Curative treatment of POMP-related autoinflammation and immune dysregulation (PRAID) by hematopoietic stem cell transplantation

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Notes: Journal of clinical immunology. - 41 (2021) , 1664–1667, ISSN: 1573-2592

Event: Veröffentlichung

(where): Freiburg

(who): Universität

(when): 2021

Creator: Meinhardt, Andrea
Ramos, Paula C.
Dohmen, R. Jürgen
Lucas, Nadja
Lee-Kirsch, Min Ae
Becker, Benjamin
Laffolie, Jan de
Cunha, Tomás
Niehues, Tim
Salzer, Ulrich
Yoshimi-Nöllke, Ayami
Erlacher, Miriam
Peters, Anke M. J.
Ehl, Stephan
Strahm, Brigitte
Speckmann, Carsten

DOI: 10.1007/s10875-021-01067-7

URN: urn:nbn:de:bsz:25-freidok-2191771

Rights: Kein Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:38 AM CEST

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Associated

Meinhardt, Andrea
Ramos, Paula C.
Dohmen, R. Jürgen
Lucas, Nadja
Lee-Kirsch, Min Ae
Becker, Benjamin
Laffolie, Jan de
Cunha, Tomás
Niehues, Tim
Salzer, Ulrich
Yoshimi-Nöllke, Ayami
Erlacher, Miriam
Peters, Anke M. J.
Ehl, Stephan
Strahm, Brigitte
Speckmann, Carsten
Universität

Time of origin

2021

Other Objects (12)

Curative Treatment of POMP-Related Autoinflammation and Immune Dysregulation (PRAID) by Hematopoietic Stem Cell Transplantation

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Cell versus cytokine – directed therapies for hemophagocytic lymphohistiocytosis (HLH) in inborn errors of immunity

Curative Treatment of POMP-Related Autoinflammation and Immune Dysregulation (PRAID) by Hematopoietic Stem Cell Transplantation

Autoimmune lymphoproliferative immunodeficiencies (ALPID) in childhood: breakdown of immune homeostasis and immune dysregulation

Immune‐mediated pathology as a consequence of impaired immune reactions: the IMPATH paradox

Immune dysregulation in patients with PTEN hamartoma tumor syndrome: analysis of FOXP3 regulatory T cells

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Germline STAT3 gain-of-function mutations in primary immunodeficiency: Impact on the cellular and clinical phenotype

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Curative Treatment of POMP-Related Autoinflammation and Immune Dysregulation (PRAID) by Hematopoietic Stem Cell Transplantation

Autoimmune lymphoproliferative immunodeficiencies (ALPID) in childhood: breakdown of immune homeostasis and immune dysregulation

Immune‐mediated pathology as a consequence of impaired immune reactions: the IMPATH paradox

Immune dysregulation in patients with PTEN hamartoma tumor syndrome: analysis of FOXP3 regulatory T cells

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Disease pathophysiology in murine models of primary hemophagocytic lymphohistiocytosis: triggers and effectors

Germline STAT3 gain-of-function mutations in primary immunodeficiency: Impact on the cellular and clinical phenotype

Efficacy of T cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosis

JAKi salvage therapy followed by curative cord blood transplantation in a XIAP-deficient infant with relapsing HLH

Cell versus cytokine – directed therapies for hemophagocytic lymphohistiocytosis (HLH) in inborn errors of immunity

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Curative treatment of POMP-related autoinflammation and immune dysregulation (PRAID) by hematopoietic stem cell transplantation

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Other Objects (12)

Curative Treatment of POMP-Related Autoinflammation and Immune Dysregulation (PRAID) by Hematopoietic Stem Cell Transplantation

Autoimmune lymphoproliferative immunodeficiencies (ALPID) in childhood: breakdown of immune homeostasis and immune dysregulation

Autoimmune lymphoproliferative immunodeficiencies (ALPID) in childhood: breakdown of immune homeostasis and immune dysregulation

Immune‐mediated pathology as a consequence of impaired immune reactions: the IMPATH paradox

Immune‐mediated pathology as a consequence of impaired immune reactions: the IMPATH paradox

Immune dysregulation in patients with PTEN hamartoma tumor syndrome: analysis of FOXP3 regulatory T cells

Prospective newborn screening for SCID in Germany: A first analysis by the pediatric immunology working group (API)

Disease pathophysiology in murine models of primary hemophagocytic lymphohistiocytosis: triggers and effectors

Germline STAT3 gain-of-function mutations in primary immunodeficiency: Impact on the cellular and clinical phenotype

Efficacy of T cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosis

JAKi salvage therapy followed by curative cord blood transplantation in a XIAP-deficient infant with relapsing HLH

Cell versus cytokine – directed therapies for hemophagocytic lymphohistiocytosis (HLH) in inborn errors of immunity

Curative Treatment of POMP-Related Autoinflammation and Immune Dysregulation (PRAID) by Hematopoietic Stem Cell Transplantation

Autoimmune lymphoproliferative immunodeficiencies (ALPID) in childhood: breakdown of immune homeostasis and immune dysregulation

Autoimmune lymphoproliferative immunodeficiencies (ALPID) in childhood: breakdown of immune homeostasis and immune dysregulation

Immune‐mediated pathology as a consequence of impaired immune reactions: the IMPATH paradox

Immune‐mediated pathology as a consequence of impaired immune reactions: the IMPATH paradox

Immune dysregulation in patients with PTEN hamartoma tumor syndrome: analysis of FOXP3 regulatory T cells

Prospective newborn screening for SCID in Germany: A first analysis by the pediatric immunology working group (API)

Disease pathophysiology in murine models of primary hemophagocytic lymphohistiocytosis: triggers and effectors

Germline STAT3 gain-of-function mutations in primary immunodeficiency: Impact on the cellular and clinical phenotype

Efficacy of T cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosis

JAKi salvage therapy followed by curative cord blood transplantation in a XIAP-deficient infant with relapsing HLH

Cell versus cytokine – directed therapies for hemophagocytic lymphohistiocytosis (HLH) in inborn errors of immunity

Curative Treatment of POMP-Related Autoinflammation and Immune Dysregulation (PRAID) by Hematopoietic Stem Cell Transplantation

Autoimmune lymphoproliferative immunodeficiencies (ALPID) in childhood: breakdown of immune homeostasis and immune dysregulation

Autoimmune lymphoproliferative immunodeficiencies (ALPID) in childhood: breakdown of immune homeostasis and immune dysregulation

Immune‐mediated pathology as a consequence of impaired immune reactions: the IMPATH paradox

Immune‐mediated pathology as a consequence of impaired immune reactions: the IMPATH paradox

Immune dysregulation in patients with PTEN hamartoma tumor syndrome: analysis of FOXP3 regulatory T cells

Prospective newborn screening for SCID in Germany: A first analysis by the pediatric immunology working group (API)

Disease pathophysiology in murine models of primary hemophagocytic lymphohistiocytosis: triggers and effectors

Germline STAT3 gain-of-function mutations in primary immunodeficiency: Impact on the cellular and clinical phenotype

Efficacy of T cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosis

JAKi salvage therapy followed by curative cord blood transplantation in a XIAP-deficient infant with relapsing HLH

Cell versus cytokine – directed therapies for hemophagocytic lymphohistiocytosis (HLH) in inborn errors of immunity

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