E-LIB Suche - Ergebnisse für: Pennekamp, Werner

1

Intra-individual, randomised comparison of the MRI contrast..:

Pennekamp, Werner ; Roggenland, Daniela ; Hering, Steffen...
European Radiology. 21 (2010) 5 - p. 1058-1067 , 2010

Link: https://doi.org/10.1007/..

2

Implantation of the CoreValve self-expanding valve prosthes..:

Bojara, Waldemar ; Mumme, Achim ; Gerckens, Ulrich...
Clinical Research in Cardiology. 98 (2009) 3 - p. 201-204 , 2009

Link: https://doi.org/10.1007/..

3

PATIENT-SPECIFIC SIMULATION MODEL TO RESEARCH THE IMPACT OF..:

Bongert, Markus ; Geller, Marius ; Pennekamp, Werner..
Journal of Biomechanics. 41 (2008) - p. S242 , 2008

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

4

Elastofibroma dorsi – differential diagnosis in chest wall ..:

Daigeler, Adrien ; Vogt, Peter Maria ; Busch, Kay...
World Journal of Surgical Oncology. 5 (2007) 1 - p. , 2007

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

5

Elastofibroma dorsi – differential diagnosis in chest wall ..:

Daigeler, Adrien ; Vogt, Peter ; Busch, Kay...
http://www.wjso.com/content/5/1/15. , 2007

Link: http://www.wjso.com/cont..

6

Elastofibroma dorsi – differential diagnosis in chest wall ..:

Steinau Hans-Ulrich ; Steinstraesser Lars ; Lehnhardt Marcus...
http://www.wjso.com/content/5/1/15. , 2007

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

7

CFAP45 deficiency causes situs abnormalities and asthenospe..:

Dougherty, Gerard W. ; Mizuno, Katsutoshi ; Nöthe-Menchen, Tabea...
Nature Communications. 11 (2020) 1 - p. , 2020

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

8

Recessive DNAH9 Loss-of-Function Mutations Cause Laterality..:

Loges, Niki T. ; Antony, Dinu ; Maver, Ales...
The American Journal of Human Genetics. 103 (2018) 6 - p. 995-1008 , 2018

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

9

TTC25 Deficiency Results in Defects of the Outer Dynein Arm..:

Wallmeier, Julia ; Shiratori, Hidetaka ; Dougherty, Gerard W....
The American Journal of Human Genetics. 99 (2016) 2 - p. 460-469 , 2016

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

10

Mutations in CCNO and MCIDAS lead to a mucociliary clearanc..:

Wallmeier, J ; Boon, M ; Mutairi, D...
Molecular and Cellular Pediatrics. 2 (2015) Suppl 1 - p. A15 , 2015

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

11

Gene discovery for motile cilia disorders: mutation spectru..:

Onoufriadis, A ; Hjeij, R ; Watson, CM...
Cilia. 4 (2015) S1 - p. , 2015

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

12

Ciliary function and motor protein composition of human fal..:

Raidt, Johanna ; Werner, Claudius ; Menchen, Tabea...
Human Reproduction. 30 (2015) 12 - p. 2871-2880 , 2015

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

13

Mutations in CCNO result in congenital mucociliary clearanc..:

Wallmeier, Julia ; Al-Mutairi, Dalal A ; Chen, Chun-Ting...
Nature Genetics. 46 (2014) 6 - p. 646-651 , 2014

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

14

CCDC151 Mutations Cause Primary Ciliary Dyskinesia by Disru..:

Hjeij, Rim ; Onoufriadis, Alexandros ; Watson, Christopher M....
The American Journal of Human Genetics. 95 (2014) 3 - p. 257-274 , 2014

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

15

DYX1C1 is required for axonemal dynein assembly and ciliary..:

UK10K ; Tarkar, Aarti ; Loges, Niki T...
Nature Genetics. 45 (2013) 9 - p. 995-1003 , 2013

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