BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 4103557)

  • 21. Charcot-Marie-Tooth disease associated with "essential tremor": Report of 7 cases and a review of the literature.
    Salisachs P
    J Neurol Sci; 1976 May; 28(1):17-40. PubMed ID: 932772
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Somatosensory evoked potentials and sensory and motor conduction in Friedreich's ataxia].
    Vacek J; Vymazal J; Nevsímalová S
    Cesk Neurol Neurochir; 1980 May; 43(3):161-7. PubMed ID: 7397868
    [No Abstract]   [Full Text] [Related]  

  • 23. Electrophysiological and histological follow-up study in 15 Friedreich's ataxia patients.
    Santoro L; Perretti A; Crisci C; Ragno M; Massini R; Filla A; De Michele G; Caruso G
    Muscle Nerve; 1990 Jun; 13(6):536-40. PubMed ID: 2366825
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Roussy-Levy hereditary areflexic dysstasia. Its historical relation to Friedreich's disease, Charcot-Marie-Tooth atrophy and Dejerine-Sottas hypertrophic neuritis; the present status of the original family; the nosologic role of this entity].
    Lapresle J
    Rev Neurol (Paris); 1982; 138(12):967-78. PubMed ID: 6763298
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Friedreich's ataxia in northern Italy: I. Clinical, neurophysiological and in vivo biochemical studies.
    D'Angelo A; DiDonato S; Negri G; Beulche F; Uziel G; Boeri R
    Can J Neurol Sci; 1980 Nov; 7(4):359-65. PubMed ID: 7214251
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Clinical contribution to the knowledge of the forms of passage or of association between Friedreich's disease and Charcot-Marie-Tooth amyotrophy].
    URAS A; GAGGINO G
    Rass Med Sarda; 1960; 62():203-14. PubMed ID: 13840430
    [No Abstract]   [Full Text] [Related]  

  • 27. Very late-onset Friedreich's ataxia with minimal GAA1 expansion mimicking multiple system atrophy of cerebellar type.
    Berciano J; Infante J; García A; Polo JM; Volpini V; Combarros O
    Mov Disord; 2005 Dec; 20(12):1643-5. PubMed ID: 16092110
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The peripheral neuropathy of Friedreich's ataxia.
    Preswick G
    Electroencephalogr Clin Neurophysiol; 1968 Oct; 25(4):399. PubMed ID: 4176572
    [No Abstract]   [Full Text] [Related]  

  • 29. [The two siblings of Friedreich's ataxia with proximal neurogenic muscular atrophy (author's transl)].
    Ikeda S; Hanyu N; Oguchi K; Yanagisawa N; Tsukagoshi H
    Rinsho Shinkeigaku; 1980 Apr; 20(4):280-5. PubMed ID: 7408332
    [No Abstract]   [Full Text] [Related]  

  • 30. Visual evoked potential abnormalities in Charcot-Marie-Tooth disease and comparison with Friedreich's ataxia.
    Carroll WM; Jones SJ; Halliday AM
    J Neurol Sci; 1983 Sep; 61(1):123-33. PubMed ID: 6631447
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Motor evoked potentials by magnetic stimulation in hereditary and sporadic ataxia.
    Mondelli M; Rossi A; Scarpini C; Guazzi GC
    Electromyogr Clin Neurophysiol; 1995 Nov; 35(7):415-24. PubMed ID: 8549432
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Are Friedreich's disease, Charcot-Marie disease and Déjérine-Sottas disease distinct nosologic entities? Two familial cases with associated syndromes].
    BULGARELLI R; LEVA R
    Minerva Pediatr; 1954 Jul; 6(13):497-502. PubMed ID: 13203336
    [No Abstract]   [Full Text] [Related]  

  • 33. [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]  

  • 34. [Disorders of neural conduction in Friedreich's ataxia. Comparison with the results in other ataxias and heredo-familial diseases].
    Cruz Martínez A
    Rev Clin Esp; 1974 Aug; 134(3):249-58. PubMed ID: 4438729
    [No Abstract]   [Full Text] [Related]  

  • 35. Spinal deformity associated with heritable neurological conditions: spinal muscular atrophy, Friedreich's ataxia, familial dysautonomia, and Charcot-Marie-Tooth disease.
    Hensinger RN; MacEwen GD
    J Bone Joint Surg Am; 1976 Jan; 58(1):13-24. PubMed ID: 1249100
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Cortical and peripheral responses evoked by stimulation of the nerve in pathology of the posterior funiculi].
    Bergamini L; Bergamasco B; Fra L; Gandiglio G; Mombelli AM; Mutani R
    Rev Neurol (Paris); 1966 Jul; 115(1):99-112. PubMed ID: 5957655
    [No Abstract]   [Full Text] [Related]  

  • 37. Clinical and electrodiagnostic features of Charcot-Marie-Tooth syndrome.
    Brust JC; Lovelace RE; Devi S
    Acta Neurol Scand Suppl; 1978; 68():1-142. PubMed ID: 212921
    [No Abstract]   [Full Text] [Related]  

  • 38. [Friedreich's ataxia: recent developments and prospects for treatment].
    Legros B; Manto MU
    Rev Med Brux; 1999 Apr; 20(2):73-9. PubMed ID: 10335100
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [SYNDROME OF SPINO-CEREBELLAR DEGENERATION WITH OPTIC ATROPHY AND DISTAL AMYOTROPHY OF THE CHARCOT-MARIE-TOOTH TYPE IN A 4-YEAR-OLD CHILD].
    BERNARD R; MOUREN P; SOULAYROL R; PINSARD N
    Pediatrie; 1963; 18():816-21. PubMed ID: 14106624
    [No Abstract]   [Full Text] [Related]  

  • 40. [Case of Friedreich disease with Charcot-Marie amyotrophy clinical study].
    MAHOUDEAU D; DAUM S; LEMPERIERE
    Rev Neurol (Paris); 1950 Oct; 83(4):281-4. PubMed ID: 14816901
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.