Search

Your search keyword '"S. Gudowius"' showing total 25 results

Search Constraints

Start Over You searched for: Author "S. Gudowius" Remove constraint Author: "S. Gudowius"
25 results on '"S. Gudowius"'

Search Results

1. First-line antiretroviral therapy with a protease inhibitor versus non-nucleoside reverse transcriptase inhibitor and switch at higher versus low viral load in HIV-infected children: an open-label, randomised phase 2/3 trial

2. Systemischer Lupus erythematodes im Kindesalter

Catalog

Books, media, physical & digital resources

3. Kollagenosen im Kindesalter

4. Immune reconstitution inflammatory syndrome (IRIS) due to Bacille Calmette Guerin (BCG) in an HIV-positive child

5. MHC class II deficiency cured by unrelated mismatched umbilical cord blood transplantation: case report and review of 68 cases in the literature

10. [Connective tissue diseases in childhood]

11. Diagnostic difficulties in childhood bilateral thalamic astrocytomas

13. MHC class II deficiency cured by unrelated mismatched umbilical cord blood transplantation: case report and review of 68 cases in the literature.

14. Saving the red baby: successful allogeneic cord blood transplantation in Omenn syndrome.

15. An immunodeficiency disease with RAG mutations and granulomas.

16. High nerve growth factor receptor (p75NTR) expression is a favourable prognostic factor in paediatric B cell precursor-acute lymphoblastic leukaemia.

17. Survivin and its prognostic significance in pediatric acute B-cell precursor lymphoblastic leukemia.

18. A single intravenous dose of prednisolone induces phosphatidylserine externalization, loss of surface marker expression and a 24-h net increase in human peripheral blood lymphocytes ex vivo.

19. Topical tacrolimus is effective against eczema in Wiskott-Aldrich syndrome (WAS).

20. Identification of candidate target antigens for antibody-based immunotherapy in childhood B-cell precursor ALL.

22. Delayed diagnosis and complications of Fanconi anaemia at advanced age--a paradigm.

23. Nuclear factor kappaB essential modulator-deficient child with immunodeficiency yet without anhidrotic ectodermal dysplasia.

24. Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase I.

25. Diagnostic difficulties in childhood bilateral thalamic astrocytomas.