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Chapter 45 Red Blood Cell Membrane Disorders 647
Bianchi P, Fermo E, Vercellati C, et al: Diagnostic power of laboratory Gallagher PG: Disorders of red cell volume regulation. Curr Opin Hematol
tests for hereditary spherocytosis: a comparison study in 150 patients 20:201–207, 2013.
grouped according to molecular and clinical characteristics. Haematologica Garnett C, Bain BJ: South-East Asian ovalocytosis. Am J Hematol 88:328,
97:516–523, 2012. 2013.
Bolton-Maggs PH, Langer JC, Iolascon A, et al: Guidelines for the diagnosis Glogowska E, Gallagher PG: Disorders of erythrocyte volume homeostasis.
and management of hereditary spherocytosis—2011 update. Br J Hae- Int J Lab Hematol 37(S1):85–91, 2015.
matol 156:37–49, 2012. Glogowska E, Lezon-Geyda K, Maksimova Y, et al: Mutations in the Gardos
Brugnara C, Mohandas N: Red cell indices in classification and treatment of channel (KCNN4) are associated with hereditary xerocytosis. Blood
anemias: from M.M. Wintrobes’s original 1934 classification to the third 126:1281–1284, 2015.
millennium. Curr Opin Hematol 20:222–230, 2013. King MJ, Garcon L, Hoyer JD, et al: ICSH guidelines for the laboratory
Buesing KL, Tracy ET, Kiernan C, et al: Partial splenectomy for hereditary diagnosis of nonimmune hereditary red cell membrane disorders. Int J
spherocytosis: a multi-institutional review. J Pediatr Surg 46:178–183, Lab Hematol 37:304–325, 2015.
2011. Mayeur-Rousse C, Gentil M, Botton J, et al: Testing for hereditary sphe-
Christensen RD, Yaish HM, Gallagher PG: A pediatrician’s practical guide rocytosis: a French experience. Haematologica 97:e48–e49, author reply
to diagnosing and treating hereditary spherocytosis in neonates. Pediatrics e52, 2012.
135:1107–1114, 2015. Rapetti-Mauss R, Lacoste C, Picard V, et al: A mutation in the Gardos
Cluitmans JC, Tomelleri C, Yapici Z, et al: Abnormal red cell structure and channel is associated with hereditary xerocytosis. Blood 126:1273–1280,
function in neuroacanthocytosis. PLoS ONE 10:e0125580, 2015. 2015.
Colin Y, Le Van Kim C, El Nemer W: Red cell adhesion in human diseases. Rice HE, Englum BR, Rothman J, et al: Clinical outcomes of splenectomy
Curr Opin Hematol 21:186–192, 2014. in children: report of the splenectomy in congenital hemolytic anemia
Cordat E, Reithmeier RA: Structure, function, and trafficking of SLC4 and registry. Am J Hematol 90:187–192, 2015.
SLC26 anion transporters. Curr Top Membr 73:1–67, 2014. Sakamoto TM, Canalli AA, Traina F, et al: Altered red cell and platelet adhe-
Da Costa L, Galimand J, Fenneteau O, et al: Hereditary spherocytosis, ellip- sion in hemolytic diseases: hereditary spherocytosis, paroxysmal nocturnal
tocytosis, and other red cell membrane disorders. Blood Rev 27:167–178, hemoglobinuria and sickle cell disease. Clin Biochem 46:1798–1803,
2013. 2013.
Das A, Bansal D, Ahluwalia J, et al: Risk factors for thromboembolism and Seims AD, Breckler FD, Hardacker KD, et al: Partial versus total splenectomy
pulmonary artery hypertension following splenectomy in children with in children with hereditary spherocytosis. Surgery 154:849–853, discus-
hereditary spherocytosis. Pediatr Blood Cancer 61:29–33, 2014. sion 53-55, 2013.
De Franceschi L, Bosman GJ, Mohandas N: Abnormal red cell features Walker RH, Schulz VP, Tikhonova IR, et al: Genetic diagnosis of neuroac-
associated with hereditary neurodegenerative disorders: the neuroacantho- anthocytosis disorders using exome sequencing. Mov Disord 27:539–543,
cytosis syndromes. Curr Opin Hematol 21:201–209, 2014. 2012.
Gallagher PG: Abnormalities of the erythrocyte membrane. Pediatr Clin
North Am 60:1349–1362, 2013.

