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8. Red blood cell Gardos channel (KCNN4): the essential determinant of erythrocyte dehydration in hereditary xerocytosis. Rapetti-Mauss R; Picard V; Guitton C; Ghazal K; Proulle V; Badens C; Soriani O; Garçon L; Guizouarn H Haematologica; 2017 Oct; 102(10):e415-e418. PubMed ID: 28619848 [No Abstract] [Full Text] [Related]
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10. Multiple thrombosis in a patient with Gardos channelopathy and a new KCNN4 mutation. Mansour-Hendili L; Egée S; Monedero-Alonso D; Bouyer G; Godeau B; Badaoui B; Lunati A; Noizat C; Aissat A; Kiger L; Mekki C; Picard V; Moutereau S; Fanen P; Bartolucci P; Garçon L; Galactéros F; Funalot B Am J Hematol; 2021 Sep; 96(9):E318-E321. PubMed ID: 34004026 [No Abstract] [Full Text] [Related]
11. Senicapoc: a potent candidate for the treatment of a subset of hereditary xerocytosis caused by mutations in the Gardos channel. Rapetti-Mauss R; Soriani O; Vinti H; Badens C; Guizouarn H Haematologica; 2016 Nov; 101(11):e431-e435. PubMed ID: 27443288 [No Abstract] [Full Text] [Related]
12. Severe hemolytic anemia in a newborn: Look out for rare Gardos channelopathies due to KCNN4 mutation. Munaretto V; Martella M; Francescato S; Reggiani G; Boaro MP; Bianchi P; Fermo E; Barcellini W; Sainati L; Colombatti R Pediatr Blood Cancer; 2023 Aug; 70(8):e30325. PubMed ID: 37132095 [No Abstract] [Full Text] [Related]
13. Dehydrated hereditary stomatocytosis: Prenatal management of ascites and pleural effusions. Le Vaillant C; Riteau AS; Eveillard M; Beneteau C Taiwan J Obstet Gynecol; 2018 Apr; 57(2):323-324. PubMed ID: 29673682 [No Abstract] [Full Text] [Related]
14. A novel PIEZO1 mutation in a patient with dehydrated hereditary stomatocytosis: a case report and a brief review of literature. Zama D; Giulietti G; Muratore E; Andolfo I; Russo R; Iolascon A; Pession A Ital J Pediatr; 2020 Jul; 46(1):102. PubMed ID: 32703298 [TBL] [Abstract][Full Text] [Related]
15. Hereditary xerocytosis and familial haemolysis due to mutation in the PIEZO1 gene: a simple diagnostic approach. Sandberg MB; Nybo M; Birgens H; Frederiksen H Int J Lab Hematol; 2014 Aug; 36(4):e62-5. PubMed ID: 24314002 [No Abstract] [Full Text] [Related]
16. Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels. Albuisson J; Murthy SE; Bandell M; Coste B; Louis-Dit-Picard H; Mathur J; Fénéant-Thibault M; Tertian G; de Jaureguiberry JP; Syfuss PY; Cahalan S; Garçon L; Toutain F; Simon Rohrlich P; Delaunay J; Picard V; Jeunemaitre X; Patapoutian A Nat Commun; 2013; 4():1884. PubMed ID: 23695678 [TBL] [Abstract][Full Text] [Related]
17. Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in India. More TA; Dongerdiye R; Devendra R; Warang PP; Kedar PS Ann Hematol; 2020 Apr; 99(4):715-727. PubMed ID: 32112123 [TBL] [Abstract][Full Text] [Related]
18. Common PIEZO1 Allele in African Populations Causes RBC Dehydration and Attenuates Plasmodium Infection. Ma S; Cahalan S; LaMonte G; Grubaugh ND; Zeng W; Murthy SE; Paytas E; Gamini R; Lukacs V; Whitwam T; Loud M; Lohia R; Berry L; Khan SM; Janse CJ; Bandell M; Schmedt C; Wengelnik K; Su AI; Honore E; Winzeler EA; Andersen KG; Patapoutian A Cell; 2018 Apr; 173(2):443-455.e12. PubMed ID: 29576450 [TBL] [Abstract][Full Text] [Related]
19. Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1. Andolfo I; Alper SL; De Franceschi L; Auriemma C; Russo R; De Falco L; Vallefuoco F; Esposito MR; Vandorpe DH; Shmukler BE; Narayan R; Montanaro D; D'Armiento M; Vetro A; Limongelli I; Zuffardi O; Glader BE; Schrier SL; Brugnara C; Stewart GW; Delaunay J; Iolascon A Blood; 2013 May; 121(19):3925-35, S1-12. PubMed ID: 23479567 [TBL] [Abstract][Full Text] [Related]