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Journal Abstract Search
211 related items for PubMed ID: 8576556
1. Genetic heterogeneity of hereditary motor and sensory neuropathy type VI. Ippel EF, Wittebol-Post D, Jennekens FG, Bijlsma JB. J Child Neurol; 1995 Nov; 10(6):459-63. PubMed ID: 8576556 [Abstract] [Full Text] [Related]
2. [The genetics of type 1 Charcot-Marie-Tooth disease, the hereditary focal neuropathies and the hereditary distal motor neuropathies]. Sevilla T. Rev Neurol; 1995 Nov; 30(1):71-9. PubMed ID: 10743001 [Abstract] [Full Text] [Related]
3. A family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci. Bellone E, Rodolico C, Toscano A, Di Maria E, Cassandrini D, Pizzuti A, Pigullo S, Mazzeo A, Macaione V, Girlanda P, Vita G, Ajmar F, Mandich P. Neuromuscul Disord; 2002 Mar; 12(3):286-91. PubMed ID: 11801401 [Abstract] [Full Text] [Related]
5. Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I loci. Auer-Grumbach M, Wagner K, Timmerman V, De Jonghe P, Hartung HP. Neurology; 2000 Jan 11; 54(1):45-52. PubMed ID: 10636124 [Abstract] [Full Text] [Related]
6. A distinct congenital motor and sensory neuropathy (neuronal type) with dysmorphic features in a father and two sons. A variant of Charcot-Marie-Tooth disease. Ruiz C, Rivas F, Ramírez-Casillas G, Vázquez-Santana R, Mendoza-Chalita B, Feria-Velasco A, Tapia-Arizmendi G, Cantú JM. Clin Genet; 1987 Feb 11; 31(2):109-13. PubMed ID: 3470161 [Abstract] [Full Text] [Related]
7. [Clinical practice of hereditary motor neuropathy (HMN) and hereditary sensory and autonomic neuropathy (HSAN)]. Takashima H. Rinsho Shinkeigaku; 2014 Feb 11; 54(12):957-9. PubMed ID: 25672680 [Abstract] [Full Text] [Related]
8. Autosomal recessive hereditary motor and sensory neuropathy with mental retardation, optic atrophy and pyramidal signs. MacDermot KD, Walker RW. J Neurol Neurosurg Psychiatry; 1987 Oct 11; 50(10):1342-7. PubMed ID: 3479531 [Abstract] [Full Text] [Related]
10. Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophy. Chalmers RM, Riordan-Eva P, Wood NW. J Neurol Neurosurg Psychiatry; 1997 Apr 11; 62(4):385-7. PubMed ID: 9120454 [Abstract] [Full Text] [Related]
11. Molecular genetics of distal hereditary motor neuropathies. Irobi J, De Jonghe P, Timmerman V. Hum Mol Genet; 2004 Oct 01; 13 Spec No 2():R195-202. PubMed ID: 15358725 [Abstract] [Full Text] [Related]
12. [Hereditary neuropathy with dominant inheritance, giant axons and cardiac involvement]. Gabriel M, Vogel P, Goebel HH. Klin Padiatr; 1986 Oct 01; 198(1):17-20. PubMed ID: 3007857 [Abstract] [Full Text] [Related]
13. Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2. Züchner S, De Jonghe P, Jordanova A, Claeys KG, Guergueltcheva V, Cherninkova S, Hamilton SR, Van Stavern G, Krajewski KM, Stajich J, Tournev I, Verhoeven K, Langerhorst CT, de Visser M, Baas F, Bird T, Timmerman V, Shy M, Vance JM. Ann Neurol; 2006 Feb 01; 59(2):276-81. PubMed ID: 16437557 [Abstract] [Full Text] [Related]
14. [Molecular genetics of inherited neuropathies]. Takashima H. Rinsho Shinkeigaku; 2006 Jan 01; 46(1):1-18. PubMed ID: 16541790 [Abstract] [Full Text] [Related]
17. [Hereditary motor and sensory neuropathy. I. Principles of classification and clinical picture]. Badurska B, Jedrzejowska H, Ryniewicz B, Drac H. Neurol Neurochir Pol; 1986 Jul 01; 20(1):24-8. PubMed ID: 3012388 [Abstract] [Full Text] [Related]
18. [Hereditary sensory and motor neuropathy and hereditary sensory and autonomic neuropathies: recent advances]. Stojkovic T. Rev Neurol (Paris); 2011 Dec 01; 167(12):948-50. PubMed ID: 22100327 [Abstract] [Full Text] [Related]
19. Hereditary motor-sensory neuropathy (HMSN): possible X-linked dominant inheritance. Phillips LH, Kelly TE, Schnatterly P, Parker D. Neurology; 1985 Apr 01; 35(4):498-502. PubMed ID: 3856757 [Abstract] [Full Text] [Related]