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2. Charcot-Marie-Tooth's disease with severe trophic and sensory disorders. Study of a case following along a half a century with anatomical studies. Barraquer-Bordas L; Navarro C; Salisachs P Acta Neurol Latinoam; 1981; 27(3-4):177-89. PubMed ID: 6965173 [TBL] [Abstract][Full Text] [Related]
3. 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]
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. Severe sensory changes, and trophic disorder, in peroneal muscular atrophy (Charcot-Marie-Tooth type). ENGLAND AC; DENNY-BROWN D AMA Arch Neurol Psychiatry; 1952 Jan; 67(1):1-22. PubMed ID: 14877348 [No Abstract] [Full Text] [Related]
6. [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]
7. [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]
12. 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]
13. Progressive muscular atrophy of the peroneal type (Charcot-Marie-Tooth disease) orthopaedic management and end-result study. JACOBS JE; CARR CR J Bone Joint Surg Am; 1950 Jan; 32A(1):27-38, illust. PubMed ID: 15401720 [No Abstract] [Full Text] [Related]
14. Treatment of pes cavus in a patient with Charcot-Marie-Tooth disease. Colon MJ; Whitton KE; Schwartz N J Foot Surg; 1980; 19(1):41-4. PubMed ID: 7240666 [No Abstract] [Full Text] [Related]
15. [Charcot-Marie-Tooth amyotrophy in 2 brothers]. MORETTI GF; STAEFFEN J; LORRAIN J; ROUX M; ROUSSEAU J J Med Bord; 1961 Nov; 138():1440-8. PubMed ID: 14475928 [No Abstract] [Full Text] [Related]
16. [Surgical treatment of foot deformities in children with Charcot-Marie neural amyotrophy]. Liandres ZA; Koniukhov MP Ortop Travmatol Protez; 1977 Mar; (3):60-4. PubMed ID: 583660 [No Abstract] [Full Text] [Related]
18. On a possible relationship between hereditary ataxia and peroneal muscular atrophy; with a critical review of the problems of intermediate forms in the degenerative disorders of the central nervous system. ROTH M Brain; 1948 Dec; 71(Pt. 4):416-33. PubMed ID: 18114340 [No Abstract] [Full Text] [Related]
19. [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]
20. [Possibilities of orthopedic treatment of hand deformities in Charcot-Marie-Tooth neural amyotrophy]. Andruson MV; Goloborod'ko SA; Al'shanova LS Ortop Travmatol Protez; 1988 Jan; (1):47-8. PubMed ID: 3362525 [No Abstract] [Full Text] [Related] [Next] [New Search]