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2. Incidence and Clinical Features of TRPV4-Linked Axonal Neuropathies in a USA Cohort of Charcot-Marie-Tooth Disease Type 2. Deng S; Feely SME; Shi Y; Zhai H; Zhan L; Siddique T; Deng HX; Shy ME Neuromolecular Med; 2020 Mar; 22(1):68-72. PubMed ID: 31468327 [TBL] [Abstract][Full Text] [Related]
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4. A TRPV4 mutation caused Charcot-Marie-Tooth disease type 2C with scapuloperoneal muscular atrophy overlap syndrome and scapuloperoneal spinal muscular atrophy in one family: a case report and literature review. Chen H; Sun C; Zheng Y; Yin J; Gao M; Zhao C; Lin J BMC Neurol; 2023 Jun; 23(1):250. PubMed ID: 37391745 [TBL] [Abstract][Full Text] [Related]
5. 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]
7. Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4. Deng HX; Klein CJ; Yan J; Shi Y; Wu Y; Fecto F; Yau HJ; Yang Y; Zhai H; Siddique N; Hedley-Whyte ET; Delong R; Martina M; Dyck PJ; Siddique T Nat Genet; 2010 Feb; 42(2):165-9. PubMed ID: 20037587 [TBL] [Abstract][Full Text] [Related]
8. Novel TRPV4 mutation in a large Chinese family with congenital distal spinal muscular atrophy, skeletal dysplasia and scaly skin. Liu Y; Yan X; Chen Y; He Z; Ouyang Y J Neurol Sci; 2020 Dec; 419():117153. PubMed ID: 33075594 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. TRPV4 related scapuloperoneal spinal muscular atrophy: Report of an Italian family and review of the literature. Biasini F; Portaro S; Mazzeo A; Vita G; Fabrizi GM; Taioli F; Toscano A; Rodolico C Neuromuscul Disord; 2016; 26(4-5):312-5. PubMed ID: 26948711 [TBL] [Abstract][Full Text] [Related]
11. TRPV4-pathy manifesting both skeletal dysplasia and peripheral neuropathy: a report of three patients. Cho TJ; Matsumoto K; Fano V; Dai J; Kim OH; Chae JH; Yoo WJ; Tanaka Y; Matsui Y; Takigami I; Monges S; Zabel B; Shimizu K; Nishimura G; Lausch E; Ikegawa S Am J Med Genet A; 2012 Apr; 158A(4):795-802. PubMed ID: 22419508 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Natural history of TRPV4-Related disorders: From skeletal dysplasia to neuromuscular phenotype. Ürel-Demir G; Şimşek-Kiper PÖ; Öncel İ; Utine GE; Haliloğlu G; Boduroğlu K Eur J Paediatr Neurol; 2021 May; 32():46-55. PubMed ID: 33774370 [TBL] [Abstract][Full Text] [Related]
15. Spondyloepimetaphyseal dysplasia-Maroteaux type due to dominant TRPV4 mutation: expanding the phenotype with a case report. Uzman CY; Çankaya T; Güleryüz H; Ülgenalp A; Bozkaya ÖG Skeletal Radiol; 2023 Jan; 52(1):115-118. PubMed ID: 35776137 [TBL] [Abstract][Full Text] [Related]
16. Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutation. Koutsis G; Lynch D; Manole A; Karadima G; Reilly MM; Houlden H; Panas M J Neurol; 2015 Aug; 262(8):1972-5. PubMed ID: 26048687 [No Abstract] [Full Text] [Related]
18. CMT2C with vocal cord paresis associated with short stature and mutations in the TRPV4 gene. Chen DH; Sul Y; Weiss M; Hillel A; Lipe H; Wolff J; Matsushita M; Raskind W; Bird T Neurology; 2010 Nov; 75(22):1968-75. PubMed ID: 21115951 [TBL] [Abstract][Full Text] [Related]
19. The remarkable phenotypic variability of the p.Arg269HiS variant in the TRPV4 gene. Jędrzejowska M; Dębek E; Kowalczyk B; Halat P; Kostera-Pruszczyk A; Ciara E; Jezela-Stanek A; Rydzanicz M; Gasperowicz P; Gos M Muscle Nerve; 2019 Jan; 59(1):129-133. PubMed ID: 30230566 [TBL] [Abstract][Full Text] [Related]