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26. [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]
27. [Identification of a new genetic entity in the form of an autosomal dominant axonal Charcot-Marie-Tooth disease associated with periodic paralyses and pyramidal syndrome]. Chokri B; Salem M; Faycel H Tunis Med; 2005 Sep; 83(9):547-55. PubMed ID: 16383201 [TBL] [Abstract][Full Text] [Related]
28. [Two cases of Charcot-Marie amyotrophy]. GUERRA M; ANTUNES L Gaz Med Port; 1953; 6(4):687-96. PubMed ID: 13142233 [No Abstract] [Full Text] [Related]
29. [Progressive distal amyotrophy (Charcot-Marie-Tooth type) with hyperalbuminosis of the cerebrospinal fluid]. Marconi GP; Menchi D Riv Patol Nerv Ment; 1965 Jun; 86(3):354-75. PubMed ID: 5868833 [No Abstract] [Full Text] [Related]
30. The value of electromyography in the aetiological diagnosis of hypotonia in infants and toddlers. Cetin E; Cuisset JM; Tiffreau V; Vallée L; Hurtevent JF; Thevenon A Ann Phys Rehabil Med; 2009; 52(7-8):546-55. PubMed ID: 19713169 [TBL] [Abstract][Full Text] [Related]
31. Mild early onset axonal Charcot-Marie-Tooth disease not linked to other axonal Charcot-Marie-Tooth loci. Kochanski A; Kennerson M; Kawulak M; Ryniewicz B; Rowinska-Marcinska K; Walizada G; Nowakowski A; Hausmanowa-Petrusewicz I; Nicholson GA Neurology; 2005 Feb; 64(3):533-5. PubMed ID: 15699389 [TBL] [Abstract][Full Text] [Related]
32. [Charcot-Marie type of neural progressive muscular atrophy following electric injury]. MACCAGNANI F; VIZIOLI R Riv Neurol; 1954; 24(3):381-7. PubMed ID: 13225458 [No Abstract] [Full Text] [Related]
33. Modafinil reduces fatigue in Charcot-Marie-Tooth disease type 1A: a case series. Carter GT; Han JJ; Mayadev A; Weiss MD Am J Hosp Palliat Care; 2006; 23(5):412-6. PubMed ID: 17060310 [TBL] [Abstract][Full Text] [Related]
34. [Spinal muscular atrophy associated with olivopontocerebellar hypoplasia. A case report]. Serra-Ortega A; Torres A; Segreo M Rev Neurol; 2005 Jan 16-31; 40(2):90-2. PubMed ID: 15712162 [TBL] [Abstract][Full Text] [Related]
35. [Results of treatment of foot deformities in a patient with the neural form of progressive muscular atrophy of the Charcot-Marie type]. Kramarenko GN Ortop Travmatol Protez; 1965 Jul; 26(7):63-6. PubMed ID: 5859700 [No Abstract] [Full Text] [Related]
36. [Urinary elimination of 11-hydroxy- and 11-dehydroxy-corticoids in Charcot-Marie-Tooth-type progressive peroneal atrophy]. CHIARELLI A; CIUCCARELLI C; PIZZOFERRATO A Bull Sci Med (Bologna); 1963; 135():142-8. PubMed ID: 14020769 [No Abstract] [Full Text] [Related]
37. Charcot-Marie-Tooth disease. Buteică E; Roşulescu E; Stănoiu B; Burada F; Stănoiu C; Zăvăleanu M Rom J Morphol Embryol; 2008; 49(1):115-9. PubMed ID: 18273515 [TBL] [Abstract][Full Text] [Related]
39. [Acropathia ulcero-mutilans, Charcot-Marie type of amyotrophic frusta & alexia in a pair of monozygotic twins]. MONTANINI R Riv Neurol; 1958; 28(6):593-609. PubMed ID: 13646503 [No Abstract] [Full Text] [Related]