E-LIB Suche - Ergebnisse für: Widmeier, Eugen

1

OXGR1 is a candidate disease gene for human calcium oxalate..:

Majmundar, Amar J. ; Widmeier, Eugen ; Heneghan, John F....
Genetics in Medicine. 25 (2023) 3 - p. 100351 , 2023

Link: https://doi.org/10.1016/..

2

Extracorporeal membrane oxygenation during the first three ..:

Widmeier, Eugen ; Wengenmayer, Tobias ; Maier, Sven...
Artificial Organs. 46 (2022) 9 - p. 1876-1885 , 2022

Link: https://doi.org/10.1111/..

3

Extracorporeal membrane oxygenation during the coronavirus ..:

Widmeier, Eugen ; Wengenmayer, Tobias ; Maier, Sven...
Artificial Organs. 46 (2022) 11 - p. 2329-2333 , 2022

Link: https://doi.org/10.1111/..

4

Incidence and predictors of delirium on the intensive care ..:

Jäckel, Markus ; Aicher, Nico ; Rilinger, Jonathan...
Scientific Reports. 11 (2021) 1 - p. , 2021

Link: https://doi.org/10.1038/..

5

RecessiveNOS1APvariants impair actin remodeling and cause g..:

Majmundar, Amar J. ; Buerger, Florian ; Forbes, Thomas A....
Science Advances. 7 (2021) 1 - p. , 2021

Link: https://doi.org/10.1126/..

6

Mobile ECMO retrieval of patients during the COVID‐19 pande..:

Widmeier, Eugen ; Duerschmied, Daniel ; Benk, Christoph...
Artificial Organs. 45 (2021) 10 - p. 1168-1172 , 2021

Link: https://doi.org/10.1111/..

7

Generation of Monogenic Candidate Genes for Human Nephrotic..:

Klämbt, Verena ; Mao, Youying ; Schneider, Ronen...
Kidney International Reports. 6 (2021) 2 - p. 460-471 , 2021

Link: https://doi.org/10.1016/..

8

Loss ofAnks6leads to YAP deficiency and liver abnormalities:

Airik, Merlin ; Schüler, Markus ; McCourt, Blake...
Human Molecular Genetics. 29 (2020) 18 - p. 3064-3080 , 2020

Link: https://doi.org/10.1093/..

9

Complete remission of Cdx-2 positive primary testicular car..:

Widmeier, Eugen ; Füllgraf, Hannah ; Waller, Cornelius F.
BMC Urology. 20 (2020) 1 - p. , 2020

Link: https://doi.org/10.1186/..

10

Subcutaneous Enoxaparin Safely Facilitates Bedside Sustaine..:

Neumann-Haefelin, Elke ; Widmeier, Eugen ; Bansbach, Joachim...
Critical Care Explorations. 2 (2020) 6 - p. e0155 , 2020

Link: https://doi.org/10.1097/..

11

DLG5 variants are associated with multiple congenital anoma..:

Marquez, Jonathan ; Mann, Nina ; Arana, Kathya...
Journal of Medical Genetics. 58 (2020) 7 - p. 453-464 , 2020

Link: https://doi.org/10.1136/..

12

Mutations in six nephrosis genes delineate a pathogenic pat..:

Ashraf, Shazia ; Kudo, Hiroki ; Rao, Jia...
Nature Communications. 9 (2018) 1 - p. , 2018

Link: https://doi.org/10.1038/..

13

Genetic variants in the LAMA5 gene in pediatric nephrotic s..:

Braun, Daniela A ; Warejko, Jillian K ; Ashraf, Shazia...
Nephrology Dialysis Transplantation. 34 (2018) 3 - p. 485-493 , 2018

Link: https://doi.org/10.1093/..

14

Panel sequencing distinguishes monogenic forms of nephritis..:

Schapiro, David ; Daga, Ankana ; Lawson, Jennifer A...
Nephrology Dialysis Transplantation. 34 (2018) 3 - p. 474-485 , 2018

Link: https://doi.org/10.1093/..

15

Mutations in WDR4 as a new cause of Galloway–Mowat syndrome:

Braun, Daniela A. ; Shril, Shirlee ; Sinha, Aditi...
American Journal of Medical Genetics Part A. 176 (2018) 11 - p. 2460-2465 , 2018

Link: https://doi.org/10.1002/..