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11. Hereditary neuropathies in children: the contribution of the new genetics. Ouvrier RA Semin Pediatr Neurol; 1996 Jun; 3(2):140-51. PubMed ID: 8795847 [TBL] [Abstract][Full Text] [Related]
12. Hereditary sensory and autonomic neuropathy type IV. Karande S; Satam N Indian Pediatr; 2005 Jun; 42(6):608-9. PubMed ID: 15995280 [No Abstract] [Full Text] [Related]
13. 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]
14. [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]
15. Hereditary sensory and autonomic neuropathies. Familial dysautonomia and other HSANs. Axelrod FB Clin Auton Res; 2002 May; 12 Suppl 1():I2-14. PubMed ID: 12102459 [No Abstract] [Full Text] [Related]
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17. 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]
18. Ataxia with ophthalmoplegia or sensory neuropathy is frequently caused by POLG mutations. Schulte C; Synofzik M; Gasser T; Schöls L Neurology; 2009 Sep; 73(11):898-900. PubMed ID: 19752458 [No Abstract] [Full Text] [Related]
19. 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]
20. Hereditary sensory neuropathy manifesting as possible child abuse. Makari GS; Carroll JE; Burton EM Pediatrics; 1994 May; 93(5):842-4. PubMed ID: 8165095 [No Abstract] [Full Text] [Related] [Next] [New Search]