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.
223 related articles for article (PubMed ID: 15455439)
1. A novel RAB7 mutation associated with ulcero-mutilating neuropathy. Houlden H; King RH; Muddle JR; Warner TT; Reilly MM; Orrell RW; Ginsberg L Ann Neurol; 2004 Oct; 56(4):586-90. PubMed ID: 15455439 [TBL] [Abstract][Full Text] [Related]
2. Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation. Rotthier A; Baets J; De Vriendt E; Jacobs A; Auer-Grumbach M; Lévy N; Bonello-Palot N; Kilic SS; Weis J; Nascimento A; Swinkels M; Kruyt MC; Jordanova A; De Jonghe P; Timmerman V Brain; 2009 Oct; 132(Pt 10):2699-711. PubMed ID: 19651702 [TBL] [Abstract][Full Text] [Related]
3. 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; 54(1):45-52. PubMed ID: 10636124 [TBL] [Abstract][Full Text] [Related]
4. 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 [TBL] [Abstract][Full Text] [Related]
5. SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies. Klein CJ; Wu Y; Kruckeberg KE; Hebbring SJ; Anderson SA; Cunningham JM; Dyck PJ; Klein DM; Thibodeau SN; Dyck PJ J Neurol Neurosurg Psychiatry; 2005 Jul; 76(7):1022-4. PubMed ID: 15965219 [TBL] [Abstract][Full Text] [Related]
6. [Molecular genetics of inherited neuropathies]. Takashima H Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790 [TBL] [Abstract][Full Text] [Related]
7. Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I). Houlden H; King R; Blake J; Groves M; Love S; Woodward C; Hammans S; Nicoll J; Lennox G; O'Donovan DG; Gabriel C; Thomas PK; Reilly MM Brain; 2006 Feb; 129(Pt 2):411-25. PubMed ID: 16364956 [TBL] [Abstract][Full Text] [Related]
8. A novel RAB7 mutation in a Chinese family with Charcot-Marie-Tooth type 2B disease. Wang X; Han C; Liu W; Wang P; Zhang X Gene; 2014 Jan; 534(2):431-4. PubMed ID: 24498653 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. A novel Lys141Thr mutation in small heat shock protein 22 (HSPB8) gene in Charcot-Marie-Tooth disease type 2L. Nakhro K; Park JM; Kim YJ; Yoon BR; Yoo JH; Koo H; Choi BO; Chung KW Neuromuscul Disord; 2013 Aug; 23(8):656-63. PubMed ID: 23796487 [TBL] [Abstract][Full Text] [Related]
11. Functional characterization of Rab7 mutant proteins associated with Charcot-Marie-Tooth type 2B disease. Spinosa MR; Progida C; De Luca A; Colucci AM; Alifano P; Bucci C J Neurosci; 2008 Feb; 28(7):1640-8. PubMed ID: 18272684 [TBL] [Abstract][Full Text] [Related]
12. Human Rab7 mutation mimics features of Charcot-Marie-Tooth neuropathy type 2B in Drosophila. Janssens K; Goethals S; Atkinson D; Ermanoska B; Fransen E; Jordanova A; Auer-Grumbach M; Asselbergh B; Timmerman V Neurobiol Dis; 2014 May; 65():211-9. PubMed ID: 24521780 [TBL] [Abstract][Full Text] [Related]
13. Charcot Marie Tooth 2B Peripheral Sensory Neuropathy: How Rab7 Mutations Impact NGF Signaling? Liu H; Wu C Int J Mol Sci; 2017 Feb; 18(2):. PubMed ID: 28165391 [TBL] [Abstract][Full Text] [Related]
14. Charcot-Marie-Tooth Type 2B: A New Phenotype Associated with a Novel Saveri P; De Luca M; Nisi V; Pisciotta C; Romano R; Piscosquito G; Reilly MM; Polke JM; Cavallaro T; Fabrizi GM; Fossa P; Cichero E; Lombardi R; Lauria G; Magri S; Taroni F; Pareyson D; Bucci C Cells; 2020 Apr; 9(4):. PubMed ID: 32326241 [TBL] [Abstract][Full Text] [Related]
15. New mutation of gap junction protein beta1 (GJB1) gene in X-linked hereditary motor and sensory neuropathy. Umehara F; Arimura Y; Osame M; Minato S; Nakahara K J Peripher Nerv Syst; 2006 Mar; 11(1):96-7. PubMed ID: 16519791 [No Abstract] [Full Text] [Related]
16. Characterization of the Rab7K157N mutant protein associated with Charcot-Marie-Tooth type 2B. De Luca A; Progida C; Spinosa MR; Alifano P; Bucci C Biochem Biophys Res Commun; 2008 Jul; 372(2):283-7. PubMed ID: 18501189 [TBL] [Abstract][Full Text] [Related]
19. Phenotype of Charcot-Marie-Tooth disease Type 2. Bienfait HM; Baas F; Koelman JH; de Haan RJ; van Engelen BG; Gabreëls-Festen AA; Ongerboer de Visser BW; Meggouh F; Weterman MA; De Jonghe P; Timmerman V; de Visser M Neurology; 2007 May; 68(20):1658-67. PubMed ID: 17502546 [TBL] [Abstract][Full Text] [Related]
20. A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V. Houlden H; King RH; Hashemi-Nejad A; Wood NW; Mathias CJ; Reilly M; Thomas PK Ann Neurol; 2001 Apr; 49(4):521-5. PubMed ID: 11310631 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]