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8. Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3. Kornak U; Mademan I; Schinke M; Voigt M; Krawitz P; Hecht J; Barvencik F; Schinke T; Gießelmann S; Beil FT; Pou-Serradell A; Vílchez JJ; Beetz C; Deconinck T; Timmerman V; Kaether C; De Jonghe P; Hübner CA; Gal A; Amling M; Mundlos S; Baets J; Kurth I Brain; 2014 Mar; 137(Pt 3):683-92. PubMed ID: 24459106 [TBL] [Abstract][Full Text] [Related]
9. Indifference rather than insensitivity to pain. Klein CJ; Sinnreich M; Dyck PJ Ann Neurol; 2003 Mar; 53(3):417-8; author reply 418-9. PubMed ID: 12601714 [No Abstract] [Full Text] [Related]
10. [A familial case with hereditary pressure-sensitive neuropathy, with "tomacula"--the first case in Japan]. Minauchi Y; Kohka M; Igata A; Ohkatsu Y Rinsho Shinkeigaku; 1982 Oct; 22(10):918-25. PubMed ID: 6963557 [No Abstract] [Full Text] [Related]
11. Charcot-Marie-Tooth disease (hereditary motor sensory neuropathies) and hereditary sensory and autonomic neuropathies. Bertorini T; Narayanaswami P; Rashed H Neurologist; 2004 Nov; 10(6):327-37. PubMed ID: 15518599 [TBL] [Abstract][Full Text] [Related]
12. [Case of hereditary sensory neuropathy with atypical clinical course]. Sawicka E; Czyzewski K; Drac H Neurol Neurochir Pol; 1979; 13(5):541-8. PubMed ID: 293503 [TBL] [Abstract][Full Text] [Related]
13. No mutation in the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with hereditary sensory and autonomic neuropathy type V. Toscano E; Simonati A; Indo Y; Andria G Ann Neurol; 2002 Aug; 52(2):224-7. PubMed ID: 12210794 [TBL] [Abstract][Full Text] [Related]
14. Late-onset hereditary sensory neuropathy type I due to SPTLC1 mutation: autopsy findings. Lindahl AJ; Lhatoo SD; Campbell MJ; Nicholson G; Love S Clin Neurol Neurosurg; 2006 Dec; 108(8):780-3. PubMed ID: 16271825 [TBL] [Abstract][Full Text] [Related]
15. Early-onset severe hereditary sensory and autonomic neuropathy type 1 with S331F SPTLC1 mutation. Suh BC; Hong YB; Nakhro K; Nam SH; Chung KW; Choi BO Mol Med Rep; 2014 Feb; 9(2):481-6. PubMed ID: 24247255 [TBL] [Abstract][Full Text] [Related]
16. Three patients in a Chinese family with hereditary sensory neuropathy mimicking leprosy. Shen J; Zhang G; Yang R; Hu T; Zhou M Lepr Rev; 2008 Dec; 79(4):441-6. PubMed ID: 19274992 [No Abstract] [Full Text] [Related]
17. Hereditary neuropathies in childhood: morphologic hallmarks and pathophysiologic mechanisms. Gabreëls-Festin A J Child Neurol; 1999 Jan; 14(1):52-3. PubMed ID: 10223855 [No Abstract] [Full Text] [Related]
18. Disease mechanisms in hereditary sensory and autonomic neuropathies. Verpoorten N; De Jonghe P; Timmerman V Neurobiol Dis; 2006 Feb; 21(2):247-55. PubMed ID: 16183296 [TBL] [Abstract][Full Text] [Related]
19. Oral manifestations, dental management, and a rare homozygous mutation of the PRDM12 gene in a boy with hereditary sensory and autonomic neuropathy type VIII: a case report and review of the literature. Elhennawy K; Reda S; Finke C; Graul-Neumann L; Jost-Brinkmann PG; Bartzela T J Med Case Rep; 2017 Aug; 11(1):233. PubMed ID: 28807049 [TBL] [Abstract][Full Text] [Related]