Weinstock C, Anliker M, von Zabern I. CD59: a long-known complement inhibitor has advanced to a blood group system. Immunohematology 2015;31:145–51.WeinstockCAnlikerMvon ZabernI.CD59: a long-known complement inhibitor has advanced to a blood group system. Immunohematology2015;31:145–51.10.21307/immunohematology-2019-083Search in Google Scholar
Anliker M, von Zabern I, Höchsmann B, et al. A new blood group antigen is defined by anti-CD59, detected in a CD59-deficient patient. Transfusion 2014;54:1817–22.AnlikerMvon ZabernIHöchsmannB, A new blood group antigen is defined by anti-CD59, detected in a CD59-deficient patient. Transfusion2014;54:1817–22.10.1111/trf.12531531720124383981Search in Google Scholar
Höchsmann B, Dohna-Schwake C, Kyrieleis HA, Pannicke U, Schrezenmeier H. Targeted therapy with eculizumab for inherited CD59 deficiency. N Engl J Med 2014;370:90–2.HöchsmannBDohna-SchwakeCKyrieleisHAPannickeUSchrezenmeierH.Targeted therapy with eculizumab for inherited CD59 deficiency. N Engl J Med2014;370:90–2.10.1056/NEJMc130810424382084Search in Google Scholar
Yamashina M, Ueda E, Kinoshita T, et al. Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria. N Engl J Med 1990;323:1184–9.YamashinaMUedaEKinoshitaT, Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria. N Engl J Med1990;323:1184–9.10.1056/NEJM1990102532317071699124Search in Google Scholar
Nevo Y, Ben-Zeev B, Tabib A, et al. CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathy. Blood 2013;121:129–35.NevoYBen-ZeevBTabibA, CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathy. Blood2013;121:129–35.10.1182/blood-2012-07-44185723149847Search in Google Scholar
Motoyama N, Okada N, Yamashina M, Okada H. Paroxysmal nocturnal hemoglobinuria due to hereditary nucleotide deletion in the HRF20 (CD59) gene. Eur J Immunol 1992;22:2669–73.MotoyamaNOkadaNYamashinaMOkadaH.Paroxysmal nocturnal hemoglobinuria due to hereditary nucleotide deletion in the HRF20 (CD59) gene. Eur J Immunol1992;22:2669–73.10.1002/eji.18302210291382994Search in Google Scholar
Ben-Zeev B, Tabib A, Nissenkorn A, et al. Devastating recurrent brain ischemic infarctions and retinal disease in pediatric patients with CD59 deficiency. Eur J Paediatr Neurol 2015;19:688–93.Ben-ZeevBTabibANissenkornA, Devastating recurrent brain ischemic infarctions and retinal disease in pediatric patients with CD59 deficiency. Eur J Paediatr Neurol2015;19:688–93.10.1016/j.ejpn.2015.07.00126233519Search in Google Scholar
Haliloglu G, Maluenda J, Sayinbatur B, et al. Early-onset chronic axonal neuropathy, strokes, and hemolysis: inherited CD59 deficiency. Neurology 2015;84:1220–4.HalilogluGMaluendaJSayinbaturB, Early-onset chronic axonal neuropathy, strokes, and hemolysis: inherited CD59 deficiency. Neurology2015;84:1220–4.10.1212/WNL.000000000000139125716358Search in Google Scholar
Klemann C, Kirschner J, Ammann S, et al. CD59 deficiency presenting as polyneuropathy and Moyamoya syndrome with endothelial abnormalities of small brain vessels. Eur J Paediatr Neurol 2018;22:870–7.KlemannCKirschnerJAmmannS, CD59 deficiency presenting as polyneuropathy and Moyamoya syndrome with endothelial abnormalities of small brain vessels. Eur J Paediatr Neurol2018;22:870–7.10.1016/j.ejpn.2018.04.00329843966Search in Google Scholar
Ardicli D, Taskiran EZ, Kosukcu C, et al. Neonatal-onset recurrent Guillain-Barre syndrome-like disease: clues for inherited CD59 deficiency. Neuropediatrics 2017;48:477–81.ArdicliDTaskiranEZKosukcuC, Neonatal-onset recurrent Guillain-Barre syndrome-like disease: clues for inherited CD59 deficiency. Neuropediatrics2017;48:477–81.10.1055/s-0037-160448328800659Search in Google Scholar
Tone M, Walsh LA, Waldmann H. Gene structure of human CD59 and demonstration that discrete mRNAs are generated by alternative polyadenylation. J Mol Biol 1992;227:971–6.ToneMWalshLAWaldmannH.Gene structure of human CD59 and demonstration that discrete mRNAs are generated by alternative polyadenylation. J Mol Biol1992;227:971–6.10.1016/0022-2836(92)90239-GSearch in Google Scholar
Holguin MH, Martin CB, Eggett T, Parker CJ. Analysis of the gene that encodes the complement regulatory protein, membrane inhibitor of reactive lysis (CD59): identification of an alternatively spliced exon and characterization of the transcriptional regulatory regions of the promoter. J Immunol 1996;157:1659–68.HolguinMHMartinCBEggettTParkerCJ.Analysis of the gene that encodes the complement regulatory protein, membrane inhibitor of reactive lysis (CD59): identification of an alternatively spliced exon and characterization of the transcriptional regulatory regions of the promoter. J Immunol1996;157:1659–68.Search in Google Scholar
International Society of Blood Transfusion, Working Party Red Cell Immunogenetics and Blood Group Terminology. Names for CD59 (ISBT 035) blood group alleles v1 0 160701 2018; http://www.isbtweb.org/working-parties/red-cell-immunogenetics-and-blood-group-terminology.International Society of Blood Transfusion, Working Party Red Cell Immunogenetics and Blood Group Terminology. Names for CD59 (ISBT 035) blood group alleles v1 0 1607012018; http://www.isbtweb.org/working-parties/red-cell-immunogenetics-and-blood-group-terminology.Search in Google Scholar
Li XF, Lin FQ, Li JP. Identification of c.238 A>G (p.Arg80Gly) of CD59 blood group gene. Transfusion 2018;58:3033–4.LiXFLinFQLiJP.Identification of c.238 A>G (p.Arg80Gly) of CD59 blood group gene. Transfusion2018;58:3033–4.10.1111/trf.1496030325039Search in Google Scholar
