234 related articles for article (PubMed ID: 6675357)
21. Electromyographic findings in lower extremities of patients with high spinal cord injury.
Taylor RG; Kewalramani LS; Fowler WM
Arch Phys Med Rehabil; 1974 Jan; 55(1):16-23. PubMed ID: 4809014
[No Abstract] [Full Text] [Related]
22. Charcot-Marie-Tooth disease mimicking ocular myasthenia gravis.
Spector RH; Smith JL; Chavis PS
Ann Ophthalmol; 1978 Aug; 10(8):1033-8. PubMed ID: 697278
[TBL] [Abstract][Full Text] [Related]
23. [Diagnosis of a myopathic disease in adult].
Eymard B
Rev Prat; 2008 Dec; 58(20):2229-43. PubMed ID: 19209654
[TBL] [Abstract][Full Text] [Related]
24. [3 cases of scapulo-peroneal neurogenic amyotrophy (Dawidenkow's syndrome). Nosological situation in relation to Charcot-Marie-Tooth disease].
Serratrice G; Pellissier JF; Pouget J
Rev Neurol (Paris); 1984; 140(12):738-40. PubMed ID: 6097982
[TBL] [Abstract][Full Text] [Related]
25. [Charcot-Marie-Tooth disease].
Krstić S; Vidaković Z; Ignjatović M
Neuropsihijatrija; 1976; 24(1-4):121-8. PubMed ID: 1031197
[No Abstract] [Full Text] [Related]
26. [The importance of studying stimulation parameters in amyotrophic lateral sclerosis and Charcot-Marie-Tooth neural amyotrophy].
Kyral V; Pára F
Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove Suppl; 1980; 23(4):415-22. PubMed ID: 6971479
[No Abstract] [Full Text] [Related]
27. A case of distal spinal muscular atrophy with unusual clinical course.
Testa D; Carenini L
Acta Neurol (Napoli); 1983 Oct; 5(5):398-401. PubMed ID: 6660063
[No Abstract] [Full Text] [Related]
28. Juvenile type of distal and segmental muscular atrophy of upper extremities.
Sobue I; Saito N; Iida M; Ando K
Ann Neurol; 1978 May; 3(5):429-32. PubMed ID: 727722
[TBL] [Abstract][Full Text] [Related]
29. [Familial scapuloperoneal-type myopathy associated with a marked elevation of serum creatine kinase and hepatomegaly].
Maruoka A; Ideguchi H; Nawata H; Goto I; Ibayashi H
Rinsho Shinkeigaku; 1989 Mar; 29(3):325-31. PubMed ID: 2752661
[TBL] [Abstract][Full Text] [Related]
30. [Myocardial lesions in several forms of progressive muscular atrophy].
Popov'ian MD; Dubinskaia EE; Proshina OV; Tul'skaia MP; Loginova LA
Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(3):330-5. PubMed ID: 6720172
[TBL] [Abstract][Full Text] [Related]
31. [Myopathis muscle tissue changes in cases of Charcot-Marie-Tooth progressive neuritic muscular atrophy].
Cazzato G; Testa G
Acta Neurol (Napoli); 1969; 24(2):171-99. PubMed ID: 5386340
[No Abstract] [Full Text] [Related]
32. [Automatic analysis of needle EMG in the differential diagnosis of neuromuscular diseases].
Babkin PS; Gekht BM; Polukazakov SN; Fedotov VP
Zh Nevropatol Psikhiatr Im S S Korsakova; 1986; 86(11):1623-8. PubMed ID: 3811721
[TBL] [Abstract][Full Text] [Related]
33. [Familial neurogenic amyotrophy, similar to Charcot-Marie-Tooth disease. Clinical and ultrastructural study].
Vital C; Julien J; Vallat JM; Le Blanc M
Rev Neurol (Paris); 1970 Jan; 122(1):15-28. PubMed ID: 5433253
[No Abstract] [Full Text] [Related]
34. [Myopathy in the adult form of glycogenosis II. Two case reports and review of the literature].
Horstmann S; Meier C; Mumenthaler M; Gitzelmann R
Fortschr Neurol Psychiatr; 1990 Sep; 58(9):343-50. PubMed ID: 2175729
[TBL] [Abstract][Full Text] [Related]
35. [Nemaline myopathy. A case report and revision of literature (author's transl)].
Rodríguez Costa T; Pascual Castroviejo I; Gutiérrez Molina M; Nistal M; López Martín V
An Esp Pediatr; 1975; 8(3):275-84. PubMed ID: 1155858
[TBL] [Abstract][Full Text] [Related]
36. Roussy-Levy hereditary areflexic dystasis presenting as Charcot-Marie-Tooth syndrome.
Murdoch JL; Beighton PH
Birth Defects Orig Artic Ser; 1971 Feb; 7(2):106-7. PubMed ID: 5173115
[No Abstract] [Full Text] [Related]
37. Tibial muscular dystrophy with late adult onset in a Spanish family.
Pardal-Fernández JM; Jerez-García P; Rallo-Gutiérrez B; Puentes-Gil JM; Godes-Medrano B; Marco-Giner J
Electromyogr Clin Neurophysiol; 2005; 45(5):285-90. PubMed ID: 16218196
[TBL] [Abstract][Full Text] [Related]
38. [Incidence and clinical polymorphism of Charcot-Marie neural amyotrophy in the Amur region].
Khomenko EI
Zh Nevropatol Psikhiatr Im S S Korsakova; 1982; 82(11):22-6. PubMed ID: 7180298
[No Abstract] [Full Text] [Related]
39. [Recessive distal myopathies. Five cases].
Arenas C; Bautista J; Galán J; Casado JL; Salazar JA; Romero M; Segura DI; Chinchón I
Neurologia; 1995 Jan; 10(1):1-6. PubMed ID: 7893506
[TBL] [Abstract][Full Text] [Related]
40. Quadriceps myopathy in two brothers: rare familial myopathy confirmed by muscle biopsy.
Finelli PF
R I Med J (1976); 1979 Apr; 62(4):125-9. PubMed ID: 286404
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
