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Person

Joachim Kunz (1974-)

Arzt

Name	Joachim Kunz
Time	1974- (Date of birth and death)
Place	Heidelberg (Wirkungsort) Deutschland
Gender	männlich
Academic degree	Dr. med. (Univ. Tübingen) (2002) PD (Universität Heidelberg) (2020)
Profession	Arzt (characteristic profession)
Variant	Joachim Bernd Kunz (Vorl. Diss.) (vollständiger Name) Joachim B. Kunz J. B. Kunz J. Kunz
Related	Universitätsklinikum Heidelberg Zentrum für Kinder- und Jugendmedizin (Heidelberg) (2009-)
Further information	Arzt für Pädiatrische Hämatologie und Onkologie, Schwerpunkt: Seltene Anämien
Source	https://www.klinikum.uni-heidelberg.de/personen/dr-med-joachim-kunz-886 (Stand: 08.05.2020)
Record type	Person
GND-Identifier	124297730
Record ID	124297730
Involved in show all Treatment of adult ALL patients with third-generation CD19-directed CAR T cells: results of a pivotal trial Perspektiven in der Therapie der β-Hämoglobinopathien Perspektiven in der Therapie der β-Hämoglobinopathien Pediatric T-ALL type-1 and type-2 relapses develop along distinct pathways of clonal evolution Pyruvatkinasemangel der Erythrozyten in Deutschland : Klinische Merkmale und Lebensqualität der Patienten 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 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 Introduction of universal newborn screening for sickle cell disease in Germany - a brief narrative review Chromatin accessibility landscape of pediatric T‐lymphoblastic leukemia and human T‐cell precursors Sickle cell disease in Germany: results from a national registry Sickle cell disease in Germany: results from a national registry Sickle cell disease in Germany: Results from a national registry Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate kinase deficiency natural history study Simultaneous Computed Tomography-Guided Biopsy and Radiofrequency Ablation of Solitary Pulmonary Malignancy in High-Risk Patients Aktualisierte Handlungsempfehlung nach der Leitlinie „Anämiediagnostik im Kindesalter“ MAP3K7 is recurrently deleted in pediatric T-lymphoblastic leukemia and affects cell proliferation independently of NF-κB PDX models recapitulate the genetic and epigenetic landscape of pediatric T‐cell leukemia Simultaneous computed tomography-guided biopsy and radiofrequency ablation of solitary pulmonary malignancy in high-risk patients Pharmakologische und kinetische Analyse der Mikroautophagocytose in vitro Pharmakologische und kinetische Analyse der Mikroautophagocytose in vitro

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Katalog der Deutschen Nationalbibliothek

Joachim Kunz (1974-)

Treatment of adult ALL patients with third-generation CD19-directed CAR T cells: results of a pivotal trial

Perspektiven in der Therapie der β-Hämoglobinopathien

Perspektiven in der Therapie der β-Hämoglobinopathien

Pediatric T-ALL type-1 and type-2 relapses develop along distinct pathways of clonal evolution

Pyruvatkinasemangel der Erythrozyten in Deutschland : Klinische Merkmale und Lebensqualität der Patienten

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

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

Introduction of universal newborn screening for sickle cell disease in Germany - a brief narrative review

Chromatin accessibility landscape of pediatric T‐lymphoblastic leukemia and human T‐cell precursors

Sickle cell disease in Germany: results from a national registry

Sickle cell disease in Germany: results from a national registry

Sickle cell disease in Germany: Results from a national registry

Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate kinase deficiency natural history study

Simultaneous Computed Tomography-Guided Biopsy and Radiofrequency Ablation of Solitary Pulmonary Malignancy in High-Risk Patients

Aktualisierte Handlungsempfehlung nach der Leitlinie „Anämiediagnostik im Kindesalter“

MAP3K7 is recurrently deleted in pediatric T-lymphoblastic leukemia and affects cell proliferation independently of NF-κB

PDX models recapitulate the genetic and epigenetic landscape of pediatric T‐cell leukemia

Simultaneous computed tomography-guided biopsy and radiofrequency ablation of solitary pulmonary malignancy in high-risk patients

Pharmakologische und kinetische Analyse der Mikroautophagocytose in vitro

Pharmakologische und kinetische Analyse der Mikroautophagocytose in vitro