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.
11. Data on three of the original patients of Roussy and Levy (1926). Salisachs P; Findley LJ; Codina M; La Torre P; Martinez-Lage JM Muscle Nerve; 1982 Oct; 5(8):663-4. PubMed ID: 7155179 [No Abstract] [Full Text] [Related]
12. [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]
13. [Charcot-Marie-Tooth disease. Genetical, clinical and electrodiagnostic study of 2 families]. Krstić S; Vidaković Z; Ignjatović M Srp Arh Celok Lek; 1975 Sep; 103(9):769-77. PubMed ID: 1228922 [No Abstract] [Full Text] [Related]
17. 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]
18. A family with Charcot-Marie-Tooth disease and Leber's optic atrophy. McLeod JG; Low PA; Morgan JA Proc Aust Assoc Neurol; 1975; 12():23-5. PubMed ID: 1215391 [TBL] [Abstract][Full Text] [Related]
19. [Clinicoelectrophysiological aspects of hereditary amyotrophies]. Avakian GN; Podobedova NS; Bystrova ES Zh Nevropatol Psikhiatr Im S S Korsakova; 1981; 81(11):1639-42. PubMed ID: 6275641 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]