Publikationen zu speziellen Erkrankungen aus der Hämatologie und Hämostasiologie

Hier finden Sie eine Zusammenstellung wichtiger nationaler und internationaler Publikationen zu den einzelnen hämatologischen Erkrankungen im Kindes- und Jugendalter.

Autor: Julia Dobke, erstellt am: 18.11.2011, Redaktion: Julia Dobke, Zuletzt geändert: 21.07.2016

Anämien

Übersichtsartikel Anämien

  1. Hicks LK, Bering H, Carson KR, Haynes AE, Kleinerman J, Kukreti V, Ma A, Mueller BU, O'Brien SH, Panepinto JA, Pasquini MC, Rajasekhar A, Sarode R, Wood WA: Five hematologic tests and treatments to question. Blood 2014, 124: 3524 [PMID: 25472968]
  2. Hicks LK, Bering H, Carson KR, Kleinerman J, Kukreti V, Ma A, Mueller BU, O'Brien SH, Pasquini M, Sarode R, Solberg L Jr, Haynes AE, Crowther MA: The ASH Choosing Wisely® campaign: five hematologic tests and treatments to question. Blood 2013, 122: 3879 [PMID: 24307720]
  3. Milman N: Anemia--still a major health problem in many parts of the world!. Ann Hematol 2011, 90: 369 [PMID: 21221586]

Literatur zur Autoimmun- hämolytischen Anämie (AIHA)

  1. Berentsen S, Tjønnfjord GE: Diagnosis and treatment of cold agglutinin mediated autoimmune hemolytic anemia. Blood reviews 2012, [Epub ahead of print] [PMID: 22330255]
  2. Garbe E, Andersohn F, Bronder E, Klimpel A, Thomae M, Schrezenmeier H, Hildebrandt M, Späth-Schwalbe E, Grüneisen A, Mayer B, Salama A, Kurtal H: Drug induced immune haemolytic anaemia in the Berlin Case-Control Surveillance Study. British journal of haematology 2011, 154: 644 [PMID: 21749359]
  3. Aladjidi N, Leverger G, Leblanc T, Picat MQ, Michel G, Bertrand Y, Bader-Meunier B, Robert A, Nelken B, Gandemer V, Savel H, Stephan JL, Fouyssac F, Jeanpetit J, Thomas C, Rohrlich P, Baruchel A, Fischer A, Chêne G, Perel Y, Centre de Référence National des Cytopénies Auto-immunes de l'Enfant (CEREVANCE): New insights into childhood autoimmune hemolytic anemia: a French national observational study of 265 children. Haematologica 2011, 96: 655 [PMID: 21228033]
  4. Pruss A, Salama A, Ahrens N, Hansen A, Kiesewetter H, Koscielny J, Dörner T: Immune hemolysis-serological and clinical aspects. Clinical and experimental medicine 2003, 3: 55 [PMID: 14598182]

Literatur zur Diamond-Blackfan-Anämie

  1. Vlachos A, Muir E: How I treat Diamond-Blackfan anemia. Blood 2010, 116: 3715 [PMID: 20651069]
  2. Vlachos A, Ball S, Dahl N, Alter BP, Sheth S, Ramenghi U, Meerpohl J, Karlsson S, Liu JM, Leblanc T, Paley C, Kang EM, Leder EJ, Atsidaftos E, Shimamura A, Bessler M, Glader B, Lipton JM, Participants of Sixth Annual Daniella Maria Arturi International Consensus Conference: Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference. British journal of haematology 2008, 142: 859 [PMID: 18671700]
  3. Faivre L, Meerpohl J, Da Costa L, Marie I, Nouvel C, Gnekow A, Bender-Götze C, Bauters F, Coiffier B, Peaud PY, Rispal P, Berrebi A, Berger C, Flesch M, Sagot P, Varet B, Niemeyer C, Tchernia G, Leblanc T: High-risk pregnancies in Diamond-Blackfan anemia: a survey of 64 pregnancies from the French and German registries. Haematologica 2006, 91: 530 [PMID: 16537118]

Literatur zur Dyserythropoetischen Anämie

  1. Grandchamp B, Hetet G, Kannengiesser C, Oudin C, Beaumont C, Rodrigues-Ferreira S, Amson R, Telerman A, Nielsen P, Kohne E, Balser C, Heimpel H: A novel type of congenital hypochromic anemia associated with a nonsense mutation in the STEAP3/TSAP6 gene. Blood 2011, 118: 6660 [PMID: 22031863]
  2. Schwarz K, Iolascon A, Verissimo F, Trede NS, Horsley W, Chen W, Paw BH, Hopfner KP, Holzmann K, Russo R, Esposito MR, Spano D, De Falco L, Heinrich K, Joggerst B, Rojewski MT, Perrotta S, Denecke J, Pannicke U, Delaunay J, Pepperkok R, Heimpel H: Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II. Nature genetics 2009, 41: 936 [PMID: 19561605]
  3. Heimpel H, Anselstetter V, Chrobak L, Denecke J, Einsiedler B, Gallmeier K, Griesshammer A, Marquardt T, Janka-Schaub G, Kron M, Kohne E: Congenital dyserythropoietic anemia type II: epidemiology, clinical appearance, and prognosis based on long-term observation. Blood 2003, 102: 4576 [PMID: 12933587]
  4. Wickramasinghe SN: Congenital dyserythropoietic anaemias: clinical features, haematological morphology and new biochemical data. Blood reviews 1998, 12: 178 [PMID: 9745888]

Literatur zur Fanconi-Anämie

  1. Alter BP: Fanconi anemia and the development of leukemia. Best practice & research. Clinical haematology 2014, 27(3-4): 214 [PMID: 25455269]
  2. Yoshimi A, Niemeyer C, Baumann I, Schwarz-Furlan S, Schindler D, Ebell W, Strahm B: High incidence of Fanconi anaemia in patients with a morphological picture consistent with refractory cytopenia of childhood. British journal of haematology 2013, 160: 109 [PMID: 23043447]
  3. Myers K, Davies SM, Harris RE, Spunt SL, Smolarek T, Zimmerman S, McMasters R, Wagner L, Mueller R, Auerbach AD, Mehta PA: The clinical phenotype of children with Fanconi anemia caused by biallelic FANCD1/BRCA2 mutations. Pediatric blood & cancer 2012, 58: 462 [PMID: 21548014]

Literatur zur sekundären Eisenüberladung

  1. Cario H, Grosse R, Janssen G, Jarisch A, Meerpohl J, Strauss G, German hematology societies (GPOH and DGHO): [Guidelines for diagnosis and treatment of secondary iron overload in patients with congenital anemia]. Klinische Padiatrie 2010, 222: 399 [PMID: 20862634]

Literatur zur Sichelzellkrankheit

  1. Danaee A, Inusa B, Howard J, Robinson S: Hyperhemolysis in Patients With Hemoglobinopathies: A Single-Center Experience and Review of the Literature. Transfusion medicine reviews 2015, 29: 220 [PMID: 26209603]
  2. Frömmel C, Brose A, Klein J, Blankenstein O, Lobitz S: Newborn screening for sickle cell disease: technical and legal aspects of a German pilot study with 38,220 participants. BioMed research international 2014, 2014, 695828 [PMID: 25147811]
  3. Alvarez O, Rodriguez MM, Jordan L, Sarnaik S: Renal medullary carcinoma and sickle cell trait: A systematic review. Pediatric blood & cancer 2015, 62: 1694 [PMID: 26053587]
  4. De Franceschi L, Mura P, Schweiger V, Vencato E, Quaglia FM, Delmonte L, Evangelista M, Polati E, Olivieri O, Finco G: Fentanyl Buccal Tablet: A New Breakthrough Pain Medication in Early Management of Severe Vaso-Occlusive Crisis in Sickle Cell Disease. Pain practice 2015, Epub ahead of print [PMID: 26009799]
  5. Fasano RM, Meier ER, Hulbert ML: Cerebral vasculopathy in children with sickle cell anemia. Blood cells, molecules & diseases 2015, 54: 17 [PMID: 25294561]
  6. Brandow AM, Farley RA, Panepinto JA: Early insights into the neurobiology of pain in sickle cell disease: A systematic review of the literature. Pediatric blood & cancer 2015, 62: 1501 [PMID: 25976161]
  7. Bhatia M, Sheth S: Hematopoietic stem cell transplantation in sickle cell disease: patient selection and special considerations. Journal of blood medicine 2015, 6: 229 [PMID: 26203293]
  8. Gualandro SF, Fonseca GH, Yokomizo IK, Gualandro DM, Suganuma LM: Cohort study of adult patients with haemoglobin SC disease: clinical characteristics and predictors of mortality. British journal of haematology 2015, 125: 3401 [PMID: 26255986]
  9. Tormey CA, Hendrickson JE: Routine non-ABO blood group antigen genotyping in sickle cell disease: the new frontier in pretransfusion testing? Transfusion 2015, 55(6 Pt 2): 1374 [PMID: 26094720]
  10. Minniti CP, Kato GJ: Critical Reviews: How we treat sickle cell patients with leg ulcers. American journal of hematology 2015, [PMID: 26257201]
  11. Conran N: High Foetal Haemoglobin in Sickle Cell Disease: Not so Protective? EBioMedicine 2015, 2: 102 [PMID: 26137548]
  12. Brousse V, Buffet P, Rees D: The spleen and sickle cell disease: the sick(led) spleen. British journal of haematology 2014, 166: 165 [PMID: 24862308]
  13. Lobitz S, Frömmel C, Brose A, Klein J, Blankenstein O: Incidence of sickle cell disease in an unselected cohort of neonates born in Berlin, Germany. European journal of human genetics 2014, 22: 1051 [PMID: 24398797]
  14. Wykes C, Arasaretnam A, O'Driscoll S, Farnham L, Moniz C, Rees DC: Vitamin D deficiency and its correction in children with sickle cell anaemia. Annals of hematology 2014, [PMID: 24981689]
  15. Ulph F, Cullinan T, Qureshi N, Kai J: Parents' responses to receiving sickle cell or cystic fibrosis carrier results for their child following newborn screening. European journal of human genetics : EJHG 2014 [PMID: 25005733]
  16. Dowling MM, Noetzel MJ, Rodeghier MJ, Quinn CT, Hirtz DG, Ichord RN, Kwiatkowski JL, Roach ES, Kirkham FJ, Casella JF, Debaun MR: Headache and Migraine in Children with Sickle Cell Disease Are Associated with Lower Hemoglobin and Higher Pain Event Rates But Not Silent Cerebral Infarction. The Journal of pediatrics 2014, E-pub ahead of print [PMID: 24529619]
  17. Gladwin MT, Barst RJ, Gibbs JS, Hildesheim M, Sachdev V, Nouraie M, Hassell KL, Little JA, Schraufnagel DE, Krishnamurti L, Novelli E, Girgis RE, Morris CR, Berman Rosenzweig E, Badesch DB, Lanzkron S, Castro OL, Taylor JG 6th, Goldsmith JC, Kato GJ, Gordeuk VR, Machado RF, walk-PHaSST Investigators and Patients: Risk factors for death in 632 patients with sickle cell disease in the United States and United Kingdom. PloS one 2014, 9:e99489 [PMID: 24988120]
  18. Adams RJ: Prevention of stroke in sickle cell anemia. The Journal of law, medicine & ethics 2014, 42: 135 [PMID: 25040376]
  19. Rhodes MM, Bates DG, Andrews T, Adkins L, Thornton J, Denham JM: Abdominal pain in children with sickle cell disease. Journal of clinical gastroenterology 2014, 48: 99 [PMID: 24247814]
  20. Inusa B, Casale M, Booth C, Lucas S: Subarachnoid haemorrhage and cerebral vasculopathy in a child with sickle cell anaemia. BMJ case reports 2014, [PMID: 25336550]
  21. Meerpohl JJ, Schell LK, Rücker G, Motschall E, Fleeman N, Niemeyer CM, Bassler D: Deferasirox for managing transfusional iron overload in people with sickle cell disease. The Cochrane database of systematic reviews 2014, 5:CD007477 [PMID: 24893174]
  22. Hsieh MM, Fitzhugh CD, Weitzel RP, Link ME, Coles WA, Zhao X, Rodgers GP, Powell JD, Tisdale JF: Nonmyeloablative HLA-matched sibling allogeneic hematopoietic stem cell transplantation for severe sickle cell phenotype. JAMA 2014, 312: 48 [PMID: 25058217]
  23. Aguilar Martinez P, Angastiniotis M, Eleftheriou A, Gulbis B, Mañú Pereira Mdel M, Petrova-Benedict R, Corrons JL: Haemoglobinopathies in Europe: health & migration policy perspectives. Orphanet journal of rare diseases 2014, 9: 97 [PMID: 24980780]
  24. Nickel RS, Hendrickson JE, Haight AE: The ethics of a proposed study of hematopoietic stem cell transplant for children with . Blood 2014, 124: 861 [PMID: 24963044]
  25. Nickel RS, Hendrickson JE, Haight AE: The ethics of a proposed study of hematopoietic stem cell transplant for children with . Blood 2014, 124: 861 [PMID: 24963044]
  26. Dedeken L, Lê PQ, Azzi N, Brachet C, Heijmans C, Huybrechts S, Devalck C, Ngalula M, Ferster A: Haematopoietic stem cell transplantation for severe sickle cell disease in childhood: a single centre experience of 50 patients. British journal of haematology 2014,Epub ahead of print [PMID: 24433465]
  27. Crosby LE, Shook LM, Ware RE, Brinkman WB: Shared decision making for hydroxyurea treatment initiation in children with sickle cell anemia. Pediatric blood & cancer 2014, Epub ahead of print [PMID: 25308571]
  28. Silva Junior GB, Vieira AP, Couto Bem AX, Alves MP, Meneses GC, Martins AM, Sanches TR, Andrade LC, Seguro AC, Libório AB, Daher EF: Renal Tubular Dysfunction in Sickle Cell Disease. Kidney & blood pressure research 2014, 38: 1 [PMID: 24504378]
  29. Hirst C, Owusu-Ofori S: Prophylactic antibiotics for preventing pneumococcal infection in children with sickle cell disease. The Cochrane database of systematic reviews 2014, 11:CD003427 [PMID: 25375222]
  30. Silva Junior GB, Vieira AP, Couto Bem AX, Alves MP, Meneses GC, Martins AM, Araújo SM, Libório AV, Daher EF: Proteinuria in adults with sickle-cell disease: the role of hydroxycarbamide(hydroxyurea) as a protective agent. International journal of clinical pharmacy 2014, 36: 766 [PMID: 24934760]
  31. Telen MJ, Afenyi-Annan A, Garrett ME, Combs MR, Orringer EP, Ashley-Koch AE: Alloimmunization in sickle cell disease: changing antibody specificities and association with chronic pain and decreased survival. Transfusion 2014, Epub ahead of print [PMID: 25444611]
  32. Gokarn N, Manwani D, Friedmann P, Borenstein SH, Jan D, Renaud E: Outcomes after early splenectomy for hematological disorders. Journal of laparoendoscopic & advanced surgical techniques. Part A 2014, 24: 897 [PMID: 25275796]
  33. Ware RE: Hydroxycarbamide: Clinical aspects. Comptes rendus biologies 2013, 336: 177 [PMID: 23643402]
  34. Uprety D, Baber A, Foy M: Ketamine infusion for sickle cell pain crisis refractory to opioids: a case report and review of literature. Annals of hematology 2013, epub ahead of print [PMID: 24232306]
  35. Naik RP, Streiff MB, Haywood C Jr, Nelson JA, Lanzkron S: Venous thromboembolism in adults with sickle cell disease: a serious and under-recognized complication. The American journal of medicine 2013, 126: 443 [PMID: 23582935]
  36. Quinn CT: Sickle cell disease in childhood: from newborn screening through transition to adult medical care. Pediatric clinics of North America 2013, 60: 1363 [PMID: 24237976]
  37. Bodas P, Huang A, O Riordan MA, Sedor JR, Dell KM: The prevalence of hypertension and abnormal kidney function in children with sickle cell disease --a cross sectional review. BMC nephrology 2013, 14: 237 [PMID: 24168027]
  38. Manwani D, Frenette PS: Vaso-occlusion in sickle cell disease: pathophysiology and novel targeted therapies. Blood 2013, 122: 3892 [PMID: 24052549]
  39. McGann PT, Nero AC, Ware RE: Current management of sickle cell anemia. Cold Spring Harbor perspectives in medicine 2013, 3 [PMID: 23709685]
  40. Majumdar S, Thompson W, Ahmad N, Gordon C, Addison C: The use and effectiveness of complementary and alternative medicine for pain in sickle cell anemia. Complementary therapies in clinical practice 2013, 19: 184 [PMID: 24199970]
  41. Sommet J, Missud F, Holvoet L, Ithier G, Lorrot M, Benkerrou M, Faye A: Morbidity among child travellers with sickle-cell disease visiting tropical areas: an observational study in a French tertiary care centre. Archives of disease in childhood 2013, epub ahead of print [PMID: 23661574]
  42. Hamideh D, Alvarez O: Sickle Cell Disease Related Mortality in the United States (1999-2009). Pediatric blood & cancer 2013, epub ahead of print [PMID: 23637037]
  43. Mynarek M, Bettoni da Cunha Riehm C, Brinkmann F, Weißenborn K, Tell-Lüersen M, Heuft HG, Maecker-Kolhoff B, Sykora KW: Normalized Transcranial Doppler Velocities, Stroke Prevention and Improved Pulmonary Function after Stem Cell Transplantation in Children with Sickle Cell Anemia. Klinische Padiatrie 2013, 225: 127 [PMID: 23625683]
  44. Ballas SK, Gupta K, Adams-Graves P: Sickle cell pain: a critical reappraisal. Blood 2012, 120: 3647 [PMID: 22923496]
  45. Lucarelli G, Isgro`, A, Sodani P, Gaziev, J: Hematopoietic Stem Cell Transplantation in Thalassemia and Sickle Cell Anemia. Cold Spring Harb Perspect Med 2012, 2: a011825 [PMID: 22553502]
  46. Rodeghiero F, Ruggeri M: Short- and long-term risks of splenectomy for benign haematological disorders: should we revisit the indications? British journal of haematology 2012l; 158: 16 [PMID: 22571181]
  47. Smith-Whitley, Kim, Thompson, Alexis A : Indications and complications of transfusions in sickle cell disease. Pediatric blood & cancer 2012, 59, 358 [DOI: 10.1002/pbc.24179]
  48. Strouse JJ, Heeney MM: Hydroxyurea for the treatment of sickle cell disease: efficacy, barriers, toxicity, and management in children. Pediatric blood & cancer 2012, 59: 365 [PMID: 22517797]
  49. Locatelli F, Pagliara D: Allogeneic hematopoietic stem cell transplantation in children with sickle cell disease. Pediatric blood & cancer 2012, 59: 372 [PMID: 22544533]
  50. Maigne G, Ferlicot S, Galacteros F, Belenfant X, Ulinski T, Niaudet P, Ronco P, Godeau B, Durrbach A, Sahali S, Lang P, Lambotte O, Audard V: Glomerular lesions in patients with sickle cell disease. Medicine 2010, 89: 18 [PMID: 20075701]
  51. National Toxicology Program: NTP-CERHR monograph on the potential human reproductive and developmental effects of hydroxyurea. NTP CERHR MON 2008,:vii-viii, v, ix-III1 [PMID: 19407858]

Literatur zu Thalassämien

  1. Baronciani D, Angelucci E, Potschger U, Gaziev J, Yesilipek A, Zecca M, Orofino MG, Giardini C, Al-Ahmari A, Marktel S, de la Fuente J, Ghavamzadeh A, Hussein AA, Targhetta C, Pilo F, Locatelli F, Dini G, Bader P, Peters C: Hemopoietic stem cell transplantation in thalassemia: a report from the European Society for Blood and Bone Marrow Transplantation Hemoglobinopathy Registry, 2000-2010. Bone Marrow Transplant 2016 [Epub ahead of print] [PMID: 26752139]
  2. Mashhadi MA, Heidari Z, Sepehri Z, Bakhshipour AR, Karimkoshte A: The selenium status in thalassemia patients in South East of iran. Int J Hematol Oncol Stem Cell Res 2014 Oct 1; 8: 1 [PMID: 25774261]
  3. Origa R, Sollaino MC, Borgna-Pignatti C, Piga A, Feliu Torres A, Masile V, Galanello R: α-Globin Gene Quadruplication and Heterozygous β-Thalassemia: A Not So Rare Cause of Thalassemia Intermedia. Acta haematologica 2013, 131: 162 [PMID: 24217654]
  4. Lucarelli G, Isgro`, A, Sodani P, Gaziev, J: Hematopoietic Stem Cell Transplantation in Thalassemia and Sickle Cell Anemia. Cold Spring Harb Perspect Med 2012, 2: a011825 [PMID: 22553502]
  5. Voskaridou E, Ladis V, Kattamis A, Hassapopoulou E, Economou M, Kourakli A, Maragkos K, Kontogianni K, Lafioniatis S, Vrettou E, Koutsouka F, Papadakis A, Mihos A, Eftihiadis E, Farmaki K, Papageorgiou O, Tapaki G, Maili P, Theohari M, Drosou M, Kartasis Z, Aggelaki M, Basileiadi A, Adamopoulos I, Lafiatis I, Galanopoulos A, Xanthopoulidis G, Dimitriadou E, Mprimi A, Stamatopoulou M, Haile ED, Tsironi M, Anastasiadis A, Kalmanti M, Papadopoulou M, Panori E, Dimoxenou P, Tsirka A, Georgakopoulos D, Drandrakis P, Dionisopoulou D, Ntalamaga A, Davros I, Karagiorga M, on behalf of the Greek Haemoglobinopathies Study Group: A national registry of haemoglobinopathies in Greece: Deducted demographics, trends in mortality and affected births. Annals of hematology 2012, epub ahead of print [DOI: 10.1007/s00277-012-1465-7]
  6. Rachmilewitz EA, Giardina PJ: How I treat thalassemia. Blood 2011, 118: 3479 [PMID: 21813448]
  7. Ginzburg Y, Rivella S: {beta}-thalassemia: a model for elucidating the dynamic regulation of ineffective erythropoiesis and iron metabolism. Blood 2011, 118: 4321 [PMID: 21768301]
  8. Kelly MJ, Pennarola BW, Rodday AM, Parsons SK, on behalf of the Journeys to Recovery Study, the HSCT-CHESS™ Study: Health-related quality of life (HRQL) in children with sickle cell disease and thalassemia following hematopoietic stem cell transplant (HSCT). Pediatric blood & cancer 2011 Dec 19; [PMID: 22183952]
  9. Kohne E, Kleihauer E: Hämoglobinopathien - eine Langzeitstudie über vier Jahrzehnte. Dtsch Arztebl Int 2010, 107: 65 [DOI: 10.3238/arztebl.2010.0065]
  10. Borgna-Pignatti C: Modern treatment of thalassaemia intermedia. British journal of haematology 2007, 138: 291 [PMID: 17565568]
  11. Rund D, Rachmilewitz E: Beta-thalassemia. The New England journal of medicine 2005, 353: 1135 [PMID: 16162884]
  12. Vetter B, Schwarz C, Kohne E, Kulozik AE: Beta-thalassaemia in the immigrant and non-immigrant German populations. British journal of haematology 1997, 97: 266 [PMID: 9163586]
Guidelines for the Management of Non Transfusion Dependent Thalassaemia (NTDT) (2013) (2.7 MB)
Leitlinie der Thalassaemia international federation zu nicht-transfusionsabhängigen Thalassämien.

Literatur zur Aplastischen Anämie

  1. Urban C, Lackner H, Müller E, Benesch M, Strenger V, Sovinz P, Schwinger W: Stem cell transplantation in 6 children with parvovirus B19- induced severe aplastic anaemia or myelodysplastic syndrome. Klinische Padiatrie 2011, 223: 332 [PMID: 22052631]
  2. Niemeyer CM, Baumann I: Classification of childhood aplastic anemia and myelodysplastic syndrome. Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program 2011, 2011, 84 [PMID: 22160017]

Literatur zu Bluttransfusionen bei chronischen Anämien

  1. Agrawal AK, Hsu E, Quirolo K, Neumayr LD, Flori HR: Red blood cell transfusion in pediatric patients with severe chronic anemia: How slow is necessary? Pediatric blood & cancer 2012, 58: 466 [PMID: 21793178]

Literatur zur refraktären Eisenmangelanämie

  1. Lehmberg K, Grosse R, Muckenthaler MU, Altamura S, Nielsen P, Schmid H, Graubner U, Oyen F, Zeller W, Schneppenheim R, Janka GE: Administration of recombinant erythropoietin alone does not improve the phenotype in iron refractory iron deficiency anemia patients. Annals of hematology 2013, 92: 387 [PMID: 23180434]

Erkrankungen der Leukozyten

Literatur zu chronischen Neutropenien

  1. Göhring G, Karow A, Steinemann D, Wilkens L, Lichter P, Zeidler C, Niemeyer C, Welte K, Schlegelberger B: Chromosomal aberrations in congenital bone marrow failure disorders--an early indicator for leukemogenesis? Annals of hematology 2007, 86: 733 [PMID: 17653548]
  2. Beekman R, Valkhof MG, Sanders MA, van Strien PM, Haanstra JR, Broeders L, Geertsma-Kleinekoort WM, Veerman AJ, Valk PJ, Verhaak RG, Löwenberg B, Touw IP: Sequential gain of mutations in severe congenital neutropenia progressing to acute myeloid leukemia. Blood 2012, 119: 5071 [PMID: 22371884]
  3. Kelly MJ, Pennarola BW, Rodday AM, Parsons SK, on behalf of the Journeys to Recovery Study, the HSCT-CHESS™ Study: Health-related quality of life (HRQL) in children with sickle cell disease and thalassemia following hematopoietic stem cell transplant (HSCT). Pediatric blood & cancer 2011 Dec 19; [PMID: 22183952]
  4. Klein C, Welte K: Genetic insights into congenital neutropenia. Clinical reviews in allergy & immunology 2010, 38: 68 [PMID: 19440858]
  5. Boztug K, Welte K, Zeidler C, Klein C: Congenital neutropenia syndromes. Immunology and allergy clinics of North America 2008, 28: 259-75, vii-viii [PMID: 18424332]
  6. Gerth HU, Juergens KU, Dirksen U, Gerss J, Schober O, Franzius C: Significant benefit of multimodal imaging: PET/CT compared with PET alone in staging and follow-up of patients with Ewing tumors. Journal of nuclear medicine : official publication, Society of Nuclear Medicine 2007, 48: 1932 [PMID: 18006618]
  7. Bohn G, Welte K, Klein C: Severe congenital neutropenia: new genes explain an old disease. Current opinion in rheumatology 2007, 19: 644 [PMID: 17917547]
  8. Link DC, Kunter G, Kasai Y, Zhao Y, Miner T, McLellan MD, Ries RE, Kapur D, Nagarajan R, Dale DC, Bolyard AA, Boxer LA, Welte K, Zeidler C, Donadieu J, Bellanné-Chantelot C, Vardiman JW, Caligiuri MA, Bloomfield CD, DiPersio JF, Tomasson MH, Graubert TA, Westervelt P, Watson M, Shannon W, Baty J, Mardis ER, Wilson RK, Ley TJ: Distinct patterns of mutations occurring in de novo AML versus AML arising in the setting of severe congenital neutropenia. Blood 2007, 110: 1648 [PMID: 17494858]
  9. Germeshausen M, Skokowa J, Ballmaier M, Zeidler C, Welte K: G-CSF receptor mutations in patients with congenital neutropenia. Current opinion in hematology 2008, 15: 332 [PMID: 18536571]
  10. James RM, Kinsey SE: The investigation and management of chronic neutropenia in children. Archives of disease in childhood 2006, 91: 852 [PMID: 16990357]
  11. Rosenberg PS, Alter BP, Bolyard AA, Bonilla MA, Boxer LA, Cham B, Fier C, Freedman M, Kannourakis G, Kinsey S, Schwinzer B, Zeidler C, Welte K, Dale DC, Severe Chronic Neutropenia International Registry: The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long-term G-CSF therapy. Blood 2006, 107: 4628 [PMID: 16497969]
  12. Cotter M, Gulmann C, Jeffers M, Smith OP: Increased bone marrow angiogenesis in children with severe chronic neutropenia treated with granulocyte colony-stimulating factor. Journal of pediatric hematology/oncology 2004, 26: 504 [PMID: 15284588]
  13. Cottle TE, Fier CJ, Donadieu J, Kinsey SE: Risk and benefit of treatment of severe chronic neutropenia with granulocyte colony-stimulating factor. Seminars in hematology 2002, 39: 134 [PMID: 11957197]
  14. Dale DC, Bolyard AA, Aprikyan A: Cyclic neutropenia. Seminars in hematology 2002, 39: 89 [PMID: 11957190]
  15. Boztug K, Welte K, Zeidler C, Klein C: Congenital neutropenia syndromes. Immunology and allergy clinics of North America 2008, 28: 259-75, vii-viii [PMID: 18424332]
  16. Zeidler C, Welte K: Kostmann syndrome and severe congenital neutropenia. Seminars in hematology 2002, 39: 82 [PMID: 11957189]
  17. Schiller M, Böhm M, Zeidler C, Germeshausen M, Welte K, Luger TA, Bonsmann G: [Cyclic neutropenia. Detection of a mutation in the gene for neutrophil elastase (ELA2)]. Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete 2001, 52: 790 [PMID: 11572070]
  18. Carlsson G, Fasth A: Infantile genetic agranulocytosis, morbus Kostmann: presentation of six cases from the original . Acta paediatrica (Oslo, Norway : 1992) 2001, 90: 757 [PMID: 11519978]
  19. Zeidler C, Boxer L, Dale DC, Freedman MH, Kinsey S, Welte K: Management of Kostmann syndrome in the G-CSF era. British journal of haematology 2000, 109: 490 [PMID: 10886193]
  20. Zeidler C, Schwinzer B, Welte K: [Severe congenital neutropenia: trends in diagnosis and therapy]. Klinische Padiatrie 2000, 212: 145 [PMID: 10994541]
  21. Horwitz M, Benson KF, Person RE, Aprikyan AG, Dale DC: Mutations in ELA2, encoding neutrophil elastase, define a 21-day biological clock in cyclic haematopoiesis. Nature genetics 1999, 23: 433 [PMID: 10581030]

Erkrankungen der Thrombozyten

Literatur zur Idiopathischen Immunthrombozytopenie (ITP)

  1. Lorenzana A, Armin S, Sharma A, Allarakhia I, Witkowski A: Cerebral Infarctions After Intravenous Immunoglobulin Therapy for ITP in a Child. Pediatric neurology 2014, 50: 188 [PMID: 24262342]
  2. Rohmer B, Valla FV, Baleydier F, Launay V, Dommange-Romero F, Pondarré C: Newly Diagnosed Immune Thrombocytopenic Purpura in Childhood: Successful Implementation of a Limited Intervention Strategy in the Setting of Pediatric Emergency Care. The Journal of pediatrics 2014, Epub ahead of print [PMID: 25454932]
  3. Labarque V, Van Geet C: Clinical practice: immune thrombocytopenia in paediatrics. European journal of pediatrics 2014, 173: 163 [PMID: 24390128]
  4. Seidel MG, Urban C, Sipurzynski J, Beham-Schmid C, Lackner H, Benesch M: High response rate but short-term effect of romiplostim in paediatric refractory chronic immune thrombocytopenia. British journal of haematology 2014, E-pub ahead of print [PMID: 24484542]
  5. Neunert CE: Individualized treatment for immune thrombocytopenia: predicting bleeding risk. Seminars in hematology 2013, 50 Suppl 1:S55 [PMID: 23664518]
  6. Grace RF, Bennett CM, Ritchey AK, Jeng M, Thornburg CD, Lambert MP, Neier M, Recht M, Kumar M, Blanchette V, Klaassen RJ, Buchanan GR, Kurth MH, Nugent DJ, Thompson AA, Stine K, Kalish LA, Neufeld EJ: Response to steroids predicts response to rituximab in pediatric chronic immune thrombocytopenia. Pediatric blood & cancer 2012, 58: 221 [PMID: 21674758]
  7. Grace RF, Long M, Kalish LA, Neufeld EJ: Applicability of 2009 international consensus terminology and criteria for immune thrombocytopenia to a clinical pediatric population. Pediatric blood & cancer 2012, 58: 216 [PMID: 21674757]
  8. George JN: Children with ITP: Looking beyond the platelet count. Pediatric blood & cancer 2012, 58: 323 [PMID: 21898785]
  9. Provan D, Stasi R, Newland AC, Blanchette VS, Bolton-Maggs P, Bussel JB, Chong BH, Cines DB, Gernsheimer TB, Godeau B, Grainger J, Greer I, Hunt BJ, Imbach PA, Lyons G, McMillan R, Rodeghiero F, Sanz MA, Tarantino M, Watson S, Young J, Kuter DJ: International consensus report on the investigation and management of primary immune thrombocytopenia. Blood 2010, 115: 168 [PMID: 19846889]
  10. Laws HJ, Janssen G, Borkhardt A: Reassessment of treatment modalities for paediatric patients with chronic immune thrombocytopenia. Hamostaseologie 2009, 29: 171 [PMID: 19404521]
  11. Rodeghiero F, Stasi R, Gernsheimer T, Michel M, Provan D, Arnold DM, Bussel JB, Cines DB, Chong BH, Cooper N, Godeau B, Lechner K, Mazzucconi MG, McMillan R, Sanz MA, Imbach P, Blanchette V, Kühne T, Ruggeri M, George JN: Standardization of terminology, definitions and outcome criteria in immune thrombocytopenic purpura of adults and children: report from an international working group. Blood 2009, 113: 2386 [PMID: 19005182]
  12. Salama A, Kiesewetter H, Kalus U, Movassaghi K, Meyer O: Massive platelet transfusion is a rapidly effective emergency treatment in patients with refractory autoimmune thrombocytopenia. Thrombosis and haemostasis 2008, 100: 762 [PMID: 18989518]
  13. Rajantie J, Zeller B, Treutiger I, Rosthöj S, NOPHO ITP working group and five national study groups: Vaccination associated thrombocytopenic purpura in children. Vaccine 2007, 25: 1838 [PMID: 17126957]
  14. Imbach P, Kühne T, Müller D, Berchtold W, Zimmerman S, Elalfy M, Buchanan GR: Childhood ITP: 12 months follow-up data from the prospective registry I of the Intercontinental Childhood ITP Study Group (ICIS). Pediatric blood & cancer 2006, 46: 351 [PMID: 16086422]
  15. Buchanan GR, Adix L: Current challenges in the management of children with idiopathic thrombocytopenic purpura. Pediatric blood & cancer 2006, 47(5 Suppl): 681 [PMID: 16933253]
  16. Tarantino MD: The treatment of immune thrombocytopenic purpura in children. Current hematology reports 2006, 5: 89 [PMID: 16537052]
  17. Rosthøj S, Hedlund-Treutiger I, Rajantie J, Zeller B, Jonsson OG, Elinder G, Wesenberg F, Henter JI, NOPHO ITP Working Group: Duration and morbidity of newly diagnosed idiopathic thrombocytopenic purpura in children: A prospective Nordic study of an unselected cohort. The Journal of pediatrics 2003, 143: 302 [PMID: 14517509]
  18. Buchanan GR, Adix L: Grading of hemorrhage in children with idiopathic thrombocytopenic purpura. The Journal of pediatrics 2002, 141: 683 [PMID: 12410198]
  19. Bolton-Maggs PH, Dickerhoff R, Vora AJ: The nontreatment of childhood ITP (or . Seminars in thrombosis and hemostasis 2001, 27: 269 [PMID: 11446660]
  20. Dickerhoff R, von Rücker A: The clinical course of immune thrombocytopenic purpura in children who did not receive intravenous immunoglobulins or sustained prednisone treatment. J Pediatr 2000, 137: 629 [DOI: 10.1067/mpd.2000.110123]
  21. Lilleyman JS: Management of childhood idiopathic thrombocytopenic purpura. British journal of haematology 1999, 105: 871 [PMID: 10554795]
  22. Kühne T, Freedman J, Semple JW, Doyle J, Butchart S, Blanchette VS: Platelet and immune responses to oral cyclic dexamethasone therapy in childhood chronic immune thrombocytopenic purpura. The Journal of pediatrics 1997, 130: 17 [PMID: 9003846]
  23. Kühl J: Ergebnisse der Pädiatrischen Neuro-Onkologie III, Berichte von der Tagung der Arbeitsgruppe für Hirntumoren im Kindesalter der Gesellschaft für Pädiatrische Onkologie und Hämatologie und der Gesellschaft für Neuropädiatrie am 13./14. Juni 1997 in Würzburg. GPOH 1997

Literatur zu Thrombozytenfunktionsstörungen

 Suche nach Artikeln in den letzten sechs Monaten in PubMed (externes Informationsangebot)
  1. Knöfler R, Eberl W, Schulze H, Bakchoul T, Bergmann F, Gehrisch S, Geisen C, Gottstein S, Halimeh S, Harbrecht U, Kappert G, Kirchmaier C, Kehrel B, Lösche W, Krause M, Mahnel R, Meyer O, Pilgrimm AK, Pillitteri D, Rott H, Santoso S, Siegemund A, Schambeck C, Scheer M, Schmugge M, Scholl T, Strauss G, Zieger B, Zotz R, Hermann M, Streif W: [Diagnosis of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)]. Hamostaseologie 2014, 34: 201 [PMID: 24903476]
  2. Streif W, Knöfler R, Eberl W, Andres O, Bakchoul T, Bergmann F, Beutel K, Dittmer R, Gehrisch S, Gottstein S, Halimeh S, Haselböck J, Hassenpflug WA, Heine S, Holzhauer S, King S, Kirchmaier CM, Krause M, Kreuz W, Lösche W, Mahnel R, Maurer M, Nimtz-Talaska A, Olivieri M, Rott H, Schambeck ChM, Schedel A, Schilling FH, Schmugge M, Schneppenheim R, Scholz U, Scholz T, Schulze H, Siegemund A, Strauß G, Sykora KW, Wermes C, Wiegering V, Wieland I, Zieger B, Zotz RB, Paediatric Committee of the Society of Thrombosis and Haemostasis Research: [Therapy of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)]. Hamostaseologie 2014, 34: 269-75, quiz 276 [PMID: 25370176]
  3. Limperger V, Klostermeier UC, Kenet G, Holzhauer S, Alhenc Gelas M, Finckh U, Junker R, Heller C, Zieger B, Kurnik K, Knöfler R, Mesters R, Halimeh S, Nowak-Göttl U: Clinical and laboratory characteristics of children with venous thromboembolism and protein C-deficiency: an observational Israeli-German cohort study. British journal of haematology 2014, 167: 385 [PMID: 25039884]
  4. Bidlingmaier C, Olivieri M,Kurnik, K: Hautblutungen bei Kindern Ist es eine Gerinnungsstörung? Monatsschrift Kinderheilkunde 2012, 160 , 538 [DOI: 10.1007/s00112-012-2631-7]
  5. Nurden AT, Freson K, Seligsohn U: Inherited platelet disorders. Haemophilia 2012, 18 Suppl 4: 154 [PMID: 22726100]
  6. Halimeh S: Menorrhagia and bleeding disorders in adolescent females. Hamostaseologie 2012, 32: 45 [PMID: 22127528]
  7. Althaus K, Najm J, Greinacher A: MYH9 Related Platelet Disorders - Often Unknown and Misdiagnosed. Klinische Padiatrie 2011, 223, 120 [DOI: 10.1055/s-0031-1275664]
  8. Cox K, Price V, Kahr WH: Inherited platelet disorders: a clinical approach to diagnosis and management. Expert review of hematology 2011, 4: 455 [PMID: 21801136]
  9. Tauer JT, Gneuss A, Lohse JE, Jürgens T, Knöfler R: Evaluation of desmopressin effect on primary haemostasis in pediatric patients with aspirin-like defect as hereditary thrombocytopathy. Klinische Padiatrie 2011, 223: 169 [PMID: 21509710]
  10. Schädlich D, Friebel D, Schallner J, Gehrisch S, Siegert G, Kuhlisch E, Knöfler R: [Evaluation of haemostasis in children treated with valproic acid]. Hamostaseologie 2010, 30 Suppl 1:S132 [PMID: 21042677]
  11. Lohse J, Schweigel J, Naeke A, Lee-Kirsch MA, Siegert G, Bergmann S, Kuhlisch E, Suttorp M, Knöfler R: Platelet function in obese children and adolescents. Hamostaseologie 2010, 30 Suppl 1:S126 [PMID: 21042676]
  12. Knöfler R, Streif W: Strategies in Clinical and Laboratory Diagnosis of Inherited Platelet Function Disorders in Children. Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie 2010, 37: 231 [PMID: 21113245]
  13. Streif W, Knöfler R, Eberl W: Inherited disorders of platelet function in pediatric clinical practice: a diagnostic challenge. Klinische Padiatrie 2010, 222: 203 [PMID: 20514633]
  14. Rolf N, Bugert P, Gehrisch S, Siegert G, Suttorp M, Knöfler R: [Clinical and laboratory aspects of the Aspirin-like defect as hereditary thrombocytopathy]. Hamostaseologie 2009, 29: 177 [PMID: 19404514]
  15. Hanebutt FL, Rolf N, Loesel A, Kuhlisch E, Siegert G, Knoefler R: Evaluation of desmopressin effects on haemostasis in children with congenital bleeding disorders. Haemophilia 2008, 14: 524 [PMID: 18284449]
  16. Knöfler R, Olivieri M, Weickardt S, Eberl W, Streif W, THROMKID Studiengruppe der Gesellschaft für Thrombose- und Hämostaseforschung eV: [First results of the THROMKID study: a quality project for the registration of children und adolescents with hereditary platelet function defects in Germany, Austria, and Switzerland]. Hamostaseologie 2007, 27: 48 [PMID: 17279276]
  17. Zotz R B, Scharf R E: Rekombinanter Faktor VIIa bei Patienten mit Plättchenfunktionsstörungen oder Thrombozytopenien. Hämostaseologie 2007, 27; 237 [ISSN: 0720-9355]
  18. Tiede A: [Perioperative hemostasis management]. Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen 2007, 78: 69-79; quiz 80 [PMID: 17216504]
  19. Gadner H, Gaedicke G, Niemeyer CH, Ritter J (Hrsg): Pädiatrische Hämatologie und Onkologie. Springer-Verlag 2006 [URI: http://www.springer.com/ medicine/ pediatrics/ book/ 978-3-540-03702-6]
  20. Dale DC, Bolyard AA, Schwinzer BG, Pracht G, Bonilla MA, Boxer L, Freedman MH, Donadieu J, Kannourakis G, Alter BP, Cham BP, Winkelstein J, Kinsey SE, Zeidler C, Welte K: The Severe Chronic Neutropenia International Registry: 10-Year Follow-up Report. Supportive cancer therapy 2006 Jul 1; 3: 220 [PMID: 18632498]
  21. Hohlfeld Th: Hämostasestörungen durch Analgetika, Antiphlogistika und Antirheumatika. Hämostasiologie 2001, 01, 22 [URI: http://www.schattauer.de/ de/ magazine/ uebersicht/ zeitschriften-a-z/ haemostaseologie/ inhalt/ archiv/ issue/ 509/ manuscript/ 1671/ show.html]

Thrombophilie

  1. Holzhauer S, Goldenberg NA, Junker R, Heller C, Stoll M, Manner D, Mesters R, Krümpel A, Stach M, Nowak-Göttl U: Inherited thrombophilia in children with venous thromboembolism and the familial risk of thromboembolism: an observational study. Blood 2012, Epub ahead of print [PMID: 22581447]

Gerinnungsstörungen

Literatur zur Hämophilie

  1. Klamroth R, Holzhauer S, Zimmermann R, Heller C, Kurnik K, Beriate® Pharmacovigilance Group: Beriate® P in the treatment of patients with haemophilia A: results of a long-term pharmacovigilance study. Thrombosis research 2014, 134 Suppl 1:S16 [PMID: 24418255]
  2. Halimeh S, Bidlingmaier C, Heller C, Gutsche S, Holzhauer S, Kenet G, Kurnik K, Manner D, Iorio A, Nowak-Göttl U: Risk factors for high-titer inhibitor development in children with hemophilia A: results of a cohort study. BioMed research international 2013, 2013, 901975 [PMID: 24199202]
  3. Mannucci PM, Mancuso ME, Santagostino E: How we choose factor VIII to treat hemophilia. Blood 2012, 119: 4108 [PMID: 22411872]

Literatur zur Diffentialdiagnostik

  1. Bidlingmaier C, Olivieri M,Kurnik, K: Hautblutungen bei Kindern Ist es eine Gerinnungsstörung? Monatsschrift Kinderheilkunde 2012, 160 , 538 [DOI: 10.1007/s00112-012-2631-7]

Literatur zum Von Willebrand Syndrom

  1. Tiede A, Rand JH, Budde U, Ganser A, Federici AB: How I treat the acquired von Willebrand syndrome. Blood 2011, 117: 6777 [PMID: 21540459]

Hämophagozytische Lymphhistiozytose

Literatur zur Hämophagozytischen Lymphhistiozytose

  1. Janka GE: Familial and acquired hemophagocytic lymphohistiocytosis. Annual review of medicine 2012, 63: 233 [PMID: 22248322]
  2. Trottestam H, Berglöf E, Horne A, Onelöv E, Beutel K, Lehmberg K, Sieni E, Silfverberg T, Aricò M, Janka G, Henter JI: Risk factors for early death in children with haemophagocytic lymphohistiocytosis. Acta paediatrica (Oslo, Norway : 1992) 2012, 101: 313 [PMID: 22017632]
  3. Pagel J, Beutel K, Lehmberg K, Koch F, Maul-Pavicic A, Rohlfs AK, Al-Jefri A, Beier R, Bomme Ousager L, Ehlert K, Gross-Wieltsch U, Jorch N, Kremens B, Pekrun A, Sparber-Sauer M, Mejstrikova E, Wawer A, Ehl S, zur Stadt U, Janka G: Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5). Blood 2012, 119: 6016 [PMID: 22451424]
  4. Trottestam H, Horne A, Aricò M, Egeler RM, Filipovich AH, Gadner H, Imashuku S, Ladisch S, Webb D, Janka G, Henter JI, Histiocyte Society: Chemoimmunotherapy for hemophagocytic lymphohistiocytosis: long-term results of the HLH-94 treatment protocol. Blood 2011, 118: 4577 [PMID: 21900192]
  5. Jordan MB, Allen CE, Weitzman S, Filipovich AH, McClain KL: How I treat hemophagocytic lymphohistiocytosis. Blood 2011, 118: 4041 [PMID: 21828139]
  6. Janka GE: Hemophagocytic syndromes. Blood reviews 2007, 21: 245 [PMID: 17590250]

Noonan Syndrom

Literatur zum Noonan Syndrom

  1. Briggs BJ, Dickerman JD: Bleeding disorders in Noonan syndrome. Pediatric blood & cancer 2012, 58: 167 [PMID: 22012616]