDO S; TAKEUCHI K; SONODA T; OKANIWA T
    No To Shinkei; 1964 Dec; 16():1029-35. PubMed ID: 14278773
    [No Abstract]   [Full Text] [Related]  

  • 3. [Charcot-Marie type of neural progressive muscular atrophy following electric injury].
    MACCAGNANI F; VIZIOLI R
    Riv Neurol; 1954; 24(3):381-7. PubMed ID: 13225458
    [No Abstract]   [Full Text] [Related]  

  • 4. [Progressive neural muscular atrophy (amyotrophy of Charcot-Marie-Tooth)].
    STOJILJKOVIC S; ROKNIC M
    Med Glas; 1961; 15():335-6. PubMed ID: 13917368
    [No Abstract]   [Full Text] [Related]  

  • 5. Progressive neuropathic (peroneal) muscular atrophy (Charcot-Marie-Tooth disease); histological findings in muscle biopsy specimens in fourteen cases, with notes on clinical diagnosis and familial occurrence.
    BRODAL A; BOYESEN S; FROVIG AG
    AMA Arch Neurol Psychiatry; 1953 Jul; 70(1):1-29. PubMed ID: 13057401
    [No Abstract]   [Full Text] [Related]  

  • 6. [Two cases of neural progressive muscular atrophy].
    TANSELLA G
    G Med Mil; 1950; 97(2):164-73. PubMed ID: 15421522
    [No Abstract]   [Full Text] [Related]  

  • 7. [Neurogenic muscular atrophy of Charcot-Marie-Tooth-Hoffman type, associated with bilateral optic atrophy].
    BRIHAYE M; NENQUIN-KLAASSEN E; BERTHOLET G
    Acta Neurol Psychiatr Belg; 1956 May; 56(5):302-12. PubMed ID: 13339286
    [No Abstract]   [Full Text] [Related]  

  • 8. [The urinary 17-ketosteroids in Charcot-Marie-Tooth-type peroneal progressive muscular atrophy].
    PIZZOFERRATO A; CIUCCARELLI C; CHIARELLI A
    Bull Sci Med (Bologna); 1963; 135():149-53. PubMed ID: 13943903
    [No Abstract]   [Full Text] [Related]  

  • 9. Cavus versus planus in the neuropathic foot (peroneal muscular atrophy reconsidered).
    Siegel IM
    Muscle Nerve; 1996 Jun; 19(6):797. PubMed ID: 8609940
    [No Abstract]   [Full Text] [Related]  

  • 10. [Contribution to the study of heredo-familial dystrophic syndrome; case of the association of Charcot-Marie type of amyotrophia with Friedreich's disease].
    SANGUINETI I
    Sist Nerv; 1950; 2(2):141-4. PubMed ID: 12984164
    [No Abstract]   [Full Text] [Related]  

  • 11. A VIRGINIA KINSHIP WITH HEREDITARY SENSORY NEUROPATHY: PERONEAL MUSCULAR ATROPHY AND PES CAVUS.
    DYCK PJ; KENNEL AJ; MAGAL IV; KRAYBILL EN
    Mayo Clin Proc; 1965 Sep; 40():685-94. PubMed ID: 14341177
    [No Abstract]   [Full Text] [Related]  

  • 12. [EXAMINATION OF NORMAL PARENTS OF PATIENTS WITH PROGRESSIVE MUSCULAR ATROPHY].
    KRYSHOVA NA; OZERESKOVSKAIA NG
    Vopr Psikhiatr Nevropatol; 1964; 10():108-20. PubMed ID: 14286649
    [No Abstract]   [Full Text] [Related]  

  • 13. [CASE OF MYELOPATHIC MUSCULAR ATROPHY THOUGHT AT FIRST TO BE PROGRESSIVE MUSCULAR DYSTROPHY--A VIEW OF THE RELATION BETWEEN KUGELBERG-WELANDER'S MUSCULAR ATROPHY AND WERDNIG-HOFFMANN DISEASE].
    FURUKAWA S; MAMIYA S
    Nihon Shonika Gakkai Zasshi; 1963 Nov; 67():745-8. PubMed ID: 14096316
    [No Abstract]   [Full Text] [Related]  

  • 14. [Posterior ganglio-radicular semeiology in Charcot-Marie-Tooth amyotrophy; trophic disorders, fulgurant pains, sensory disorders].
    BARRAQUER-FERRE L; BARRAQUER-BORDAS L
    Acta Neurol Psychiatr Belg; 1953 Jan; 53(1):55-70. PubMed ID: 13039975
    [No Abstract]   [Full Text] [Related]  

  • 15. [CASE OF CHARCOT-MARIE MUSCULAR ATROPHY IN A FAMILY FROM VALAIS].
    LORENZ J
    J Genet Hum; 1964 Sep; 13():207-13. PubMed ID: 14230030
    [No Abstract]   [Full Text] [Related]  

  • 16. [Genetic aspects of primary myopathies, infantile progressive spinal atrophy (Werdnig-Hoffman atrophy) and neural atrophy (Charcot-Marie-Tooth disease)].
    HANHART E
    Acta Neurol Psychiatr Belg; 1954 Feb; 54(2):91-119. PubMed ID: 13157965
    [No Abstract]   [Full Text] [Related]  

  • 17. HEREDITARY PROXIMAL SPINAL MUSCULAR ATROPHY. BIOCHEMICAL INVESTIGATIONS.
    IONASESCU V; LUCA N; PETRESCU A; CALCAIANU G
    Confin Neurol; 1965; 25():79-86. PubMed ID: 14267799
    [No Abstract]   [Full Text] [Related]  

  • 18. Type I spinal muscular atrophy can mimic sensory-motor axonal neuropathy.
    Anagnostou E; Miller SP; Guiot MC; Karpati G; Simard L; Dilenge ME; Shevell MI
    J Child Neurol; 2005 Feb; 20(2):147-50. PubMed ID: 15794183
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Charcot-Marie amyotrophia].
    BOGAERT LV
    Rev Neurol (Paris); 1952; 86(6 bis):745-53. PubMed ID: 13004633
    [No Abstract]   [Full Text] [Related]  

  • 20. [The nosological situation of hereditary motor and sensory neuropathies (HMSN, Charcot-Marie-Tooth disease, neural muscular atrophy)].
    Warzok R; Wattig B; Schwesinger G; Schneeweiss H; Heydenreich F
    Zentralbl Allg Pathol; 1990; 136(6):549-62. PubMed ID: 2281721
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.