Kunz, Joachim Dr. med.; PDUniversität HeidelbergHeidelberg
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Publications in heiBIB 
- Mirza, Adil: Gene therapy in transfusion-dependent non-β0/β0 genotype β-thalassemia : first real-world experience of beti-cel / Adil Mirza, Mona-Lisa Ritsert, Gloria Tao, Himal Thakar, Stephan Lobitz, Sabine Heine, Leila Koscher… , 14 January 2025. - 10 S. : Diagramme
In: Blood advances, ISSN 2473-9537. 9(2025), 1 vom: Jan., Seite 29-38
DOI: 10.1182/bloodadvances.2024014104
- Kwiatkowski, Janet: Betibeglogene autotemcel gene therapy in patients with transfusion-dependent, severe genotype β-thalassaemia (HGB-212) : a non-randomised, multicentre, single-arm, open-label, single-dose, phase 3 trial / Janet L Kwiatkowski, Mark C Walters, Suradej Hongeng, Evangelia Yannaki, Andreas E Kulozik, Joachim … , 30 November-6 December 2024. - 12 S. : Illustrationen
In: The lancet, ISSN 1474-547X. 404(2024), 10468 vom: Dez., Seite 2175-2186
DOI: 10.1016/S0140-6736(24)01884-1
- Kunz, Joachim: Sickle cell disease / Joachim B. Kunz, Laura Tagliaferri, October 2024. - 13 S. : Illustrationen
In: Transfusion medicine and hemotherapy, ISSN 1660-3818. 51(2024), 5 vom: Okt., Seite 332-344
DOI: 10.1159/000540149
- Allard, Pierre Nicolas: The German sickle cell disease registry reveals a surprising risk of acute splenic sequestration and an increased transfusion requirement in patients with compound heterozygous sickle cell disease HbS/β-thalassaemia and no or low HbA expression / Pierre Allard, Laura Tagliaferri, Vivienn Weru, Holger Cario, Stephan Lobitz, Regine Grosse, Matthia… , October 2024. - 9 S. : Illustrationen
In: European journal of haematology, ISSN 1600-0609. 113(2024), 4 vom: Okt., Seite 501-509
DOI: 10.1111/ejh.14259
- Montalembert, Mariane de: Sickle cell health awareness, perspectives, and experiences (SHAPE) survey : perspectives of adolescent and adult patients, caregivers, and healthcare professionals on the burden of sickle cell disease / Mariane de Montalembert, Alan Anderson, Fernando F. Costa, Baba P. D. Inusa, Wasil Jastaniah, Joachi… , August 2024. - 11 S. : Diagramme
In: European journal of haematology, ISSN 1600-0609. 113(2024), 2 vom: Aug., Seite 172-182
DOI: 10.1111/ejh.14211
- Kunz, Joachim: Perspektiven in der Therapie der β-Hämoglobinopathien / Priv.-Doz. Dr. Joachim Kunz ; unter Mitarbeit von Prof. Dr. Holger Cario, Dr. Dani Hakimeh, Dr. Andr… . - 1. Auflage. -
Bremen ; London ; Boston: UNI-MED Verlag AG, 2023. - 112 Seiten : Illustrationen, ISBN 978-3-8374-1653-4
(UNI-MED Science)
- Schubert, Maria-Luisa: Treatment of adult ALL patients with third-generation CD19-directed CAR T cells : results of a pivotal trial / Maria-Luisa Schubert, Anita Schmitt, Angela Hückelhoven-Krauss, Brigitte Neuber, Alexander Kunz, Phi… , 22 July 2023. - 17 S. : Illustrationen
In: Journal of hematology & oncology, ISSN 1756-8722. 16(2023), Artikel-ID 79, Seite 1-17
DOI: 10.1186/s13045-023-01470-0
- Mañú Pereira, María del Mar: Sickle cell disease landscape and challenges in the EU : the ERN-EuroBloodNet perspective / María del Mar Mañú Pereira, Raffaella Colombatti, Federico Alvarez, Pablo Bartolucci, Celeste Bento,… , August 2023. - 8 S. : Illustrationen
In: The lancet, ISSN 2352-3026. 10(2023), 8 vom: Aug., Seite e687-e694
DOI: 10.1016/S2352-3026(23)00182-5
- Tesorero, Rafael: A high-throughput newborn screening approach for SCID, SMA, and SCD combining multiplex qPCR and tandem mass spectrometry / Rafael Tesorero, Joachim Janda, Friederike Hörster, Patrik Feyh, Ulrike Mütze, Jana Hauke, Kathrin S… , March 10, 2023. - 16 S.
In: PLOS ONE, ISSN 1932-6203. 18(2023), 3 vom: März, Artikel-ID e0283024, Seite 1-16
DOI: 10.1371/journal.pone.0283024
- Wildenberg, Niklas Philipp: Hb Santa Juana (β 108(G10) Asn > Ser) : a low oxygen affinity hemoglobin variant in a family of Bosnian background / N.P. Wildenberg, C. Rossi, A.E. Kulozik and J.B. Kunz, 03 Mar 2023. - 4 S.
In: Hematology, ISSN 1607-8454. 28(2023), 1 vom: März, Artikel-ID 2184120, Seite 1-4
DOI: 10.1080/16078454.2023.2184120
- Allard, Pierre Nicolas: Genetic modifiers of fetal hemoglobin affect the course of sickle cell disease in patients treated with hydroxyurea / Pierre Allard, Nareen Alhaj, Stephan Lobitz, Holger Cario, Andreas Jarisch, Regine Grosse, Lena Oeve… , July, 2022. - 12 S.
In: Haematologica, ISSN 1592-8721. 107(2022), 7, Seite 1577-1588
DOI: 10.3324/haematol.2021.278952
- Johann, Pascal-David: Cui Bono? : Identifying patient groups that may benefit from granulocyte transfusions in pediatric hematology and oncology / Pascal D. Johann, MD, Patrick Wuchter, MD, Lenka Trojanova, MD, Dominik Sturm, MD, Kevin Hai-Ning Lu… , October 2022. - 8 S.
In: Journal of pediatric hematology - oncology, ISSN 1536-3678. 44(2022), 7, Seite e968-e975
DOI: 10.1097/MPH.0000000000002349
- Brissot, Pierre: Une anémie ferriprive génétique rare : le syndrome IRIDA / P. Brissot, J. Kunz, E. Brissot, M.-B. Troadec, O. Loréal, M. Ropert, 15 January 2022. - 6 S.
In: Bulletin de l'Académie Nationale de Médecine. 206(2022), 3 vom: März, Seite 317-322
DOI: 10.1016/j.banm.2021.06.023
- Muckenthaler, Lena: Constitutional PIGA mutations cause a novel subtype of hemochromatosis in patients with neurologic dysfunction / Lena Muckenthaler, Oriana Marques, Silvia Colucci, Joachim Kunz, Piotr Fabrowski, Thomas Bast, Sandr… , 2022. - 5 S.
In: Blood, ISSN 1528-0020. 139(2022), 9, Seite 1418-1422
DOI: 10.1182/blood.2021013519
- Kunz, Joachim: Benefits of a disease management program for Sickle Cell Disease in Germany 2011-2019 : the increased use of hydroxyurea correlates with a reduced frequency of acute chest syndrome / Joachim B. Kunz, Andreas Schlotmann, Andrea Daubenbüchel, Stephan Lobitz, Andrea Jarisch, Regine Gro… , 30 September 2021. - 12 S.
In: Journal of Clinical Medicine, ISSN 2077-0383. 10(2021), 19, special issue, Artikel-ID 4543, Seite 1-12
DOI: 10.3390/jcm10194543
- Kunz, Joachim: Gene therapy of the hemoglobinopathies / Joachim B. Kunz, Andreas E. Kulozik, 11 September 2020. - 12 S. : Illustrationen
In: HemaSphere, ISSN 2572-9241. 4(2020), 5, Artikel-ID e479, Seite 1-12
DOI: 10.1097/HS9.0000000000000479
- Erarslan-Uysal, Büşra: Chromatin accessibility landscape of pediatric T-lymphoblastic leukemia and human T-cell precursors / Büşra Erarslan-Uysal, Joachim B Kunz, Tobias Rausch, Paulina Richter-Pechańska, Ianthe AEM van Belze… , 5 August 2020. - 14 S.
In: EMBO molecular medicine, ISSN 1757-4684. 12(2020,9) Artikel-Nummer e12104, 14 Seiten
DOI: 10.15252/emmm.202012104
- Kunz, Joachim: Sickle cell disease in Germany : results from a national registry / Joachim B. Kunz, Stephan Lobitz, Regine Grosse, Lena Oevermann, Dani Hakimeh, Andrea Jarisch, Holger… , 2020. - 7 S.
In: Pediatric blood & cancer, ISSN 1545-5017. 67(2020,4) Artikel-Nummer e28130, 7 Seiten
DOI: 10.1002/pbc.28130
- Kunz, Joachim: Analyse von Modellkrankheiten für das molekulare Verständnis hämatologischer Krankheiten im Kindesalter / vorgelegt von Dr. med. Joachim Kunz. -
Heidelberg, 2019. - 1 Band (verschiedene Seitenzählungen) : Illustrationen, Diagramme
- Schubert, Maria-Luisa: Treatment of patients with relapsed or refractory CD19+ lymphoid disease with T lymphocytes transduced by RV-SFG.CD19.CD28.4-1BBzeta retroviral vector : a unicentre phase I/II clinical trial protocol / Maria-Luisa Schubert, Anita Schmitt, Leopold Sellner, Brigitte Neuber, Joachim Kunz, Patrick Wuchter… , May 19 2019. - 15 S.
In: BMJ open, ISSN 2044-6055. 9(2019), 5, Artikel-ID e026644, Seite 1-15
DOI: 10.1136/bmjopen-2018-026644
- Johann, Pascal-David: Ausgeprägte Therapietoxizität bei der Behandlung einer congenitalen, akuten myeloischen Leukämie : = / Pascal Johann, Martin Thomas Dabek, Tina Heinzmann, Jens Westhoff, Andreas Kulozik, Joachim Kunz, 18. März 2019. - 3 S.
In: Klinische Pädiatrie, ISSN 1439-3824. 231(2019), 06, Seite 291-293
DOI: 10.1055/a-0859-7375
- Mouttet, Brice: Durable remissions in TCF3-HLF positive acute lymphoblastic leukemia with blinatumomab and stem cell transplantation / by Brice Mouttet, Luciana Vinti, Philip Ancliff, Nicole Bodmer, Benoît Brethon, Gunnar Cario, Christ… , 2019. - 14 S.
In: Haematologica, ISSN 1592-8721. 104(2019, 6) Artikel-Nummer e244-e247, 14 Seiten
DOI: 10.3324/haematol.2018.210104
- Szarzyńska‐Zawadzka, Bronisława: PTEN abnormalities predict poor outcome in children with T-cell acute lymphoblastic leukemia treated according to ALL IC-BFM protocols / Bronisława Szarzyńska‐Zawadzka, Joachim B. Kunz, Łukasz Sędek, Maria Kosmalska, Katarzyna Zdon, Prze… , 07 January 2019. - 4 S.
In: American journal of hematology, ISSN 1096-8652. 94(2019), 4, Seite E93-E96
DOI: 10.1002/ajh.25396
- Beers, E.J. (Ward) van: Prevalence and management of iron overload in pyruvate kinase deficiency : report from the Pyruvate kinase deficiency natural history study / Eduard J. van Beers, Stephanie van Straaten, D. Holmes Morton, Wilma Barcellini, Stefan W. Eber, Ber… . - 3 S.
In: Haematologica, ISSN 1592-8721. 104(2019), 2, S. e51-e53
DOI: 10.3324/haematol.2018.196295
- Kunz, Joachim: Aktualisierte Handlungsempfehlung nach der Leitlinie „Anämiediagnostik im Kindesalter“ / J. Kunz, A. Kulozik, 2020. - 3 S.
In: Monatsschrift Kinderheilkunde, ISSN 1433-0474. 168(2020), 7, Seite 644-646
DOI: 10.1007/s00112-018-0561-8
- Lobitz, Stephan: Newborn screening for sickle cell disease in Europe : recommendations from a Pan-European Consensus Conference / Stephan Lobitz, Paul Telfer, Elena Cela, Bichr Allaf, Michael Angastiniotis, Carolina Backman Johans… , 18 October 2018. - 13 S.
In: British journal of haematology, ISSN 1365-2141. 183(2018), 4, Seite 648-660
DOI: 10.1111/bjh.15600
- Richter-Pechańska, Paulina: PDX models recapitulate the genetic and epigenetic landscape of pediatric T-cell leukemia / Paulina Richter-Pechańska, Joachim B Kunz, Beat Bornhauser, Caroline von Knebel Doeberitz, Tobias Ra… , 2 November 2018. - 13 S.
In: EMBO molecular medicine, ISSN 1757-4684. 10(2018,12) Artikel-Nummer e9443, 13 Seiten
DOI: 10.15252/emmm.201809443
- Fuhrmann, Stephan: Expression of CD56 defines a distinct subgroup in childhood T-ALL with inferior outcome : Results of the ALL-BFM 2000 trial / Stephan Fuhrmann, Richard Schabath, Anja Möricke, Martin Zimmermann, Joachim B. Kunz, Andreas E. Kul… , 7 June 2018. - 8 S.
In: British journal of haematology, ISSN 1365-2141. 183(2018), 1, Seite 96-103
DOI: 10.1111/bjh.15503
- Santos, David M. Cordas dos: MAP3K7 is recurrently deleted in pediatric T-lymphoblastic leukemia and affects cell proliferation independently of NF-[kappa]B / David M. Cordas dos Santos; Juliane Eilers; Alfonso Sosa Vizcaino; Elena Orlova; Martin Zimmermann; … . -
London ; Berlin ; Heidelberg: BioMed Central ; Springer, 18 June 2018. - 1 Online-Ressource (12 Seiten)
DOI: 10.1186/s12885-018-4525-0
- Santos, David M. Cordas dos: MAP3K7 is recurrently deleted in pediatric T-lymphoblastic leukemia and affects cell proliferation independently of NF-[kappa]B / David M. Cordas dos Santos, Juliane Eilers, Alfonso Sosa Vizcaino, Elena Orlova, Martin Zimmermann, … , 18 June 2018
In: BMC cancer, ISSN 1471-2407. 18(2018) Artikel-Nummer 663, 12 Seiten
DOI: 10.1186/s12885-018-4525-0
- Kunz, Joachim: The epidemiology of sickle cell disease in Germany following recent large-scale immigration / Joachim B. Kunz, Holger Cario, Regine Grosse, Andrea Jarisch, Stephan Lobitz, Andreas E. Kulozik, July 2017. - 10 S.
In: Pediatric blood & cancer, ISSN 1545-5017. 64(2017), 7, Artikel-ID e26550
DOI: 10.1002/pbc.26550
- Tagliaferri, Laura: Newborn screening for severe combined immunodeficiency using a novel and simplified method to measure T-cell excision circles (TREC) / Laura Tagliaferri, Joachim B. Kunz, Margit Happich, Susanna Esposito, Thomas Bruckner, Daniel Hübsch… , 2017. - 5 S.
In: Clinical immunology, ISSN 1521-7035. 175(2017), Seite 51-55
DOI: 10.1016/j.clim.2016.11.016
- Richter-Pechańska, Paulina: Identification of a genetically defined ultra-high-risk group in relapsed pediatric T-lymphoblastic leukemia / P. Richter-Pechańska, J.B. Kunz, J. Hof, M. Zimmermann, T. Rausch, O.R. Bandapalli, E. Orlova, G. Sc… , 3 February 2017
In: Blood cancer journal, ISSN 2044-5385. 7(2017,2) Artikel-Nummer e523, 9 Seiten
DOI: 10.1038/bcj.2017.3
- Hof, Jana: NOTCH1 mutation, TP53 alteration and myeloid antigen expression predict outcome heterogeneity in children with first relapse of T-cell acute lymphoblastic leukemia / Jana Hof, Corinne Kox, Stefanie Groeneveld-Krentz, Obul R. Bandapalli, Leonid Karawajew, Katharina S… , July 2017. - 4 S.
In: Haematologica, ISSN 1592-8721. 102(2017), 7, Seite e249-e252
DOI: 10.3324/haematol.2016.157792
- Frismantas, Viktoras: Ex vivo drug response profiling detects recurrent sensitivity patterns in drug-resistant acute lymphoblastic leukemia / Viktoras Frismantas, Maria Pamela Dobay, Anna Rinaldi, Joelle Tchinda, Samuel H. Dunn, Joachim Kunz,… , 25 January 2017. - 12 S.
In: Blood, ISSN 1528-0020. 129(2017), 11, Seite e26-e37
DOI: 10.1182/blood-2016-09-738070
- Ratnaparkhe, Manasi: Genomic profiling of acute lymphoblastic leukemia in ataxia telangiectasia patients reveals tight link between ATM mutations and chromothripsis / M. Ratnaparkhe, M. Hlevnjak, T. Kolb, A. Jauch, K.K. Maass, F. Devens, A. Rode, V. Hovestadt, A. Kor… , 14 March 2017. - 9 S.
In: Leukemia, ISSN 1476-5551. 31(2017), 10, Seite 2048-2056
DOI: 10.1038/leu.2017.55
- Kunz, Joachim: Significant prevalence of sickle cell disease in Southwest Germany : results from a birth cohort study indicate the necessity for newborn screening / Joachim B. Kunz, Saida Awad, Margit Happich, Lena Muckenthaler, Martin Lindner, Gwendolyn Gramer, Jü… , 2016. - 6 S.
In: Annals of hematology, ISSN 1432-0584. 95(2016), 3, Seite 397-402
DOI: 10.1007/s00277-015-2573-y
- Kunz, Joachim: Pediatric T-cell lymphoblastic leukemia evolves into relapse by clonal selection, acquisition of mutations and promoter hypomethylation / Joachim B. Kunz, Tobias Rausch, Obul R. Bandapalli, Juliane Eilers, Paulina Pechanska, Stephanie Sch… , October 31, 2015. - 9 S.
In: Haematologica, ISSN 1592-8721. 100(2015), 11, Seite 1442-1450
DOI: 10.3324/haematol.2015.129692
- Bandapalli, Obul Reddy: The activating STAT5B N642H mutation is a common abnormality in pediatric T-cell acute lymphoblastic leukemia and confers a higher risk of relapse / Obul R. Bandapalli, Stephanie Schuessele, Joachim B. Kunz, Tobias Rausch, Adrian M. Stütz, Noa Tal, … , October 2014. - 5 S.
In: Haematologica, ISSN 1592-8721. 99(2014), 10, Seite e188-e192
DOI: 10.3324/haematol.2014.104992
- Kunz, Joachim: Handlungsempfehlung nach der Leitlinie „Anämiediagnostik im Kindesalter“ / J. Kunz, A. Kulozik, 29. August 2013. - 4 S.
In: Monatsschrift Kinderheilkunde, ISSN 1433-0474. 161(2013), 9, Seite 847-850
DOI: 10.1007/s00112-012-2861-8
- Schneider, Till M.: Simultaneous computed tomography-guided biopsy and radiofrequency ablation of solitary pulmonary malignancy in high-risk patients / T. Schneider, M. Puderbach, J. Kunz, A. Bischof, F.L. Giesel, H. Dienemann, F.J.F. Herth, P.A. Schna… . -
Basel: Karger, 21 Okt. 2019. - 1 Online-Ressource (8 Seiten)
DOI: 10.11588/heidok.00027242
- Kunz, Joachim: Differenzialdiagnose der kindlichen Anämie / J.B. Kunz, A.E. Kulozik. - 12 S.
In: Monatsschrift Kinderheilkunde, ISSN 1433-0474. 160(2012), 4, S. 395-406
DOI: 10.1007/s00112-012-2624-6
- Schneider, Till M.: Simultaneous computed tomography-guided biopsy and radiofrequency ablation of solitary pulmonary malignancy in high-risk patients / Till Schneider; Michael Puderbach; Joachim Kunz; Arpad Bischof; Frederik L. Giesel; Hendrik Dieneman… . -
[Basel]: Karger, 2012. - Online-Ressource
