Stephan Schultze-Strasser
Overview
Explore the profile of Stephan Schultze-Strasser including associated specialties, affiliations and a list of published articles.
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5
Citations
406
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0
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Recent Articles
1.
Bachelet D, Albert T, Mbogning C, Hassler S, Zhang Y, Schultze-Strasser S, et al.
PLoS One
. 2019 Jun;
14(6):e0218258.
PMID: 31194850
Replacement therapy in severe hemophilia A leads to factor VIII (FVIII) inhibitors in 30% of patients. Factor VIII gene (F8) mutation type, a family history of inhibitors, ethnicity and intensity...
2.
Konigs C, Schultze-Strasser S, Quaiser A, Bochennek K, Schwabe D, Klingebiel T, et al.
Front Pediatr
. 2018 May;
6:121.
PMID: 29780793
B lymphocytes are key players in humoral immunity, expressing diverse surface immunoglobulin receptors directed against specific antigenic epitopes. The development and profile of distinct subpopulations have gained awareness in the...
3.
Stein S, Scholz S, Schwable J, Sadat M, Modlich U, Schultze-Strasser S, et al.
Hum Gene Ther Clin Dev
. 2013 Jul;
24(2):86-98.
PMID: 23845071
Chronic granulomatous disease (CGD) is a primary immunodeficiency characterized by impaired antimicrobial activity in phagocytic cells. As a monogenic disease affecting the hematopoietic system, CGD is amenable to gene therapy....
4.
Schwable J, Schultze-Strasser S, Stein S, Grez M
Pharm Unserer Zeit
. 2011 Jun;
40(3):264-71.
PMID: 21698616
No abstract available.
5.
Stein S, Ott M, Schultze-Strasser S, Jauch A, Burwinkel B, Kinner A, et al.
Nat Med
. 2010 Jan;
16(2):198-204.
PMID: 20098431
Gene-modified autologous hematopoietic stem cells (HSC) can provide ample clinical benefits to subjects suffering from X-linked chronic granulomatous disease (X-CGD), a rare inherited immunodeficiency characterized by recurrent, often life-threatening bacterial...