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4. 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]
5. Overview of hereditary neuropathy with liability to pressure palsies. Chance PF Ann N Y Acad Sci; 1999 Sep; 883():14-21. PubMed ID: 10586225 [TBL] [Abstract][Full Text] [Related]
6. Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct genetic disorders. Chance PF; Lensch MW; Lipe H; Brown RH; Brown RH; Bird TD Neurology; 1994 Dec; 44(12):2253-7. PubMed ID: 7991108 [TBL] [Abstract][Full Text] [Related]
7. Autosomal dominant Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: detection of the recombination in Slovene patients and exclusion of the potentially recessive Thr118Met PMP22 point mutation. Leonardis L; Zidar J; Ekici A; Peterlin B; Rautenstrauss B Int J Mol Med; 1998 Feb; 1(2):495-501. PubMed ID: 9852256 [TBL] [Abstract][Full Text] [Related]
8. [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]
10. 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]
12. Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study. Nelis E; Van Broeckhoven C; De Jonghe P; Löfgren A; Vandenberghe A; Latour P; Le Guern E; Brice A; Mostacciuolo ML; Schiavon F; Palau F; Bort S; Upadhyaya M; Rocchi M; Archidiacono N; Mandich P; Bellone E; Silander K; Savontaus ML; Navon R; Goldberg-Stern H; Estivill X; Volpini V; Friedl W; Gal A Eur J Hum Genet; 1996; 4(1):25-33. PubMed ID: 8800924 [TBL] [Abstract][Full Text] [Related]
13. Mutation analysis of the nerve specific promoter of the peripheral myelin protein 22 gene in CMT1 disease and HNPP. Nelis E; De Jonghe P; De Vriendt E; Patel PI; Martin JJ; Van Broeckhoven C J Med Genet; 1998 Jul; 35(7):590-3. PubMed ID: 9678704 [TBL] [Abstract][Full Text] [Related]
14. Hereditary neuropathy with liability to pressure palsies (HNPP) patients of Korean ancestry with chromosome 17p11.2-p12 deletion. Kim SM; Chung KW; Choi BO; Yoon ES; Choi JY; Park KD; Sunwoo IN Exp Mol Med; 2004 Feb; 36(1):28-35. PubMed ID: 15031668 [TBL] [Abstract][Full Text] [Related]
15. A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies. Lorenzetti D; Pareyson D; Sghirlanzoni A; Roa BB; Abbas NE; Pandolfo M; Di Donato S; Lupski JR Am J Hum Genet; 1995 Jan; 56(1):91-8. PubMed ID: 7825607 [TBL] [Abstract][Full Text] [Related]
16. A novel 3'-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies. Meuleman J; Pou-Serradell A; Löfgren A; Ceuterick C; Martin JJ; Timmerman V; Van Broeckhoven C; De Jonghe P Neuromuscul Disord; 2001 May; 11(4):400-3. PubMed ID: 11369192 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Charcot-Marie-Tooth disease and related peripheral neuropathies. De Jonghe P; Timmerman V; Nelis E; Martin JJ; Van Broeckhoven C J Peripher Nerv Syst; 1997; 2(4):370-87. PubMed ID: 10975746 [TBL] [Abstract][Full Text] [Related]
19. Noncanonical splice-site variant in peripheral myelin protein 22 gene (PMP22) in a patient with hereditary neuropathy with liability to pressure palsies. Kawamoto N; Hamada Y; Kobayashi S; Naruse H; Ishiura H; Matsukawa T; Mitsui J; Tsuji S; Sonoo M; Toda T J Peripher Nerv Syst; 2023 Sep; 28(3):513-517. PubMed ID: 37170477 [TBL] [Abstract][Full Text] [Related]
20. Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities. Gouider R; LeGuern E; Emile J; Tardieu S; Cabon F; Samid M; Weissenbach J; Agid Y; Bouche P; Brice A Neurology; 1994 Dec; 44(12):2250-2. PubMed ID: 7991107 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]