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]