Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Publikationen

Suchbegriffe: PRIMARY IMMUNODEFICIENCY, . Treffer: 19

2020

Tesch, VK; Abolhassani, H; Shadur, B; Zobel, J; Mareika, Y; Sharapova, S; Karakoc-Aydiner, E; Rivière, JG; Garcia-Prat, M; Moes, N; Haerynck, F; Gonzales-Granado, LI; Santos Pérez, JL; Mukhina, A; Shcherbina, A; Aghamohammadi, A; Hammarström, L; Dogu, F; Haskologlu, S; İkincioğulları, AI; Köstel Bal, S; Baris, S; Kilic, SS; Karaca, NE; Kutukculer, N; Girschick, H; Kolios, A; Keles, S; Uygun, V; Stepensky, P; Worth, A; van Montfrans, JM; Peters, AMJ; Meyts, I; Adeli, M; Marzollo, A; Padem, N; Khojah, AM; Chavoshzadeh, Z; Avbelj Stefanija, M; Bakhtiar, S; Florkin, B; Meeths, M; Gamez, L; Grimbacher, B; Seppänen, MRJ; Lankester, A; Gennery, AR; Seidel, MG; Inborn Errors, Clinical, and Registry Working Parties of the European Society for Blood and Marrow Transplantation and the European Society for Immunodeficiencies Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score.
J Allergy Clin Immunol. 2020; 145(5):1452-1463 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Thaventhiran, JED; Lango Allen, H; Burren, OS; Rae, W; Greene, D; Staples, E; Zhang, Z; Farmery, JHR; Simeoni, I; Rivers, E; Maimaris, J; Penkett, CJ; Stephens, J; Deevi, SVV; Sanchis-Juan, A; Gleadall, NS; Thomas, MJ; Sargur, RB; Gordins, P; Baxendale, HE; Brown, M; Tuijnenburg, P; Worth, A; Hanson, S; Linger, RJ; Buckland, MS; Rayner-Matthews, PJ; Gilmour, KC; Samarghitean, C; Seneviratne, SL; Sansom, DM; Lynch, AG; Megy, K; Ellinghaus, E; Ellinghaus, D; Jorgensen, SF; Karlsen, TH; Stirrups, KE; Cutler, AJ; Kumararatne, DS; Chandra, A; Edgar, JDM; Herwadkar, A; Cooper, N; Grigoriadou, S; Huissoon, AP; Goddard, S; Jolles, S; Schuetz, C; Boschann, F; Primary Immunodeficiency Consortium for the NIHR Bioresource; Lyons, PA; Hurles, ME; Savic, S; Burns, SO; Kuijpers, TW; Turro, E; Ouwehand, WH; Thrasher, AJ; Smith, KGC Whole-genome sequencing of a sporadic primary immunodeficiency cohort.
Nature. 2020; 583(7814):90-95 [OPEN ACCESS]
PubMed PUBMED Central FullText FullText_MUG

 

2019

Bakhtiar, S; Fekadu, J; Seidel, MG; Gambinieri, E Allogeneic Hematopoietic Stem Cell Transplantation for Congenital Immune Dysregulatory Disorders.
Front Pediatr. 2019; 7: 461-461. [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Hauck, F; Gennery, AR; Seidel, MG Editorial: The Relationship Between Cancer Predisposition and Primary Immunodeficiency
FRONT IMMUNOL. 2019; 10: 1781 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Seidel, MG; Kindle, G; Gathmann, B; Quinti, I; Buckland, M; van Montfrans, J; Scheible, R; Rusch, S; Gasteiger, LM; Grimbacher, B; Mahlaoui, N; Ehl, S; ESID Registry Working Party and collaborators The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity.
J Allergy Clin Immunol Pract. 2019; 7(6):1763-1770
Web of Science PubMed FullText FullText_MUG

 

2018

Hauck, F; Voss, R; Urban, C; Seidel, MG Intrinsic and extrinsic causes of malignancies in patients with primary immunodeficiency disorders.
J Allergy Clin Immunol. 2018; 141(1):59-68
Web of Science PubMed FullText FullText_MUG

 

Kindler, O; Quehenberger, F; Benesch, M; Seidel, MG The Iceberg Map of germline mutations in childhood cancer: focus on primary immunodeficiencies.
Curr Opin Pediatr. 2018; 30(6):855-863
Web of Science PubMed FullText FullText_MUG

 

Schwinger, W; Urban, C; Ulreich, R; Sperl, D; Karastaneva, A; Strenger, V; Lackner, H; Boztug, K; Albert, MH; Benesch, M; Seidel, MG The Phenotype and Treatment of WIP Deficiency: Literature Synopsis and Review of a Patient With Pre-transplant Serial Donor Lymphocyte Infusions to Eliminate CMV.
Front Immunol. 2018; 9(94):2554-2554 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Tesch, VK; IJspeert, H; Raicht, A; Rueda, D; Dominguez-Pinilla, N; Allende, LM; Colas, C; Rosenbaum, T; Ilencikova, D; Baris, HN; Nathrath, MHM; Suerink, M; Januszkiewicz-Lewandowska, D; Ragab, I; Azizi, AA; Wenzel, SS; Zschocke, J; Schwinger, W; Kloor, M; Blattmann, C; Brugieres, L; van der Burg, M; Wimmer, K; Seidel, MG No Overt Clinical Immunodeficiency Despite Immune Biological Abnormalities in Patients With Constitutional Mismatch Repair Deficiency.
Front Immunol. 2018; 9: 1506-1506. [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

2016

Gámez-Díaz, L; August, D; Stepensky, P; Revel-Vilk, S; Seidel, MG; Noriko, M; Morio, T; Worth, AJ; Blessing, J; Van de Veerdonk, F; Feuchtinger, T; Kanariou, M; Schmitt-Graeff, A; Jung, S; Seneviratne, S; Burns, S; Belohradsky, BH; Rezaei, N; Bakhtiar, S; Speckmann, C; Jordan, M; Grimbacher, B The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency.
J ALLERGY CLIN IMMUN. 2016; 137(1): 223-230.
Web of Science PubMed FullText FullText_MUG

 

Ghosh, S; Seidel, MG Editorial: Current Challenges in Immune and Other Acquired Cytopenias of Childhood.
Front Pediatr. 2016; 4(3):3-3 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Schatorjé, E; van der Flier, M; Seppänen, M; Browning, M; Morsheimer, M; Henriet, S; Neves, JF; Vinh, DC; Alsina, L; Grumach, A; Soler-Palacin, P; Boyce, T; Celmeli, F; Goudouris, E; Hayman, G; Herriot, R; Förster-Waldl, E; Seidel, M; Simons, A; de Vries, E Primary immunodeficiency associated with chromosomal aberration - an ESID survey.
Orphanet J Rare Dis. 2016; 11(1):110-110 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

2014

Schatorjé, EJ; Gathmann, B; van Hout, RW; de Vries, E; PedPAD consortium The PedPAD study: boys predominate in the hypogammaglobulinaemia registry of the ESID online database.
Clin Exp Immunol. 2014; 176(3):387-393 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Seidel, MG; Duerr, C; Woutsas, S; Schwerin-Nagel, A; Sadeghi, K; Neesen, J; Uhrig, S; Santos-Valente, E; Pickl, WF; Schwinger, W; Urban, C; Boztug, K; Förster-Waldl, E A novel immunodeficiency syndrome associated with partial trisomy 19p13.
J Med Genet. 2014; 51(4):254-263 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

2012

de Vries, E; European Society for Immunodeficiencies (ESID) members Patient-centred screening for primary immunodeficiency, a multi-stage diagnostic protocol designed for non-immunologists: 2011 update.
Clin Exp Immunol. 2012; 167(1): 108-119. [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Gathmann, B; Binder, N; Ehl, S; Kindle, G; ESID Registry Working Party The European internet-based patient and research database for primary immunodeficiencies: update 2011.
Clin Exp Immunol. 2012; 167(3): 479-491. [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Sperl, D; Benesch, M; Urban, C; Lackner, H; Sovinz, P; Speicher, MR; Uhrig, S; Schwarzbraun, T; Schwinger, W; zur Stadt, U; Beutel, K; Janka, G; Scarpatetti, M; Seidel, MG Fatal EBV infection and variable clinical manifestations in an XLP-1 pedigree - rapid diagnosis of primary immunodeficiencies may save lives.
Klin Padiatr. 2012; 224(6):386-389 (- Case Report)
Web of Science PubMed FullText FullText_MUG

 

2011

Beitzke, M; Enzinger, C; Windpassinger, C; Pfeifer, D; Fazekas, F; Woellner, C; Grimbacher, B; Kroisel, PM Community acquired Staphylococcus aureus meningitis and cerebral abscesses in a patient with a Hyper-IgE and a Dubowitz-like syndrome.
J Neurol Sci. 2011; 309(1-2):12-15 (- Case Report)
Web of Science PubMed FullText FullText_MUG

 

1988

Fuchs, D; Ebell, W; Friedrich, W; Hausen, A; Reibnegger, G; Werner, ER; Wachter, H Urinary neopterin in infants with primary immunodeficiency.
Immunobiology. 1988; 177(1):1-6
Web of Science PubMed Google Scholar

 

© Med Uni Graz Impressum