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.
11. 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]
12. PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies. van Paassen BW; van der Kooi AJ; van Spaendonck-Zwarts KY; Verhamme C; Baas F; de Visser M Orphanet J Rare Dis; 2014 Mar; 9():38. PubMed ID: 24646194 [TBL] [Abstract][Full Text] [Related]
13. Identification of Genetic Causes of Inherited Peripheral Neuropathies by Targeted Gene Panel Sequencing. Nam SH; Hong YB; Hyun YS; Nam da E; Kwak G; Hwang SH; Choi BO; Chung KW Mol Cells; 2016 May; 39(5):382-8. PubMed ID: 27025386 [TBL] [Abstract][Full Text] [Related]
14. Whole-exome sequencing is a valuable diagnostic tool for inherited peripheral neuropathies: Outcomes from a cohort of 50 families. Hartley T; Wagner JD; Warman-Chardon J; Tétreault M; Brady L; Baker S; Tarnopolsky M; Bourque PR; Parboosingh JS; Smith C; McInnes B; Innes AM; Bernier F; Curry CJ; Yoon G; Horvath GA; Bareke E; Gillespie M; ; ; Majewski J; Bulman DE; Dyment DA; Boycott KM Clin Genet; 2018 Feb; 93(2):301-309. PubMed ID: 28708278 [TBL] [Abstract][Full Text] [Related]
15. 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]
18. Pediatric inherited peripheral neuropathy: a prospective study at a Spanish referral center. Argente-Escrig H; Frasquet M; Vázquez-Costa JF; Millet-Sancho E; Pitarch I; Tomás-Vila M; Espinós C; Lupo V; Sevilla T Ann Clin Transl Neurol; 2021 Sep; 8(9):1809-1816. PubMed ID: 34323022 [TBL] [Abstract][Full Text] [Related]
19. Genetics of inherited peripheral neuropathies and the next frontier: looking backwards to progress forwards. Parmar JM; Laing NG; Kennerson ML; Ravenscroft G J Neurol Neurosurg Psychiatry; 2024 Oct; 95(11):992-1001. PubMed ID: 38744462 [TBL] [Abstract][Full Text] [Related]
20. Rapid detection of duplication/deletion of the PMP22 gene in patients with Charcot-Marie-Tooth disease Type 1A and hereditary neuropathy with liability to pressure palsy by real-time quantitative PCR using SYBR Green I dye. Kim SW; Lee KS; Jin HS; Lee TM; Koo SK; Lee YJ; Jung SC J Korean Med Sci; 2003 Oct; 18(5):727-32. PubMed ID: 14555828 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]