Suchergebnisse - "Berner, Jakob"

PubPharm (6)

1

Evans syndrome caused by a deleterious mutation affecting the adaptor protein SASH3

enthalten in: British journal of haematology | 2023

von Novak, W. | Berner, J. | Svaton, M. | +13

2

Dominant inherited β-thalassemia intermedia in a Polish family due to a novel frameshift mutation in HBB

enthalten in: Pediatric blood & cancer | 2023

von Novak, W. | Sunder-Plassmann, R. | Berner, J. | +6

3

Phosphomevalonate kinase deficiency expands the genetic spectrum of systemic autoinflammatory diseases

enthalten in: The Journal of allergy and clinical immunology | 2023

von Berner, J. | van de Wetering, C. | Jimenez Heredia, R. | +10

4

Human repair-related Schwann cells adopt functions of antigen-presenting cells in vitro

enthalten in: Glia | 2022

von Berner, J. | Weiss, T. | Sorger, H. | +9

5

Human repair-related Schwann cells adopt functions of antigen-presenting cells in vitro

enthalten in: bioRxiv.org | 2022

von Berner, J. | Weiss, T. | Sorger, H. | +8

6

Human repair‐related Schwann cells adopt functions of antigen‐presenting cells in vitro

enthalten in: Glia | 2022

von Berner, J. | Weiss, T. | Sorger, H. | +9

1
[1]