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Person

Carsten Speckmann (1977-)

Arzt

Name	Carsten Speckmann
Time	1977- (Date of birth and death)
Place	Krefeld (Geburtsort)
Academic degree	Dr. med. (Univ. Freiburg (Breisgau)) (2004)
Profession	Arzt (characteristic profession)
Further information	Habil. Fach Kinderheilkunde (Pädiatrische Immunologie), Universität Freiburg (Breisgau) 2014
Record type	Person
GND-Identifier	129532118
Record ID	129532118
Involved in show all Successful long-term enzyme replacement therapy in a patient with delayed-onset ADA deficiency Impact of newborn screening for SCID on the management of congenital athymia The different faces of GATA2 deficiency: implications for therapy and surveillance Variable syndromic immunodeficiency in patients with Biallelic PRIM1 mutations JAKi Salvage Therapy Followed by Curative Cord Blood Transplantation in a XIAP-Deficient Infant with Relapsing HLH Prospective Newborn Screening for SCID in Germany: A First Analysis by the Pediatric Immunology Working Group (API) Corrigendum: Do common infections trigger disease-onset or -severity in CTLA-4 insufficiency? Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency JAKi salvage therapy followed by curative cord blood transplantation in a XIAP-deficient infant with relapsing HLH Newborn screening for severe combined immunodeficiencies (SCID) in Germany = Neugeborenenscreening auf schwere kombinierte Immundefekte (SCID) in Deutschland Prospective newborn screening for SCID in Germany: A first analysis by the pediatric immunology working group (API) Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50 Do common infections trigger disease-onset or -severity in CTLA-4 insufficiency? Hematopoietic cell transplantation in severe combined immunodeficiency: the SCETIDE 2006-2014 European cohort International retrospective study of allogeneic hematopoietic cell transplantation for activated PI3K-delta syndrome Curative Treatment of POMP-Related Autoinflammation and Immune Dysregulation (PRAID) by Hematopoietic Stem Cell Transplantation Ledipasvir/Sofosbuvir Eradicates Hepatitis C in an Immunodeficient STAT3-GOF Patient A distinct CD38+CD45RA+ population of CD4+, CD8+, and double-negative T cells is controlled by FAS Activation-induced deaminase is critical for the establishment of DNA methylation patterns prior to the germinal center reaction Agammaglobulinemia with normal B-cell numbers in a patient lacking Bob1 Curative treatment of POMP-related autoinflammation and immune dysregulation (PRAID) by hematopoietic stem cell transplantation Daratumumab therapy for post-HSCT immune-mediated cytopenia: experiences from two pediatric cases and review of literature Ledipasvir/Sofosbuvir eradicates hepatitis C in an immunodeficient STAT3-GOF patient Outcome of chronic granulomatous disease ‐ conventional treatment vs stem cell transplantation Pulmonary granulomatosis of genetic origin Long-term robustness of a T-cell system emerging from somatic rescue of a genetic block in T-cell development Modeling MyD88 deficiency in vitro provides new insights in Its function Modeling MyD88 deficiency In vitro provides new insights in its function Ruxolitinib controls lymphoproliferation and Diabetes in a STAT3-GOF patient Tuberculosis-associated HLH in an 8-month-old infant: a case report and review Ulceration in prolidase deficiency: successful treatment with anticoagulants Hematopoietic stem cell transplantation for CD40 ligand deficiency: results from an EBMT/ESID-IEWP-SCETIDE-PIDTC study High levels of IL-18 and IFN-γ in chronically inflamed tissue in chronic granulomatous disease Secondary C1q deficiency in activated PI3Kδ syndrome type 2 The German National Registry of Primary Immunodeficiencies (2012-2017) The German National Registry of Primary Immunodeficiencies (2012-2017) The German national registry of primary immunodeficiencies (2012–2017) A RAB27A 5′ untranslated region structural variant associated with late-onset hemophagocytic lymphohistiocytosis and normal pigmentation Germline deletion of CIN85 in humans with X chromosome – linked antibody deficiency Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency Variable impairment of platelet functions in patients with severe, genetically linked immune deficiencies Clinical and molecular heterogeneity of RTEL1 deficiency Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: a large patient cohort study Corrigendum: Clinical and molecular heterogeneity of RTEL1 deficiency Evolution of disease activity and biomarkers on and off rapamycin in 28 patients with autoimmune lymphoproliferative syndrome Immundefizienz und Autoimmunität : ein klinisch relevantes Paradox In-vivo-Detektion und Quantifikation retroviral markierter humaner hämatopoetischer Stammzellklone in der Gentherapie In-vivo-Detektion und Quantifikation retroviral markierter humaner hämatopoetischer Stammzellklone in der Gentherapie

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Katalog der Deutschen Nationalbibliothek

Carsten Speckmann (1977-)

Successful long-term enzyme replacement therapy in a patient with delayed-onset ADA deficiency

Impact of newborn screening for SCID on the management of congenital athymia

The different faces of GATA2 deficiency: implications for therapy and surveillance

Variable syndromic immunodeficiency in patients with Biallelic PRIM1 mutations

JAKi Salvage Therapy Followed by Curative Cord Blood Transplantation in a XIAP-Deficient Infant with Relapsing HLH

Prospective Newborn Screening for SCID in Germany: A First Analysis by the Pediatric Immunology Working Group (API)

Corrigendum: Do common infections trigger disease-onset or -severity in CTLA-4 insufficiency?

Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency

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

Newborn screening for severe combined immunodeficiencies (SCID) in Germany = Neugeborenenscreening auf schwere kombinierte Immundefekte (SCID) in Deutschland

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

Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50

Do common infections trigger disease-onset or -severity in CTLA-4 insufficiency?

Hematopoietic cell transplantation in severe combined immunodeficiency: the SCETIDE 2006-2014 European cohort

International retrospective study of allogeneic hematopoietic cell transplantation for activated PI3K-delta syndrome

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

Ledipasvir/Sofosbuvir Eradicates Hepatitis C in an Immunodeficient STAT3-GOF Patient

A distinct CD38+CD45RA+ population of CD4+, CD8+, and double-negative T cells is controlled by FAS

Activation-induced deaminase is critical for the establishment of DNA methylation patterns prior to the germinal center reaction

Agammaglobulinemia with normal B-cell numbers in a patient lacking Bob1

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

Daratumumab therapy for post-HSCT immune-mediated cytopenia: experiences from two pediatric cases and review of literature

Ledipasvir/Sofosbuvir eradicates hepatitis C in an immunodeficient STAT3-GOF patient

Outcome of chronic granulomatous disease ‐ conventional treatment vs stem cell transplantation

Pulmonary granulomatosis of genetic origin

Long-term robustness of a T-cell system emerging from somatic rescue of a genetic block in T-cell development

Modeling MyD88 deficiency in vitro provides new insights in Its function

Modeling MyD88 deficiency In vitro provides new insights in its function

Ruxolitinib controls lymphoproliferation and Diabetes in a STAT3-GOF patient

Tuberculosis-associated HLH in an 8-month-old infant: a case report and review

Ulceration in prolidase deficiency: successful treatment with anticoagulants

Hematopoietic stem cell transplantation for CD40 ligand deficiency: results from an EBMT/ESID-IEWP-SCETIDE-PIDTC study

High levels of IL-18 and IFN-γ in chronically inflamed tissue in chronic granulomatous disease

Secondary C1q deficiency in activated PI3Kδ syndrome type 2

The German National Registry of Primary Immunodeficiencies (2012-2017)

The German National Registry of Primary Immunodeficiencies (2012-2017)

The German national registry of primary immunodeficiencies (2012–2017)

A RAB27A 5′ untranslated region structural variant associated with late-onset hemophagocytic lymphohistiocytosis and normal pigmentation

Germline deletion of CIN85 in humans with X chromosome – linked antibody deficiency

Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study

Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency

Variable impairment of platelet functions in patients with severe, genetically linked immune deficiencies

Clinical and molecular heterogeneity of RTEL1 deficiency

Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: a large patient cohort study

Corrigendum: Clinical and molecular heterogeneity of RTEL1 deficiency

Evolution of disease activity and biomarkers on and off rapamycin in 28 patients with autoimmune lymphoproliferative syndrome

Immundefizienz und Autoimmunität : ein klinisch relevantes Paradox

In-vivo-Detektion und Quantifikation retroviral markierter humaner hämatopoetischer Stammzellklone in der Gentherapie

In-vivo-Detektion und Quantifikation retroviral markierter humaner hämatopoetischer Stammzellklone in der Gentherapie