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2. Vocal cord paresis and diaphragmatic dysfunction are severe and frequent symptoms of GDAP1-associated neuropathy. Sevilla T; Jaijo T; Nauffal D; Collado D; Chumillas MJ; Vilchez JJ; Muelas N; Bataller L; Domenech R; Espinós C; Palau F Brain; 2008 Nov; 131(Pt 11):3051-61. PubMed ID: 18812441 [TBL] [Abstract][Full Text] [Related]
3. A Sporadic Case of Charcot-Marie-Tooth Disease Type 2 with Left Vocal Fold Palsy due to Mitofusin 2 Mutation. Kanemaru K; Ogawa G; Mochizuki H; Nakazato M; Shiomi K Intern Med; 2019 Jul; 58(14):2091-2093. PubMed ID: 30996168 [TBL] [Abstract][Full Text] [Related]
4. Charcot-Marie-Tooth Disease type 1 and pediatric true vocal fold paralysis. Boseley ME; Bloch I; Hartnick CJ Int J Pediatr Otorhinolaryngol; 2006 Feb; 70(2):345-7. PubMed ID: 16084600 [TBL] [Abstract][Full Text] [Related]
5. [A case of X-linked bulbospinal muscular atrophy with bilateral abductor vocal cord paralysis]. Tomiyasu K; Saito T; Nukazawa T; Ito H; Kowa H Rinsho Shinkeigaku; 1996 May; 36(5):683-6. PubMed ID: 8905990 [TBL] [Abstract][Full Text] [Related]
7. [Anesthetic and postoperative management of Charcot-Marie-Tooth disease associated with vocal cord paralysis]. Watanabe T; Yamashita M; Kondo Y; Sato S; Mizutani T; Watanabe T; Naito H Masui; 1982 May; 31(5):530-4. PubMed ID: 7131729 [No Abstract] [Full Text] [Related]
8. Vocal cord and diaphragm paralysis, as clinical features of a French family with autosomal recessive Charcot-Marie-Tooth disease, associated with a new mutation in the GDAP1 gene. Stojkovic T; Latour P; Viet G; de Seze J; Hurtevent JF; Vandenberghe A; Vermersch P Neuromuscul Disord; 2004 Apr; 14(4):261-4. PubMed ID: 15019704 [TBL] [Abstract][Full Text] [Related]
9. Congenital bilateral vocal fold paralysis and Charcot-Marie-Tooth disease. Lewis AF; Carron JD; Vedanarayanan V Ann Otol Rhinol Laryngol; 2010 Jan; 119(1):47-9. PubMed ID: 20128187 [TBL] [Abstract][Full Text] [Related]
10. Vocal fold paresis of Charcot-Marie-Tooth disease. Sulica L; Blitzer A; Lovelace RE; Kaufmann P Ann Otol Rhinol Laryngol; 2001 Nov; 110(11):1072-6. PubMed ID: 11713921 [TBL] [Abstract][Full Text] [Related]
11. Laryngeal neuropathy of Charcot-Marie-Tooth disease: further observations and novel mutations associated with vocal fold paresis. Benson B; Sulica L; Guss J; Blitzer A Laryngoscope; 2010 Feb; 120(2):291-6. PubMed ID: 19950375 [TBL] [Abstract][Full Text] [Related]
12. Disorders of pulmonary function, sleep, and the upper airway in Charcot-Marie-Tooth disease. Aboussouan LS; Lewis RA; Shy ME Lung; 2007; 185(1):1-7. PubMed ID: 17294338 [TBL] [Abstract][Full Text] [Related]
13. [A case of hereditary motor and sensory neuropathy with vocal cords palsy and diaphragmatic weakness]. Fukuda H; Kitani M; Imaoka K Rinsho Shinkeigaku; 1993 Feb; 33(2):175-81. PubMed ID: 8319389 [TBL] [Abstract][Full Text] [Related]
14. Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family. Santoro L; Manganelli F; Di Maio L; Barbieri F; Carella M; D'Adamo P; Casari G Neuromuscul Disord; 2002 May; 12(4):399-404. PubMed ID: 12062259 [TBL] [Abstract][Full Text] [Related]
15. Vocal cord paralysis in Charcot-Marie-Tooth type 4b1 disease associated with a novel mutation in the myotubularin-related protein 2 gene: A case report and review of the literature. Zambon AA; Natali Sora MG; Cantarella G; Cerri F; Quattrini A; Comi G; Previtali SC; Bolino A Neuromuscul Disord; 2017 May; 27(5):487-491. PubMed ID: 28190646 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. A case of Creutzfeldt-Jacob disease with bilateral vocal fold abductor paralysis. Li L; Saigusa H; Nagayama H; Nakamura T; Aino I; Komachi T; Yamaguchi S J Voice; 2009 Sep; 23(5):635-8. PubMed ID: 18468847 [TBL] [Abstract][Full Text] [Related]