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13 in total

1. Cation depletion by the sodium pump in red cells with pathologic cation leaks. Sickle cells and xerocytes.

Authors: C H Joiner; O S Platt; S E Lux
Journal: J Clin Invest Date: 1986-12 Impact factor: 14.808

2. Red blood cell Gardos channel (KCNN4): the essential determinant of erythrocyte dehydration in hereditary xerocytosis.

Authors: Raphaël Rapetti-Mauss; Véronique Picard; Corinne Guitton; Khaldoun Ghazal; Valérie Proulle; Catherine Badens; Olivier Soriani; Loïc Garçon; Hélène Guizouarn
Journal: Haematologica Date: 2017-06-15 Impact factor: 9.941

3. Abnormality of erythrocyte membrane protein in a case of congenital stomatocytosis.

Authors: U Bienzle; S Bhadki; H Knüfermann; D Niethammer; E Kleihauer
Journal: Klin Wochenschr Date: 1977-06-15

4. Animal model of human disease. Congenital hemolytic anemia.

Authors: S M Fletch; P H Pinkerton
Journal: Am J Pathol Date: 1973-06 Impact factor: 4.307

5. Role of the spleen in congenital stomatocytosis associated with high sodium-low potassium erythrocytes.

Authors: W Schröter; K Ungefehr; W Tillmann
Journal: Klin Wochenschr Date: 1981-02-16

6. Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis.

Authors: Ryan Zarychanski; Vincent P Schulz; Brett L Houston; Yelena Maksimova; Donald S Houston; Brian Smith; Jesse Rinehart; Patrick G Gallagher
Journal: Blood Date: 2012-04-23 Impact factor: 22.113

7. Exercise-induced hemolysis in xerocytosis. Erythrocyte dehydration and shear sensitivity.

Authors: O S Platt; S E Lux; D G Nathan
Journal: J Clin Invest Date: 1981-09 Impact factor: 14.808

8. Missing band 7 membrane protein in two patients with high Na, low K erythrocytes.

Authors: W M Lande; P V Thiemann; W C Mentzer
Journal: J Clin Invest Date: 1982-12 Impact factor: 14.808

9. Non-immune interaction of erythrophilic IgG fractions with human red blood cells.

Authors: S Dagan; A Beretz; M Fridkin; Y Burstein; Z Spirer
Journal: Mol Cell Biochem Date: 1985-02 Impact factor: 3.396

Review 10. Human phenotypes caused by PIEZO1 mutations; one gene, two overlapping phenotypes?

Authors: Silvia Martin-Almedina; Sahar Mansour; Pia Ostergaard
Journal: J Physiol Date: 2018-01-31 Impact factor: 5.182