These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
23. Four siblings with type II hereditary sensory and autonomic neuropathy. Basu S; Paul DK; Basu S Indian Pediatr; 2002 Sep; 39(9):870-4. PubMed ID: 12368536 [No Abstract] [Full Text] [Related]
24. Congenital sensory neuropathy as a differential diagnosis for phagocytic immunodeficiency. Gharagozlou M; Zandieh F; Tabatabaei P; Zamani G Iran J Allergy Asthma Immunol; 2006 Mar; 5(1):35-7. PubMed ID: 17242503 [TBL] [Abstract][Full Text] [Related]
25. [Hereditary neuropathies]. Mellgren SI; Vedeler C Tidsskr Nor Laegeforen; 2003 Sep; 123(18):2585-7. PubMed ID: 14714050 [TBL] [Abstract][Full Text] [Related]
26. 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]
27. Non-healing ulcers in the foot. Shah SV; Bavdekar AV J Assoc Physicians India; 1984 Apr; 32(4):377-8. PubMed ID: 6589221 [No Abstract] [Full Text] [Related]
28. Hereditary sensory autonomic neuropathy Type IV. Dua T; Sharma J; Singhal T; Arya VB Indian Pediatr; 2005 Mar; 42(3):281-4. PubMed ID: 15817982 [TBL] [Abstract][Full Text] [Related]
29. [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]
31. Hereditary sensory autonomic neuropathy--type II in siblings. Balachandran C; Sabitha L; Kantharaj GR Indian J Lepr; 1996; 68(4):373-4. PubMed ID: 9001907 [No Abstract] [Full Text] [Related]
32. Congenital insensitivity to pain (hereditary sensory and autonomic neuropathy type V): a rare case report. Singla S; Marwah N; Dutta S J Dent Child (Chic); 2008; 75(2):207-11. PubMed ID: 18647521 [TBL] [Abstract][Full Text] [Related]
33. A case of a hereditary, late progressing sensory autonomic neuropathy. Cinar Y; Hekimoglu F; Ince B; Ince U; Onganer E Clin Neuropathol; 1998; 17(1):12-4. PubMed ID: 9496534 [TBL] [Abstract][Full Text] [Related]
34. [A case of hereditary sensory autonomic neuropathy type II with late onset]. Shimoya K; Ishimoto S; Ohnishi A; Yamamoto T Rinsho Shinkeigaku; 1999 May; 39(5):551-4. PubMed ID: 10424148 [TBL] [Abstract][Full Text] [Related]
35. [Congenital insensitivity to pain, anhidrosis and premature loss of baby teeth as a symptoms of rare neuropathy]. Ahmed M; Hietala M; Huoponen K; Juntunen M; Jääskeläinen S; Penttinen M; Syrjänen S; Karjalainen S Duodecim; 2005; 121(13):1429-32. PubMed ID: 16134716 [No Abstract] [Full Text] [Related]
36. SPTLC1 is mutated in hereditary sensory neuropathy, type 1. Bejaoui K; Wu C; Scheffler MD; Haan G; Ashby P; Wu L; de Jong P; Brown RH Nat Genet; 2001 Mar; 27(3):261-2. PubMed ID: 11242106 [TBL] [Abstract][Full Text] [Related]
37. Is there involvement of the central nervous system in hereditary sensory radicular neuropathy? Hageman G; Hilhorst BG; Rozeboom AR Clin Neurol Neurosurg; 1992; 94(1):49-54. PubMed ID: 1321699 [TBL] [Abstract][Full Text] [Related]
38. [Hereditary neuropathy with a tendency to pressure palsy]. Wulff CH Tidsskr Nor Laegeforen; 1982 Aug; 102(23):1153-5. PubMed ID: 6963030 [No Abstract] [Full Text] [Related]
39. [Clinical aspects of ulcero-mutilating acropathy]. Reich P; Weber I; Wolf K Dermatol Monatsschr; 1987; 173(3):135-40. PubMed ID: 3474180 [No Abstract] [Full Text] [Related]
40. Late onset hereditary sensory and autonomic neuropathy with cognitive impairment associated with Y163X prion mutation. Themistocleous AC; Kennett R; Husain M; Palace J; Mead S; Bennett DL J Neurol; 2014 Nov; 261(11):2230-3. PubMed ID: 25287017 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]