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.
192 related articles for article (PubMed ID: 31993930)
1. PMP22 Gene-Associated Neuropathies: Phenotypic Spectrum in a Cohort from India. Nagappa M; Sharma S; Govindaraj P; Chickabasaviah YT; Siram R; Shroti A; Debnath M; Sinha S; Bindu PS; Taly AB J Mol Neurosci; 2020 May; 70(5):778-789. PubMed ID: 31993930 [TBL] [Abstract][Full Text] [Related]
2. Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. Taioli F; Cabrini I; Cavallaro T; Acler M; Fabrizi GM Brain; 2011 Feb; 134(Pt 2):608-17. PubMed ID: 21252112 [TBL] [Abstract][Full Text] [Related]
3. Clinical and molecular genetic characteristics of 24 families of hereditary neuropathy with liability to pressure palsy and literature review. Cao W; Huang S; Zhao H; Li Z; Zhu X; Liu L; Zhang R Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2023 Oct; 48(10):1572-1582. PubMed ID: 38432886 [TBL] [Abstract][Full Text] [Related]
4. Charcot-Marie-Tooth disease and related inherited neuropathies. Murakami T; Garcia CA; Reiter LT; Lupski JR Medicine (Baltimore); 1996 Sep; 75(5):233-50. PubMed ID: 8862346 [TBL] [Abstract][Full Text] [Related]
5. Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients. Hattori N; Yamamoto M; Yoshihara T; Koike H; Nakagawa M; Yoshikawa H; Ohnishi A; Hayasaka K; Onodera O; Baba M; Yasuda H; Saito T; Nakashima K; Kira J; Kaji R; Oka N; Sobue G; Brain; 2003 Jan; 126(Pt 1):134-51. PubMed ID: 12477701 [TBL] [Abstract][Full Text] [Related]
11. Clinical and Molecular Characterization of PMP22 point mutations in Taiwanese patients with Inherited Neuropathy. Liao YC; Tsai PC; Lin TS; Hsiao CT; Chao NC; Lin KP; Lee YC Sci Rep; 2017 Nov; 7(1):15363. PubMed ID: 29127354 [TBL] [Abstract][Full Text] [Related]
12. [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]
13. [Molecular genetics of inherited neuropathies]. Takashima H Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790 [TBL] [Abstract][Full Text] [Related]
14. Tetraspan myelin protein PMP22 and demyelinating peripheral neuropathies: new facts and hypotheses. Müller HW Glia; 2000 Jan; 29(2):182-5. PubMed ID: 10625337 [TBL] [Abstract][Full Text] [Related]
15. A novel PMP22 insertion mutation causing Charcot-Marie-Tooth disease type 3: A case report. Han L; Huang Y; Nie Y; Li J; Chen G; Tu S; Shen P; Chen C Medicine (Baltimore); 2021 Mar; 100(11):e25163. PubMed ID: 33726003 [TBL] [Abstract][Full Text] [Related]
16. Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in Japan. Abe A; Numakura C; Kijima K; Hayashi M; Hashimoto T; Hayasaka K J Hum Genet; 2011 May; 56(5):364-8. PubMed ID: 21326314 [TBL] [Abstract][Full Text] [Related]
17. Correlation between the histopathologic, genotypic, and phenotypic features of hereditary peripheral neuropathies in childhood. Ouvrier R J Child Neurol; 1996 Mar; 11(2):133-46. PubMed ID: 8881991 [TBL] [Abstract][Full Text] [Related]
18. Distinct disease mechanisms in peripheral neuropathies due to altered peripheral myelin protein 22 gene dosage or a Pmp22 point mutation. Giambonini-Brugnoli G; Buchstaller J; Sommer L; Suter U; Mantei N Neurobiol Dis; 2005 Apr; 18(3):656-68. PubMed ID: 15755691 [TBL] [Abstract][Full Text] [Related]
19. Mutation analysis of PMP22 in Slovak patients with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies. Resko P; Radvansky J; Odnogova Z; Baldovic M; Minarik G; Polakova H; Palffy R; Kadasi L Gen Physiol Biophys; 2011 Dec; 30(4):379-88. PubMed ID: 22131320 [TBL] [Abstract][Full Text] [Related]
20. Pmp22 mutant allele-specific siRNA alleviates demyelinating neuropathic phenotype in vivo. Lee JS; Chang EH; Koo OJ; Jwa DH; Mo WM; Kwak G; Moon HW; Park HT; Hong YB; Choi BO Neurobiol Dis; 2017 Apr; 100():99-107. PubMed ID: 28108290 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]