219 related articles for article (PubMed ID: 26534810)
1. Hereditary peripheral neuropathies diagnosed by next-generation sequencing.
Høyer H; Busk ØL; Holla ØL; Strand L; Russell MB; Skjelbred CF; Braathen GJ
Tidsskr Nor Laegeforen; 2015 Nov; 135(20):1838-44. PubMed ID: 26534810
[TBL] [Abstract][Full Text] [Related]
2. [Clinical practice of hereditary motor neuropathy (HMN) and hereditary sensory and autonomic neuropathy (HSAN)].
Takashima H
Rinsho Shinkeigaku; 2014; 54(12):957-9. PubMed ID: 25672680
[TBL] [Abstract][Full Text] [Related]
3. Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies.
Dohrn MF; Glöckle N; Mulahasanovic L; Heller C; Mohr J; Bauer C; Riesch E; Becker A; Battke F; Hörtnagel K; Hornemann T; Suriyanarayanan S; Blankenburg M; Schulz JB; Claeys KG; Gess B; Katona I; Ferbert A; Vittore D; Grimm A; Wolking S; Schöls L; Lerche H; Korenke GC; Fischer D; Schrank B; Kotzaeridou U; Kurlemann G; Dräger B; Schirmacher A; Young P; Schlotter-Weigel B; Biskup S
J Neurochem; 2017 Dec; 143(5):507-522. PubMed ID: 28902413
[TBL] [Abstract][Full Text] [Related]
4. Assessment of Targeted Next-Generation Sequencing as a Tool for the Diagnosis of Charcot-Marie-Tooth Disease and Hereditary Motor Neuropathy.
Lupo V; García-García F; Sancho P; Tello C; García-Romero M; Villarreal L; Alberti A; Sivera R; Dopazo J; Pascual-Pascual SI; Márquez-Infante C; Casasnovas C; Sevilla T; Espinós C
J Mol Diagn; 2016 Mar; 18(2):225-34. PubMed ID: 26752306
[TBL] [Abstract][Full Text] [Related]
5. Diagnostic yield of advanced genetic testing in patients with hereditary neuropathies: A retrospective single-site study.
Felice KJ; Whitaker CH; Khorasanizadeh S
Muscle Nerve; 2021 Oct; 64(4):454-461. PubMed ID: 34232518
[TBL] [Abstract][Full Text] [Related]
6. Molecular diagnosis of inherited peripheral neuropathies by targeted next-generation sequencing: molecular spectrum delineation.
Bacquet J; Stojkovic T; Boyer A; Martini N; Audic F; Chabrol B; Salort-Campana E; Delmont E; Desvignes JP; Verschueren A; Attarian S; Chaussenot A; Delague V; Levy N; Bonello-Palot N
BMJ Open; 2018 Oct; 8(10):e021632. PubMed ID: 30373780
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [Advances in the molecular genetics of the hereditary neuropathies].
Palau F; Cuesta A; Pedrola L
Rev Neurol; 2002 Aug 1-15; 35(3):246-53. PubMed ID: 12235587
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. [Molecular genetics of inherited neuropathies].
Takashima H
Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
[TBL] [Abstract][Full Text] [Related]
12. Inherited peripheral neuropathy.
Keller MP; Chance PF
Semin Neurol; 1999; 19(4):353-62. PubMed ID: 10716658
[TBL] [Abstract][Full Text] [Related]
13. Genetic epidemiology of Charcot-Marie-Tooth disease.
Braathen GJ
Acta Neurol Scand Suppl; 2012; (193):iv-22. PubMed ID: 23106488
[TBL] [Abstract][Full Text] [Related]
14. [Diagnosis of monogenic diseases of the peripheral nervous system].
Haupt A; Epplen JT
Dtsch Med Wochenschr; 1996 Nov; 121(47):1469-72. PubMed ID: 8983897
[No Abstract] [Full Text] [Related]
15. [Genetic distribution in Chinese patients with hereditary peripheral neuropathy].
Liu XX; Duan XH; Zhang S; Sun AP; Zhang YS; Fan DS
Beijing Da Xue Xue Bao Yi Xue Ban; 2022 Oct; 54(5):874-883. PubMed ID: 36241230
[TBL] [Abstract][Full Text] [Related]
16. [Hereditary sensory and motor neuropathy and hereditary sensory and autonomic neuropathies: recent advances].
Stojkovic T
Rev Neurol (Paris); 2011 Dec; 167(12):948-50. PubMed ID: 22100327
[TBL] [Abstract][Full Text] [Related]
17. Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases: an update.
Tazir M; Hamadouche T; Nouioua S; Mathis S; Vallat JM
J Neurol Sci; 2014 Dec; 347(1-2):14-22. PubMed ID: 25454638
[TBL] [Abstract][Full Text] [Related]
18. Diagnosis and new treatments in genetic neuropathies.
Reilly MM; Shy ME
J Neurol Neurosurg Psychiatry; 2009 Dec; 80(12):1304-14. PubMed ID: 19917815
[TBL] [Abstract][Full Text] [Related]
19. Hereditary sensory neuropathies.
Houlden H; Blake J; Reilly MM
Curr Opin Neurol; 2004 Oct; 17(5):569-77. PubMed ID: 15367861
[TBL] [Abstract][Full Text] [Related]
20. Hereditary Neuropathies.
Eggermann K; Gess B; Häusler M; Weis J; Hahn A; Kurth I
Dtsch Arztebl Int; 2018 Feb; 115(6):91-97. PubMed ID: 29478438
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
