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4. Distal spinal muscular atrophy with vocal cord paralysis (dSMA-VII) is not linked to the MPD2 locus on chromosome 5q31. McEntagart M; Spurlock G; Jackson C; Harper P; Rahman N J Med Genet; 2000 Aug; 37(8):E14. PubMed ID: 10922394 [No Abstract] [Full Text] [Related]
5. [Chronic spinal amyotrophy with paralysis of the vocal cords: Young-Harper syndrome]. Serratrice G; Pellissier JF; Gastaut JL; Desnuelle C Rev Neurol (Paris); 1984; 140(11):657-8. PubMed ID: 6505493 [TBL] [Abstract][Full Text] [Related]
6. Autosomal dominant distal spinal muscular atrophy: an Italian family not linked to 12q24 and 7p14. De Angelis MV; Gatta V; Stuppia L; Passamonti L; Gambi D; Uncini A Neuromuscul Disord; 2002 Jan; 12(1):26-30. PubMed ID: 11731281 [TBL] [Abstract][Full Text] [Related]
7. [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]
8. [Autosomal dominant adult-onset spinal muscular atrophy with vocal cord paralysis: a case report]. Sakajiri K; Iwasa K; Okino S; Takamori M Rinsho Shinkeigaku; 2000 Jul; 40(7):712-6. PubMed ID: 11186910 [TBL] [Abstract][Full Text] [Related]
9. Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance. Boylan KB; Cornblath DR Ann Neurol; 1992 Sep; 32(3):404-7. PubMed ID: 1416812 [TBL] [Abstract][Full Text] [Related]
10. Congenital vocal cord paralysis with possible autosomal recessive inheritance: case report and review of the literature. Koppel R; Friedman S; Fallet S Am J Med Genet; 1996 Aug; 64(3):485-7. PubMed ID: 8862626 [TBL] [Abstract][Full Text] [Related]
11. TRPV4 mutations in children with congenital distal spinal muscular atrophy. Fiorillo C; Moro F; Brisca G; Astrea G; Nesti C; Bálint Z; Olschewski A; Meschini MC; Guelly C; Auer-Grumbach M; Battini R; Pedemonte M; Romano A; Menchise V; Biancheri R; Santorelli FM; Bruno C Neurogenetics; 2012 Aug; 13(3):195-203. PubMed ID: 22526352 [TBL] [Abstract][Full Text] [Related]
12. Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14. McEntagart M; Norton N; Williams H; Teare MD; Dunstan M; Baker P; Houlden H; Reilly M; Wood N; Harper PS; Futreal PA; Williams N; Rahman N Am J Hum Genet; 2001 May; 68(5):1270-6. PubMed ID: 11294660 [TBL] [Abstract][Full Text] [Related]
13. Autosomal dominantly inherited adductor laryngeal paralysis--a new syndrome with a suggestion of linkage to HLA. Mace M; Williamson E; Worgan D Clin Genet; 1978 Nov; 14(5):265-70. PubMed ID: 709905 [TBL] [Abstract][Full Text] [Related]
14. Autosomal dominant inheritance of Gerhardt's syndrome in three generations of a family. Morelli G; Mesolella C; Cavaliere ML; Stabile M; Ventruto V J Med Genet; 1980 Aug; 17(4):325. PubMed ID: 7205912 [No Abstract] [Full Text] [Related]
15. Clinical and genetic heterogeneity in peroneal muscular atrophy associated with vocal cord weakness. McEntagart M; Dunstan M; Bell C; Boltshauser E; Donaghy M; Harper PS; Williams N; Teare MD; Rahman N J Neurol Neurosurg Psychiatry; 2002 Dec; 73(6):762-5. PubMed ID: 12438487 [TBL] [Abstract][Full Text] [Related]