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.
25. PCR-based strategy for the diagnosis of hereditary neuropathy with liability to pressure palsies and Charcot-Marie-Tooth disease type 1A. Young P; Stögbauer F; Wiebusch H; Löfgren A; Timmerman V; Van Broeckhoven C; Ringelstein EB; Assmann G; Funke H Neurology; 1998 Mar; 50(3):760-3. PubMed ID: 9521270 [TBL] [Abstract][Full Text] [Related]
26. Molecular diagnosis of Charcot-Marie-Tooth 1A disease and hereditary neuropathy with liability to pressure palsies by quantifying CMT1A-REP sequences: consequences of recombinations at variant sites on chromosomes 17p11.2-12. Vandenberghe A; Latour P; Chauplannaz G; Chapon F; Pouget J; Dumas R; Laguenay A; Ollagnon E; Bost M; Duthel S; Chazot G; Boucherat M Clin Chem; 1996 Jul; 42(7):1021-5. PubMed ID: 8674184 [TBL] [Abstract][Full Text] [Related]
27. A de novo case of hereditary neuropathy with liability to pressure palsies (HNPP) of maternal origin: a new mechanism for deletion in 17p11.2? LeGuern E; Gouider R; Ravisé N; Lopes J; Tardieu S; Gugenheim M; Abbas N; Bouche P; Agid Y; Brice A Hum Mol Genet; 1996 Jan; 5(1):103-6. PubMed ID: 8789446 [TBL] [Abstract][Full Text] [Related]
28. Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies. Chance PF; Fischbeck KH Hum Mol Genet; 1994; 3 Spec No():1503-7. PubMed ID: 7849745 [TBL] [Abstract][Full Text] [Related]
29. Molecular basis of hereditary neuropathies. Chance PF Phys Med Rehabil Clin N Am; 2001 May; 12(2):277-91. PubMed ID: 11345007 [TBL] [Abstract][Full Text] [Related]
32. DNA deletion associated with hereditary neuropathy with liability to pressure palsies. Chance PF; Alderson MK; Leppig KA; Lensch MW; Matsunami N; Smith B; Swanson PD; Odelberg SJ; Disteche CM; Bird TD Cell; 1993 Jan; 72(1):143-51. PubMed ID: 8422677 [TBL] [Abstract][Full Text] [Related]
33. Inherited neuropathies: Charcot-Marie-Tooth disease and related disorders. Chance PF; Lupski JR Baillieres Clin Neurol; 1994 Aug; 3(2):373-85. PubMed ID: 7952853 [TBL] [Abstract][Full Text] [Related]
34. Overview of Hereditary Neuropathy with Liability to Pressure Palsies. Chance PF Ann N Y Acad Sci; 1999 Oct; 883(1):14-21. PubMed ID: 29086948 [TBL] [Abstract][Full Text] [Related]
35. Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy. Chance PF Neuromolecular Med; 2006; 8(1-2):159-74. PubMed ID: 16775374 [TBL] [Abstract][Full Text] [Related]
36. The 5' regulatory sequence of the PMP22 in the patients with Charcot-Marie-Tooth disease. Sinkiewicz-Darol E; Kabzińska D; Moszyńska I; Kochański A Acta Biochim Pol; 2010; 57(3):373-7. PubMed ID: 20842290 [TBL] [Abstract][Full Text] [Related]
37. [Hereditary neuropathy with liability to pressure palsies: study of six Spanish families]. Pou Serradell A; Monells J; Téllez MJ; Fossas P; Löfgren A; Meuleman J; Timmerman V; De Jonghe P; Ceuterick C; Martin JJ Rev Neurol (Paris); 2002 May; 158(5 Pt 1):579-88. PubMed ID: 12072826 [TBL] [Abstract][Full Text] [Related]
38. Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descent. Timmerman V; Rautenstrauss B; Reiter LT; Koeuth T; Löfgren A; Liehr T; Nelis E; Bathke KD; De Jonghe P; Grehl H; Martin JJ; Lupski JR; Van Broeckhoven C J Med Genet; 1997 Jan; 34(1):43-9. PubMed ID: 9032649 [TBL] [Abstract][Full Text] [Related]
39. Novel PCR-based diagnostic tools for Charcot-Marie-Tooth type 1A and hereditary neuropathy with liability to pressure palsies. Stronach EA; Clark C; Bell C; Löfgren A; McKay NG; Timmerman V; Van Broeckhoven C; Haites NE J Peripher Nerv Syst; 1999; 4(2):117-22. PubMed ID: 10442687 [TBL] [Abstract][Full Text] [Related]
40. Asian hereditary neuropathy patients with peripheral myelin protein-22 gene aneuploidy. Ohnishi A; Li LY; Fukushima Y; Mori T; Mori M; Endo C; Yoshimura T; Sonobe M; Flandermeyer R; Lebo RV Am J Med Genet; 1995 Oct; 59(1):51-8. PubMed ID: 8849012 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]