{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,9,21]],"date-time":"2022-09-21T05:54:39Z","timestamp":1663739679545},"reference-count":43,"publisher":"Georg Thieme Verlag KG","issue":"19","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Dtsch Med Wochenschr"],"published-print":{"date-parts":[[2022,9]]},"DOI":"10.1055\/a-1767-8423","type":"journal-article","created":{"date-parts":[[2022,9,20]],"date-time":"2022-09-20T23:25:03Z","timestamp":1663716303000},"page":"1266-1276","source":"Crossref","is-referenced-by-count":0,"title":["Kongenitale h\u00e4molytische An\u00e4mien durch Membran- und\u00a0Enzymdefekte der Erythrozyten"],"prefix":"10.1055","volume":"147","author":[{"given":"Franziska","family":"G\u00e9nevaux","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Annika","family":"Bertsch","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lisa","family":"Wiederer","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Stefan","family":"Eber","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"194","published-online":{"date-parts":[[2022,9,20]]},"reference":[{"key":"ref1","doi-asserted-by":"publisher","first-page":"367","DOI":"10.1111\/j.1365-2141.2008.07091.x","article-title":"Disorders of red cell membrane","volume":"141","author":"X An","year":"2008","journal-title":"Br J Haematol"},{"key":"ref2","doi-asserted-by":"publisher","first-page":"668","DOI":"10.1136\/archdischild-2013-305748","article-title":"Diagnostic and therapeutic challenges of primary autoimmune haemolytic anaemia in children","volume":"99","author":"J M Vagace","year":"2014","journal-title":"Arch Dis Child"},{"key":"ref3","doi-asserted-by":"publisher","first-page":"201","DOI":"10.1097\/MOH.0b013e32835f6870","article-title":"Disorders of red cell volume regulation","volume":"20","author":"P G Gallagher","year":"2013","journal-title":"Curr Opin Hematol"},{"key":"ref4","volume-title":"Hereditary Spherocytosis","author":"E A Zamora","year":"2022"},{"key":"ref5","doi-asserted-by":"publisher","first-page":"167","DOI":"10.1016\/j.blre.2013.04.003","article-title":"Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders","volume":"27","author":"L Da Costa","year":"2013","journal-title":"Blood Rev"},{"key":"ref6","doi-asserted-by":"publisher","first-page":"1411","DOI":"10.1016\/s0140-6736(08)61588-3","article-title":"Hereditary spherocytosis","volume":"372","author":"S Perrotta","year":"2008","journal-title":"Lancet"},{"key":"ref8","doi-asserted-by":"publisher","first-page":"556","DOI":"10.1016\/j.gene.2017.07.009","article-title":"Novel mutations in patients with hereditary red blood cell membrane disorders using next-generation sequencing","volume":"627","author":"Y He","year":"2017","journal-title":"Gene"},{"key":"ref9","doi-asserted-by":"publisher","first-page":"138","DOI":"10.1016\/j.tracli.2010.05.006","article-title":"Hereditary spherocytosis","volume":"17","author":"A Iolascon","year":"2010","journal-title":"Transfus Clin Biol"},{"key":"ref10","doi-asserted-by":"publisher","first-page":"60","DOI":"10.1159\/000486229","article-title":"Molecular Genetic Mechanisms of Hereditary Spherocytosis: Current Perspectives","volume":"139","author":"B J He","year":"2018","journal-title":"Acta Haematol"},{"key":"ref11","doi-asserted-by":"publisher","first-page":"37","DOI":"10.1111\/j.1365-2141.2011.08921.x","article-title":"Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update","volume":"156","author":"P H Bolton-Maggs","year":"2012","journal-title":"Br J Haematol"},{"key":"ref12","doi-asserted-by":"publisher","first-page":"e306","DOI":"10.1097\/MPH.0000000000002211","article-title":"Clinical Features and Outcome of Children With Hereditary Spherocytosis","volume":"44","author":"M A Kili\u00e7","year":"2022","journal-title":"J Pediatric Hematol Oncol"},{"key":"ref13","doi-asserted-by":"publisher","first-page":"137","DOI":"10.1186\/1756-0500-7-137","article-title":"Human parvovirus B19-induced aplastic crisis in an adult patient with hereditary spherocytosis: a case report and review of the literature","volume":"7","author":"Y Kobayashi","year":"2014","journal-title":"BMC Res Notes"},{"key":"ref14","doi-asserted-by":"publisher","DOI":"10.1177\/2050312114547093","article-title":"Hereditary spherocytosis: Consequences of delayed diagnosis","volume":"2","author":"S C Steward","year":"2014","journal-title":"SAGE Open Medicine"},{"key":"ref15","doi-asserted-by":"crossref","first-page":"118","DOI":"10.1053\/j.seminhematol.2004.01.002","article-title":"Hereditary spherocytosis--defects in proteins that connect the membrane skeleton to the lipid bilayer","volume":"41","author":"S Eber","year":"2004","journal-title":"Semin Hematol"},{"key":"ref16","doi-asserted-by":"publisher","first-page":"697","DOI":"10.1111\/ijlh.12906","article-title":"Screening of hereditary spherocytosis and pyruvate kinase deficiency by automated blood count using erythrocytic and reticulocytic parameters","volume":"40","author":"V Bob\u00e9e","year":"2018","journal-title":"Int J Lab Hematol"},{"key":"ref17","doi-asserted-by":"crossref","first-page":"307","DOI":"10.4103\/0377-4929.162836","article-title":"Mean reticulocyte volume enhances the utility of red cell mean sphered cell volume in differentiating peripheral blood spherocytes of hereditary spherocytosis from other causes","volume":"58","author":"S C Nair","year":"2015","journal-title":"Ind J Pathol Microbiol"},{"key":"ref18","doi-asserted-by":"publisher","first-page":"627","DOI":"10.1586\/ehm.11.51","article-title":"Splenectomy for hereditary spherocytosis: complete, partial or not at all?","volume":"4","author":"M Casale","year":"2011","journal-title":"Expert Rev Hematol"},{"key":"ref19","doi-asserted-by":"publisher","first-page":"1616","DOI":"10.1182\/blood-2015-11-679357","article-title":"Long-term follow-up of subtotal splenectomy for hereditary spherocytosis: a single-center study","volume":"127","author":"T Pincez","year":"2016","journal-title":"Blood"},{"key":"ref20","doi-asserted-by":"publisher","first-page":"E340","DOI":"10.1002\/ajh.25223","article-title":"Subtotal and total splenectomy for hereditary pyropoikilocytosis: Benefits and outcomes","volume":"93","author":"T Pincez","year":"2018","journal-title":"Am J Hematol"},{"key":"ref21","doi-asserted-by":"crossref","first-page":"791","DOI":"10.1111\/j.1365-2141.2005.05956.x","article-title":"Near-total splenectomy for hereditary spherocytosis: clinical prospects in relation to disease severity","volume":"132","author":"G A Stoehr","year":"2006","journal-title":"Brit J Haematol"},{"key":"ref22","doi-asserted-by":"publisher","first-page":"466","DOI":"10.1002\/bjs.6008","article-title":"Mode of splenectomy and immunogenicity of meningococcal vaccination in patients with hereditary spherocytosis","volume":"95","author":"G A Stoehr","year":"2008","journal-title":"Brit J Surg"},{"key":"ref23","doi-asserted-by":"publisher","first-page":"e00358","DOI":"10.1002\/rcr2.358","article-title":"Surgical resection of extramedullary haematopoiesis in the posterior mediastinum","volume":"6","author":"R Matsumoto","year":"2018","journal-title":"Respirol Case Rep"},{"key":"ref25","doi-asserted-by":"publisher","first-page":"1427","DOI":"10.3748\/wjg.15.1427","article-title":"Acute pancreatitis: etiology and common pathogenesis","volume":"15","author":"G J Wang","year":"2009","journal-title":"World J Gastroenterol"},{"key":"ref26","doi-asserted-by":"publisher","first-page":"107","DOI":"10.1002\/ajh.24929","article-title":"Hereditary stomatocytosis: An underdiagnosed condition","volume":"93","author":"I Andolfo","year":"2018","journal-title":"Am J Hematol"},{"key":"ref28","doi-asserted-by":"publisher","first-page":"e127","DOI":"10.1097\/mph.0000000000001025","article-title":"An Infant With Unusually High Unconjugated Hyperbilirubinemia Due to Coexistence of Hereditary Spherocytosis and Gilbert Syndrome","volume":"40","author":"I Butorac Ahel","year":"2018","journal-title":"J Ped Hematol Oncol"},{"key":"ref29","doi-asserted-by":"publisher","first-page":"471","DOI":"10.3233\/ch-141889","article-title":"Erythrocyte deformability and hereditary elliptocytosis","volume":"58","author":"A Vay\u00e1","year":"2014","journal-title":"Clin Hemorheol Microcirc"},{"key":"ref30","doi-asserted-by":"publisher","first-page":"4","DOI":"10.1016\/j.bcmd.2016.07.003","article-title":"Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis","volume":"61","author":"O Niss","year":"2016","journal-title":"Blood Cells Mol Dis"},{"key":"ref31","doi-asserted-by":"publisher","first-page":"142","DOI":"10.1053\/j.seminhematol.2004.01.003","article-title":"Hereditary elliptocytosis: spectrin and protein 4.1R","volume":"41","author":"P G Gallagher","year":"2004","journal-title":"Semin Hematol"},{"key":"ref32","doi-asserted-by":"publisher","first-page":"410","DOI":"10.1111\/j.1600-0609.2008.01118.x","article-title":"Hereditary stomatocytosis","volume":"81","author":"V Singh","year":"2008","journal-title":"Eur J Haematol"},{"key":"ref33","doi-asserted-by":"publisher","first-page":"123","DOI":"10.1007\/3-540-29036-2_9","volume-title":"Angeborene Erythrozytenmembrandefekte","author":"S Eber","year":"2006"},{"key":"ref34","doi-asserted-by":"publisher","first-page":"183","DOI":"10.2147\/jbm.S179764","article-title":"Dehydrated hereditary stomatocytosis: clinical perspectives","volume":"10","author":"H Frederiksen","year":"2019","journal-title":"J Blood Med"},{"key":"ref35","doi-asserted-by":"publisher","first-page":"266","DOI":"10.1002\/ajh.24212","article-title":"Dehydrated hereditary stomatocytosis","volume":"91","author":"D M Layton","year":"2016","journal-title":"Am J Hematol"},{"key":"ref36","doi-asserted-by":"publisher","first-page":"e52","DOI":"10.1097\/mpg.0000000000002077","article-title":"Dehydrated Hereditary Stomatocytosis Presenting as Severe Perinatal Ascites and Cholestasis","volume":"68","author":"J Halma","year":"2019","journal-title":"J Pediatr Gastroenterol Nutr"},{"key":"ref37","doi-asserted-by":"publisher","first-page":"102","DOI":"10.1186\/s13052-020-00864-x","article-title":"A novel PIEZO1 mutation in a patient with dehydrated hereditary stomatocytosis: a case report and a brief review of literature","volume":"46","author":"D Zama","year":"2020","journal-title":"Ital J Pediatr"},{"key":"ref38","doi-asserted-by":"publisher","first-page":"620","DOI":"10.1111\/bjh.15272","article-title":"Dehydrated hereditary stomatocytosis causing fetal hydrops and perinatal ascites","volume":"182","author":"B Jenner","year":"2018","journal-title":"Brit J Haematol"},{"key":"ref39","doi-asserted-by":"publisher","first-page":"721","DOI":"10.3324\/haematol.11469","article-title":"Pyruvate kinase deficiency","volume":"92","author":"Z Alberto","year":"2007","journal-title":"Haematologica"},{"key":"ref40","volume-title":"Blood: Principles and Practice of Hematology","author":"R I Handin","year":"1995"},{"key":"ref41","doi-asserted-by":"publisher","first-page":"1620","DOI":"10.1055\/s-2008-1055521","article-title":"Diagnosis of pyruvate kinase deficiency in the presence of an elevated reticulocyte count","volume":"120","author":"A Pekrun","year":"1995","journal-title":"Dtsch Med Wochenschr"},{"key":"ref42","doi-asserted-by":"publisher","first-page":"1432","DOI":"10.1056\/NEJMoa2116634","article-title":"Mitapivat versus Placebo for Pyruvate Kinase Deficiency","volume":"386","author":"H Al-Samkari","year":"2022","journal-title":"N Engl J Med"},{"key":"ref43","doi-asserted-by":"publisher","first-page":"375","DOI":"10.1046\/j.1365-2141.2003.03980.x","article-title":"Pyrimidine 5\u2032 Nucleotidase Deficiency","volume":"120","author":"D C Rees","year":"2003","journal-title":"Br J Haematol"},{"key":"ref44","doi-asserted-by":"publisher","first-page":"713","DOI":"10.2165\/11536520-000000000-00000","article-title":"Medications and glucose-6-phosphate dehydrogenase deficiency: an evidence-based review","volume":"33","author":"I Youngster","year":"2010","journal-title":"Drug Saf"},{"key":"ref45","doi-asserted-by":"publisher","first-page":"59","DOI":"10.1007\/s00112-015-0020-8","article-title":"An\u00e4mien","volume":"164","author":"S Eber","year":"2016","journal-title":"Monatsschr Kinderheilk"},{"key":"ref46","doi-asserted-by":"publisher","first-page":"4034","DOI":"10.1182\/blood-2005-04-1622","article-title":"The energy-less red blood cell is lost: erythrocyte enzyme abnormalities of glycolysis","volume":"106","author":"R van Wijk","year":"2005","journal-title":"Blood"}],"container-title":["DMW - Deutsche Medizinische Wochenschrift"],"original-title":[],"language":"de","link":[{"URL":"http:\/\/www.thieme-connect.de\/products\/ejournals\/pdf\/10.1055\/a-1767-8423.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,9,20]],"date-time":"2022-09-20T23:26:21Z","timestamp":1663716381000},"score":1,"resource":{"primary":{"URL":"http:\/\/www.thieme-connect.de\/DOI\/DOI?10.1055\/a-1767-8423"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2022,9]]},"references-count":43,"journal-issue":{"issue":"19","published-online":{"date-parts":[[2022,9,20]]},"published-print":{"date-parts":[[2022,9]]}},"URL":"https:\/\/doi.org\/10.1055\/a-1767-8423","archive":["Portico","CLOCKSS"],"relation":{},"ISSN":["0012-0472","1439-4413"],"issn-type":[{"value":"0012-0472","type":"print"},{"value":"1439-4413","type":"electronic"}],"subject":[],"published":{"date-parts":[[2022,9]]}}}