Personal information

Websites & social links

https://www.uniklinik-freiburg.de/cci/forschung/carsten-speckmann.html?L=528

Keywords

primary immunodeficiencies, stem cell transplantation

Countries

Germany

Activities

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Employment (1)

University Medical Center Freiburg: Freiburg, DE

Consultant Immunology / Stem Cell Transplantation (Pediatric Hematology and Oncology)
Employment
Source: Self-asserted source
Carsten Speckmann

Works (50 of 70)

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Page 1 of 2

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

Journal of Clinical Immunology
2023-08 | Journal article
DOI: 10.1007/s10875-023-01522-7
Contributors: Maria Elena Maccari; Camille Tron; Carsten Speckmann; Julian Thalhammer; Stephan Ehl; Anke Peters; Brigitte Strahm
Source: check_circle
Crossref

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

Journal of Clinical Immunology
2023-07 | Journal article
DOI: 10.1007/s10875-023-01450-6
Contributors: Carsten Speckmann; Uta Nennstiel; Manfred Hönig; Michael H. Albert; Sujal Ghosh; Catharina Schuetz; Inken Brockow; Friederike Hörster; Tim Niehues; Stephan Ehl et al.
Source: check_circle
Crossref

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

2022-12-29 | Preprint
DOI: 10.21203/rs.3.rs-2394259/v1
Contributors: Carsten Speckmann; Uta Nennstiel; Manfred Hönig; Michael H. Albert; Sujal Ghosh; Catharina Schütz; Inken Brockow; Friederike Hörster; Tim Niehues; Stephan Ehl et al.
Source: check_circle
Crossref

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

The Journal of allergy and clinical immunology
2019-01 | Journal article
DOI: 10.1016/j.jaci.2018.12.1010
PMID: 30660643
Contributors: Ferrua F; Galimberti S; Courteille V; Slatter MA; Booth C; Moshous D; Neven B; Blanche S; Laberko A; Shcherbina A et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Epigenetic immune cell counting in human blood samples for immunodiagnostics.

Science translational medicine
2018-08 | Journal article
DOI: 10.1126/scitranslmed.aan3508
PMID: 30068569
Contributors: Baron U; Werner J; Schildknecht K; Schulze JJ; Mulu A; Liebert UG; Sack U; Speckmann C; Gossen M; Wong RJ et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

CD57 identifies T cells with functional senescence before terminal differentiation and relative telomere shortening in patients with activated PI3 kinase delta syndrome.

Immunology and cell biology
2018-06 | Journal article
DOI: 10.1111/imcb.12169
PMID: 29790605
Contributors: Cura Daball P; Ventura Ferreira MS; Ammann S; Klemann C; Lorenz MR; Warthorst U; Leahy TR; Conlon N; Roche J; Soler-Palacín P et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjects.

The Journal of allergy and clinical immunology
2018-05 | Journal article
DOI: 10.1016/j.jaci.2018.02.055
PMID: 29729943
Contributors: Schwab C; Gabrysch A; Olbrich P; Patiño V; Warnatz K; Wolff D; Hoshino A; Kobayashi M; Imai K; Takagi M et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

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

The Journal of experimental medicine
2018-04 | Journal article
DOI: 10.1084/jem.20170534
PMID: 29636373
PMC: PMC5940257
Contributors: Keller B; Shoukier M; Schulz K; Bhatt A; Heine I; Strohmeier V; Speckmann C; Engels N; Warnatz K; Wienands J
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

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

The Journal of allergy and clinical immunology
2018-03 | Journal article
DOI: 10.1016/j.jaci.2018.02.031
PMID: 29522846
PMC: PMC6034010
Contributors: Tesi B; Rascon J; Chiang SCC; Burnyte B; Löfstedt A; Fasth A; Heizmann M; Juozapaite S; Kiudeliene R; Kvedaraite E et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

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

The Journal of allergy and clinical immunology
2018-03 | Journal article
DOI: 10.1016/j.jaci.2018.02.007
PMID: 29477728
PMC: PMC6058308
Contributors: Lawless D; Geier CB; Farmer JR; Lango Allen H; Thwaites D; Atschekzei F; Brown M; Buchbinder D; Burns SO; Butte MJ et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea.

Inflammatory bowel diseases
2017-12 | Journal article
DOI: 10.1097/mib.0000000000001235
PMID: 28930861
Contributors: Petersen BS; August D; Abt R; Alddafari M; Atarod L; Baris S; Bhavsar H; Brinkert F; Buchta M; Bulashevska A et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

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

Haematologica
2017-12 | Journal article
DOI: 10.3324/haematol.2017.176974
PMID: 29242293
PMC: PMC5830379
Contributors: Nagy M; Mastenbroek TG; Mattheij NJA; de Witt S; Clemetson KJ; Kirschner J; Schulz AS; Vraetz T; Speckmann C; Braun A et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

ORAI1 mutations abolishing store-operated Ca2+ entry cause anhidrotic ectodermal dysplasia with immunodeficiency.

The Journal of allergy and clinical immunology
2017-11 | Journal article
DOI: 10.1016/j.jaci.2017.10.031
PMID: 29155098
Contributors: Lian J; Cuk M; Kahlfuss S; Kozhaya L; Vaeth M; Rieux-Laucat F; Picard C; Benson MJ; Jakovcevic A; Bilic K et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Corrigendum: Clinical and Molecular Heterogeneity of RTEL1 Deficiency.

Frontiers in Immunology
2017-10 | Journal article
DOI: 10.3389/fimmu.2017.01250
PMID: 28989339
PMC: PMC5630696
Contributors: Speckmann C; Sahoo SS; Rizzi M; Hirabayashi S; Karow A; Serwas NK; Hoemberg M; Damatova N; Schindler D; Vannier JB et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis.

Journal of clinical immunology
2017-09 | Journal article
DOI: 10.1007/s10875-017-0443-1
PMID: 28936583
Contributors: Ammann S; Lehmberg K; Zur Stadt U; Klemann C; Bode SFN; Speckmann C; Janka G; Wustrau K; Rakhmanov M; Fuchs I et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

The BEACH protein LRBA is required for hair bundle maintenance in cochlear hair cells and for hearing.

EMBO reports
2017-09 | Journal article
DOI: 10.15252/embr.201643689
PMID: 28893864
PMC: PMC5666617
Contributors: Vogl C; Butola T; Haag N; Hausrat TJ; Leitner MG; Moutschen M; Lefèbvre PP; Speckmann C; Garrett L; Becker L et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Hemophagocytic lymphohistiocytosis as presenting manifestation of profound combined immunodeficiency due to an ORAI1 mutation.

The Journal of allergy and clinical immunology
2017-06 | Journal article
DOI: 10.1016/j.jaci.2017.05.039
PMID: 28633876
PMC: PMC5723226
Contributors: Klemann C; Ammann S; Heizmann M; Fuchs S; Bode SF; Heeg M; Fuchs H; Lehmberg K; Zur Stadt U; Roll C et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Clinical and Molecular Heterogeneity of RTEL1 Deficiency.

Frontiers in Immunology
2017-05 | Journal article
DOI: 10.3389/fimmu.2017.00449
PMID: 28507545
PMC: PMC5410638
Contributors: Speckmann C; Sahoo SS; Rizzi M; Hirabayashi S; Karow A; Serwas NK; Hoemberg M; Damatova N; Schindler D; Vannier JB et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

IgG4-related disease in autoimmune lymphoproliferative syndrome.

Clinical immunology (Orlando, Fla.)
2017-05 | Journal article
DOI: 10.1016/j.clim.2017.05.003
PMID: 28478106
Contributors: van de Ven AAJM; Seidl M; Drendel V; Schmitt-Graeff A; Voll RE; Rensing-Ehl A; Speckmann C; Ehl S; Warnatz K; Kollert F
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Symptomatic Cytomegalovirus Infections in the First Year of Life: When Is Antiviral Therapy Conceived to Be Justified?

The Pediatric infectious disease journal
2017-02 | Journal article
DOI: 10.1097/inf.0000000000001407
PMID: 28079836
Contributors: Schuster K; Goelz R; Speckmann C; Henneke P
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Human RAD52 - a novel player in DNA repair in cancer and immunodeficiency.

Haematologica
2016-12 | Journal article
DOI: 10.3324/haematol.2016.155838
PMID: 27979922
PMC: PMC5286958
Contributors: Ghosh S; Hönscheid A; Dückers G; Ginzel S; Gohlke H; Gombert M; Kempkes B; Klapper W; Kuhlen M; Laws HJ et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Newborn screening for severe combined immunodeficiency using a novel and simplified method to measure T-cell excision circles (TREC).

Clinical immunology (Orlando, Fla.)
2016-12 | Journal article
DOI: 10.1016/j.clim.2016.11.016
PMID: 27916705
Contributors: Tagliaferri L; Kunz JB; Happich M; Esposito S; Bruckner T; Hübschmann D; Okun JG; Hoffmann GF; Schulz A; Kappe J et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

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

Haematologica
2016-10 | Journal article
DOI: 10.3324/haematol.2016.153411
PMID: 27789675
PMC: PMC5286954
Contributors: Klemann C; Esquivel M; Magerus-Chatinet A; Lorenz MR; Fuchs I; Neveux N; Castelle M; Rohr J; da Cunha CB; Ebinger M et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis.

The Journal of allergy and clinical immunology
2016-09 | Journal article
DOI: 10.1016/j.jaci.2016.07.040
PMID: 27658761
PMC: PMC6311415
Contributors: Speckmann C; Doerken S; Aiuti A; Albert MH; Al-Herz W; Allende LM; Scarselli A; Avcin T; Perez-Becker R; Cancrini C et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation.

The Journal of allergy and clinical immunology
2016-09 | Journal article
DOI: 10.1016/j.jaci.2016.07.039
PMID: 27697500
PMC: PMC5374029
Contributors: de la Morena MT; Leonard D; Torgerson TR; Cabral-Marques O; Slatter M; Aghamohammadi A; Chandra S; Murguia-Favela L; Bonilla FA; Kanariou M et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

XIAP deficiency and MEFV variants resulting in an autoinflammatory lymphoproliferative syndrome.

BMJ case reports
2016-09 | Journal article
DOI: 10.1136/bcr-2016-216922
PMID: 27681353
PMC: PMC5051366
Contributors: Christiansen M; Ammann S; Speckmann C; Mogensen TH
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

X-linked Inhibitor of Apoptosis Complicated by Granulomatous Lymphocytic Interstitial Lung Disease (GLILD) and Granulomatous Hepatitis.

Journal of clinical immunology
2016-08 | Journal article
DOI: 10.1007/s10875-016-0320-3
PMID: 27492372
Contributors: Steele CL; Doré M; Ammann S; Loughrey M; Montero A; Burns SO; Morris EC; Gaspar B; Gilmour K; Bibi S et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

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

The Journal of allergy and clinical immunology
2016-07 | Journal article
DOI: 10.1016/j.jaci.2016.06.021
PMID: 27555459
PMC: PMC5292996
Contributors: Coulter TI; Chandra A; Bacon CM; Babar J; Curtis J; Screaton N; Goodlad JR; Farmer G; Steele CL; Leahy TR et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Activated PI3Kδ syndrome type 2: Two patients, a novel mutation, and review of the literature.

Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
2016-05 | Journal article
DOI: 10.1111/pai.12585
PMID: 27116393
Contributors: Olbrich P; Lorenz M; Cura Daball P; Lucena JM; Rensing-Ehl A; Sanchez B; Führer M; Camacho-Lovillo M; Melon M; Schwarz K et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Hyperactive mTOR pathway promotes lymphoproliferation and abnormal differentiation in autoimmune lymphoproliferative syndrome.

Blood
2016-04 | Journal article
DOI: 10.1182/blood-2015-11-685024
PMID: 27099149
Contributors: Völkl S; Rensing-Ehl A; Allgäuer A; Schreiner E; Lorenz MR; Rohr J; Klemann C; Fuchs I; Schuster V; von Bueren AO et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Disturbed B-lymphocyte selection in autoimmune lymphoproliferative syndrome.

Blood
2016-02 | Journal article
DOI: 10.1182/blood-2015-04-642488
PMID: 26907631
Contributors: Janda A; Schwarz K; van der Burg M; Vach W; Ijspeert H; Lorenz MR; Elgizouli M; Pieper K; Fisch P; Hagel J et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency.

The Journal of allergy and clinical immunology
2016-01 | Journal article
DOI: 10.1016/j.jaci.2015.09.025
PMID: 26768763
Contributors: Gámez-Díaz L; August D; Stepensky P; Revel-Vilk S; Seidel MG; Noriko M; Morio T; Worth AJJ; Blessing J; Van de Veerdonk F et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Transplantation from a symptomatic carrier sister restores host defenses but does not prevent colitis in NEMO deficiency.

Clinical immunology (Orlando, Fla.)
2016-01 | Journal article
DOI: 10.1016/j.clim.2016.01.010
PMID: 26812624
PMC: PMC6101191
Contributors: Klemann C; Pannicke U; Morris-Rosendahl DJ; Vlantis K; Rizzi M; Uhlig H; Vraetz T; Speckmann C; Strahm B; Pasparakis M et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Preserved effector functions of human ORAI1- and STIM1-deficient neutrophils.

The Journal of allergy and clinical immunology
2015-12 | Journal article
DOI: 10.1016/j.jaci.2015.09.047
PMID: 26670474
PMC: PMC4860117
Contributors: Elling R; Keller B; Weidinger C; Häffner M; Deshmukh SD; Zee I; Speckmann C; Ehl S; Schwarz K; Feske S et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Activating PI3Kδ mutations in a cohort of 669 patients with primary immunodeficiency.

Clinical and experimental immunology
2015-11 | Journal article
DOI: 10.1111/cei.12706
PMID: 26437962
Contributors: Elgizouli M; Lowe DM; Speckmann C; Schubert D; Hülsdünker J; Eskandarian Z; Dudek A; Schmitt-Graeff A; Wanders J; Jørgensen SF et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Gray platelet syndrome can mimic autoimmune lymphoproliferative syndrome.

Blood
2015-10 | Journal article
DOI: 10.1182/blood-2015-06-654145
PMID: 26472737
PMC: PMC4683566
Contributors: Rensing-Ehl A; Pannicke U; Zimmermann SY; Lorenz MR; Neven B; Fuchs I; Salzer U; Speckmann C; Strauss A; Maaβ E et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Omenn syndrome associated with a functional reversion due to a somatic second-site mutation in CARD11 deficiency.

Blood
2015-08 | Journal article
DOI: 10.1182/blood-2015-03-631374
PMID: 26289640
PMC: PMC4654427
Contributors: Fuchs S; Rensing-Ehl A; Pannicke U; Lorenz MR; Fisch P; Jeelall Y; Rohr J; Speckmann C; Vraetz T; Farmand S et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Diagnostic and therapeutic challenges in a child with complete interferon-γ receptor 1 deficiency.

Pediatric blood & cancer
2015-07 | Journal article
DOI: 10.1002/pbc.25625
PMID: 26173802
PMC: PMC4651008
Contributors: Olbrich P; Martínez-Saavedra MT; Perez-Hurtado JM; Sanchez C; Sanchez B; Deswarte C; Obando I; Casanova JL; Speckmann C; Bustamante J et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Disturbed B-lymphocytes selection in autoimmune lymphoproliferative syndrome.

Molecular and cellular pediatrics
2015-07 | Journal article
DOI: 10.1186/2194-7791-2-S1-A23
PMC: PMC4715105
Contributors: Janda A; Schwarz K; van der Burg M; Vach W; Ijspeert H; Lorenz MR; Elgizouli M; Pieper K; Fisch P; Hagel J et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling.

Clinical immunology (Orlando, Fla.)
2015-07 | Journal article
DOI: 10.1016/j.clim.2015.07.002
PMID: 26187144
Contributors: Hauck F; Blumenthal B; Fuchs S; Lenoir C; Martin E; Speckmann C; Vraetz T; Mannhardt-Laakmann W; Lambert N; Gil M et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Symptomatic males and female carriers in a large Caucasian kindred with XIAP deficiency.

Journal of clinical immunology
2015-05 | Journal article
DOI: 10.1007/s10875-015-0166-0
PMID: 25943627
Contributors: Dziadzio M; Ammann S; Canning C; Boyle F; Hassan A; Cale C; Elawad M; Fiil BK; Gyrd-Hansen M; Salzer U et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis.

Haematologica
2015-05 | Journal article
DOI: 10.3324/haematol.2014.121608
PMID: 26022711
PMC: PMC4486233
Contributors: Bode SF; Ammann S; Al-Herz W; Bataneant M; Dvorak CC; Gehring S; Gennery A; Gilmour KC; Gonzalez-Granado LI; Groß-Wieltsch U et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Pathogenic fungi regulate immunity by inducing neutrophilic myeloid-derived suppressor cells.

Cell host & microbe
2015-03 | Journal article
DOI: 10.1016/j.chom.2015.02.007
PMID: 25771792
PMC: PMC4400268
Contributors: Rieber N; Singh A; Öz H; Carevic M; Bouzani M; Amich J; Ost M; Ye Z; Ballbach M; Schäfer I et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Reversible pancytopenia and immunodeficiency in a patient with hereditary folate malabsorption.

Pediatric blood & cancer
2014-12 | Journal article
DOI: 10.1002/pbc.25364
PMID: 25504888
Contributors: Erlacher M; Grünert SC; Cseh A; Steinfeld R; Salzer U; Lausch E; Nosswitz U; Dückers G; Niehues T; Ehl S et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations.

Nature medicine
2014-10 | Journal article
DOI: 10.1038/nm.3746
PMID: 25329329
PMC: PMC4668597
Contributors: Schubert D; Bode C; Kenefeck R; Hou TZ; Wing JB; Kennedy A; Bulashevska A; Petersen BS; Schäffer AA; Grüning BA et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Patients with T⁺/low NK⁺ IL-2 receptor γ chain deficiency have differentially-impaired cytokine signaling resulting in severe combined immunodeficiency.

European journal of immunology
2014-08 | Journal article
DOI: 10.1002/eji.201444689
PMID: 25042067
Contributors: Fuchs S; Rensing-Ehl A; Erlacher M; Vraetz T; Hartjes L; Janda A; Rizzi M; Lorenz MR; Gilmour K; de Saint-Basile G et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

A new functional assay for the diagnosis of X-linked inhibitor of apoptosis (XIAP) deficiency.

Clinical and experimental immunology
2014-06 | Journal article
DOI: 10.1111/cei.12306
PMID: 24611904
Contributors: Ammann S; Elling R; Gyrd-Hansen M; Dückers G; Bredius R; Burns SO; Edgar JD; Worth A; Brandau H; Warnatz K et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Abnormally differentiated CD4+ or CD8+ T cells with phenotypic and genetic features of double negative T cells in human Fas deficiency.

Blood
2014-06 | Journal article
DOI: 10.1182/blood-2014-03-564286
PMID: 24894771
Contributors: Rensing-Ehl A; Völkl S; Speckmann C; Lorenz MR; Ritter J; Janda A; Abinun M; Pircher H; Bengsch B; Thimme R et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia.

American journal of human genetics
2014-06 | Journal article
DOI: 10.1016/j.ajhg.2014.05.007
PMID: 24931394
PMC: PMC4085583
Contributors: Stray-Pedersen A; Backe PH; Sorte HS; Mørkrid L; Chokshi NY; Erichsen HC; Gambin T; Elgstøen KB; Bjørås M; Wlodarski MW et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central

Diagnosis of immunodeficiency caused by a purine nucleoside phosphorylase defect by using tandem mass spectrometry on dried blood spots.

The Journal of allergy and clinical immunology
2014-04 | Journal article
DOI: 10.1016/j.jaci.2014.01.040
PMID: 24767876
Contributors: la Marca G; Canessa C; Giocaliere E; Romano F; Malvagia S; Funghini S; Moriondo M; Valleriani C; Lippi F; Ombrone D et al.
Source: Self-asserted source
Carsten Speckmann via Europe PubMed Central
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Peer review (6 reviews for 2 publications/grants)

Review activity for Bone marrow transplantation (1)
Review activity for Journal of clinical immunology. (5)
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