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Rudnik, Thomas
38  Ergebnisse:
Personensuche X
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1

["Uhrwerk Orange"]:

Rudnik, Thomas ; Bachmann, Peter W. ; Burgess, Anthony.. , 2007
Exemplar:  Zentrale/Mediathek: pf 0244
 
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2

SARS-CoV-2 Genomic Surveillance Reveals Little Spread From ..:

Valesano, Andrew L ; Fitzsimmons, William J ; Blair, Christopher N...
Open Forum Infectious Diseases.  8 (2021)  11 - p. , 2021
Link: https://doi.org/10.1093/..
 
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3

A feasibility study of dual-task strategy training to impro..:

Wollesen, Bettina ; Rudnik, Silvan ; Gulberti, Alessandro...
Scientific Reports.  11 (2021)  1 - p. , 2021
Link: https://doi.org/10.1038/..
 
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4

Loss of ERE binding activity by estrogen receptor‐α alters ..:

Rudnik, Volha ; Sanyal, Arunik ; Syed, Farhan A....
Journal of Cellular Biochemistry.  103 (2007)  3 - p. 896-907 , 2007
Link: https://doi.org/10.1002/..
 
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5

Familial acute aortic dissection associated with a novel AC..:

Strecker, Thomas ; Wiesmueller, Felix ; Rudnik-Schöneborn, Sabine...
Virchows Archiv.  482 (2022)  2 - p. 437-443 , 2022
Link: https://doi.org/10.1007/..
 
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6

Controlled release of celecoxib inhibits inflammation, bone..:

Tellegen, A. R. ; Rudnik-Jansen, I. ; Pouran, B....
Drug Delivery.  25 (2018)  1 - p. 1438-1447 , 2018
Link: https://doi.org/10.1080/..
 
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7

Clinical and morphological variability of the E396K mutatio..:

Elbracht, Miriam ; Senderek, Jan ; Schara, Ulrike...
Clinical Neuropathology.  33 (2014)  9 - p. 335-343 , 2014
Link: https://doi.org/10.5414/..
 
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8

Pontocerebellar hypoplasia type 1: Clinical spectrum and re..:

Rudnik-Schöneborn, Sabine ; Senderek, Jan ; Jen, Joanna C....
Neurology.  80 (2013)  5 - p. 438-446 , 2013
Link: https://doi.org/10.1212/..
 
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9

Primary pulmonary hypertension, congenital heart defect, ce..:

Reutter, Heiko ; Bagci, Soyhan ; Müller, Andreas...
European Journal of Medical Genetics.  55 (2012)  1 - p. 27-31 , 2012
Link: https://doi.org/10.1016/..
 
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10

A new splice site mutation in the SMN1 gene causes discrepa..:

Eggermann, Thomas ; Eggermann, Katja ; Elbracht, Miriam..
Neuromuscular Disorders.  18 (2008)  2 - p. 146-149 , 2008
Link: https://doi.org/10.1016/..
 
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11

The 4G/5G polymorphism in the plasminogen activator inhibit..:

Muetze, Sabine ; Eggermann, Thomas ; Leeners, Brigitte...
Journal of Thrombosis and Thrombolysis.  27 (2007)  2 - p. 141-145 , 2007
Link: https://doi.org/10.1007/..
 
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12

Neither maternal nor fetal mutation (E474Q) in the α-subuni..:

Mütze, Sabine ; Ahillen, Ines ; Rudnik-Schoeneborn, Sabine...
Journal of Perinatal Medicine.  35 (2007)  1 - p. , 2007
Link: https://doi.org/10.1515/..
 
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13

Mutations of the LMNA gene can mimic autosomal dominant pro..:

Rudnik-Schöneborn, Sabine ; Botzenhart, Elke ; Eggermann, Thomas...
Neurogenetics.  8 (2006)  2 - p. 137-142 , 2006
Link: https://doi.org/10.1007/..
 
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14

Mutations in SIL1 cause Marinesco-Sjögren syndrome, a cereb..:

Senderek, Jan ; Krieger, Michael ; Stendel, Claudia...
Nature Genetics.  37 (2005)  12 - p. 1312-1314 , 2005
Link: https://doi.org/10.1038/..
 
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15

PKHD1mutations in autosomal recessive polycystic kidney dis..:

Bergmann, Carsten ; Senderek, Jan ; Küpper, Fabian...
Human Mutation.  23 (2004)  5 - p. 453-463 , 2004
Link: https://doi.org/10.1002/..
 
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