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.
119 related articles for article (PubMed ID: 22065612)
1. Striking phenotypic variability in familial TRPV4-axonal neuropathy spectrum disorder. Aharoni S; Harlalka G; Offiah A; Shuper A; Crosby AH; McEntagart M Am J Med Genet A; 2011 Dec; 155A(12):3153-6. PubMed ID: 22065612 [No Abstract] [Full Text] [Related]
2. Reduced penetrance in hereditary motor neuropathy caused by TRPV4 Arg269Cys mutation. Berciano J; Baets J; Gallardo E; Zimoń M; García A; López-Laso E; Combarros O; Infante J; Timmerman V; Jordanova A; De Jonghe P J Neurol; 2011 Aug; 258(8):1413-21. PubMed ID: 21336783 [TBL] [Abstract][Full Text] [Related]
3. Phenotypic spectrum and incidence of TRPV4 mutations in patients with inherited axonal neuropathy. Echaniz-Laguna A; Dubourg O; Carlier P; Carlier RY; Sabouraud P; Péréon Y; Chapon F; Thauvin-Robinet C; Laforêt P; Eymard B; Latour P; Stojkovic T Neurology; 2014 May; 82(21):1919-26. PubMed ID: 24789864 [TBL] [Abstract][Full Text] [Related]
4. [Experience in molecular diagnostic in hereditary neuropathies in a pediatric tertiary hospital]. Fernández-Ramos JA; López-Laso E; Camino-León R; Gascón-Jiménez FJ; Jiménez-González MD Rev Neurol; 2015 Dec; 61(11):490-8. PubMed ID: 26602803 [TBL] [Abstract][Full Text] [Related]
5. Phenotypic spectrum and incidence of TRPV4 mutations in patients with inherited axonal neuropathy. Sullivan JM; Landouré G; Gaudet R; Sumner CJ Neurology; 2014 Nov; 83(21):1991. PubMed ID: 25404646 [No Abstract] [Full Text] [Related]
6. A novel WARS mutation (p.Asp314Gly) identified in a Chinese distal hereditary motor neuropathy family. Wang B; Li X; Huang S; Zhao H; Liu J; Hu Z; Lin Z; Liu L; Xie Y; Jin Q; Zhao H; Tang B; Niu Q; Zhang R Clin Genet; 2019 Aug; 96(2):176-182. PubMed ID: 31069783 [TBL] [Abstract][Full Text] [Related]
7. Comprehensive analysis of the TRPV4 gene in a large series of inherited neuropathies and controls. Fawcett KA; Murphy SM; Polke JM; Wray S; Burchell VS; Manji H; Quinlivan RM; Zdebik AA; Reilly MM; Houlden H J Neurol Neurosurg Psychiatry; 2012 Dec; 83(12):1204-9. PubMed ID: 22851605 [TBL] [Abstract][Full Text] [Related]
8. Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C. Auer-Grumbach M; Olschewski A; Papić L; Kremer H; McEntagart ME; Uhrig S; Fischer C; Fröhlich E; Bálint Z; Tang B; Strohmaier H; Lochmüller H; Schlotter-Weigel B; Senderek J; Krebs A; Dick KJ; Petty R; Longman C; Anderson NE; Padberg GW; Schelhaas HJ; van Ravenswaaij-Arts CM; Pieber TR; Crosby AH; Guelly C Nat Genet; 2010 Feb; 42(2):160-4. PubMed ID: 20037588 [TBL] [Abstract][Full Text] [Related]
9. The puzzle of TRPV4 channelopathies. Nilius B; Voets T EMBO Rep; 2013 Feb; 14(2):152-63. PubMed ID: 23306656 [TBL] [Abstract][Full Text] [Related]
10. [Hereditary motor and sensory neuropathy type 4A]. Shagina OA; Dadali EL; Fedotov VP; Tiburkova TB; Poliakov AV Zh Nevrol Psikhiatr Im S S Korsakova; 2010; 110(5 Pt 1):13-6. PubMed ID: 21322820 [TBL] [Abstract][Full Text] [Related]
13. The distal hereditary motor neuropathies. Rossor AM; Kalmar B; Greensmith L; Reilly MM J Neurol Neurosurg Psychiatry; 2012 Jan; 83(1):6-14. PubMed ID: 22028385 [TBL] [Abstract][Full Text] [Related]
14. Axonal neuropathy-associated TRPV4 regulates neurotrophic factor-derived axonal growth. Jang Y; Jung J; Kim H; Oh J; Jeon JH; Jung S; Kim KT; Cho H; Yang DJ; Kim SM; Kim IB; Song MR; Oh U J Biol Chem; 2012 Feb; 287(8):6014-24. PubMed ID: 22187434 [TBL] [Abstract][Full Text] [Related]
15. A novel Feng SY; Li LY; Feng SM; Zou ZY Ann Clin Transl Neurol; 2019 Feb; 6(2):401-405. PubMed ID: 30847374 [TBL] [Abstract][Full Text] [Related]
16. Hereditary neuropathy with liability to pressure palsy (HNPP): report of a family with a new point mutation in PMP22 gene. Fusco C; Spagnoli C; Salerno GG; Pavlidis E; Frattini D; Pisani F Ital J Pediatr; 2017 Oct; 43(1):97. PubMed ID: 29078790 [TBL] [Abstract][Full Text] [Related]
17. Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies. Zimoń M; Baets J; Auer-Grumbach M; Berciano J; Garcia A; Lopez-Laso E; Merlini L; Hilton-Jones D; McEntagart M; Crosby AH; Barisic N; Boltshauser E; Shaw CE; Landouré G; Ludlow CL; Gaudet R; Houlden H; Reilly MM; Fischbeck KH; Sumner CJ; Timmerman V; Jordanova A; Jonghe PD Brain; 2010 Jun; 133(Pt 6):1798-809. PubMed ID: 20460441 [TBL] [Abstract][Full Text] [Related]
18. Identification of a de novo insertional mutation in P0 in a patient with a Déjérine-Sottas syndrome (DSS) phenotype. Rautenstrauss B; Nelis E; Grehl H; Pfeiffer RA; Van Broeckhoven C Hum Mol Genet; 1994 Sep; 3(9):1701-2. PubMed ID: 7530550 [No Abstract] [Full Text] [Related]
19. A case of congenital spinal muscular atrophy with pain due to a mutation in TRPV4. Fleming J; Quan D Neuromuscul Disord; 2016 Dec; 26(12):841-843. PubMed ID: 27751652 [TBL] [Abstract][Full Text] [Related]
20. HSMNR belongs to the most frequent types of hereditary neuropathy in the Czech Republic and is twice more frequent than HMSNL. Šafka Brožková D; Haberlová J; Mazanec R; Laštůvková J; Seeman P Clin Genet; 2016 Aug; 90(2):161-5. PubMed ID: 26822750 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]